Name: paraffin-embedded and frozen sections of drosophila adult muscles
Uploaded: 2010-12-27T17:30:00
Duration: 7 min 28 s
Description: Watch this Scientific Journal Video about Paraffin-Embedded and Frozen Sections of Drosophila Adult Muscles at JoVE.com

हम हमें क्रायो - सूक्ष्म तक्षणी का उपयोग करने के लिए अनुमति देने के लिए प्रो Eichele धन्यवाद. मैक्स प्लैंक - Gesselschaft कार्य द्वारा वित्त पोषित किया गया था.

1. तैयार <ol><li> हौसले Carnoy लगानेवाला 06:03:01 अनुपात में क्रमशः निरपेक्ष इथेनॉल, क्लोरोफॉर्म और हिमनदों एसिटिक एसिड के संयोजन द्वारा तैयार 3. यह, के रूप में के रूप में अच्छी तरह से submerging कॉलर के लिए सभी समाधान कांच धुंधला जार में रखा जाना चाहिए (सिफारिश के लिए अभिकर्मकों अनुभाग देखें). </li><li> तैयार एल्यूमीनियम पन्नी कॉलर के लिए सही आकार को पाकेट के अंदर डालता है. </li><li> 2 X 40% इथेनॉल, 70% इथेनॉल, 2 एक्स 100% इथेनॉल, methylbenzoate (एमबी), 50/50 v / v एमबी और आयल, 2 एक्स आयल धुंधला: जार में निम्नलिखित समाधान तैयार करें. 60-65 सी. सेंटीग्रेड और एक मशीन सेट में एमबी आयल कंटेनरों प्लेस </li><li> गर्म आयल पन्नी जेब में 60-65 डिग्री सेल्सियस के लिए डालना </li></ol> 2. कॉलर में मक्खियों फिक्सिंग <ol><li> जहाँ आप मक्खी के लिए प्रविष्टि बिंदु देख सकते हैं एक ऊर्ध्वाधर स्थिति में टेप का उपयोग द्विनेत्री के तहत कॉलर 4 संलग्न . </li><li> Anesthetize कार्बन या हाइपोथर्मिया के माध्यम से डाइऑक्साइड एक बर्फ ब्लॉक का उपयोग कर का उपयोग मक्खियों. मक्खियों को स्थिर नहीं सावधान रहो. </li><li> संदंश का प्रयोग, ठीक उन्मुख कॉलर (और ब्लेड और ब्लेड नीचे पेट के शीर्ष पर सिर और छाती) में अपने पंख और जगह हथियाने के द्वारा अलग - अलग मक्खियों लेने. 10-20 मक्खियों कॉलर में आसानी से फिट होना चाहिए. </li></ol> नोट: यदि आप कई जीनोटाइप का विश्लेषण कर रहे हैं, कॉलर संख्या और इसी जीनोटाइप के एक नोट बनाने के लिए मत भूलना. 3. ड्रोसोफिला Thoraxes के आयल धारा <ol><li> Carnoy समाधान के लिए स्थानांतरित करना कॉलर और 4 में ऊतकों को ठीक ° सी रात खत्म. </li><li> निर्धारण के बाद, इथेनॉल की बढ़ती सांद्रता का उपयोग नमूना निर्जलीकरण. 10 मिनट 40 (2 बार)%, 70% और 100% (2 बार) कमरे के तापमान पर इथेनॉल में प्रत्येक डूब कॉलर के लिए. MB और एमबी + आयल समाधान (1:1) में प्रत्येक में 30 मिनट के लिए अगले सेते कॉलर और फिर 60 मिनट प्रत्येक के लिए दो आयल की 60-65 में परिवर्तन ° सी. में कॉलर घुसपैठ पन्नी जेब में तेजी से स्थानांतरित कॉलर और पिघला (60-65 डिग्री सेल्सियस) आयल के साथ भरें. यह कमरे के तापमान पर प्लेस और आयल मुश्किल बनने के लिए (यह सबसे अच्छा है रात भर छोड़ है) की अनुमति है. ध्यान दें कि कॉलर अलग झुकाव में पन्नी जेब में रखा जा सकता है वर्गों आप की जरूरत है (अनुदैर्ध्य या अनुप्रस्थ) के उन्मुखीकरण के आधार पर. </li><li> पन्नी से कॉलर के साथ सूखी आयल ब्लॉक खोलना और धीरे आयल ब्लॉक से कॉलर अलग. एक तेज ब्लेड या स्केलपेल की मदद के साथ सावधानी से मक्खी ऊतक आसपास से अतिरिक्त आयल में कटौती. </li><li> 7-10 सुक्ष्ममापी अनुभाग कदम के साथ एक रोटेशन सूक्ष्म तक्षणी पर आयल ब्लॉक कट और कटौती ऊतक एक 37 डिग्री सेल्सियस पानी के स्नान में फ्लैट फ्लोट करने की अनुमति. ध्रुवीय स्लाइड पर sectioned ऊतक प्लेस और रात खत्म सुखाने की अनुमति. ये स्लाइड hematoxyline और eosin के साथ धुंधला के लिए इस्तेमाल किया जा सकता है (चित्रा 1A-D) toluidine नीले, एनिलिन नीले या अन्य मर जाता है ऊतक संरचनाओं कल्पना करने के लिए, के रूप में अच्छी तरह के रूप में एंटीबॉडी धुंधला के लिए (चित्रा 1E-ई ``). </li></ol> 4. ड्रोसोफिला Thoraxes के Cryosections <ol><li> आयल वर्गों के साथ के रूप में, एक कॉलर और फैशन एक एल्यूमीनियम पन्नी जेब में मक्खियों को तैयार है. एक ठंड कूलर के लिए नमूने तैयार करने के लिए की जरूरत होगी. सुनिश्चित करें कि कूलर -60 के आसपास है डिग्री सेल्सियस, इस तापमान तक पहुँचने के लिए अनुमति देने के लिए एक छोटे से इथेनॉल और सूखी बर्फ का उपयोग करें. प्रयोग शुरू करने से पहले एक घंटे क्रायो - एम्बेडिंग माध्यम की बोतल (ऊतक टेक अक्टूबर यौगिक) उल्टा क्रम में इसे शांत करने के लिए और हवा के बुलबुले के गठन को कम करने के लिए एक 4 डिग्री सेल्सियस फ्रिज में डाल दिया. </li><li> पन्नी जेब किया गया है कि पूर्व ठंड कूलर के अंदर कई मिनट के लिए ठंडा और तेजी यौगिक क्रायो - एम्बेडिंग के साथ भरने के लिए मक्खियों के साथ कॉलर स्थानांतरित करना. 3-10 मिनट के लिए नमूना फ्रीज चलो. ध्यान कूलर के अंदर गठित ब्लॉक खोलना, धीरे एम्बेडिंग ब्लॉक से कॉलर अलग और -20 डिग्री सेल्सियस पर यह कम से कम एक दिन के लिए डाल दिया. </li><li> 10-15 सुक्ष्ममापी की एक अनुभाग मोटाई के साथ -15 और -18 डिग्री सेल्सियस के बीच क्रायो - सूक्ष्म तक्षणी पर जमी मांसपेशियों कट. Polarized स्लाइड पर प्लेस और जब तक आगे की प्रक्रिया करने के लिए तैयार -20 डिग्री सेल्सियस पर रखने. हम 4% formaldehyde पीबीएस समाधान में एंटीबॉडी धुंधला करने से पहले कमरे के तापमान पर 10 मिनट के लिए ऊतक फिक्सिंग सुझाव देते हैं. </li></ol> 5. लिपिड जांच में ड्रोसोफिला स्नायु लिपिड बूंदों तेल लाल हे Sieber और Thummel 5 से अपनाया प्रोटोकॉल का उपयोग करने cryosections पर दाग के साथ पता लगाया जा सकता है. <ol><li> निर्धारण के बाद, पानी के साथ स्लाइड्स दो बार धोने के 5 मिनट, 10 मिनट के लिए 3 घंटे में तेल लाल हे कमरे के तापमान पर दाग सेते के लिए propylene glycol में equilibrated के लिए. तो नमूने propylene glycol और पीबीएस में 30 मिनट में 5 मिनट के लिए 2 बार धो लो. 30% ग्लिसरॉल में माउंट. </li></ol> 6. प्रतिनिधि परिणाम: <img src="/files/ftp_upload/2438/2438fig1.jpg" alt="चित्रा 1" /> अंजीर1 ure. Parrafin - एम्बेडेड वर्गों Hematoxyline और eosine दाग अनुप्रस्थ (एबी) अनुदैर्ध्य और अप्रत्यक्ष उड़ान मांसपेशियों के वर्गों (सीडी). ए और सी सामान्य संरचित मांसपेशियों से पता चलता है. आकार और आकारिकी की मांसपेशियों द्वारा असामान्य बी और डी क्रमशः (काला तीर) पर प्रतिनिधित्व कर रहे हैं. विरोधी LamC परमाणु लिफाफा मार्कर और DAPI, दाग परमाणु (एफई) के साथ ड्रोसोफिला छाती दाग की अनुप्रस्थ अनुभाग . सामान्य के बढ़े हुए दृश्य (लाल तीर) और बिगड़ी मांसपेशियों (पीले तीर) (एफ). जी ड्रोसोफिला आंत्र पथ दाग के LamC और DAPI के साथ अनुभाग का प्रतिनिधित्व करता है. <img src="/files/ftp_upload/2438/2438fig2.jpg" alt="चित्रा 2" /> चित्रा 2. जमे हुए वर्गों ए ड्रोसोफिला तेल लाल हे, लिपिड बूंदों लेबल के साथ दाग छाती के ट्रांसवर्स जमी वर्गों . बी अप्रत्यक्ष उड़ान मांसपेशियों के अनुदैर्ध्य जमे हुए वर्गों के साथ दाग विरोधी महानिदेशक, मांसपेशी sarcolemma मार्कर और DAPI.

<ol>
	<li>Miller, A. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=The+internal+anatomy+and+histology+of+the+imago+of+Drosophila+melanogaster.">The internal anatomy and histology of the imago of Drosophila melanogaster.</a> , (1950).</li><li>Shcherbata, H. R. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Dissecting+muscle+and+neuronal+disorders+in+a+Drosophila+model+of+muscular+dystrophy.">Dissecting muscle and neuronal disorders in a Drosophila model of muscular dystrophy.</a> The EMBO journal. 26, 481-481 (2007).</li><li>Kucherenko, M. M. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Genetic+modifier+screens+reveal+new+components+that+interact+with+the+Drosophila+dystroglycan-dystrophin+complex.">Genetic modifier screens reveal new components that interact with the Drosophila dystroglycan-dystrophin complex.</a> PloS one. 3, e2418-e2418 (2008).</li><li>Puchtler, H., Waldrop, F. S., Conner, H. M., Terry, M. S. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Carnoy+fixation:+practical+and+theoretical+considerations.">Carnoy fixation: practical and theoretical considerations.</a> Histochemie. 16, 361-36 (1968).</li><li>Ashburner, M. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=.">.</a> Drosophila - A Laboratory Manual. , (1989).</li><li>Sieber, M. H., Thummel, C. S. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=The+DHR96+nuclear+receptor+controls+triacylglycerol+homeostasis+in+Drosophila.">The DHR96 nuclear receptor controls triacylglycerol homeostasis in Drosophila.</a> Cell metabolism. 10, 481-481 (2009).</li></ol>

ब्याज की कोई संघर्ष की घोषणा की.

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		<div>
		<table border="1">
		<thead>
		<tr>
		<th>Material Name</th>
		<th>Type</th>
		<th>Company</th>
		<th>Catalogue Number</th>
		<th>Comment</th>
		</tr>
		</thead>
		<tbody>
		
<tr>
<td>Stainless steel collars</td>
<td>&nbsp;</td>
<td>self-made</td>
<td>&nbsp;</td>
<td>Specially constructed</td>
</tr>
<tr>
<td>Forceps</td>
<td>&nbsp;</td>
<td>Fine Science Tools GmbH</td>
<td>11295-10</td>
<td>&nbsp;</td>
<tr>
<td>Aluminum foil</td>
<td>&nbsp;</td>
<td>Any</td>
<td>&nbsp;</td>
<td>&nbsp;</td>
<tr>
<td>Blade or scalpel</td>
<td>&nbsp;</td>
<td>Any</td>
<td>&nbsp;</td>
<td>&nbsp;</td>
<tr>
<td>Wheaton macro staining jar</td>
<td>&nbsp;</td>
<td>Wheaton Science Products </td>
<td>900200</td>
<td>&nbsp;</td>
<tr>
<td>Microtome</td>
<td>&nbsp;</td>
<td>Carl Zeiss</td>
<td>&nbsp;</td>
<td>Model: Hyrax M25</td>
</tr>
<tr>
<td>Cryo-microtome</td>
<td>&nbsp;</td>
<td>Leica </td>
<td>&nbsp;</td>
<td>Model CM3050S</td>
</tr>
<tr>
<td>60-65&deg;C Incubator</td>
<td>&nbsp;</td>
<td>Any</td>
<td>&nbsp;</td>
<td>Large enough to hold at least 4 staining jars</td>
</tr>
<tr>
<td>Freezing cooler with metal block</td>
<td>&nbsp;</td>
<td>Any</td>
<td>&nbsp;</td>
<td>Store at -80&deg;C</td>
</tr>
<tr>
<td>Super-frost slides</td>
<td>&nbsp;</td>
<td>Thermo Fisher Scientific</td>
<td>9161155</td>
<td>&nbsp;</td>
<tr>
<td>Cover slips</td>
<td>&nbsp;</td>
<td>Any </td>
<td>&nbsp;</td>
<td>Recommend 24 X 40 mm</td>
</tr>
<tr>
<td>Chloroform</td>
<td>&nbsp;</td>
<td>Sigma-Aldrich</td>
<td>288306</td>
<td>Analytical grade </td>
</tr>
<tr>
<td>Glacial acetic acid</td>
<td>&nbsp;</td>
<td>Merck</td>
<td>100063</td>
<td>Analytical grade</td>
</tr>
<tr>
<td>Ethanol</td>
<td>&nbsp;</td>
<td>Merck</td>
<td>100983</td>
<td>Analytical grade</td>
</tr>
<tr>
<td>Methylbenzoate</td>
<td>&nbsp;</td>
<td>Sigma-Aldrich</td>
<td>M29908-500G</td>
<td>Analytical grade</td>
</tr>
<tr>
<td>Paraplast plus</td>
<td>&nbsp;</td>
<td>Sigma-Aldrich</td>
<td>76258</td>
<td>Paraffin</td>
</tr>
<tr>
<td>Tissue-Teck O.C.T. compound</td>
<td>&nbsp;</td>
<td>Sakura</td>
<td>4583</td>
<td>&nbsp;</td>
<tr>
<td>16% formaldehyde, methanol free</td>
<td>&nbsp;</td>
<td>Polysciences</td>
<td>18814</td>
<td>&nbsp;</td>
<tr>
<td>Glycerol</td>
<td>&nbsp;</td>
<td>Sigma-Aldrich</td>
<td>G5150-1L</td>
<td>&nbsp;</td>		</tbody>
		</table>
		</div>

paraffin-embedded and frozen sections of drosophila adult muscles

मानव में पेशी अपविकास और myopathies के आणविक लक्षण वर्णन मांसपेशियों की बीमारी की जटिलता और मांसपेशियों के विनिर्देशन के आनुवांशिक विश्लेषण से पता चला है, और मॉडल प्रणाली में गठन कार्य मांसपेशियों के शरीर क्रिया विज्ञान में बहुमूल्य अंतर्दृष्टि प्रदान की है. इसलिए, पहचान और आणविक तंत्र है कि मांसपेशियों की क्षति आबाद निस्र्पक के लिए महत्वपूर्ण है. वयस्क ड्रोसोफिला बहु फाइबर मांसपेशियों की संरचना समान है हड्डीवाला धारीदार 1 मांसपेशियों और ड्रोसोफिला के आनुवंशिक tractability यह एक महान प्रणाली dystrophic मांसपेशियों आकारिकी का विश्लेषण और बुढ़ापे वयस्क में पेशी समारोह को प्रभावित प्रक्रियाओं 2 मक्खियों विशेषताएँ बना दिया है. यहाँ हम आयल एम्बेडेड और ड्रोसोफिला वक्ष मांसपेशियों के वर्गों जमे हुए तैयार करने के लिए histological तकनीक मौजूद है . ये तैयारियाँ शास्त्रीय histological धब्बे के साथ सना हुआ हो सकता है और प्रोटीन का पता लगाने के रंगों के साथ लेबल ऊतक के लिए अनुमति देते हैं, और विशेष रूप से cryosections बरकरार मांसपेशियों में प्रोटीन की immunohistochemical पता लगाने के लिए आदर्श होते हैं. यह मांसपेशियों के ऊतकों की संरचना, morphological दोष की पहचान है, और मांसपेशियों / ड्रोसोफिला वयस्क मांसपेशियों में न्यूरॉन विशिष्ट प्रोटीन के लिए अभिव्यक्ति पैटर्न का पता लगाने के के विश्लेषण के लिए अनुमति देता है. इन तकनीकों में भी थोड़ा शरीर के अन्य भागों के सेक्शनिंग करने के लिए संशोधित किया जा सकता है.

Watch this Scientific Journal Video about Paraffin-Embedded and Frozen Sections of Drosophila Adult Muscles at JoVE.com

Paraffin-Embedded and Frozen Sections of Drosophila Adult Muscles

मांसपेशियों की क्षति अंतर्निहित तंत्र की पहचान महत्वपूर्ण है. यहाँ हम आयल एम्बेडेड और ड्रोसोफिला वक्ष मांसपेशियों के वर्गों जमे हुए तैयार करने के लिए histological तकनीक मौजूद है. यह मांसपेशियों की आकारिकी और प्रोटीन और अन्य मांसपेशी कोशिका घटकों के स्थानीयकरण के विश्लेषण की अनुमति देता है.

के आयल - एंबेडेड और जमे हुए वर्गों ड्रोसोफिला वयस्क स्नायु

The molecular characterization of muscular dystrophies and myopathies in humans has revealed the complexity of muscle disease and genetic analysis of ...

paraffin-embedded-and-frozen-sections-of-drosophila-adult-muscles

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Biology

Paraffin-Embedded and Frozen Sections of Drosophila Adult Muscles

Whole Cell Recordings from Brain of Adult Drosophila

In this video, we demonstrate the procedure for isolating whole brains from adult Drosophila in preparation for recording from single neurons. We begin by describing the dissecting solution and capture of the adult females used in our studies. The procedure for removing the whole brain intact, including both optic lobes, is illustrated. Dissection of the overlying trachea is also shown.  The isolated brain is not only small but needs special care in handling at this stage to prevent damage to the neurons, many of which are close to the outer surface of the tissue. We show how a special holder we developed is used to stabilize the brain in the recording chamber. A standard electrophysiology set up is used for recording from single neurons or pairs of neurons. A fluorescent image, viewed through the recording microscope, from a GAL4 line driving GFP expression (GH146) illustrates how projection neurons (PNs) are identified in the live brain. A high power Nomarski image shows a view of a single neuron that is being targeted for whole cell recording. When the brain is successfully removed without damage, the majority of the neurons are spontaneously active, firing action potentials and/or exhibiting spontaneous synaptic input. This in situ preparation, in which whole cell recording of identified neurons in the whole brain can be combined with genetic and pharmacological manipulations, is a useful model for exploring cellular physiology and plasticity in the adult CNS.

This video demonstrates the procedure for isolating whole brains from adult Drosophila in preparation for recording from single neurons using standard whole cell technology. It includes images of GFP labeled cells and neurons viewed during recording.

वयस्क ड्रोसोफिला के मस्तिष्क से पूरे सेल रिकॉर्डिंग

In this video, we demonstrate the procedure for isolating whole brains from adult Drosophila in preparation for recording from single neurons. We begin by ...

High-Resolution Video Tracking of Locomotion in Adult Drosophila Melanogaster

Flies provide an important model for studying complex behavior due to the plethora of genetic tools available to researchers in this field. Studying locomotor behavior in Drosophila melanogaster relies on the ability to be able to quantify changes in motion during or in response to a given task. For this reason, a high-resolution video tracking system, such as the one we describe in this paper, is a valuable tool for measuring locomotion in real-time. Our protocol involves the use of an initial air pulse to break the flies momentum, followed by a thirty second filming period in a square chamber. A tracking program is then used to calculate the instantaneous speed of each fly within the chamber in 10 msec increments. Analysis software then compiles this data, and outputs a variety of parameters such as average speed, max speed, time spent in motion, acceleration, etc. This protocol will discuss proper feeding and management of flies for behavioral tasks, handling flies without anesthetization or immobilization, setting up a controlled environment, and running the assay from start to finish.

The study of complex locomotor behavior in Drosophila melanogaster is dependent upon the ability to quantify changes in a given fly's movement. This article demonstrates how to do this using a high-resolution tracking system.

उच्च संकल्प प्रौढ़ ड्रोसोफिला मेलानोगास्टर में हरकत की वीडियो ट्रैकिंग

Flies provide an important model for studying complex behavior due to the plethora of genetic tools available to researchers in this field.  Studying ...

Preparation of Developing and Adult Drosophila Brains and Retinae for Live Imaging

The Drosophila brain and visual system are widely utilized model systems to study neuronal development, function and degeneration. Here we show three preparations of the brain and visual system that cover the range from the developing eye disc-brain complex in the developing pupae to individual eye and brain dissection from adult flies. All protocols are optimized for the live culture of the preparations. However, we also present the conditions for fixed tissue immunohistochemistry where applicable. Finally, we show live imaging conditions for these preparations using conventional and resonant 4D confocal live imaging in a perfusion chamber. Together, these protocols provide a basis for live imaging on different time scales ranging from functional intracellular assays on the scale of minutes to developmental or degenerative processes on the scale of many hours.

Preparation of Developing and Adult Drosophila Brains and Retinae for Live Imaging

This protocol describes three Drosophila preparations: 1) adult brain dissection, 2) adult retina dissection and 3) developing eye disc- brain complexes dissection. Emphasis is laid on special preparation techniques and conditions for live imaging, although all preparations can be used for fixed tissue immunohistochemistry.

विकास और वयस्क की तैयारी ड्रोसोफिला दिमाग और लाइव इमेजिंग के लिए Retinae

The Drosophila brain and visual system are widely utilized model systems to study neuronal development, function and degeneration. Here we show three ...

Dissection of Oenocytes from Adult Drosophila melanogaster

In Drosophila melanogaster, as in other insects, a waxy layer on the outer surface of the cuticle, composed primarily of hydrocarbon compounds, provides protection against desiccation and other environmental challenges. Several of these cuticular hydrocarbon (CHC) compounds also function as semiochemical signals, and as such mediate pheromonal communications between members of the same species, or in some instances between different species, and influence behavior. Specialized cells referred to as oenocytes are regarded as the primary site for CHC synthesis. However, relatively little is known regarding the involvement of the oenocytes in the regulation of the biosynthetic, transport, and deposition pathways contributing to CHC output. Given the significant role that CHCs play in several aspects of insect biology, including chemical communication, desiccation resistance, and immunity, it is important to gain a greater understanding of the molecular and genetic regulation of CHC production within these specialized cells. The adult oenocytes of D. melanogaster are located within the abdominal integument, and are metamerically arrayed in ribbon-like clusters radiating along the inner cuticular surface of each abdominal segment. In this video article we demonstrate a dissection technique used for the preparation of oenocytes from adult D. melanogaster. Specifically, we provide a detailed step-by-step demonstration of (1) how to fillet prepare an adult Drosophila abdomen, (2) how to identify the oenocytes and discern them from other tissues, and (3) how to remove intact oenocyte clusters from the abdominal integument. A brief experimental illustration of how this preparation can be used to examine the expression of genes involved in hydrocarbon synthesis is included. The dissected preparation demonstrated herein will allow for the detailed molecular and genetic analysis of oenocyte function in the adult fruit fly.

Dissection of Oenocytes from Adult Drosophila melanogaster

In insects, the oenocytes produce cuticular hydrocarbon compounds. These compounds protect against desiccation and facilitate chemical communication. Here we demonstrate a dissection technique used to isolate the oenocytes from adult Drosophila melanogaster, and illustrate how this preparation can be utilized to study genes involved in hydrocarbon synthesis.

वयस्क से Oenocytes के विच्छेदन ड्रोसोफिला मेलानोगास्टर</em

In Drosophila melanogaster, as in other insects, a waxy layer on the outer surface of the cuticle, composed primarily of hydrocarbon compounds, provides ...

DNA Extraction from Paraffin Embedded Material for Genetic and Epigenetic Analyses

Disease development and progression are characterized by frequent genetic and epigenetic aberrations including chromosomal rearrangements, copy number gains and losses and DNA methylation. Advances in high-throughput, genome-wide profiling technologies, such as microarrays, have significantly improved our ability to identify and detect these specific alterations. However as technology continues to improve, a limiting factor remains sample quality and availability. Furthermore, follow-up clinical information and disease outcome are often collected years after the initial specimen collection. Specimens, typically formalin-fixed and paraffin embedded (FFPE), are stored in hospital archives for years to decades. DNA can be efficiently and effectively recovered from paraffin-embedded specimens if the appropriate method of extraction is applied. High quality DNA extracted from properly preserved and stored specimens can support quantitative assays for comparisons of normal and diseased tissues and generation of genetic and epigenetic signatures 1. To extract DNA from paraffin-embedded samples, tissue cores or microdissected tissue are subjected to xylene treatment, which dissolves the paraffin from the tissue, and then rehydrated using a series of ethanol washes. Proteins and harmful enzymes such as nucleases are subsequently digested by proteinase K. The addition of lysis buffer, which contains denaturing agents such as sodium dodecyl sulfate (SDS), facilitates digestion 2. Nucleic acids are purified from the tissue lysate using buffer-saturated phenol and high speed centrifugation which generates a biphasic solution. DNA and RNA remain in the upper aqueous phase, while proteins, lipids and polysaccharides are sequestered in the inter- and organic-phases respectively. Retention of the aqueous phase and repeated phenol extractions generates a clean sample. Following phenol extractions, RNase A is added to eliminate contaminating RNA. Additional phenol extractions following incubation with RNase A are used to remove any remaining enzyme. The addition of sodium acetate and isopropanol precipitates DNA, and high speed centrifugation is used to pellet the DNA and facilitate isopropanol removal. Excess salts carried over from precipitation can interfere with subsequent enzymatic assays, but can be removed from the DNA by washing with 70% ethanol, followed by centrifugation to re-pellet the DNA 3. DNA is re-suspended in distilled water or the buffer of choice, quantified and stored at -20&deg;C. Purified DNA can subsequently be used in downstream applications which include, but are not limited to, PCR, array comparative genomic hybridization 4 (array CGH), methylated DNA Immunoprecipitation (MeDIP) and sequencing, allowing for an integrative analysis of tissue/tumor samples.

This video demonstrates the protocol for DNA extraction from formalin-fixed paraffin-embedded material. This is a multi-day procedure in which tissue sections are deparaffinized with xylene, rehydrated with ethanol and treated with proteinase K to purify and isolate DNA for subsequent gene-specific or genome-wide analysis.

जेनेटिक और Epigenetic विश्लेषण के लिए आयल एंबेडेड सामग्री से डीएनए निष्कर्षण

Disease development and progression are characterized by frequent genetic and epigenetic aberrations including chromosomal rearrangements, copy number ...

Preparation of Adult Drosophila Eyes for Thin Sectioning and Microscopic Analysis

Drosophila has long been used as model system to study development, mainly due to the ease with which it is genetically tractable. Over the years, a plethora of mutant strains and technical tricks have been developed to allow sophisticated questions to be asked and answered in a reasonable amount of time. Fundamental insight into the interplay of components of all known major signaling pathways has been obtained in forward and reverse genetic Drosophila studies. The fly eye has proven to be exceptionally well suited for mutational analysis, since, under laboratory conditions, flies can survive without functional eyes. Furthermore, the surface of the insect eye is composed of some 800 individual unit eyes (facets or ommatidia) that form a regular, smooth surface when looked at under a dissecting microscope. Thus, it is easy to see whether a mutation might affect eye development or growth by externally looking for the loss of the smooth surface ('rough eye' phenotype; Fig. 1) or overall eye size, respectively (for examples of screens based on external eye morphology see e.g.1). Subsequent detailed analyses of eye phenotypes require fixation, plastic embedding and thin-sectioning of adult eyes.
The Drosophila eye develops from the so-called eye imaginal disc, a bag of epithelial cells that proliferate and differentiate during larval and pupal stages (for review see e.g. 2). Each ommatidium consists of 20 cells, including eight photoreceptors (PR or R-cells; Fig. 2), four lens-secreting cone cells, pigment cells ('hexagon' around R-cell cluster) and a bristle. The photoreceptors of each ommatidium, most easily identified by their light sensitive organelles, the rhabdomeres, are organized in a trapezoid made up of the six "outer" (R1-6) and two "inner" photoreceptors (R7/8; R8 [Fig. 2] is underneath R7 and thus only seen in sections from deeper areas of the eye). The trapezoid of each facet is precisely aligned with those of its neighbors and the overall anteroposterior and dorsoventral axes of the eye (Fig. 3A). In particular, the ommatidia of the dorsal and ventral (black and red arrows, respectively) halves of the eye are mirror images of each other and correspond to two chiral forms established during planar cell polarity signaling (for review see e.g. 3).
The method to generate semi-thin eye sections (such as those presented in Fig. 3) described here is slightly modified from the one originally described by Tomlinson and Ready4. It allows the morphological analysis of all cells except for the transparent cone cells. In addition, the pigment of R-cells (blue arrowheads in Fig. 2 and 3) can be used as a cell-autonomous marker for the genotype of a R-cell, thus genetic requirements of genes in a subset of R-cells can readily be determined5,6.

Preparation of Adult Drosophila Eyes for Thin Sectioning and Microscopic Analysis

A standard approach to prepare adult Drosophila eyes for semi-thin sectioning and light microscopic analysis is presented here. The protocol can be used for gross morphological analysis of eye defects, or with the indicated adjustments can be used to determine genetic requirements of genes in specific cell types of the eye (e.g. clonal analysis of photoreceptors) or for electron microscopic analysis.

प्रौढ़ की तैयारी ड्रोसोफिला आंखें पतली सेक्शनिंग और सूक्ष्म विश्लेषण के लिए

Drosophila has long been used as model system to study development, mainly due to the ease with which it is genetically tractable. Over the years, a ...

Proteomic Sample Preparation from Formalin Fixed and Paraffin Embedded Tissue

Preserved clinical material is a unique source for proteomic investigation of human disorders. Here we describe an optimized protocol allowing large scale quantitative analysis of formalin fixed and paraffin embedded (FFPE) tissue. The procedure comprises four distinct steps. The first one is the preparation of sections from the FFPE material and microdissection of cells of interest. In the second step the isolated cells are lysed and processed using 'filter aided sample preparation' (FASP) technique. In this step, proteins are depleted from reagents used for the sample lysis and are digested in two-steps using endoproteinase LysC and trypsin. 
After each digestion, the peptides are collected in separate fractions and their content is determined using a highly sensitive fluorescence measurement. Finally, the peptides are fractionated on 'pipette-tip' microcolumns. The LysC-peptides are separated into 4 fractions whereas the tryptic peptides are separated into 2 fractions. In this way prepared samples allow analysis of proteomes from minute amounts of material to a depth of 10,000 proteins. Thus, the described workflow is a powerful technique for studying diseases in a system-wide-fashion as well as for identification of potential biomarkers and drug targets.

Archival formalin fixed and paraffin embedded (FFPE) clinical samples are valuable material for investigation of diseases. Here we demonstrate a sample preparation workflow allowing in-depth proteomic analysis of microdissected FFPE tissue.

Formalin से प्रोटिओमिक नमूना तैयार आयल एम्बेडेड ऊतक फिक्स्ड और

Preserved clinical material is a unique source for proteomic investigation of human disorders. Here we describe an optimized protocol allowing large scale ...

qPCR Is a Sensitive and Rapid Method for Detection of Cytomegaloviral DNA in Formalin-fixed, Paraffin-embedded Biopsy Tissue

It is crucial to identify cytomegalovirus (CMV) infection in the gastrointestinal (GI) tract of immunosuppressed patients, given their greater risk for developing severe infection. Many laboratory methods for the detection of CMV infection have been developed, including serology, viral culture, and molecular methods. Often, these methods reflect systemic involvement with CMV and do not specifically identify local tissue involvement. Therefore, detection of CMV infection in the GI tract is frequently done by traditional histology of biopsy tissue. Hematoxylin and eosin (H&#38;E) staining in conjunction with immunohistochemistry (IHC) have remained the mainstays of examining these biopsies. H&#38;E and IHC sometimes result in atypical (equivocal) staining patterns, making interpretation difficult. It was shown that quantitative polymerase chain reaction (qPCR) for CMV can successfully be performed on formalin-fixed, paraffin-embedded (FFPE) biopsy tissue for very high sensitivity and specificity. The goal of this protocol is to demonstrate how to perform qPCR testing for the detection of CMV in FFPE biopsy tissue in a clinical laboratory setting. This method is likely to be of great benefit for patients in cases of equivocal staining for CMV in GI biopsies.

This protocol describes qPCR detection of cytomegalovirus in formalin-fixed, paraffin-embedded biopsy tissue, which is rapid, sensitive, specific, and useful for interpreting equivocal hematoxylin and eosin or immunohistochemical staining patterns.

qPCR formalin-तय, आयल एम्बेडेड बायोप्सी ऊतक में Cytomegaloviral डीएनए का पता लगाने के लिए एक संवेदनशील और तेजी से विधि है

It is crucial to identify cytomegalovirus (CMV) infection in the gastrointestinal (GI) tract of immunosuppressed patients, given their greater risk for ...

Indirect Immunofluorescence on Frozen Sections of Mouse Mammary Gland

Indirect immunofluorescence is used to detect and locate proteins of interest in a tissue. The protocol presented here describes a complete and simple method for the immune detection of proteins, the mouse lactating mammary gland being taken as an example. A protocol for the preparation of the tissue samples, especially concerning the dissection of mouse mammary gland, tissue fixation and frozen tissue sectioning, are detailed. A standard protocol to perform indirect immunofluorescence, including an optional antigen retrieval step, is also presented. The observation of the labeled tissue sections as well as image acquisition and post-treatments are also stated. This procedure gives a full overview, from the collection of animal tissue to the cellular localization of a protein. Although this general method can be applied to other tissue samples, it should be adapted to each tissue/primary antibody couple studied.

The indirect immunofluorescence protocol described in this article allows the detection and the localization of proteins in the mouse mammary gland. A complete method is given to prepare mammary gland samples, to perform immunohistochemistry, to image the tissue sections by fluorescence microscopy, and to reconstruct images.

माउस स्तन ग्रंथि के जमे हुए वर्गों पर अप्रत्यक्ष इम्यूनोफ्लोरेसेंस

Indirect immunofluorescence is used to detect and locate proteins of interest in a tissue. The protocol presented here describes a complete and simple ...

Employing Digital Droplet PCR to Detect BRAF V600E Mutations in Formalin-fixed Paraffin-embedded Reference Standard Cell Lines

ddPCR is a highly sensitive PCR method that utilizes a water-oil emulsion system. Using a droplet generator, an extracted nucleic acid sample is partitioned into ~20,000 nano-sized, water-in-oil droplets, and PCR amplification occurs in individual droplets. The ddPCR approach is in identifying sequence mutations, copy number alterations, and select structural rearrangements involving targeted genes. Here, we demonstrate the use of ddPCR as a powerful technique for precisely quantitating rare BRAF V600E mutations in FFPE reference standard cell lines, which is helpful in identifying individuals with cancer. In conclusion, ddPCR technique offers the potential to precisely profile the specific rare mutations in different genes in various types of FFPE samples.

The goal of this video is to demonstrate how to perform&#160;automated DNA extraction from formalin-fixed paraffin-embedded (FFPE) reference standard cell lines and digital droplet PCR&#160;(ddPCR) analysis to detect rare mutations in a clinical setting. Detecting mutations in FFPE samples demonstrates the clinical utility of ddPCR in FFPE samples.