The authors would like to acknowledge Dr. Michael Easterling (Social and Scientific Systems, Inc., Durham, NC) for his assistance with the validation of this method and Dr. Tiago Ferreira (McGill University, Montreal, Quebec, Canada) for his continual assistance with the Sholl application.

All animal use and procedures for this study were approved by the NIEHS Laboratory Animal Care and Use Committee and conducted in an Association for Assessment and Accreditation of Laboratory Animal Care-accredited facility.
1. Excise Mammary Glands
<ol>
	<li>Pre-label all slides using a xylene-proof method (pencil works best). Cover them with mounting solution at the end to preserve the label.</li>
	<li>Euthanize the animal by an Institutional Animal Care and Use Committee-approved method.</li>
	<li>After euthanasia, place the animal on its back on a dissecting board (Figure 1). Stretch and pin down all four limbs, with the rear limbs forming an inverted V (holding pins or small-gauge needles work well).</li>
	<li>Spray the abdomen liberally with 70% ethanol to keep hair out of the mammary sample.</li>
	<li>Using forceps, pull up the abdominal skin at the midline and make a small incision with dissecting scissors, being careful not to puncture the peritoneum.
	<ol>
		<li>Beginning at the incision, cut the skin up to the neck region and then distally to the front limb. Cut down to the inguinal region and then distally to the first joint of the rear limb on the same side; this incision usually separates mammary glands 5 and 6. Avoid cutting the peritoneum.</li>
		<li>Pull back the skin with the attached mammary fat pad using forceps, gently separating it from the peritoneum using the blunt end of dissecting scissors. Separate as far dorsally as possible to fully expose the 4th and 5th inguinal mammary glands on the underside of the skin; pin the skin to the dissecting board (Figure 2).</li>
		<li>Gently grasp the mammary tissue of the 5th gland with the rounded side of curved forceps and slowly trim the gland away from the skin, being careful not to nick the gland or the skin.</li>
		<li>Continue to trim, moving dorsally until the 4th and 5th glands have been completely lifted from the skin. Ensure that the nipple region is removed with the rest of the gland, as this serves as the starting point for the Sholl analysis. Cut the mammary tissue away from the body where it is attached at gland 4.</li>
	</ol>
	</li>
	<li>Once the gland is removed from the animal, spread it evenly on an electrostatically charged, 25 mm x 75 mm x 1 mm microscopy slide, with the side that was adjacent to the skin facing down. 
	NOTE: For glands from older or lactating animals, a 51 x 75 x 1 mm slide may be required.</li>
	<li>While wearing gloves, gently squeeze out any air bubbles. Cover the gland with a plastic paraffin film and another microscope slide and compress the gland to adhere it to the slide. 
	NOTE: A 50 mL conical tube filled with water serves as a suitable weight. The amount of time required to adhere to the slide depends on the thickness of the gland. Thin, postnatal day (PND) 4 glands should be compressed for a minimum of 30 min, while thicker, adult glands may require as much as 2-5 h.</li>
</ol>
2. Prepare Mammary Whole-Mounts
<ol>
	<li>Prepare the carmine alum solution at least 24 h in advance, as it requires boiling and refrigeration.
	<ol>
		<li>Dissolve 1 g of carmine alum and 2.5 g of aluminum potassium sulfate (AlK(SO4)2&#183;12H2O) in 500 mL of distilled water and boil for 20 min in a 1-L flask. Bring the final volume to 500 mL using distilled water.</li>
		<li>Filter the solution through filter paper under a vacuum and refrigerate for storage. 
		NOTE: Carmine alum solution can be reused but should be discarded when the color begins to fade.</li>
	</ol>
	</li>
	<li>Prior to fixation, peel the paraffin film off the gland, being careful not to pull the gland off the slide. Place the slide(s) in a glass slide-staining jar and immerse in fixative (100% ethanol, chloroform, and glacial acetic acid in a 6:3:1 ratio) for 12-48 h, depending on the thickness of the glands.</li>
	<li>Pour off the fixative and soak the glands in 70% ethanol for 15 min. Gradually rehydrate the glands by pouring out 1/3 of the ethanol solution and replacing it with distilled water. Soak for 5 min. Repeat this process three times.</li>
	<li>After the final rinse, pour off all the ethanol/water solution and replace it with 100% distilled water. Soak the glands for 5 min.</li>
	<li>Pour off the distilled water and immerse the glands in the carmine alum solution. Stain the glands for 12-24 h, depending on the thickness. 
	NOTE: The glands cannot be over-stained, but the staining time for multiple batches should be the same, so that the staining intensity is the same.</li>
	<li>Pour off the carmine alum solution and rinse the glands in 100% distilled water for 30 s. Gradually dehydrate the glands by soaking them in 70% ethanol for 15 min, 95% ethanol for 15 min, and 100% ethanol for 20 min.</li>
	<li>Clear the glands of fat by soaking them in xylene for 12-72 h, depending on the thickness. 
	NOTE: The glands should be translucent (clear). If any opaque (whitish) areas remain, continue soaking in xylene until translucent. If lactating or otherwise very thick glands are being stained and cleared, the xylene may need to be replaced once to fully clear the glands.</li>
	<li>Mount the slides with a xylene-based mounting medium by pipetting enough medium to just cover the gland. Add a coverslip, ensuring that no air bubbles form.</li>
	<li>Allow the slides to dry. As the mounting medium dries, it will contract under the coverslip, and it may be necessary to add additional mounting medium. Once no additional medium is required, allow the slides to dry completely; this may take 2-3 weeks.</li>
	<li>Once the slides are completely dry, any residual mounting medium can be removed with a cotton swab and a small amount of xylene. Be careful not to use too much xylene, as this can dissolve the mounting medium and loosen the coverslip. If this happens and air bubbles collect under the coverslip, the coverslip should be removed in xylene and the mounting process should be repeated.</li>
</ol>
3. Prepare Whole-mount Images for Analysis
<ol>
	<li>Capture images of whole-mounts (Figure 3) using a macroscope or dissecting microscope and a digital camera with the appropriate software. 
	NOTE: While any magnification that captures the entire glandular epithelium can be selected, it is imperative to capture all whole-mount images that will be compared to each other at the same magnification.</li>
	<li>Download ImageJ software (or FIJI software)6.</li>
	<li>Open the mammary whole-mount image in ImageJ by clicking &#34;File&#34;&#160;&#8594; &#34;Open.&#34; Select the Freehand tool and trace around the glandular epithelium. Select &#34;Edit&#34;&#160;&#8594; &#34;Clear Outside.&#34;
	<ol>
		<li>Remove the lymph nodes by tracing around the node and using the Freehand tool and &#34;Edit&#34;&#160;&#8594; &#34;Cut.&#34;</li>
	</ol>
	</li>
	<li>Separate the color channels by selecting &#34;Image&#34;&#160;&#8594; &#34;Color&#34; &#8594; &#34;Split Channels.&#34; Select the channel with the best contrast, typically the blue channel. 
	NOTE: An RGB image consists of a stack of the red, green, and blue components of that image. This action separates these components into three 8-bit grayscale images.</li>
	<li>Subtract the background by selecting &#34;Process&#34;&#160;&#8594; &#34;Subtract Background.&#34; Choose the desired parameters and then click &#34;Preview&#34; to preview the changes. 
	NOTE: &#34;Subtract Background&#34; removes smooth, continuous backgrounds. Additionally, &#34;Process&#34; &#8594; &#34;Filters&#34; &#8594; &#34;Unsharp Mask&#34; can be used to create contrast.</li>
	<li>Choose one of the following methods for automatically removing noise: despeckle or remove outliers. 
	NOTE: ImageJ offers a third method for automatic noise removal: remove NaNs. However, the remove NaNs command is not applicable since it uses 32-bit images, and the current method uses 8-bit images.
	<ol>
		<li>Remove noise using the despeckle command by selecting &#34;Process&#34; &#8594; &#34;Noise&#34;&#160;&#8594; &#34;Despeckle.&#34; 
		NOTE: This is equivalent to adding a median filter, which replaces each pixel with the median value in its 3&#8197;&#215;&#8197;3 neighborhood.</li>
		<li>Remove noise using the remove outliers command by selecting &#34;Process&#34; &#8594; &#34;Noise&#34; &#8594; &#34;Remove Outliers.&#34; 
		NOTE: This process replaces a pixel with the median of the pixels in the immediate surroundings if it deviates from the median by more than a certain value (the threshold).</li>
	</ol>
	</li>
	<li>Remove any remaining noise manually (Figure 4).
	<ol>
		<li>Open a copy of the original image and use this as a guide for what is and what is not noise. Click the double-red-arrow button at the far right of the toolbar. Select the Drawing Tools; the Drawing Tool buttons will now appear in the toolbar.</li>
		<li>Click the Eraser tool. Adjust the eraser diameter by right-clicking the Eraser tool button. Hold the left mouse button to erase noise. 
		NOTE: Only one session of erasing can be undone. Once the left mouse button is released and clicked again, the previous erase cannot be undone.</li>
	</ol>
	</li>
	<li>Adjust the threshold by selecting &#34;Image&#34; &#8594; &#34;Adjust&#34; &#8594; &#34;Threshold.&#34; Move the sliders to adjust the minimum (upper slider) and maximum (lower slider) threshold values until an adequate depiction of the gland is achieved. 
	NOTE: Setting the threshold value segments grayscale images into features of interest and background.
	<ol>
		<li>Click Apply. If necessary, remove additional noise at this point by following steps 3.6.1 and 3.6.2.</li>
	</ol>
	</li>
	<li>Reconstruct the portions of the glandular epithelium that were removed by thresholding and noise removal (Figure 5).
	<ol>
		<li>Conduct image reconstruction carefully and on a minimal basis to maintain the integrity of the original image. Refer to the original image for a reference as to what is and what is not epithelium.</li>
		<li>Click the Spray Can tool (on the toolbar with the Drawing Tools). Adjust the spray diameter and rate by right-clicking on the Spray Can tool button. Carefully fill in missing sections of gland by clicking or holding down on the left mouse button.</li>
	</ol>
	</li>
	<li>Create a skeletonized image of the gland for conducting the Sholl Analysis. Ensure that the thresholded image is binary by selecting &#34;Process&#34; &#8594; &#34;Binary&#34;&#160;&#8594; &#34;Make Binary.&#34;
	<ol>
		<li>If the image is white on a black background, select &#34;Process&#34;&#160;&#8594; &#34;Binary&#34;&#160;&#8594; &#34;Options&#34; and uncheck &#34;Black Background.&#34; Skeletonize the image by selecting &#34;Process&#34; &#8594; &#34;Binary&#34; &#8594; &#34;Skeletonize.&#34; 
		NOTE: This repeatedly removes pixels from the edges of the binary image until it is reduced to a single-pixel-wide shape.</li>
		<li>Dilate the image one time by selecting &#34;Process&#34; &#8594; &#34;Binary&#34; &#8594; &#34;Dilate.&#34; 
		NOTE: This fills in gaps created by thresholding and skeletonizing by adding pixels to the edges of the binary image.</li>
	</ol>
	</li>
	<li>Save the image by selecting &#34;File&#34; &#8594; &#34;Save As.&#34; Select an image type (typically jpeg), enter the filename, and click &#34;OK.&#34;</li>
	<li>Check the accuracy of the skeletonized image by overlaying the skeletonized image onto the original image (Figure 6).
	<ol>
		<li>Create an overlay by opening both the original image and the skeletonized image. Select &#34;Image&#34; &#8594; &#34;Overlay&#34; &#8594; &#34;Add Image.&#34; In the &#34;Add Image&#34; dialog box, select the skeleton image from the &#34;Image to Add&#34; dropdown menu and set the opacity at 30%.</li>
		<li>Save the image of the skeleton image overlaid onto the original by selecting &#34;File&#34; &#8594; &#34;Save As.&#34; Select an image type, enter the file name, and click &#34;OK.&#34;</li>
	</ol>
	</li>
</ol>
4. Conduct the Sholl Analysis
<ol>
	<li>Open a skeleton image and make the image binary by selecting &#34;Process&#34; &#8594; &#34;Binary&#34;&#160;&#8594; &#34;Make Binary.&#34;
	<ol>
		<li>Prior to setting the magnification scale, measure the number of pixels/mm using a micrometer for the magnification at which the images were captured.</li>
		<li>Set the measured magnification scale by selecting &#34;Analyze&#34; &#8594; &#34;Set Scale.&#34; Enter the number of pixels/mm. Set the &#34;Known Distance&#34; and the &#34;Pixel Aspect Ratio,&#34; both to 1. Enter &#34;mm&#34; for the &#34;Unit of Length&#34; and check &#34;Global&#34; (maintains the same scale for each image).</li>
	</ol>
	</li>
	<li>Determine the ending radius (enclosing radius) for the Sholl analysis by drawing a line from the start of the primary duct (center of analysis) to the most distal point of the glandular epithelium (Figure 7).
	<ol>
		<li>Use the line drawing tool in the toolbar to draw a line between the points of interest. Press the &#34;M&#34; key to take a measurement and note that a results window will open. 
		NOTE: The value in the &#34;Length&#34; column is the length of the line in mm. This value will be automatically entered as the Ending Radius when setting the Sholl parameters. The Sholl plugin will use the starting point of the line as the center of the centric rings.</li>
	</ol>
	</li>
	<li>Running the Sholl Analysis.
	<ol>
		<li>Run the analysis by selecting &#34;Plugins&#34; &#34;Advanced Sholl Analysis;&#34; a parameter window will appear.</li>
		<li>Set the Starting Radius in &#34;I. Definition of Shells&#34; to 0.00 mm; the length of the line measured in step 4.2 will automatically be entered as the &#34;Ending Radius.&#34;</li>
		<li>Set the &#34;Radius Step Size&#34; to 0.1 mm. 
		NOTE: The radius step size determines the number of rings (effectively the number of iterations); a smaller step size will increase the number of rings, while a larger step size will decrease the number of rings. The radius cannot be set too small, although an excessively small radius will result in an unnecessarily large number of rings. However, it can be set too large, which will create fewer rings and subsequently underestimate the true number of intersections. Refer to Stanko et al. (2015) for further information on determining the step size.</li>
		<li>Set the &#34;# Samples&#34; to 1 and the &#34;Integration&#34; to &#34;Mean&#34; in &#34;II. Multiple Samples per Radius.&#34;</li>
		<li>Set the &#34;Enclosing radius cutoff&#34; to 1 and check &#34;infer from starting radius&#34; for the &#34;# Primary branches&#34; in &#34;III. Descriptors and Curve Fitting.&#34; 
		NOTE: &#34;Fit profile and compute descriptors&#34; and &#34;Show fitting details&#34; can be checked as desired.</li>
		<li>Check &#34;Linear&#34; and select &#34;Best fitting degree&#34; in &#34;Profiles Without Normalization;&#34; check &#34;Most informative.&#34; Select &#34;Area for Normalized Profiles&#34; in &#34;IV. Sholl Methods.&#34;</li>
		<li>Check &#34;Create Intersections Mask&#34; in &#34;V. Output options&#34; to create a heat map of the intersections (optional).</li>
		<li>Click &#34;Cf. Segmentation&#34; to generate a preview window of the image with rings to confirm the area of analysis.</li>
	</ol>
	</li>
	<li>Click &#34;OK&#34; to run the analysis.</li>
</ol>
5. Measuring the MEA
<ol>
	<li>Measure the MEA by tracing the shortest distance around the epithelial tree (Figure 8).
	<ol>
		<li>In ImageJ with the skeleton image of the gland open, click the Polygon tool. Click on a point on the perimeter of the epithelial tree to begin the polygon, move around the perimeter of the gland, and click to add a line segment.</li>
		<li>When the entire epithelial area has been circumvented, double-click to close the polygon. Press the &#34;M&#34; key to open a results window; the value in the &#34;Area&#34; column is the MEA.</li>
	</ol>
	</li>
	<li>In cases where the glandular epithelium has extended beyond the lymph node, subtract the lymph node area (LNA) from the MEA when calculating the branching density.
	<ol>
		<li>Measure the LNA by tracing the lymph node in the same manner as the epithelial tree and pressing &#34;M.&#34; 
		NOTE: The LNA must be subtracted from the MEA in these cases because the lymph node prevents the analysis from counting intersections within the LNA. When the epithelium has not reached the lymph node, the LNA is zero.</li>
	</ol>
	</li>
</ol>
6. Reporting Data
<ol>
	<li>Report values for the enclosing radius, MEA, N, k, and branching density. 
	NOTE: The enclosing radius is determined in step 4.2 and the MEA is determined in step 5.1.
	<ol>
		<li>Run the analysis to generate a Sholl results window. 
		NOTE: The reported N is the value for the sum inters. The reported k is the value for the Sholl regression coefficient (semi-log). The Sholl analysis will return a value for k over any measured region of the glandular epithelium. To obtain an accurate value for k over the full epithelium, the ductal ends must be present.</li>
		<li>Modify the Sholl analysis for the mammary gland by using the output value for N to calculate the branching density (the fundamental endpoint of this method). Calculate the branching density using the formula N/(MEA-LNA) and report the value as N/mm2.</li>
	</ol>
	</li>
</ol>

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	<li>Sholl, D. A. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Dendritic+organization+of+the+neurons+in+the+visual+and+motor+cortices+of+the+cat.">Dendritic organization of the neurons in the visual and motor cortices of the cat.</a> J Anat. 87 (4), 387-406 (1953).</li><li>Ferreira, T. A., Iacono, L. L., Gross, C. T. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Serotonin+receptor+1A+modulates+actin+dynamics+and+restricts+dendritic+growth+in+hippocampal+neurons.">Serotonin receptor 1A modulates actin dynamics and restricts dendritic growth in hippocampal neurons.</a> Eur J Neurosci. 32 (1), 18-26 (2010).</li><li>Stanko, J. P., Easterling, M. R., Fenton, S. E. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Application+of+Sholl+analysis+to+quantify+changes+in+growth+and+development+in+rat+mammary+gland+whole+mounts.">Application of Sholl analysis to quantify changes in growth and development in rat mammary gland whole mounts.</a> Reprod Toxicol. 54, 129-135 (2015).</li><li>Assis, S., Warri, A., Cruz, M. I., Hilakivi-Clarke, L. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Changes+in+Mammary+Gland+Morphology+and+Breast+Cancer+Risk+in+Rats.">Changes in Mammary Gland Morphology and Breast Cancer Risk in Rats.</a> J. Vis. Exp. (44), e2260 (2010).</li><li>Plante, I., Stewart, M. K., Laird, D. W. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Evaluation+of+Mammary+Gland+Development+and+Function+in+Mouse+Models.">Evaluation of Mammary Gland Development and Function in Mouse Models.</a> J. Vis. Exp. (53), e2828 (2011).</li><li>ImageJ User Guide. IJ 1.46r. ImageJ Available from: <a target="_blank" href="https://imagej.nih.gov/ij/docs/guide/146.html">https://imagej.nih.gov/ij/docs/guide/146.html</a> (2012)</li><li>Tucker, D. K., Foley, J. F., Hayes-Bouknight, S. A., Fenton, S. 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L. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Persistent+abnormalities+in+the+rat+mammary+gland+following+gestational+and+lactational+exposure+to+2,3,7,8-tetrachlorodibenzo-p-dioxin+(TCDD).">Persistent abnormalities in the rat mammary gland following gestational and lactational exposure to 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD).</a> Toxicol Sci. 67 (1), 63-74 (2002).</li><li>Murray, T. J., Maffini, M. V., Ucci, A. A., Sonnenschein, C., Soto, A. 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A., Russo, J. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=In+utero+exposure+to+butyl+benzyl+phthalate+induces+modifications+in+the+morphology+and+the+gene+expression+profile+of+the+mammary+gland:+an+experimental+study+in+rats.">In utero exposure to butyl benzyl phthalate induces modifications in the morphology and the gene expression profile of the mammary gland: an experimental study in rats.</a> Environ Health. 10 (1), 5 (2011).</li><li>Johnson, M. D., Mueller, S. C. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Three+dimensional+multiphoton+imaging+of+fresh+and+whole+mount+developing+mouse+mammary+glands.">Three dimensional multiphoton imaging of fresh and whole mount developing mouse mammary glands.</a> BMC Cancer. 13, 373 (2013).</li><li>Enoch, R. R., Stanko, J. P., Greiner, S. 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The authors have nothing to disclose.

From birth until puberty, mammary gland growth is allometric. After puberty, the mammary gland develops through extensive ductal branching and elongation, which continue until the mammary epithelium occupies the entire fat pad. Branching characteristics are an important aspect of mammary gland development, and the ability to objectively quantify these characteristics can be highly useful for assessing normal mammary development and for identifying abnormal development following early life exposures to mammary toxicants.<...

Mammary gland branching is a characteristic that is commonly assessed as an indicator of gland development, but it is difficult to objectively quantify. In 1953, Sholl1 described a method for measuring neuronal dendritic arborization in the visual and motor cortices of the cat, and a plugin for this technique was developed by Ferriera et al2. Because both neurons and mammary glands exhibit a similar tree-like structure, the plugin was employed to quantify mammary epithelial branching densities in 2D images of the peripubertal rat mammary gland. The peripubertal stage was chosen for analysis because weaning is a life stage that is often assessed in academic laboratories and test guideline studies. The Sholl analysis is a plugin distributed with FIJI, which is the open-source image processing package ImageJ, with additional plugins included. The plugin creates a series of concentric rings encircling a predefined center (typically the soma of a neuron or the origin of the primary duct of a mammary gland) and extending out to the distal-most portion of the object (the enclosing radius). It then counts the number of intersections (N) that occur on each of the rings. The plugin also returns a Sholl regression coefficient (k), which is a measurement of the rate of decay of epithelial branching.
Using ImageJ, a skeletonized image of a mammary gland whole-mount is created and the mammary epithelial area (MEA) is measured. The image is analyzed using the Sholl analysis plugin, and values for N and k, among other values not utilized here, are returned. Mammary epithelial branching density is determined by calculating N/MEA. The extent to which branching continues in the outer regions of the glandular epithelium is the branching complexity and is an indicator of uniform distal epithelial growth. As k is a measure of the distal decrease in epithelial branching, it is an effective measure of the branching complexity and a reliable indicator of mammary development.
This protocol describes a computer-assisted method for creating skeletonized images of mammary gland whole-mounts and quantitatively evaluating mammary branching characteristics in peripubertal male and female rats. This method is relatively rapid and does not require the use of specialized microscopy equipment. Development and validation of this method are described in Stanko et al. (2015)3. This report also describes preparation of rat mammary gland whole=mounts. Similar mammary whole-mount procedures have been described in de Assis et al. (2010)4 and Plante et al. (2011)5.

<table border="0" cellpadding="0" cellspacing="0" width="1069">
	<tbody>
		<tr height="21">
			<td height="21" style="height:21px;width:245px;">Dissecting board</td>
			<td style="width:161px;">NA</td>
			<td style="width:224px;">NA</td>
			<td style="width:439px;">A piece of styrofoam roughly 10&#34;x12&#34; is suitable.</td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:245px;">Dissecting T-Pins</td>
			<td>Daigger</td>
			<td style="width:224px;">EF7419A</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:245px;">Spray bottle with ethanol</td>
			<td>NA</td>
			<td style="width:224px;">NA</td>
			<td>70% ethanol is suitable.</td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:245px;">Curved dissecting scissors</td>
			<td>Fine Science Tools</td>
			<td style="width:224px;">14569-09</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:245px;">Straight dissecing scissors</td>
			<td>Fine Science Tools</td>
			<td style="width:224px;">14568-09</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:245px;">Curved forceps</td>
			<td>Fine Science Tools</td>
			<td style="width:224px;">11003-12</td>
			<td></td>
		</tr>
		<tr height="160">
			<td height="160" style="height:160px;width:245px;">Superfrost Plus 24x75x1 mm microscope slides</td>
			<td>ThermoFisher Scientific</td>
			<td>4951PLUS-001</td>
			<td style="width:439px;">Thermo Scientific Superfrost Plus &#38; Colorfrost Plus slides hold tissue sections on permanently without the need for expensive coatings in IHC and Anatomical Pathology applications. This treatment reduces tissue loss during staining as well as hours of slide preparation. Slides electro-statically attract frozen tissue sections and cytology preparations and feature a chemistry similar to silane, although optimized to improve application performance. 
			https://www.thermofisher.com/order/catalog/product/4951PLUS4.&#160;</td>
		</tr>
		<tr height="42">
			<td height="42" style="height:42px;width:245px;">Fisherfinest Premium Cover Glass 24x60x1 mm</td>
			<td>Fisher scientific</td>
			<td style="width:224px;">12-548-5P</td>
			<td></td>
		</tr>
		<tr height="42">
			<td height="42" style="height:42px;width:245px;">Bemis Parafilm M Laboratory Wrapping Film</td>
			<td>Fisher scientific</td>
			<td style="width:224px;">13-374-12</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;">Chloroform</td>
			<td>Sigma-Aldrich</td>
			<td>C2432</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;">Glacial acetic acid</td>
			<td>Sigma-Aldrich</td>
			<td>A9967</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:245px;">Ethanol absolute, &#8805;99.8% (GC)&#160;</td>
			<td>Sigma-Aldrich</td>
			<td style="width:224px;">24102</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;">Xylene</td>
			<td>Sigma-Aldrich</td>
			<td>214736</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;">Carmine alum&#160;</td>
			<td>Sigma-Aldrich</td>
			<td>C1022</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;">Aluminum potassium sulfate&#160;</td>
			<td>Sigma-Aldrich</td>
			<td>A6435</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:245px;">Permount mounting media</td>
			<td>Fisher Scientific</td>
			<td style="width:224px;">SP15</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:245px;">Macroscope</td>
			<td>Leica</td>
			<td>Z16 APO&#160;</td>
			<td rowspan="3" style="width:439px;">This is the image capturing hardware and software used in this laboratory.&#160; As there are many different options, the methods and applications may vary between laboratories.</td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:245px;">Digital camera</td>
			<td>Leica</td>
			<td style="width:224px;">DFC295</td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:245px;">Camera software</td>
			<td>Leica</td>
			<td style="width:224px;">Leica Application Suite v3.1&#160;</td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:245px;">ImageJ software</td>
			<td>Open source</td>
			<td>http://imagej.net/Welcome</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:245px;">Sholl analysis&#160;</td>
			<td>Open source</td>
			<td>http://imagej.net/Sholl_Analysis</td>
			<td></td>
		</tr>
	</tbody>
</table>

quantifying branching density in rat mammary gland whole-mounts using the sholl analysis method

An increasing number of studies are utilizing the rodent mammary gland as an endpoint for assessing the developmental toxicity of a chemical exposure. The effects these exposures have on mammary gland development are typically evaluated using either basic dimensional measurements or by scoring morphological characteristics. However, the broad range of methods for interpreting developmental changes could lead to inconsistent translations across laboratories. A common method of assessment is needed so that proper interpretations can be formed from data being compared across studies. The present study describes the application of the Sholl analysis method to quantify mammary gland branching characteristics. The Sholl method was originally developed for use in quantifying neuronal dendritic patterns. By using ImageJ, an open-source image analysis software package, and a plugin developed for this analysis, the mammary gland branching density and the complexity of a mammary gland from a peripubertal female rat were determined. The methods described here will enable the use of the Sholl analysis as an effective tool for quantifying an important characteristic of mammary gland development.

The values for the measured enclosed radius, MEA, N, k, and calculated branching density for the mammary gland analyzed in this protocol are reported in Table 1. The Sholl analysis generates linear and semi-log plots of the number of intersections at each radius (Figure 9) and, if selected, a heat map of the intersections (Figure 10). Less-developed glands exhibit fewer intersections within the same MEA ...

Watch this Scientific Journal Video about Quantifying Branching Density in Rat Mammary Gland Whole-mounts Using the Sholl Analysis Method at JoVE.com

Quantifying Branching Density in Rat Mammary Gland Whole-mounts Using the Sholl Analysis Method

Mammary gland development in the rodent has typically been evaluated using descriptive assessments or by measuring basic physical attributes. Branching density is an indicator of mammary development that is difficult to quantify objectively. This protocol describes a reliable method for the quantitative assessment of mammary gland branching characteristics.

An increasing number of studies are utilizing the rodent mammary gland as an endpoint for assessing the developmental toxicity of a chemical exposure. The ...

quantifying-branching-density-rat-mammary-gland-whole-mounts-using

Research

JoVE Journal

Developmental Biology

14.1K Views.  National Institute of Environmental Health Sciences. Mammary gland development in the rodent has typically been evaluated using descriptive assessments or by measuring basic physical attributes. Branching density is an indicator of mammary development that is difficult to quantify objectively. This protocol describes a reliable method for the quantitative assessment of mammary gland branching characteristics. 

Video: Quantifying Branching Density in Rat Mammary Gland Whole-mounts Using the Sholl Analysis Method

Analysis of Zebrafish Larvae Skeletal Muscle Integrity with Evans Blue Dye

The zebrafish model is an emerging system for the study of neuromuscular disorders. In the study of neuromuscular diseases, the integrity of the muscle membrane is a critical disease determinant. To date, numerous neuromuscular conditions display degenerating muscle fibers with abnormal membrane integrity; this is most commonly observed in muscular dystrophies. Evans Blue Dye (EBD) is a vital, cell permeable dye that is rapidly taken into degenerating, damaged, or apoptotic cells; in contrast, it is not taken up by cells with an intact membrane. EBD injection is commonly employed to ascertain muscle integrity in mouse models of neuromuscular diseases. However, such EBD experiments require muscle dissection and/or sectioning prior to analysis. In contrast, EBD uptake in zebrafish is visualized in live, intact preparations. Here, we demonstrate a simple and straightforward methodology for performing EBD injections and analysis in live zebrafish. In addition, we demonstrate a co-injection strategy to increase efficacy of EBD analysis. Overall, this video article provides an outline to perform EBD injection and characterization in zebrafish models of neuromuscular disease.

In this study, we describe a straightforward method to perform Evans Blue Dye (EBD) analysis on zebrafish larvae. This technique is a powerful tool for the characterization of skeletal muscle integrity and delineation of zebrafish models of muscular dystrophy, and is a valuable method for the development of novel therapeutics.

The zebrafish model is an emerging system for the study of neuromuscular disorders.  In the study of neuromuscular diseases, the integrity of the muscle ...

Methods to Examine the Lymph Gland and Hemocytes in Drosophila Larvae

Many parallels exist between the Drosophila and mammalian hematopoietic systems, even though Drosophila lack the lymphoid lineage that characterize mammalian adaptive immunity. Drosophila and mammalian hematopoiesis occur in spatially and temporally distinct phases to produce several blood cell lineages. Both systems maintain reservoirs of blood cell progenitors with which to expand or replace mature lineages. The hematopoietic system allows Drosophila and mammals to respond to and to adapt to immune challenges. Importantly, the transcriptional regulators and signaling pathways that control the generation, maintenance, and function of the hematopoietic system are conserved from flies to mammals. These similarities allow Drosophila to be used to genetically model hematopoietic development and disease.
Here we detail assays to examine the hematopoietic system of Drosophila larvae. In particular, we outline methods to measure blood cell numbers and concentration, visualize a specific mature lineage in vivo, and perform immunohistochemistry on blood cells in circulation and in the hematopoietic organ. These assays can reveal changes in gene expression and cellular processes including signaling, survival, proliferation, and differentiation and can be used to investigate a variety of questions concerning hematopoiesis. Combined with the genetic tools available in Drosophila, these assays can be used to evaluate the hematopoietic system upon defined genetic alterations. While not specifically outlined here, these assays can also be used to examine the effect of environmental alterations, such as infection or diet, on the hematopoietic system.

Methods to Examine the Lymph Gland and Hemocytes in Drosophila Larvae

Drosophila and mammalian hematopoietic systems share many common features, making Drosophila an attractive genetic model to study hematopoiesis. Here we demonstrate dissection and mounting of the major larval hematopoietic organ for immunohistochemistry. We also describe methods to assay various larval hematopoietic compartments including circulating hemocytes and sessile crystal cells.

Many parallels exist between the Drosophila and mammalian hematopoietic systems, even though Drosophila lack the lymphoid lineage that characterize ...

Spatial and Temporal Analysis of Active ERK in the C. elegans Germline

The evolutionarily conserved&#160;extracellular signal transducing RTK-RAS-ERK pathway is an important kinase-signaling cascade that controls multiple cellular and developmental processes principally via activation of ERK, the terminal kinase of the pathway. Tight regulation of ERK activity is essential for normal development and homeostasis; overly active ERK results in excessive cellular proliferation, while underactive ERK causes cell death. C. elegans is a powerful model system that has helped characterize the function and regulation of RTK-RAS-ERK signaling pathway during development. In particular, the RTK-RAS-ERK pathway is essential for C. elegans germline development, which is the focus of this method. Using antibodies specific to the active, diphosphorylated form of ERK (dpERK), the stereotypical localization pattern can be visualized within the germline. Because this pattern is both spatially and temporally controlled, the ability to reproducibly assay dpERK is useful to identify regulators of the pathway that affect dpERK signal duration and amplitude and thus germline development. Here we demonstrate how to successfully dissect, stain, and image dpERK within the C. elegans gonad. This method can be adapted for spatial localization of any signaling or structural protein in the C. elegans gonad, provided an antibody compatible with immunofluorescence is available.

Spatial and Temporal Analysis of Active ERK in the C. elegans Germline

We present an immunofluorescence&#160;imaging-based method for spatial and temporal localization of active ERK in the dissected C. elegans gonad. The protocol described here can be adapted for visualization of any signaling or structural protein in the C. elegans gonad, provided a suitable antibody reagent is available.

The evolutionarily conserved&#160;extracellular signal transducing RTK-RAS-ERK pathway is an important kinase-signaling cascade that controls multiple ...

A 5-mC Dot Blot Assay Quantifying the DNA Methylation Level of Chondrocyte Dedifferentiation In Vitro

The dedifferentiation of hyaline chondrocytes into fibroblastic chondrocytes often accompanies monolayer expansion of chondrocytes in vitro. The global DNA methylation level of chondrocytes is considered to be a suitable biomarker for the loss of the chondrocyte phenotype. However, results based on different experimental methods can be inconsistent. Therefore, it is important to establish a precise, simple, and rapid method to quantify global DNA methylation levels during chondrocyte dedifferentiation.
Current genome-wide methylation analysis techniques largely rely on bisulfite genomic sequencing. Due to DNA degradation during bisulfite conversion, these methods typically require a large sample volume. Other methods used to quantify global DNA methylation levels include high-performance liquid chromatography (HPLC). However, HPLC requires complete digestion of genomic DNA. Additionally, the prohibitively high cost of HPLC instruments limits HPLC&#39;s wider application.
In this study, genomic DNA (gDNA) was extracted from human chondrocytes cultured with varying number of passages. The gDNA methylation level was detected using a methylation-specific dot blot assay. In this dot blot approach, a gDNA mixture containing the methylated DNA to be detected was spotted directly onto an N+ membrane as a dot inside a previously drawn circular template pattern. Compared with other gel electrophoresis-based blotting approaches and other complex blotting procedures, the dot blot method saves significant time. In addition, dot blots can detect overall DNA methylation level using a commercially available 5-mC antibody. We found that the DNA methylation level differed between the monolayer subcultures, and therefore could play a key role in chondrocyte dedifferentiation. The 5-mC dot blot is a reliable, simple, and rapid method to detect the general DNA methylation level to evaluate chondrocyte phenotype.

A 5-mC Dot Blot Assay Quantifying the DNA Methylation Level of Chondrocyte Dedifferentiation In Vitro

We present a method to quantify DNA methylation based on the 5-methylcytosine (5-mC) dot blot. We determined the 5-mC levels during chondrocyte dedifferentiation. This simple technique could be used to quickly determine the chondrocyte phenotype in ACI treatment.

The dedifferentiation of hyaline chondrocytes into fibroblastic chondrocytes often accompanies monolayer expansion of chondrocytes in vitro. The global ...

Transfer of Mammary Gland-forming Ability Between Mammary Basal Epithelial Cells and Mammary Luminal Cells via Extracellular Vesicles/Exosomes

Cells can communicate via exosomes, ~100-nm extracellular vesicles (EVs) that contain proteins, lipids, and nucleic acids. Non-adherent/mesenchymal mammary epithelial cell (NAMEC)-derived extracellular vesicles can be isolated from NAMEC medium via differential ultracentrifugation. Based on their density, EVs can be purified via ultracentrifugation at 110,000 x g. The EV preparation from ultracentrifugation can be further separated using a continuous density gradient to prevent contamination with soluble proteins. The purified EVs can then be further evaluated using nanoparticle-tracking analysis, which measures the size and number of vesicles in the preparation. The extracellular vesicles with a size ranging from 50 to 150 nm are exosomes. The NAMEC-derived EVs/exosomes can be ingested by mammary epithelial cells, which can be measured by flow cytometry and confocal microscopy. Some mammary stem cell properties (e.g., mammary gland-forming ability) can be transferred from the stem-like NAMECs to mammary epithelial cells via the NAMEC-derived EVs/exosomes. Isolated primary EpCAMhi/CD49flo luminal mammary epithelial cells cannot form mammary glands after being transplanted into mouse fat pads, while EpCAMlo/CD49fhi basal mammary epithelial cells form mammary glands after transplantation. Uptake of NAMEC-derived EVs/exosomes by EpCAMhi/CD49flo luminal mammary epithelial cells allows them to generate mammary glands after being transplanted into fat pads. The EVs/exosomes derived from stem-like mammary epithelial cells transfer mammary gland-forming ability to EpCAMhi/CD49flo luminal mammary epithelial cells.

This protocol describes methods for purifying, quantitating, and characterizing extracellular vesicles (EVs)/exosomes from non-adherent/mesenchymal mammary epithelial cells and for using them to transfer mammary gland-forming ability to luminal mammary epithelial cells. EVs/exosomes derived from stem-like mammary epithelial cells can transfer this cell property to cells that ingest the EVs/exosomes.

Cells can communicate via exosomes, ~100-nm extracellular vesicles (EVs) that contain proteins, lipids, and nucleic acids. Non-adherent/mesenchymal ...

Analysis of Protein-protein Interactions and Co-localization Between Components of Gap, Tight, and Adherens Junctions in Murine Mammary Glands

Cell-cell interactions play a pivotal role in preserving tissue integrity and the barrier between the different compartments of the mammary gland. These interactions are provided by junctional proteins that form nexuses between adjacent cells. Junctional protein mislocalization and reduced physical associations with their binding partners can result in the loss of function and, consequently, to organ dysfunction. Thus, identifying protein localization and protein-protein interactions (PPIs) in normal and disease-related tissues is essential to finding new evidences and mechanisms leading to the progression of diseases or alterations in developmental status. This manuscript presents a two-step method to evaluate PPIs in murine mammary glands. In protocol section 1, a method to perform co-immunofluorescence (co-IF) using antibodies raised against the proteins of interest, followed by secondary antibodies labeled with fluorochromes, is described. Although co-IF allows for the demonstration of the proximity of the proteins, it does make it possible to study their physical interactions. Therefore, a detailed protocol for co-immunoprecipitation (co-IP) is provided in protocol section 2. This method is used to determine the physical interactions between proteins, without confirming whether these interactions are direct or indirect. In the last few years, co-IF and co-IP techniques have demonstrated that certain components of intercellular junctions co-localize and interact together, creating stage-dependent junctional nexuses that vary during mammary gland development.

Intercellular junctions are requisites for mammary gland stage-specific functions and development. This manuscript provides a detailed protocol for the study of protein-protein interactions (PPIs) and co-localization using murine mammary glands. These techniques allow for the investigation of the dynamics of the physical association between intercellular junctions at different developmental stages.

Cell-cell interactions play a pivotal role in preserving tissue integrity and the barrier between the different compartments of the mammary gland. These ...

A Novel Mammary Fat Pad Transplantation Technique to Visualize the Vessel Generation of Vascular Endothelial Stem Cells

Endothelial cells (ECs) are the fundamental building blocks of the vascular architecture and mediate vascular growth and remodeling to ensure proper vessel development and homeostasis. However, studies on endothelial lineage hierarchy remain elusive due to the lack of tools to gain access as well as to directly evaluate their behavior in vivo. To address this shortcoming, a new tissue model to study angiogenesis using the mammary fat pad has been developed. The mammary gland develops mostly in the postnatal stages, including puberty and pregnancy, during which robust epithelium proliferation is accompanied by extensive vascular remodeling. Mammary fat pads provide space, matrix, and rich angiogenic stimuli from the growing mammary epithelium. Furthermore, mammary fat pads are located outside the peritoneal cavity, making them an easily accessible grafting site for assessing the angiogenic potential of exogenous cells. This work also describes an efficient tracing approach using fluorescent reporter mice to specifically label the targeted population of vascular endothelial stem cells (VESCs) in vivo. This lineage tracing method, coupled with subsequent tissue whole-mount microscopy, enable the direct visualization of targeted cells and their descendants, through which the proliferation capability can be quantified and the differentiation commitment can be fate-mapped. Using these methods, a population of bipotent protein C receptor (Procr) expressing VESCs has recently been identified in multiple vascular systems. Procr+ VESCs, giving rise to both new ECs and pericytes, actively contribute to angiogenesis during development, homeostasis, and injury repair. Overall, this manuscript describes a new mammary fat pad transplantation and in vivo lineage tracing techniques that can be used to evaluate the stem cell properties of VESCs.

This work demonstrates a novel approach to assess the proliferation, differentiation, and vessel-forming potential of vascular endothelial stem cells (VESCs) through mammary fat pad transplantation followed by whole-mount tissue preparation for microscopic observation. A lineage tracing strategy to investigate the behavior of VESCs in vivo is also presented.

Endothelial cells (ECs) are the fundamental building blocks of the vascular architecture and mediate vascular growth and remodeling to ensure proper ...

Dissection and Immunofluorescent Staining of Mushroom Body and Photoreceptor Neurons in Adult Drosophila melanogaster Brains

Nervous system development involves a sequential series of events that are coordinated by several signaling pathways and regulatory networks. Many of the proteins involved in these pathways are evolutionarily conserved between mammals and other eukaryotes, such as the fruit fly Drosophila melanogaster, suggesting that similar organizing principles exist during the development of these organisms. Importantly, Drosophila has been used extensively to identify cellular and molecular mechanisms regulating processes that are required in mammals including neurogenesis, differentiation, axonal guidance, and synaptogenesis. Flies have also been used successfully to model a variety of human neurodevelopmental diseases. Here we describe a protocol for the step-by-step microdissection, fixation, and immunofluorescent localization of proteins within the adult Drosophila brain. This protocol focuses on two example neuronal populations, mushroom body neurons and retinal photoreceptors, and includes optional steps to trace individual mushroom body neurons using Mosaic Analysis with a Repressible Cell Marker (MARCM) technique. Example data from both wild-type and mutant brains are shown along with a brief description of a scoring criteria for axonal guidance defects. While this protocol highlights two well-established antibodies for investigating the morphology of mushroom body and photoreceptor neurons, other Drosophila brain regions and the localization of proteins within other brain regions can also be investigated using this protocol.

Dissection and Immunofluorescent Staining of Mushroom Body and Photoreceptor Neurons in Adult Drosophila melanogaster Brains

This protocol describes the dissection and immunostaining of adult Drosophila melanogaster brain tissues. Specifically, this protocol highlights the use of Drosophila mushroom body and photoreceptor neurons as example neuronal subsets that can be accurately used to uncover general principles underlying many aspects of neuronal development.

Nervous system development involves a sequential series of events that are coordinated by several signaling pathways and regulatory networks. Many of the ...

Visualizing the Node and Notochordal Plate In Gastrulating Mouse Embryos Using Scanning Electron Microscopy and Whole Mount Immunofluorescence

The post-implantation mouse embryo undergoes major shape changes after the initiation of gastrulation and morphogenesis. A hallmark of morphogenesis is the formation of the transient organizers, the node and notochordal plate, from cells that have passed through the primitive streak. The proper formation of these signaling centers is essential for the development of the body plan and techniques to visualize them are of high interest to mouse developmental biologists. The node and notochordal plate lie on the ventral surface of gastrulating mouse embryos around embryonic day (E) 7.5 of development. The node is a cup-shaped structure whose cells possess a single slender cilium each. The proper subcellular localization and rotation of the cilia in the node pit determines left-right asymmetry. The notochordal plate cells also possess single cilia albeit shorter than those of the node cells. The notochordal plate forms the notochord which acts as an important signaling organizer for somitogenesis and neural patterning. Because the cells of the node and notochordal plate are transiently present on the surface and possess cilia, they can be visualized using scanning electron microscopy (SEM). Among other techniques used to visualize these structures at the cellular level is whole mount immunofluorescence (WMIF) using the antibodies against the proteins that are highly expressed in the node and notochordal plate. In this report, we describe our optimized protocols to perform SEM and WMIF of the node and notochordal plate in developing mouse embryos to help in the assessment of tissue shape and cellular organization in wild-type and gastrulation mutant embryos.

The node and notochordal plate are transient signaling organizers in developing mouse embryos that can be visualized using several techniques. Here, we describe in detail how to perform two of the techniques to study their structure and morphogenesis: 1) scanning electron microscopy (SEM); and 2) whole mount immunofluorescence (WMIF).

The post-implantation mouse embryo undergoes major shape changes after the initiation of gastrulation and morphogenesis. A hallmark of morphogenesis is ...

A Multi-Omics Extraction Method for the In-Depth Analysis of Synchronized Cultures of the Green Alga Chlamydomonas reinhardtii

Microalgae have been the focus of research for their applications in the production of high value compounds, food and fuel. Moreover, they are valuable photosynthetic models facilitating the understanding of the basic cellular processes. System wide studies enable comprehensive and in-depth understanding of molecular functions of the organisms. However, multiple independent samples and protocols are required for proteomics, lipidomics and metabolomics studies introducing higher error and variability. A robust high throughput extraction method for the simultaneous extraction of chlorophyll, lipids, metabolites, proteins and starch from a single sample of the green alga Chlamydomonas reinhardtii is presented here. The illustrated experimental setup is for Chlamydomonas cultures synchronized using 12 h/12 h light/dark conditions. Samples were collected over a 24 h cell cycle to demonstrate that the metabolites, lipids and starch data obtained using various analytical platforms are well conformed. Furthermore, protein samples collected using the same extraction protocol were used to conduct detailed proteomics analysis to evaluate their quality and reproducibility. Based on the data, it can be inferred that the illustrated method provides a robust and reproducible approach to advance understanding of various biochemical pathways and their functions with greater confidence for both basic and applied research.

A Multi-Omics Extraction Method for the In-Depth Analysis of Synchronized Cultures of the Green Alga Chlamydomonas reinhardtii

System-wide analysis of multiple biomolecules is crucial to gain functional and mechanistic insights into biological processes. Hereby, an extensive protocol is described for high throughput extraction of lipids, metabolites, proteins and starch from a single sample harvested from synchronized Chlamydomonas culture.

Microalgae have been the focus of research for their applications in the production of high value compounds, food and fuel. Moreover, they are valuable ...