We acknowledge Leena Patel and Diamond Woodard for helping in the Drosophila medium preparation and Dr. Igor Chesnokov for providing access to the camera-attached stereomicroscope.

1. Preparation of Drosophila (the tools required are depicted in Figure 2A)
<ol>
	<li>For any of the experiments described, collect Drosophila (maintained at room temperature, or 25 &#186;C) within 5 days of eclosion and place them in a vial filled with 5 - 7 mL of Drosophila food (see Materials Table), with no more than 25 flies in each vial; maintain a female:male ratio of 2:1.</li>
	<li>Sprinkle a small amount of granulated yeast to stimulate Drosophila egg produc...

<ol>
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Chapter. , 21-21 (2010).</li><li>Mitra, K., Rikhy, R., Lilly, M., Lippincott-Schwartz, J. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=DRP1-dependent+mitochondrial+fission+initiates+follicle+cell+differentiation+during+Drosophila+oogenesis.">DRP1-dependent mitochondrial fission initiates follicle cell differentiation during Drosophila oogenesis.</a> J Cell Biol. 197 (4), 487-497 (2012).</li><li>Klusza, S., Deng, W. 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J., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=A+new+mitochondrial+pool+of+cyclin+E,+regulated+by+Drp1,+is+linked+to+cell-density-dependent+cell+proliferation.">A new mitochondrial pool of cyclin E, regulated by Drp1, is linked to cell-density-dependent cell proliferation.</a> J Cell Sci. 128 (22), 4171-4182 (2015).</li><li>Mitra, K., Wunder, C., Roysam, B., Lin, G., Lippincott-Schwartz, J. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=A+hyperfused+mitochondrial+state+achieved+at+G1-S+regulates+cyclin+E+buildup+and+entry+into+S+phase.">A hyperfused mitochondrial state achieved at G1-S regulates cyclin E buildup and entry into S phase.</a> Proc Natl Acad Sci U S A. 106 (29), 11960-11965 (2009).</li><li>Shidara, Y., Hollenbeck, P. 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The authors have no competing financial interests.

Critical Steps within the Protocol
Photobleaching: Preventing undue photobleaching of fluorescent samples is absolutely necessary to performing efficient confocal microscopy. Therefore, the time used to locate samples through the eyepiece or to set image acquisition parameters through the live scanning mode should be minimized to minimize photobleaching.
Tissue damage: Since mitochondria are considered to be the sensors of cellular health, it...

Mitochondria are classically described as the cellular powerhouse, since they are the main seats of energy production in differentiated cells. Moreover, mitochondria play a critical role in metabolism, heat generation, lipid modification, calcium and redox homeostasis, the orchestration of cell signaling processes, etc1. Mitochondria also play an active role in the induction of cell death2, as well as in cell cycle regulation3. Such multi-functionality raises the following fundamental questions: a) how do mitochondria perform all these functions simultaneously and b) are there specific mitochondrial pools or subzones that are specialized for distinct functions? In this context, it is important to note that the multifunctional mitochondria are dynamic in their shape, size, and structure within individual cells and that the steady-state shape of mitochondria can vary between cell types. Decades of research from various laboratories suggest that the alteration of mitochondrial shape, size, and structure, collectively called mitochondrial dynamics, is crucial for maintaining various mitochondrial functions4,5,6. These findings raise the possibility that mitochondria may accomplish their multi-functionality by virtue of their structural dynamism.
Extensive efforts are underway to understand the mitochondrial structure-function relationship. The dynamism of mitochondrial structure is primarily maintained by their ability to undergo fission and fusion events with each other. Fission of large mitochondria converts them into smaller mitochondrial elements, while fusion between two smaller mitochondria merges them into a larger mitochondrial element7. Moreover, transient fusion of two mitochondria may occur to allow the mixing of their contents. The fission and fusion events of the inner and outer mitochondrial membranes are carefully governed by specific sets of proteins. The core fission machinery is composed of dynamin-related protein 1 (Drp1), which is recruited from the cytosol to the mitochondria by its interaction with certain bona fide mitochondrial proteins (e.g., Fis1 or Mff1), while Drp1 function can also be regulated by other proteins on the mitochondrial surface4. Although Drp1 operates on the outer membrane, its fission abilities impact the inner membrane as well. The orchestration of the fission of outer and inner mitochondrial membranes is not well understood. On the other hand, fusion of the inner membrane is governed at the core by the activities of Opa1, while mitofusins govern the fusion of the outer-membrane5. The balance of the counteracting fission and fusion events of mitochondria dictate the steady-state mitochondrial shape in a cell. For example, repression of mitochondrial fission would result in complete and unopposed fusion, while the over-activity of mitochondrial fission would result in fragmentation of mitochondria3.
The study of the mitochondrial structure-function relationship primarily involves two complimentary approaches: a) analyses of the cellular and organismal phenotypes after genetic manipulation of mitochondrial fission/fusion proteins and b) direct assessments of mitochondrial structure and function. It is noteworthy that genetic analyses may not always reveal the direct functionality of the molecule at hand (in this case, mitochondrial fission/fusion proteins), as the phenotypes may arise due to secondary effects. Therefore, it is of the utmost importance to develop and use tools to study mitochondrial structure and function directly. Any assessment of mitochondrial structure involves various microscopy tools. Use of fluorescence microscopy of live cells has greatly advanced the studies of mitochondrial dynamics, since mitochondrial dynamism can be monitored both qualitatively and quantitatively using the appropriate fluorescence microscopy tools and techniques8. Fluorescence microscopy-based tools have been developed to study mitochondrial structure and function in live and fixed Drosophila melanogaster tissues, elucidating the significance of mitochondrial dynamism in vivo9. These and related methods are described here, with the goal of studying mitochondrial structure and function in the Drosophila ovary.
The Drosophila ovary consists of germline and somatic lineages, which arise from their respective adult stem cells that reside in the germarium10,11. Sixteen syncytial germ cells (GCs) get encapsulated by somatic follicle cells (FCs) to form individual egg chambers that emerge out of the germarium (Figure 1). One of the 16 GCs get committed to become an oocyte, and the remaining 15 GCs develop into nurse cells that support the growth of the oocyte chamber, facilitating the maturation of the egg before it is laid. The majority of the FCs undergo 9 rounds of mitotic divisions before they exit the mitotic cell cycle to terminally differentiate into a patterned epithelial cell layer consisting of anterior follicle cells (AFCs), posterior follicle cells (PFCs), and main body cells (MBCs). The consecutive egg chambers are connected by stalk cells, which are differentiated cells that are also derived from the FCs early in development. Mitochondrial shape regulated by the mitochondrial fission protein Drp1 is actively involved in the process of differentiation during the normal development of the Drosophila ovarian FC layer9,12. The methods used in these studies to identify the involvement of Drp1 in Drosophila follicle cell layer development are described here.

<table border="0" cellpadding="0" cellspacing="0" width="722">
	<tbody>
		<tr height="38">
			<td height="38" style="height:38px;width:247px;">Grace&#39;s Media (Insect Dissecting Medium)</td>
			<td style="width:148px;">Fisher Scientific</td>
			<td style="width:136px;">30611031-2</td>
			<td style="width:191px;"></td>
		</tr>
		<tr height="38">
			<td height="38" style="height:38px;width:247px;">41 Paraformaldehyde AQ</td>
			<td style="width:148px;">Electronic Microscopy Sciences</td>
			<td style="width:136px;">50-259-99</td>
			<td></td>
		</tr>
		<tr height="38">
			<td height="38" style="height:38px;width:247px;">Mitotracker Green (overall mitochondrial stain)</td>
			<td style="width:148px;">Life Technologies</td>
			<td style="width:136px;">m7514</td>
			<td>Reconstitute and Aliquot</td>
		</tr>
		<tr height="38">
			<td height="38" style="height:38px;width:247px;">Tetramethylrhodamine ethyl ester perchlorate</td>
			<td style="width:148px;">Sigma Aldrich</td>
			<td style="width:136px;">87917-25MG</td>
			<td>Reconstitute and Aliquot</td>
		</tr>
		<tr height="20">
			<td height="20" style="height:20px;width:247px;">MitoSox (Mito-Ros stain)</td>
			<td style="width:148px;">Life Technologies</td>
			<td style="width:136px;">m36008</td>
			<td>Reconstitute and Aliquot</td>
		</tr>
		<tr height="20">
			<td height="20" style="height:20px;width:247px;">PolyLysine</td>
			<td style="width:148px;">MP Biomedicals</td>
			<td style="width:136px;">ICN15017625</td>
			<td></td>
		</tr>
		<tr height="20">
			<td height="20" style="height:20px;width:247px;">Fly Vials</td>
			<td style="width:148px;">Fisher Scientific</td>
			<td style="width:136px;">AS-515</td>
			<td></td>
		</tr>
		<tr height="20">
			<td height="20" style="height:20px;width:247px;">Fly Conicals</td>
			<td style="width:148px;">Fisher Scientific</td>
			<td style="width:136px;">AS-355</td>
			<td></td>
		</tr>
		<tr height="20">
			<td height="20" style="height:20px;width:247px;">Fly Vial Flugs</td>
			<td style="width:148px;">Fisher Scientific</td>
			<td style="width:136px;">AS273</td>
			<td></td>
		</tr>
		<tr height="20">
			<td height="20" style="height:20px;width:247px;">Fly Conical Flugs</td>
			<td style="width:148px;">Fisher Scientific</td>
			<td style="width:136px;">AS 277</td>
			<td></td>
		</tr>
		<tr height="38">
			<td height="38" style="height:38px;width:247px;">Jazzmix Drosophila food (Drosophila food)</td>
			<td style="width:148px;">Fisher Scientific</td>
			<td style="width:136px;">AS153</td>
			<td></td>
		</tr>
		<tr height="20">
			<td height="20" style="height:20px;width:247px;">Bovine Serum Albumin</td>
			<td style="width:148px;">Sigma Aldrich</td>
			<td style="width:136px;">A9647-50G</td>
			<td></td>
		</tr>
		<tr height="20">
			<td height="20" style="height:20px;width:247px;">Cyclin E Antibody (d-300)</td>
			<td style="width:148px;">Santa Cruz</td>
			<td style="width:136px;">sc- 33748</td>
			<td></td>
		</tr>
		<tr height="38">
			<td height="38" style="height:38px;width:247px;">ATPB antibody [3D5] - Mitochondrial Marker</td>
			<td style="width:148px;">AbCam</td>
			<td style="width:136px;">ab14730</td>
			<td></td>
		</tr>
		<tr height="38">
			<td height="38" style="height:38px;width:247px;">Cy3 AffiniPure Goat Anti-Mouse IgG (H+L)</td>
			<td style="width:148px;">Jackson ImmunoResearch</td>
			<td style="width:136px;">115-165-146</td>
			<td></td>
		</tr>
		<tr height="44">
			<td height="44" style="height:44px;width:247px;">Cy5 AffiniPure Goat Anti-Rabbit IgG (H+L)</td>
			<td style="width:148px;">Jackson ImmunoResearch</td>
			<td style="width:136px;">111-175-144</td>
			<td></td>
		</tr>
		<tr height="29">
			<td height="29" style="height:29px;width:247px;">Hoechst</td>
			<td style="width:148px;">Fisher Scientific</td>
			<td style="width:136px;">H3570</td>
			<td></td>
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		<tr height="30">
			<td height="30" style="height:30px;width:247px;">VectaShield</td>
			<td style="width:148px;">Fisher Scientific</td>
			<td style="width:136px;">H100</td>
			<td></td>
		</tr>
		<tr height="38">
			<td height="38" style="height:38px;width:247px;">Azer Scientific EverMark Select Microscope Slides</td>
			<td style="width:148px;">Fisher Scientific</td>
			<td style="width:136px;">22-026-252</td>
			<td></td>
		</tr>
		<tr height="30">
			<td height="30" style="height:30px;width:247px;">Microscope Cover Glass</td>
			<td style="width:148px;">Fisher Scientific</td>
			<td style="width:136px;">12-542-B</td>
			<td></td>
		</tr>
		<tr height="30">
			<td height="30" style="height:30px;width:247px;">Name</td>
			<td style="width:148px;">Company</td>
			<td style="width:136px;">Catalog Number</td>
			<td>Comments</td>
		</tr>
		<tr height="38">
			<td height="38" style="height:38px;width:247px;">Mat Tek Corp&#160;Glass Bottom Mircrowell Dish</td>
			<td style="width:148px;">Fisher Scientific</td>
			<td style="width:136px;">P35G-0-14-C</td>
			<td></td>
		</tr>
		<tr height="20">
			<td height="20" style="height:20px;width:247px;">Active Dried Yeast</td>
			<td style="width:148px;">Fisher Scientific</td>
			<td style="width:136px;">ICN10140001</td>
			<td></td>
		</tr>
		<tr height="20">
			<td height="20" style="height:20px;width:247px;">Confocal Microscope</td>
			<td style="width:148px;">Carl Zeiss</td>
			<td style="width:136px;">LSM 700</td>
			<td></td>
		</tr>
		<tr height="47">
			<td height="47" style="height:47px;width:247px;">Dumont #5 Forceps</td>
			<td style="width:148px;">Fine Science Technologies</td>
			<td style="width:136px;">11251-20</td>
			<td></td>
		</tr>
		<tr height="51">
			<td height="51" style="height:51px;width:247px;">Moria Nickel Plated Pin Holder</td>
			<td style="width:148px;">Fine Science Technologies</td>
			<td style="width:136px;">26016-12</td>
			<td></td>
		</tr>
		<tr height="44">
			<td height="44" style="height:44px;width:247px;">Minutien Pins</td>
			<td style="width:148px;">Fine Science Technologies</td>
			<td style="width:136px;">26002-15</td>
			<td></td>
		</tr>
		<tr height="46">
			<td height="46" style="height:46px;width:247px;">MYFP ( w[*]; P{w[+mC]=sqh-EYFP-Mito}3 )</td>
			<td style="width:148px;">Bloomington Stock Center</td>
			<td style="width:136px;">7194</td>
			<td></td>
		</tr>
		<tr height="20">
			<td height="20" style="height:20px;width:247px;">Fly Pad</td>
			<td style="width:148px;">Fly stuff</td>
			<td style="width:136px;">59-118</td>
			<td></td>
		</tr>
		<tr height="20">
			<td height="20" style="height:20px;width:247px;">Blowgun</td>
			<td style="width:148px;">Fly stuff</td>
			<td style="width:136px;">54-104</td>
			<td></td>
		</tr>
		<tr height="20">
			<td height="20" style="height:20px;width:247px;">Blowgun needle</td>
			<td style="width:148px;">Flystuff</td>
			<td style="width:136px;">54-119</td>
			<td></td>
		</tr>
		<tr height="20">
			<td height="20" style="height:20px;width:247px;">Dissecting Microscope</td>
			<td style="width:148px;">Carl Zeiss</td>
			<td style="width:136px;">Stemi 2000</td>
			<td></td>
		</tr>
		<tr height="20">
			<td height="20" style="height:20px;width:247px;">Analyses software</td>
			<td style="width:148px;">Carl Zeiss</td>
			<td style="width:136px;">Zen&#160;</td>
			<td></td>
		</tr>
		<tr height="20">
			<td height="20" style="height:20px;width:247px;">Analyses software</td>
			<td style="width:148px;">Open source</td>
			<td style="width:136px;">Image J</td>
			<td></td>
		</tr>
		<tr height="20">
			<td height="20" style="height:20px;width:247px;">Research Macro Zoom Microscope</td>
			<td style="width:148px;">Olympus</td>
			<td style="width:136px;">MVX10</td>
			<td></td>
		</tr>
		<tr height="39">
			<td height="39" style="height:39px;width:247px;">QICAM Fast 1394 Cooled Digital Camera, 12-bit, Mono&#160;</td>
			<td style="width:148px;">QImaging</td>
			<td style="width:136px;">QIC-F-M-12-C</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:247px;">QCapture Pro 5.1</td>
			<td style="width:148px;">QImaging</td>
			<td style="width:136px;"></td>
			<td></td>
		</tr>
	</tbody>
</table>

studying mitochondrial structure and function in drosophila ovaries

Analysis of the mitochondrial structure-function relationship is required for a thorough understanding of the regulatory mechanisms of mitochondrial functionality. Fluorescence microscopy is an indispensable tool for the direct assessment of mitochondrial structure and function in live cells and for studying the mitochondrial structure-function relationship, which is primarily modulated by the molecules governing fission and fusion events between mitochondria. This paper describes and demonstrates specific methods for studying mitochondrial structure and function in live as well as in fixed tissue in the model organism Drosophila melanogaster. The tissue of choice here is the Drosophila ovary, which can be isolated and made amenable for ex vivo live confocal microscopy. Furthermore, the paper describes how to genetically manipulate the mitochondrial fission protein, Drp1, in Drosophila ovaries to study the involvement of Drp1-driven mitochondrial fission in modulating the mitochondrial structure-function relationship. The broad use of such methods is demonstrated in already-published as well as in novel data. The described methods can be further extended towards understanding the direct impact of nutrients and/or growth factors on the mitochondrial properties ex vivo. Given that mitochondrial dysregulation underlies the etiology of various diseases, the described innovative methods developed in a genetically tractable model organism, Drosophila, are anticipated to contribute significantly to the understanding of the mechanistic details of the mitochondrial structure-function relationship and to the development of mitochondria-directed therapeutic strategies.

The described methods can be used to study mitochondrial structure and function in live and fixed Drosophila ovaries (Figure 2B). Provided are some examples of anticipated results obtained with the described methods.
Dissection of the Drosophila ovary: When dissected further, the severed abdomens (Figure 3B) from the whole Drosophila (Figure 3A)...

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Studying Mitochondrial Structure and Function in Drosophila Ovaries

Analysis of the mitochondrial structure-function relationship is required for a thorough understanding of the regulatory mechanisms of mitochondrial functionality. Specific methods for studying mitochondrial structure and function in live and fixed Drosophila ovaries are described and demonstrated in this paper.

Studying Mitochondrial Structure and Function in Drosophila Ovaries

Analysis of the mitochondrial structure-function relationship is required for a thorough understanding of the regulatory mechanisms of mitochondrial ...

The overall goal of this procedure, is to demonstrate methods for studying mitochondrial structure and function in live as well as in fixed tissue in the model organism drosophila melanogaster. This method can help answer key questions in the field of Mitochondrial Biology. Such as the regulatory mechanisms of mitochondrial function.The main advantage of this technique is that it performs detailed analysis of the mitochondrial structure/function relationship. After sorting out five anesthetized female flies according to the text protocol, under the dissection microscope, use two pairs of forceps to sever the thorax from the abdomen. Then, carefully transfer the abdomens to the second well of the dish.Using one pair of forceps to hold the abdomen at the posterior end, use the other pair of forceps to slowly push the ovaries out. Then use the forceps to hold an individual ovary by the opaque posterior end and carefully move it to the third well of the dish for teasing or fixing. Carefully tease the protective sheath from around the ovaries, by using a pair of forceps to hold the posterior end and lightly sweeping a teasing needle from the posterior to the anterior end.To prepare polylysene coated chambers, place two separated 20 microliter drops of polylysene on the cover glass of a glass-bottom petri dish. Air dry the plates at 37 degrees celsius for one hour, and outline the polylysine on the underside of the plate. Set the scanning parameters on the confocal microscope by opening the image acquisition software, and in the acquisition tab, set the appropriate scanning parameters.Check the time series, bleaching and regions boxes to open the individual tabs. Then, enter the appropriate acquisition parameter values into each tab. Next, place one dissected and teased ovary onto a marked polylysine coated region and use a teasing needle to spread the ovary and separate the ovarials.Place a 10 micro liter drop of insect dissecting medium on top of the ovary, making sure to cover the entire polylysine coated area. Then, cover the petri dish. Immediately after mounting the ovary, place the sample on the microscope stage and use the eye piece to quickly locate the field of interest in the live tissue.Click live to acquire a live image of the selected field of interest, then click stop to stop live scanning. If necessary, adjust the acquisition parameters so that the detected fluorescent signal is below the saturation levels with the defined background as set by adjusting the offset values. From the graphic tab, use the bezier drawing tool to draw a small ROI to demarcate the photo bleaching zone on the image acquired by scanning.Then perform image acquisition, by clicking on start experiment. To carry out live-staining with fluorescent mitochondrial dyes, dilute the stock of stains in warm dissecting medium to final working concentrations. After dissection and teasing is demonstrated earlier, place the ovaries into 200 microliters of staining solution in a well of a dissection dish.Cover the dish with aluminum foil wrapped box to protect it from light and incubate the tissue for 10 minutes. Next, wash the stained ovaries by using forceps to move them carefully into three consecutive wells containing medium without stain. For co-staining with TMRE, in the compatible overall mitrochondrial stain, carry-out staining with TMRE first, then without washing the tissue, immediately transfer the sample into the overall mitochondrial stain.After washing and mounting the ovaries as demonstrated earlier in this video, to carry out confocal imaging on the sample, check the z-sectioning box to open the tab. Turn the focus wheel towards the bottom of the sample while it is being live-scanned and click on set-first to define the bottom-most z-section. Then move the focus wheel in the opposite direction to define the top-most section.Perform image acquisition by clicking on start experiment. In the case of live xvivamicroscopy, the data should be obtained within 15 minutes of tissue mounting, otherwise, the experimental results may be affected by alterations of physiology due to insuing death of the tissue. Immediately after dissection under a fume hood place ovaries into 200 microliters of fresh room temperature PFA in the well of a glass dissecting dish.Incubate the tissue for 15 minutes to fix it. After washing the ovaries in PBS according to the text protocol, while still in PBS, tease the ovaries to carefully remove the protective fiber sheath that may hinder antigen access from the antibody. Permeabilize the teased ovaries by placing them in a microfuse tube with 500 microliters of 0.5 percent tritan x 100 in PBS.Next, place the tube in a covered box and set to rock at 25 RPM's for 30 minutes. Remove the PBS/TX according to the text protocol block the tissue by adding 200 microliters of BSA dissolved in 0.5 percent PBS/TX. Incubate the samples on the rocker at room temperature for one hour.After removing the blocking solution, add anti-rabid desycline E and anti-mouse ATPB antibodies. Incubate the tissue on the rocker at room temperature for two hours. Following the incubation, use PBS-TX to wash the ovaries three times for 15 minutes each.Then, add 200 microliters of the appropriate secondary antibodies and fresh PBS-TX and incubate at room temperature for one hour. After washing the tissue two times, add hooks to the third wash. Then with a one milliliter micropipet, remove the immuno-stained ovaries from the microfuse tube into a fresh well of a glass dissecting dish containing 200 microliters of PBS.Add one drop of glycerol based mounting medium to a glass slide and add the immuno-stained ovaries one-by-one to the mounting medium. Under a dissection microscope, while holding the opaque portion of the ovary with forceps, use a teasing needle to gently pluck the transparent ovarials from the opaque mature egg chambers. Then, remove the mature egg chambers from the mounting medium.Place a cover glass on the slide and lightly press to ensure the mounting medium spreads uniformly. Air dry the samples for 15 minutes before using nail polish to seal the edges. Finally, perform confocal microscopy as needed.As shown here, flip targeted to one of the mitochondrial clouds associated with the nerse cells leads to greater than 50 percent loss of the fluorescent signal from the blue and white ROI's surrounding the red flip ROI within 200 seconds while the yellow control ROI's minimally bleached. The drosophilla ovaries exhibited a decrease in signal with a depth of tissue, and it is important to discern the maximal depth of tissue within which the phlorophores such as TMRE and mitostain, can be detected during live imaging. A qualitative analysis from co-staining with TMRE and the overall mitochondrial stain, shows that the drisophilla germarium exhibits higher mitochondrial potential per unit mass in stage 2B.In this figure, semi-qualitative analysis demonstrates the difference in mitochondrial potential per unit mass between AFC's and the MBC's as analyzed from a stage 9 egg chamber. These images reveal that mitosox uptake occurs in the mitotic and post-mitotic drisophilla follicle cells. In this experiment, co-immuno staining identifies elevated decycline signal overlapping with the mitochondrial ATPB signal and the GFP negative DRP1 nole clones in the Germarium and in a stage 9 egg chamber.The described methods can be modified and employed to study mitochondrial structure function in other drisophilla tissues. After watching this video, you should have a good understanding of how to dissect, stain and image fixed and live drisophilla ovaries to study mitochonrial structure and function.

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23.8K Görüntüleme.  University of Alabama at Birmingham. The overall goal of this procedure, is to demonstrate methods for studying mitochondrial structure and function in live as well as in fixed tissue in the model organism drosophila melanogaster. This method can help answer key questions in the field of Mitochondrial Biology. Such as the regulatory mechanisms of mitochondrial function.The main advantage of this technique is that it performs detailed analysis of the mitochondrial structure/function relationship. After sorting out five ane...