1. הסר ביצים אינקובטור <ol style=";text-align:right;direction:rtl"><li style=";text-align:right;direction:rtl"> שמור על 37 ° C עם לחות יחסית להגדיר מעל 60%. </li><li style=";text-align:right;direction:rtl"> הסר את הביצים; להפוך ביצים 90 ° כך בסיס גדול טמון אופקי. </li></ol> 2. ביצים ספוגית לעקר <ol style=";text-align:right;direction:rtl"><li style=";text-align:right;direction:rtl"> להרוות ערימה של גזה לא סטרילי עם אתנול 70%. </li><li style=";text-align:right;direction:rtl"> השתמש 2-3 חתיכות ספוגית עד 5 ביצים. בטל כאשר גזה הוא מלוכלך. </li></ol> 3. הכנת הסרת חלבון האתר <ol style=";text-align:right;direction:rtl"><li style=";text-align:right;direction:rtl"> גזור מקום 1 &quot;x 1&quot; נייר דבק פלסטי 3M שמאל רק בסיס כדי להגן על האזור שבו אלבומין יצויר החוצה. </li></ol> 4. הסרת חלבון <ol style=";text-align:right;direction:rtl"><li style=";text-align:right;direction:rtl"> השתמש נקודת זוג מספריים לעשות חור קטן באמצע הקלטת. </li><li style=";text-align:right;direction:rtl"> בעזרת מזרק 10 סמ&quot;ק עם מד 18, 1-inch מחט, לאט לקדוח את המחט דרך החור שנעשו על ידי המספריים. </li><li style=";text-align:right;direction:rtl"> כונן את המחט כלפי מטה בזווית של 45 מעלות צלזיוס כלפי התחתון של הביצה. </li><li style=";text-align:right;direction:rtl"> הטה את המחט לכיוון מרכז ותנסחו 3-4 מ&quot;ל של חלבון. </li></ol> 5. Windowing <ol style=";text-align:right;direction:rtl"><li style=";text-align:right;direction:rtl"> גזור 3 &quot;x 3&quot; חתיכת סרט פלסטיק למתוח אותו כך שיתאים על החלק העליון של הביצה. הרחב את פינות הריבוע סביב קצוות מעוגלים של המשטח האופקי של הביצים, נזהרים שלא למשוך יותר מדי קשה. משוך את הסרט כך שהוא צמוד פני השטח של ביצים עם קפלים לא. </li><li style=";text-align:right;direction:rtl"> באמצעות זוג חד ישר 4 &quot;מספריים לנתיחה, טוויסט חור במרכז החלק התחתון של האזור שבו קלטת הוצב. לאט מדריך את הלהב התחתון של המספריים לתוך הביצה להיות בטוח כדי לשמור על עצות אל מול פנים את הקליפה. ישיר את הלהב לעבר בסיס ולאט לאט מתחילים לחתוך את הקליפה. המשך בצורה נגד כיוון השעון, לעצור רק לפני שהגיע למרכז הדף. הסר את המספריים וחזור הולך בכיוון ההפוך עד קצת קטן בלבד של ביצה נשאר מחובר. בדוק כדי לוודא את הביצית מופרית. תסגור את החלון. </li></ol> 6. סגירה, פתיחה מחדש ואיטום הביצה. <ol style=";text-align:right;direction:rtl"><li style=";text-align:right;direction:rtl"> חותכים כ 2-3 &quot;ארוך על ידי 1 / 2&quot; סרט פלסטי רחב סגר את החלון, כך שהוא מתאים בחזרה לתוך החור הזה נחתך. קחו עוד 1 x 1 &quot;חתיכת קלטת את החור שממנו ביצה היה סחוט. השתמש זוג מלקחיים לפתוח מחדש את הביצה לעשות את כל המניפולציות. כאשר אתה מוכן להחזיר את ביצי אל האינקובטור, לחתוך חתיכה של סרט כי הוא גדול מספיק כדי לאטום את החלון לכסות את המשטח האופקי שלם של הביצה. </li></ol>

<ol>
	<li>Cramer, K. S., Fraser, S. E., Rubel, E. W. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=.">.</a> Dev Biol. 224, 138-151 (2000).</li><li>Cramer, K. S., Bermingham-McDonogh, O., Krull, C. E., Rubel, E. W. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=.">.</a> Dev Biol. 269, 26-35 (2004).</li><li>Cramer, K. S., Cerretti, D. P., Siddiqui, S. A. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=.">.</a> Dev Biol. 295, 76-89 (2006).</li><li>Huffman, K. J., Cramer, K. S. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=.">.</a> Dev Neurobiol. 67, 1655-1668 (2007).</li><li>Krull, C. E. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=.">.</a> Dev Dyn. 229, 433-439 (2004).</li><li>Gerlach-Bank, L. M., Cleveland, A. R., Barald, K. F. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=.">.</a> Dev Dyn. 229, 219-230 (2004).</li></ol>

שיטה זו מאפשרת פעמים הישרדות ארוכה בעקבות מניפולציות ניסיוני. לדוגמה, צבען תיוג מחקרים מותר הישרדות E10 או במאוחר במחקר גורל מיפוי (1). בנוסף, הוא שימש במשך במחקרים electroporation אובו המספקים שינוי של רמות ביטוי הגנים והפיתוח הנדרשים כדי להמשיך בשלבי ההתפתחות מאוחר יותר (2-6). טכניקה זו ח?...

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		<th>Catalogue Number</th>
		<th>Comment</th>
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<tr>
<td>Rotating incubator</td>
<td>&nbsp;</td>
<td>Profi</td>
<td>&nbsp;</td>
<td>Maintain at 37&#176; Degrees with relative humidity set above 60%</td>
</tr>
<tr>
<td>70 % EtOH</td>
<td>&nbsp;</td>
<td>&nbsp;</td>
<td>&nbsp;</td>
<td>&nbsp;</td>
<tr>
<td>gauze</td>
<td>&nbsp;</td>
<td>&nbsp;</td>
<td>&nbsp;</td>
<td>&nbsp;</td>
<tr>
<td>3M plastic tape</td>
<td>&nbsp;</td>
<td>&nbsp;</td>
<td>&nbsp;</td>
<td>&nbsp;</td>
<tr>
<td>10cc syringe</td>
<td>&nbsp;</td>
<td>&nbsp;</td>
<td>&nbsp;</td>
<td>1/egg
</td>
</tr>
<tr>
<td>18G needles</td>
<td>&nbsp;</td>
<td>&nbsp;</td>
<td>&nbsp;</td>
<td>1&#189; inch needle, 1/syringe</td>
</tr>
<tr>
<td>Dissection scissors</td>
<td>&nbsp;</td>
<td>&nbsp;</td>
<td>&nbsp;</td>
<td>4" sharp straight blades</td>
</tr>
<tr>
<td>Fertilized Eggs</td>
<td>&nbsp;</td>
<td>&nbsp;</td>
<td>&nbsp;</td>
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windowing chicken eggs for developmental studies

המחקר של פיתוח כבר סייעו במידה רבה על ידי שימוש בעובר האפרוח כמודל ניסיוני. קלות הנגישות של העובר אפשרה לניסויים למפות גורלות התא באמצעות גישות שונות, כולל חומוס שליו מפלצות וסימון צבע מוקד. בנוסף, היא מאפשרת הפרעות המולקולרי של מספר סוגים, כולל המיקום של חלבון מצופה חרוזים המבוא של ה-DNA פלסמיד משתמש electroporation אובו. ניסויים אלה הניבו מידע חשוב על התפתחות מערכת העצבים המרכזית ואת הפריפריה. עבור רבים של מחקרים אלה, יש צורך לפתוח את קליפת הביצה ואת reclose זה מביך ללא צמיחה של העובר. העובר ניתן לבדוק בכל שלבי ההתפתחות רצופים על ידי פתיחה מחדש את קליפת הביצה. אמנם יש כמה שיטות מצוין לפתיחת ביצי תרנגולת, במאמר זה אנו להדגים שיטה אחת, כי כבר מותאם במיוחד פעמים הישרדות ארוכה. בשיטה זו, הביצה מוטלת על צדו חלון קטן הוא חתך במעטפת. לאחר הליך הניסוי, הקליפה משמשת כדי לכסות את הביצה למשך הפיתוח שלה. סרט הפלסטיק השקוף שכיסה את קליפת הביצה מגנה על העובר ומסייעת לשמור על הלחות במהלך יתרת תקופת הדגירה. שיטה זו הייתה בשימוש החל שני ימי דגירה ו אפשרה הישרדות לדורותיה עובריים בוגרת.

Watch this Scientific Journal Video about Windowing Chicken Eggs for Developmental Studies at JoVE.com

וירוסים | סרטון אוסף ביולוגיה

Windowing Chicken Eggs for Developmental Studies

קלות הנגישות של העובר אפשרה לניסויים למפות גורלות התא באמצעות גישות שונות, כולל חומוס שליו מפלצות וסימון צבע מוקד. במאמר זה אנו מדגים אחד הכנת ביצה שיטה כי כבר מותאם במיוחד פעמים הישרדות ארוכה.

עוף Windowing ביצים למחקרים התפתחותיים

The study of development has been greatly aided by the use of the chick embryo as an experimental model.  The ease of accessibility of the embryo has ...

windowing-chicken-eggs-for-developmental-studies

Research

JoVE Journal

Biology

27.7K Views.  University of California, Irvine (UCI). קלות הנגישות של העובר אפשרה לניסויים למפות גורלות התא באמצעות גישות שונות, כולל חומוס שליו מפלצות וסימון צבע מוקד. במאמר זה אנו מדגים אחד הכנת ביצה שיטה כי כבר מותאם במיוחד פעמים הישרדות ארוכה.

Video: Windowing Chicken Eggs for Developmental Studies

Obtaining Eggs from Xenopus laevis Females

The eggs of Xenopus laevis intact, lysed, and/or fractionated are useful for a wide variety of experiments. This protocol shows how to induce egg laying, collect and dejelly the eggs, and sort the eggs to remove any damaged eggs.

The eggs of Xenopus laevis intact, lysed, and/or fractionated are useful for a wide variety of experiments. This protocol shows how to induce egg laying, collect and dejelly the eggs, and sort the eggs to remove any damaged eggs.

קבלת ביצים Xenopus laevis נקבות

The eggs of Xenopus laevis intact, lysed, and/or fractionated are useful for a wide variety of experiments. This protocol shows how to induce egg laying, ...

Xenotransplantation of Human Stem Cells into the Chicken Embryo

The chicken embryo is a classical animal model for studying normal embryonic and fetal development and for xenotransplantation experiments to study the behavior of cells in a standardized in vivo environment. The main advantages of the chicken embryo include low cost, high accessibility, ease of surgical manipulation and lack of a fully developed immune system. Xenotransplantation into chicken embryos can provide valuable information about cell proliferation, differentiation and behavior, the responses of cells to signals in defined embryonic tissue niches, and tumorigenic potential. Transplanting cells into chicken embryos can also be a step towards transplantation experiments in other animal models. Recently the chicken embryo has been used to evaluate the neurogenic potential of human stem and progenitor cells following implantation into neural anlage1-6. In this video we document the entire procedure for transplanting human stem cells into the developing central nervous system of the chicken embryo. The procedure starts with incubation of fertilized eggs until embryos of the desired age have developed. The eggshell is then opened, and the embryo contrasted by injecting dye between the embryo and the yolk. Small lesions are made in the neural tube using microsurgery, creating a regenerative site for cell deposition that promotes subsequent integration into the host tissue. We demonstrate injections of human stem cells into such lesions made in the part of the neural tube that forms the hindbrain and the spinal cord, and into the lumen of the part of the neural tube that forms the brain. Systemic injections into extraembryonic veins and arteries are also demonstrated as an alternative way to deliver cells to vascularized tissues including the central nervous system. Finally we show how to remove the embryo from the egg after several days of further development and how to dissect the spinal cord free for subsequent physiological, histological or biochemical analyses.

In this paper we present a method for transplanting human stem cells into various regions of the central nervous system of the chicken embryo. This provides an in vivo model for assessing the proliferation and differentiation of various types of human stem cells in embryonic tissue environments.

Xenotransplantation בתאי גזע אנושיים לתוך העובר עוף

The chicken embryo is a classical animal model for studying normal embryonic and fetal development and for xenotransplantation experiments to study the ...

Mutagenesis and Functional Analysis of Ion Channels Heterologously Expressed in Mammalian Cells

We will demonstrate how to study the functional effects of introducing a point mutation in an ion channel. We study G protein-gated inwardly rectifying potassium (referred to as GIRK) channels, which are important for regulating the excitability of neurons. There are four different mammalian GIRK channel subunits (GIRK1-GIRK4) - we focus on GIRK2 because it forms a homotetramer. Stimulation of different types of G protein-coupled receptors (GPCRs), such as the muscarinic receptor (M2R), leads to activation of GIRK channels. Alcohol also directly activates GIRK channels. We will show how to mutate one amino acid by specifically changing one or more nucleotides in the cDNA for the GIRK channel. This mutated cDNA sequence will be amplified in bacteria, purified, and the presence of the point mutation will be confirmed by DNA sequencing. The cDNAs for the mutated and wild-type GIRK channels will be transfected into human embryonic kidney HEK293T cells cultured in vitro. Lastly, whole-cell patch-clamp electrophysiology will be used to study the macroscopic potassium currents through the ectopically expressed wild-type or mutated GIRK channels. In this experiment, we will examine the effect of a L257W mutation in GIRK2 channels on M2R-dependent and alcohol-dependent activation.

We will demonstrate how to study the effect of a single point mutation on the function of an ion channel.

Mutagenesis וניתוח פונקציונלי של תעלות יונים הביעו Heterologously בתאי יונקים

We will demonstrate how to study the functional effects of introducing a point mutation in an ion channel. We study G protein-gated inwardly rectifying ...

Gene Transfer into Older Chicken Embryos by ex ovo Electroporation

The chicken embryo provides an excellent model system for studying gene function and regulation during embryonic development. In ovo electroporation is a powerful method to over-express exogenous genes or down-regulate endogenous genes in vivo in chicken embryos1. Different structures such as DNA plasmids encoding genes2-4, small interfering RNA (siRNA) plasmids5, small synthetic RNA oligos6, and morpholino antisense oligonucleotides7 can be easily transfected into chicken embryos by electroporation. However, the application of in ovo electroporation is limited to embryos at early incubation stages (younger than stage HH20 - according to Hamburg and Hamilton)8 and there are some disadvantages for its application in embryos at later stages (older than stage HH22 - approximately 3.5 days of development). For example, the vitelline membrane at later stages is usually stuck to the shall membrane and opening a window in the shell causes rupture of the vessels, resulting in death of the embryos; older embryos are covered by vitelline and allantoic vessels, where it is difficult to access and manipulate the embryos; older embryos move vigorously and is difficult to control the orientation through a relatively small window in the shell.
In this protocol we demonstrate an ex ovo electroporation method for gene transfer into chicken embryos at late stages (older than stage HH22). For ex ovo electroporation, embryos are cultured in Petri dishes9 and the vitelline and allantoic vessels are widely spread. Under these conditions, the older chicken embryos are easily accessed and manipulated. Therefore, this method overcomes the disadvantages of in ovo electroporation applied to the older chicken embryos. Using this method, plasmids can be easily transfected into different parts of the older chicken embryos10-12.

Gene Transfer into Older Chicken Embryos by ex ovo Electroporation

A method of gene transfer into chicken embryos at later incubation stages (older than Hamburger and Hamilton stage (HH) 22) is described. This method overcomes disadvantages of in ovo electroporation applied to older chicken embryos and is a useful technique to study gene function and regulation at older developmental stages.

ין העברת לעוברי עוף מבוגרים יותר על ידי<em&gt; לג&#39;ימי לשעבר</em&gt; Electroporation

The chicken embryo provides an  excellent model system for studying gene function and regulation during  embryonic development. In ovo electroporation is ...

Separation of Spermatogenic Cell Types Using STA-PUT Velocity Sedimentation

Mammalian spermatogenesis is a complex differentiation process that occurs in several stages in the seminiferous tubules of the testes. Currently, there is no reliable cell culture system allowing for spermatogenic differentiation in vitro, and most biological studies of spermatogenic cells require tissue harvest from animal models like the mouse and rat. Because the testis contains numerous cell types - both non-spermatogenic (Leydig, Sertoli, myeloid, and epithelial cells) and spermatogenic (spermatogonia, spermatocytes, round spermatids, condensing spermatids and spermatozoa) - studies of the biological mechanisms involved in spermatogenesis require the isolation and enrichment of these different cell types. The STA-PUT method allows for the separation of a heterogeneous population of cells - in this case, from the testes - through a linear BSA gradient. Individual cell types sediment with different sedimentation velocity according to cell size, and fractions enriched for different cell types can be collected and utilized in further analyses. While the STA-PUT method does not result in highly pure fractions of cell types, e.g. as can be obtained with certain cell sorting methods, it does provide a much higher yield of total cells in each fraction (~1 x 108 cells/spermatogenic cell type from a starting population of 7-8 x 108 cells). This high yield method requires only specialized glassware and can be performed in any cold room or large refrigerator, making it an ideal method for labs that have limited access to specialized equipment like a fluorescence activated cell sorter (FACS) or elutriator.

The STA-PUT method allows for the separation of different populations of spermatogenic cells based on size and density.

הפרדה של סוגי תאי Spermatogenic שימוש בשקיעה מהירות STA-PUT

Mammalian spermatogenesis is a complex  differentiation process that occurs in several stages in the seminiferous  tubules of the testes. Currently, there ...

A Guide to Modern Quantitative Fluorescent Western Blotting with Troubleshooting Strategies

The late 1970s saw the first publicly reported use of the western blot, a technique for assessing the presence and relative abundance of specific proteins within complex biological samples. Since then, western blotting methodology has become a common component of the molecular biologists experimental repertoire. A cursory search of PubMed using the term &#8220;western blot&#8221; suggests that in excess of two hundred and twenty thousand published manuscripts have made use of this technique by the year 2014. Importantly, the last ten years have seen technical imaging advances coupled with the development of sensitive fluorescent labels which have improved sensitivity and yielded even greater ranges of linear detection. The result is a now truly Quantifiable Fluorescence based Western Blot (QFWB) that allows biologists to carry out comparative expression analysis with greater sensitivity and accuracy than ever before. Many &#8220;optimized&#8221; western blotting methodologies exist and are utilized in different laboratories. These often prove difficult to implement due to the requirement of subtle but undocumented procedural amendments. This protocol provides a comprehensive description of an established and robust QFWB method, complete with troubleshooting strategies.

The advancement of western blotting using fluorescence has allowed detection of subtle changes in protein expression enabling quantitative analyses. Here we describe a robust methodology for detection of a range of proteins across a variety of species and tissue types. A strategy to overcome common technical problems is also provided.

מדריך למודרני כמותי פלורסנט המערבי סופג עם אסטרטגיות לפתרון בעיות

The late 1970s saw the first publicly reported use of the western blot, a technique for assessing the presence and relative abundance of specific proteins ...

Tracking and Quantifying Developmental Processes in C. elegans Using Open-source Tools

Quantitatively capturing developmental processes is crucial to derive mechanistic models and key to identify and describe mutant phenotypes. Here protocols are presented for preparing embryos and adult C. elegans animals for short- and long-term time-lapse microscopy and methods for tracking and quantification of developmental processes. The methods presented are all based on C. elegans strains available from the Caenorhabditis Genetics Center and on open-source software that can be easily implemented in any laboratory independently of the microscopy system used. A reconstruction of a 3D cell-shape model using the modelling software IMOD, manual tracking of fluorescently-labeled subcellular structures using the multi-purpose image analysis program Endrov, and an analysis of cortical contractile flow using PIVlab (Time-Resolved Digital Particle Image Velocimetry Tool for MATLAB) are shown. It is discussed how these methods can also be deployed to quantitatively capture other developmental processes in different models, e.g., cell tracking and lineage tracing, tracking of vesicle flow.

Tracking and Quantifying Developmental Processes in C. elegans Using Open-source Tools

Here it is shown how to track and quantify developmental processes in C. elegans. The methods presented are based on open-source tools that can be easily implemented. It is demonstrated how to reconstruct 3D cell-shape models, how to manually track subcellular structures, and how to analyze cortical contractile flow.

מעקב וכימות תהליכים התפתחותיים ב<em&gt; C. elegans</em&gt; שימוש בכלי קוד פתוח

Quantitatively capturing developmental processes is crucial to derive mechanistic models and key to identify and describe mutant phenotypes. Here ...

Laser-assisted Lentiviral Gene Delivery to Mouse Fertilized Eggs

Lentiviruses are efficient vectors for gene delivery to mammalian cells. Following transduction, the lentiviral genome is stably incorporated into the host chromosome and is passed on to progeny. Thus, they are ideal vectors for creation of stable cell lines, in vivo delivery of indicators, and transduction of single cell fertilized eggs to create transgenic animals. However, mouse fertilized eggs and early stage embryos are protected by the zona pellucida, a glycoprotein matrix that forms a barrier against lentiviral gene delivery. Lentiviruses are too large to penetrate the zona and are typically delivered by microinjection of viral particles into the perivitelline cavity, the space between the zona and the embryonic cells. The requirement for highly skilled technologists and specialized equipment has minimized the use of lentiviruses for gene delivery to mouse embryos. This article describes a protocol for permeabilizing the mouse fertilized eggs by perforating the zona with a laser. Laser-perforation does not result in any damage to embryos and allows lentiviruses to gain access to embryonic cells for gene delivery. Transduced embryos can develop into blastocyst in vitro, and if implanted in pseudopregnant mice, develop into transgenic pups. The laser used in this protocol is effective and easy to use. Genes delivered by lentiviruses stably incorporate into mouse embryonic cells and are germline transmittable. This is an alternative method for creation of transgenic mice that requires no micromanipulation and microinjection of fertilized eggs.

Mouse fertilized eggs and early stage embryos are protected by the zona pellucida, a glycoprotein matrix that forms a barrier against gene delivery. This article describes a protocol for perforating the zona with a laser to transduce embryonic cells with lentiviral vectors and to create transgenic mice.

המסירה הגן Lentiviral לייזר בסיוע העכבר מופרית ביצים

Lentiviruses are efficient vectors for gene delivery to mammalian cells. Following transduction, the lentiviral genome is stably incorporated into the ...

Measuring Photophysiology of Attached Stage of Colacium sp. by a Cuvette-Type Fast Repetition Rate Fluorometer

Fast repetition rate fluorometer (FRRf) is a beneficial method for measuring photosystem II (PSII) photophysiology and primary productivity. Although FRRf can measure PSII absorption cross-section (&#963;PSII), maximum photochemical efficiency (Fv/Fm), effective photochemical efficiency (Fq&#8242;/Fm&#8242;), and non-photochemical quenching (NPQNSV) for various eukaryotic algae and cyanobacteria, almost all FRRf studies to date have focused on phytoplankton. Here, the protocol describes how to measure PSII photophysiology of an epizoic alga Colacium sp.&#160;Ehrenberg 1834 (Euglenophyta), in its attached stage (attached to zooplankton), using cuvette-type FRRf. First, we estimated the effects of substrate zooplankton (Scapholeberis mucronata O.F. M&#252;ller 1776, Cladocera, Daphniidae) on baseline fluorescence and &#963;PSII, Fv/Fm, Fq&#8242;/Fm&#8242;, and NPQNSV of planktonic Colacium sp. To validate this methodology, we recorded photophysiology measurements of attached Colacium sp. on S. mucronata and compared these results with its planktonic stage. Representative results showed how the protocol could determine the effects of calcium (Ca) and manganese (Mn) on Colacium sp. photophysiology and identify the various effects of Mn enrichment between attached and planktonic stages. Finally, we discuss the adaptability of this protocol to other periphytic algae.

Measuring Photophysiology of Attached Stage of Colacium sp. by a Cuvette-Type Fast Repetition Rate Fluorometer

Fast repetition rate fluorometer (FRRf) is a beneficial method for measuring photosystem II photophysiology and primary productivity. Here we describe a protocol to measure PSII photophysiology of epizoic alga, Colacium sp. on substrate zooplankton using cuvette-type FRRf.

מדידת פוטופיזיולוגיה של השלב המצורף של קולאקיום sp. על ידי פלואורומטר קצב חזרה מהירה מסוג Cuvette

Fast repetition rate fluorometer (FRRf) is a beneficial method for measuring photosystem II (PSII) photophysiology and primary productivity. Although FRRf ...

חקר ביטוי חלבונים במהלך התפתחות עדשת עוף

Microinjection of Recombinant RCAS(A) Retrovirus into Embryonic Chicken Lens

Embryonic chicken (Gallus domesticus) is a well-established animal model for the study of lens development and physiology, given its high degree of similarity with the human lens. RCAS(A) is a replication-competent chicken retrovirus that infects dividing cells, which serves as a powerful tool to study the in situ expression and function of wild-type and mutant proteins during lens development by microinjection into the empty lumen of lens vesicle at early developmental stages, restricting its action to surrounding proliferating lens cells. Compared to other approaches, such as transgenic models and ex vivo cultures, the use of an RCAS(A) replication-competent avian retrovirus provides a highly effective, rapid, and customizable system to express exogenous proteins in chick embryos. Specifically, targeted gene transfer can be confined to proliferative lens fiber cells without the need for tissue-specific promoters. In this article, we will briefly overview the steps needed for recombinant retrovirus RCAS(A) preparation, provide a detailed, comprehensive overview of the microinjection procedure, and provide sample results of the technique.

מחבר זרקור: חקירת התפתחות ותפקוד עדשה באמצעות מיקרו-הזרקה של רטרו-וירוס RCAS(A) בעדשת עוף עוברית 

This protocol paper describes the methodology of embryonic chicken lens microinjection of an RCAS(A) retrovirus as a tool for studying in situ function and expression of proteins during lens development.

מיקרו-הזרקה של רטרו-וירוס רקומביננטי RCAS(A) לעדשת עוף עוברית

Embryonic chicken (Gallus domesticus) is a well-established animal model for the study of lens development and physiology, given its high degree of ...