دعمت بدء الأموال إلى A. ديكنسون من جامعة فرجينيا كومنولث في هذا العمل. الكتاب نود أن نعترف دان Nacu لموهبته الفنية في خلق الشكل التخطيطي.

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الكتاب ليس لديهم ما يكشف.

أصبح القيطم المورق أداة مفيدة لتشريح آليات تطوير الوجهية التنموية الأساسية. ومع ذلك، هناك حاليا أي بروتوكولات واصفا حجم وشكل التغييرات في هذه المنطقة في الضفادع. فإن الطريقة الموصوفة هنا تسهم إسهاما كبيرا في مجال التنمية الوجهية عن طريق السماح للالكمي أكثر صرا...

من بين الأنواع الأكثر انتشارا وتدميرا من العيوب الخلقية الإنسان هي تلك التي تؤثر على الفم والوجه، مثل الشقوق الوجهية 1. الأطفال الذين يعانون من الهياكل الوجهية تالف الخضوع لعمليات جراحية متعددة طوال حياتهم والنضال مع تشوهات الوجه، والكلام والسمع ومشاكل تناول الطعام. وبالتالي، تسهيل البحوث العلمية الجديدة في تطوير والقحف الوجهية أمر بالغ الأهمية للوقاية والعلاج من هذه الأنواع من العيوب الخلقية في الإنسان. وقد برز القيطم المورق كأداة جديدة لتشريح الآليات التي تحكم تطوير القحفي (تشمل بعض الأمثلة 2،3،4 -11). وبالتالي، يمكن لطريقة الكمي لتحليل حجم وشكل التغييرات خلال تنمية الرأس والوجه من هذا النوع أن تكون قوية جدا 3. هنا، نقدم مثل هذا الأسلوب. الجمع بين القياسات التقليدية الحجم مع morphometrics الهندسية مقتبسة من دراسة القيطم 12 </سوب&gt; وثروة من الدراسات تحليل شكل الوجه البشري 13-15. الهدف من هذا البروتوكول هو السماح للباحثين لقياس حجم الوجه وأشكال التمييز بين الظواهر الوجهية المختلفة أثناء التطور العادية وغير العادية. وهذا التحليل يسمح للتمايز بين أفضل العيوب القحفي خفية مثل تلك الناشئة عن الآثار المستمرة للجينات و / أو العوامل البيئية. بالإضافة إلى ذلك، يمكن لهذا الأسلوب الكمي أيضا تكشف حتى تحسن طفيف أو إنقاذ عيب فموي وجهي. وبالتالي هذا يجعله دليلا مفيدا في تحليل العلاجات المحتملة. مزيج من قياسات الوجه وmorphometrics الهندسية التي نقدمها هنا يسمح للتحليل الإحصائي أشمل من كل من حجم وشكل المنطقة الوجهية من البروتوكولات الحالية التي تستخدم إلى حد كبير واحد فقط أو 15-18 الآخرين. وعلاوة على ذلك، فإننا نقدم طريقة بسيطة لتقييم كل من الإنسي والجانبية للطائراتوجه دون الحاجة إلى معدات التصوير المتطورة ثلاثية الأبعاد المستخدمة في الدراسات الحالية 13،19. نحن لشرح هذا البروتوكول على القيطم المورق الأجنة تعامل مع مثبط مستقبلات حمض الريتينويك أن يدفع تنمية الوجهية غير طبيعية والحنك المشقوق متوسط ​​2،3. وقد كشفت الكمي لأبعاد وشكل المنطقة الوجهية في هذه الأجنة التغيرات في midface التي هي مماثلة للبشر مع الشقوق الحنكية مماثلة ونماذج الماوس 20،21. ومع ذلك، فإن هذا البروتوكول يمكن استخدامها لتقييم آثار المركبات الأخرى على التنمية الوجهية مثل المواد الطبيعية، ومبيدات الأعشاب، أو بروتينات مثل عوامل النمو. وعلاوة على ذلك، حجم وشكل التغييرات الوجهية الناجمة عن اضطراب في التعبير الجيني عن طريق الخسارة أو الربح من التجارب وظيفة (باستخدام morpholinos العقاقير أو Crispers / Talens) كما يمكن كميا باستخدام هذا البروتوكول. أخيرا، قمنا بتطوير هذه الطريقة specificaLLY لتقييم القيطم التشكل. ومع ذلك، يتم تعديله بسهولة لتحليل أي الفقاريات. ويمكن أن تشمل أيضا تطبيقات أخرى باستخدام هذا البروتوكول لمقارنة وثيقي الصلة للدراسات تطورية أو بيئية. في حين أن المثال نحن نقدم هنا يستخدم هذا البروتوكول لوصف تحليل المنطقة الوجهية، يمكن بسهولة تعديله لتحليل مناطق أخرى، أجهزة، أو الهياكل. وهذا البروتوكول الكمي فموي وجهي أصبح مصدرا قيما للمجتمع البحوث، وكذلك أداة تعليمية ممتازة للطلاب الجامعيين كدليل الفيديو.

<table border="0" cellpadding="0" cellspacing="0" width="818">
	<tbody>
		<tr height="42">
			<td height="42" style="height:42px;width:304px;">Name of the reagent</td>
			<td style="width:143px;">Company</td>
			<td style="width:136px;">Catalogue number</td>
			<td style="width:236px;">Comments (optional)</td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;">Dissecting microscope</td>
			<td>Zeiss</td>
			<td></td>
			<td>fitted with AxioCamICC1 camera</td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;">Dumont #5 Inox forceps</td>
			<td>Fine Science Tools</td>
			<td>11251-10</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;">Sterile, disposable scalpel</td>
			<td>Sklar</td>
			<td>06-2015</td>
			<td></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:304px;">24-well plate</td>
			<td style="width:143px;">Fisher Scientific</td>
			<td style="width:136px;">087721</td>
			<td style="width:236px;"></td>
		</tr>
		<tr height="42">
			<td height="42" style="height:42px;width:304px;">Standard Disposable transfer pipettes</td>
			<td style="width:143px;">Fisher Scientific</td>
			<td style="width:136px;">13-711-7M</td>
			<td style="width:236px;"></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:304px;">150 mm X 15 mm Petri dishes</td>
			<td style="width:143px;">Falcon</td>
			<td style="width:136px;">351058</td>
			<td style="width:236px;"></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:304px;">Incubators</td>
			<td style="width:143px;">Ectotherm</td>
			<td style="width:136px;"></td>
			<td style="width:236px;">set to 15C or 20C&#160;</td>
		</tr>
		<tr height="60">
			<td height="60" style="height:60px;width:304px;">Modeling Clay</td>
			<td style="width:143px;">Premo, or other non-toxic modeling clay</td>
			<td style="width:136px;"></td>
			<td style="width:236px;">in black or white</td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:304px;">Straight teasing needle</td>
			<td style="width:143px;">Thermo Scientific</td>
			<td style="width:136px;">19010</td>
			<td style="width:236px;"></td>
		</tr>
		<tr height="40">
			<td height="40" style="height:40px;width:304px;">Capillary Tubing (for needles)</td>
			<td>FHC</td>
			<td>30-30-1</td>
			<td style="width:236px;">Borosil 1.0mm OD x 0.5mm ID/Fiber, 100 mm each</td>
		</tr>
		<tr height="80">
			<td height="80" style="height:80px;width:304px;">Needle Puller, Model P-97&#160;</td>
			<td style="width:143px;">Sutter Instrument Co,&#160;</td>
			<td style="width:136px;">Needle Puller: P-97 Flaming/ Bown micropipette puller Filament: FB300B</td>
			<td style="width:236px;">For filaments, use Sutter 3.00mm square box filaments, 3.0mm wide.</td>
		</tr>
		<tr height="60">
			<td height="60" style="height:60px;width:304px;">Pipettemen</td>
			<td style="width:143px;">Gilson</td>
			<td style="width:136px;">F144802, F123600, F123602</td>
			<td style="width:236px;"></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:304px;">BMS-453</td>
			<td style="width:143px;">Tocris</td>
			<td style="width:136px;">3409</td>
			<td style="width:236px;"></td>
		</tr>
		<tr height="40">
			<td height="40" style="height:40px;width:304px;">DMSO</td>
			<td style="width:143px;">American Bioanalytical</td>
			<td style="width:136px;">AB00435-01000</td>
			<td style="width:236px;"></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:304px;">Cysteine</td>
			<td style="width:143px;">Sigma-Aldrich</td>
			<td style="width:136px;">52-90-4</td>
			<td style="width:236px;"></td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:304px;">Paraformaldehyde powder</td>
			<td style="width:143px;">Sigma-Aldrich</td>
			<td style="width:136px;">158127</td>
			<td style="width:236px;"></td>
		</tr>
		<tr height="40">
			<td height="40" style="height:40px;width:304px;">Petri dishes</td>
			<td style="width:143px;">Falcom</td>
			<td style="width:136px;">353003, 351058</td>
			<td style="width:236px;">100 mm diameter and 150 mm in diameter</td>
		</tr>
		<tr height="21">
			<td height="21" style="height:21px;width:304px;">100% Ethanol</td>
			<td style="width:143px;">VWR</td>
			<td>89125-170</td>
			<td style="width:236px;"></td>
		</tr>
	</tbody>
</table>

quantification of orofacial phenotypes in xenopus

أصبح القيطم أداة هامة لتشريح الآليات التي تحكم تطوير القحفي والعيوب. وهناك طريقة لقياس تطور الوجهية تسمح لتحليل أكثر دقة من الظواهر الوجهية على إلغاء مع المواد التي يمكن وراثيا أو جزيئيا التلاعب التعبير الجيني أو وظيفة البروتين. باستخدام اثنين من صور ثلاثية الأبعاد من رؤساء الجنينية، يتم قياس حجم الأبعاد التقليدية مثل فموي وجهي العرض والطول ويتميز بتصميم داخلي متطور. وبالإضافة إلى ذلك، يتم استخدام مقياس استدارة من فتحة الفم الجنينية لوصف شكل الفم. يتم تنفيذ morphometrics هندسية من هذه الصور ثنائية الأبعاد أيضا لتقديم وجهة نظر أكثر تعقيدا من التغيرات في شكل المنطقة الوجهية. يتم تعيين المعالم إلى نقاط محددة في المنطقة الوجهية ويتم إنشاؤها الإحداثيات. ويستخدم تحليل المكون الرئيسي للحد من إحداثيات تاريخية لمكونات المبدأ الذي يميز ثم العلاجالمجموعات. يتم عرض هذه النتائج على أنها مؤامرة مبعثر فيه الأفراد مع الأشكال الوجهية مماثلة العنقودية معا. ومن المفيد أيضا إجراء تحليل التمايز وظيفة، مقارنة إحصائية مواقف المعالم بين مجموعات العلاج اثنين. يتم عرض هذا التحليل على شبكة التحول حيث ينظر التغيرات في المركز التاريخي كما ناقلات. تم فرضه شبكة على هذه النواقل بحيث يتم عرض نمط تزييفها لإظهار حيث تغيرت مواقف تاريخية كبيرة. وتستند التغييرات في شكل تحليل التمايز وظيفة على مقياس إحصائي، وبالتالي يمكن تقييمها من قبل ذات القيمة ص. هذا التحليل هو بسيط ويمكن الوصول إليها، والتي تتطلب فقط المجسام والبرامج مجانية، وبالتالي سيكون البحث والتدريس المورد الثمين.

هنا، وقد أظهر تحليل كمي لحجم وشكل فموي وجهي لمقارنة الأجنة تعامل مع مستقبلات حمض الريتينويك المانع (RAR المانع) لضوابط غير المعالجة. وعولج الأجنة مع تركيز 1 ميكرومتر من هذا المانع الكيميائية من المرحلة 24 إلي 30 (26-35 HPF)، جرفت، وثابتة في المرحلة 42 (82 HPF). ثم تم معالجتها وتحلي?...

Watch this Scientific Journal Video about Quantification of Orofacial Phenotypes in Xenopus at JoVE.com

Quantification of Orofacial Phenotypes in Xenopus

وقد تم تطوير طريقة لقياس حجم فموي وجهي وشكل الضفدع الأجنة المورق. في هذا البروتوكول، ويتم الجمع بين قياسات حجم التقليدية مع morphometrics الهندسية للسماح لتحليلات أكثر تطورا التنمية الوجهية والعيوب.

الكمي من الظواهر في الوجهية<em&gt; القيطم</em

Xenopus has become an important tool for dissecting the mechanisms governing craniofacial development and defects. A method to quantify orofacial ...

quantification-of-orofacial-phenotypes-in-xenopus

Research

JoVE Journal

Biology

Quantification of Orofacial Phenotypes in Xenopus

9.7K Views.  Virginia Commonwealth University.  وقد تم تطوير طريقة لقياس حجم فموي وجهي وشكل الضفدع الأجنة المورق. في هذا البروتوكول، ويتم الجمع بين قياسات حجم التقليدية مع morphometrics الهندسية للسماح لتحليلات أكثر تطورا التنمية الوجهية والعيوب. 

Video: Quantification of Orofacial Phenotypes in Xenopus

Microinjection of Xenopus Laevis Oocytes

Microinjection of Xenopus laevis oocytes followed by thin-sectioning electron microscopy (EM) is an excellent system for studying nucleocytoplasmic transport. Because of its large nucleus and high density of nuclear pore complexes (NPCs), nuclear transport can be easily visualized in the Xenopus oocyte. Much insight into the mechanisms of nuclear import and export has been gained through use of this system (reviewed by Pant&eacute;, 2006). In addition, we have used microinjection of Xenopus oocytes to dissect the nuclear import pathways of several viruses that replicate in the host nucleus. 
Here we demonstrate the cytoplasmic microinjection of Xenopus oocytes with a nuclear import substrate. We also show preparation of the injected oocytes for visualization by thin-sectioning EM, including dissection, dehydration, and embedding of the oocytes into an epoxy embedding resin. Finally, we provide representative results for oocytes that have been microinjected with the capsid of the baculovirus Autographa californica nucleopolyhedrovirus (AcMNPV) or the parvovirus Minute Virus of Mice (MVM), and discuss potential applications of the technique.

Here we demonstrate cytoplasmic microinjection of Xenopus laevis oocytes with a nuclear import substrate, as well as preparation of the injected oocytes for visualization by thin-sectioning electron microscopy.

Microinjection من البويضات المورق القيطم

Microinjection of Xenopus laevis oocytes followed by thin-sectioning electron microscopy (EM) is an excellent system for studying nucleocytoplasmic ...

Visualizing RNA Localization in Xenopus Oocytes

RNA localization is a conserved mechanism of establishing cell polarity. Vg1 mRNA localizes to the vegetal pole of Xenopus laevis oocytes and acts to spatially restrict gene expression of Vg1 protein. Tight control of Vg1 distribution in this manner is required for proper germ layer specification in the developing embryo. RNA sequence elements in the 3' UTR of the mRNA, the Vg1 localization element (VLE) are required and sufficient to direct transport. To study the recognition and transport of Vg1 mRNA in vivo, we have developed an imaging technique that allows extensive analysis of trans-factor directed transport mechanisms via a simple visual readout. 
To visualize RNA localization, we synthesize fluorescently labeled VLE RNA and microinject this transcript into individual oocytes. After oocyte culture to allow transport of the injected RNA, oocytes are fixed and dehydrated prior to imaging by confocal microscopy. Visualization of mRNA localization patterns provides a readout for monitoring the complete pathway of RNA transport and for identifying roles in directing RNA transport for cis-acting elements within the transcript and trans-acting factors that bind to the VLE (Lewis et al., 2008, Messitt et al., 2008). We have extended this technique through co-localization with additional RNAs and proteins (Gagnon and Mowry, 2009, Messitt et al., 2008), and in combination with disruption of motor proteins and the cytoskeleton (Messitt et al., 2008) to probe mechanisms underlying mRNA localization.

Visualizing RNA Localization in Xenopus Oocytes

Visualization of in vivo RNA transport is accomplished by microinjection of fluorescently labeled RNA transcripts into Xenopus oocytes, followed by confocal microscopy.

تصور التعريب في الحمض النووي الريبي القيطم البويضات

RNA localization is a conserved mechanism of establishing cell polarity.  Vg1 mRNA localizes to the vegetal pole of Xenopus laevis oocytes and acts to ...

Patch Clamp and Perfusion Techniques for Studying Ion Channels Expressed in Xenopus oocytes

The protocol presented here is designed to study the activation of the large conductance, voltage- and Ca2+-activated K+ (BK) channels. The protocol may also be used to study the structure-function relationship for other ion channels and neurotransmitter receptors1. BK channels are widely expressed in different tissues and have been implicated in many physiological functions, including regulation of smooth muscle contraction, frequency tuning of inner hair cells and regulation of neurotransmitter release2-6. BK channels are activated by membrane depolarization and by intracellular Ca2+ and Mg2+ 6-9. Therefore, the protocol is designed to control both the membrane voltage and the intracellular solution. In this protocol, messenger RNA of BK channels is injected into Xenopus laevis oocytes (stage V-VI) followed by 2-5 days of incubation at 18&deg;C10-13. Membrane patches that contain single or multiple BK channels are excised with the inside-out configuration using patch clamp techniques10-13. The intracellular side of the patch is perfused with desired solutions during recording so that the channel activation under different conditions can be examined. To summarize, the mRNA of BK channels is injected into Xenopus laevis oocytes to express channel proteins on the oocyte membrane; patch clamp techniques are used to record currents flowing through the channels under controlled voltage and intracellular solutions.

Patch Clamp and Perfusion Techniques for Studying Ion Channels Expressed in Xenopus oocytes

Ionic current of BK channels is recorded using patch clamp techniques. BK channels are expressed in Xenopus oocytes by injecting messenger RNA. The intracellular solution during patch clamp recordings is controlled by a perfusion system.

أعربت المشبك التصحيح وتقنيات الإرواء لدراسة في قنوات ايون القيطم البويضات

The protocol presented here is designed to study the activation of the large conductance, voltage- and Ca2+-activated K+ (BK) channels. The protocol may ...

RNAi Screening to Identify Postembryonic Phenotypes in C. elegans

C. elegans has proven to be a valuable model system for the discovery and functional characterization of many genes and gene pathways1. More sophisticated tools and resources for studies in this system are facilitating continued discovery of genes with more subtle phenotypes or roles. 
Here we present a generalized protocol we adapted for identifying C. elegans genes with postembryonic phenotypes of interest using RNAi2. This procedure is easily modified to assay the phenotype of choice, whether by light or fluorescence optics on a dissecting or compound microscope. This screening protocol capitalizes on the physical assets of the organism and molecular tools the C. elegans research community has produced. As an example, we demonstrate the use of an integrated transgene that expresses a fluorescent product in an RNAi screen to identify genes required for the normal localization of this product in late stage larvae and adults. First, we used a commercially available genomic RNAi library with full-length cDNA inserts. This library facilitates the rapid identification of multiple candidates by RNAi reduction of the candidate gene product. Second, we generated an integrated transgene that expresses our fluorecently tagged protein of interest in an RNAi-sensitive background. Third, by exposing hatched animals to RNAi, this screen permits identification of gene products that have a vital embryonic role that would otherwise mask a post-embryonic role in regulating the protein of interest. Lastly, this screen uses a compound microscope equipped for single cell resolution.

RNAi Screening to Identify Postembryonic Phenotypes in C. elegans

We describe a sensitized method to identify postembryonic regulators of protein expression and localization in C. elegans using an RNAi-based genomic screen and an integrated transgene that expresses a functional, fluorescently tagged protein.

[رني الفرز لتحديد الظواهر تال للمرحلة الجنينية في C. ايليجانس</em

C. elegans has proven to be a valuable model system for the discovery and functional characterization of many genes and gene pathways1. More sophisticated ...

Facial Transplants in Xenopus laevis Embryos

Craniofacial birth defects occur in 1 out of every 700 live births, but etiology is rarely known due to limited understanding of craniofacial development. To identify where signaling pathways and tissues act during patterning of the developing face, a 'face transplant' technique has been developed in embryos of the frog Xenopus laevis. A region of presumptive facial tissue (the "Extreme Anterior Domain" (EAD)) is removed from a donor embryo at tailbud stage, and transplanted to a host embryo of the same stage, from which the equivalent region has been removed. This can be used to generate a chimeric face where the host or donor tissue has a loss or gain of function in a gene, and/or includes a lineage label. After healing, the outcome of development is monitored, and indicates roles of the signaling pathway within the donor or surrounding host tissues. Xenopus is a valuable model for face development, as the facial region is large and readily accessible for micromanipulation. Many embryos can be assayed, over a short time period since development occurs rapidly. Findings in the frog are relevant to human development, since craniofacial processes appear conserved between Xenopus and mammals.

Facial Transplants in Xenopus laevis Embryos

A technique for transplanting "Extreme Anterior Domain" facial tissue between Xenopus laevis embryos has been developed. Tissue can be moved from one gene expression background into another, allowing the study of local requirements for craniofacial development and for signaling interactions between facial regions.

زرع الوجه في<em&gt; القيطم المورق</em&gt; الأجنة

Craniofacial birth defects occur in 1 out of every 700 live births, but etiology is rarely known due to limited understanding of craniofacial development. ...

The Xenopus Oocyte Cut-open Vaseline Gap Voltage-clamp Technique With Fluorometry

The cut-open oocyte Vaseline gap (COVG) voltage clamp technique allows for analysis of electrophysiological and kinetic properties of heterologous ion channels in oocytes. Recordings from the cut-open setup are particularly useful for resolving low magnitude gating currents, rapid ionic current activation, and deactivation. The main benefits over the two-electrode voltage clamp (TEVC) technique include increased clamp speed, improved signal-to-noise ratio, and the ability to modulate the intracellular and extracellular milieu.
Here, we employ the human cardiac sodium channel (hNaV1.5), expressed in Xenopus oocytes, to demonstrate the cut-open setup and protocol as well as modifications that are required to add voltage clamp fluorometry capability.
The properties of fast activating ion channels, such as hNaV1.5, cannot be fully resolved near room temperature using TEVC, in which the entirety of the oocyte membrane is clamped, making voltage control difficult. However, in the cut-open technique, isolation of only a small portion of the cell membrane allows for the rapid clamping required to accurately record fast kinetics while preventing channel run-down associated with patch clamp techniques.
In conjunction with the COVG technique, ion channel kinetics and electrophysiological properties can be further assayed by using voltage clamp fluorometry, where protein motion is tracked via cysteine conjugation of extracellularly applied fluorophores, insertion of genetically encoded fluorescent proteins, or the incorporation of unnatural amino acids into the region of interest1. This additional data yields kinetic information about voltage-dependent conformational rearrangements of the protein via changes in the microenvironment surrounding the fluorescent molecule.

The Xenopus Oocyte Cut-open Vaseline Gap Voltage-clamp Technique With Fluorometry

The cut-open Vaseline gap approach is used to obtain low noise recordings of ionic and gating currents from voltage-dependent ion channels expressed in Xenopus oocytes with high resolution of fast channel kinetics. With minor modification, voltage clamp fluorometry can be coupled to the cut-open oocyte protocol.

ال<em&gt; القيطم</em&gt; سيت قص مفتوحة الفازلين جاب الجهد المشبك تقنية مع التألق

The cut-open oocyte Vaseline gap (COVG) voltage clamp technique allows for analysis of electrophysiological and kinetic properties of heterologous ion ...

Reconstitution Of &#946;-catenin Degradation In Xenopus Egg Extract

Xenopus laevis egg extract is a well-characterized, robust system for studying the biochemistry of diverse cellular processes. Xenopus egg extract has been used to study protein turnover in many cellular contexts, including the cell cycle and signal transduction pathways1-3. Herein, a method is described for isolating Xenopus egg extract that has been optimized to promote the degradation of the critical Wnt pathway component, &beta;-catenin. Two different methods are described to assess &beta;-catenin protein degradation in Xenopus egg extract. One method is visually informative ([35S]-radiolabeled proteins), while the other is more readily scaled for high-throughput assays (firefly luciferase-tagged fusion proteins). The techniques described can be used to, but are not limited to, assess &beta;-catenin protein turnover and identify molecular components contributing to its turnover. Additionally, the ability to purify large volumes of homogenous Xenopus egg extract combined with the quantitative and facile readout of luciferase-tagged proteins allows this system to be easily adapted for high-throughput screening for modulators of &beta;-catenin degradation.

Reconstitution Of &amp;#946;-catenin Degradation In Xenopus Egg Extract

A method is described for analyzing protein degradation using radiolabeled and luciferase-fusion proteins in Xenopus egg extract and its adaptation for high-throughput screening for small molecule modulators of protein degradation.

إعادة تشكيل β-catenin تدهور في<em&gt; القيطم</em&gt; مستخلصات البيض

Xenopus laevis egg extract is a well-characterized, robust system for studying the biochemistry of diverse cellular processes. Xenopus egg extract has ...

نضح الدم في الضفادع الأفريقية المخالب للنسخ والبروتيوميات

Effective Rapid Blood Perfusion in Xenopus

Xenopus have been powerful model organisms for understanding vertebrate development and disease for over 100 years. Here, a rapid blood perfusion protocol in Xenopus, aimed at a consistent and drastic reduction of blood within all tissues, is defined. Perfusion is carried out by inserting a needle directly into the ventricle of the heart and pumping heparinized phosphate-buffered saline (PBS) through the vascular system. The procedure can be completed in approximately 10 min per animal. The blood is dominated by a few highly abundant proteins and cell types, creating numerous issues as these proteins mask most other molecules and cell types of interest. The reproducible characterization of adult Xenopus tissues with quantitative proteomics and single-cell transcriptomics will benefit from applying this protocol prior to organ sampling. The protocols for tissue sampling are defined in companion papers. These procedures are aimed at the standardization of practices across Xenopus of different sex, age, and health status, specifically X. laevis and X. tropicalis.

تسليط الضوء على المؤلف: نضح الدم السريع الفعال في Xenopus  

Presented here is an effective rapid blood perfusion protocol to prepare tissue samples from African clawed frogs for transcriptomics and proteomics studies.

التروية الدموية السريعة الفعالة في Xenopus

Xenopus have been powerful model organisms for understanding vertebrate development and disease for over 100 years. Here, a rapid blood perfusion protocol ...