إعداد مقدما من microinjection <ol style=";text-align:right;direction:rtl"><li style=";text-align:right;direction:rtl"> البعوض الدم : للحقن من الاثنين الى الجمعة من الإناث إطعام في يوم الخميس الماضي. </li><li style=";text-align:right;direction:rtl"> تعد الإبر الزجاج باستخدام برنامج 3 أو 2 (انظر المواد). </li><li style=";text-align:right;direction:rtl"> مد أنبوب لأجنة ذبابة الفاكهة هو قارورة الثقافة. الرطب القطن والصوف في الجزء السفلي ، مع قرص من الورق الرطب تصفية تغطية هذه الأزمة. </li><li style=";text-align:right;direction:rtl"> إعداد زلة تغطية البلاستيك عن طريق الالتزام المزدوج الجانب الشريط إلى نهاية واحدة. الشريط تقليم لتغطية زلة بحيث تنتهي عند حافة الانزلاق الغطاء. </li><li style=";text-align:right;direction:rtl"> يعد النفط مقابل تجفيف (انظر المواد) </li><li style=";text-align:right;direction:rtl"> 150 مل دورق البلاستيك مع القطن والصوف الرطب في الجزء السفلي ، مع تغطية قرص من الورق الرطب تصفية (80mm Whatman) للحفاظ على الأجنة بعد الحقن. </li></ol> إعداد زرع القسري <ol style=";text-align:right;direction:rtl"><li style=";text-align:right;direction:rtl"> جمع 60-10 الإناث تغذية الدم مع استخدام لالشافطة ونقلها إلى القارورة الثقافة ذبابة الفاكهة مع القطن الرطب ورقة الترشيح. </li><li style=";text-align:right;direction:rtl"> وضع البعوض العودة الى ظروف insectory في الظلام ، والسماح لتضع بيضها و1H 15min. </li><li style=";text-align:right;direction:rtl"> اسمحوا البالغين تطير في القفص ، وإزالة القرص رقة الترشيح مع الأجنة. </li><li style=";text-align:right;direction:rtl"> ليصطف والبيض ، وذلك بموجب نطاق تشريح. باستخدام الملقط غرامة رقم 5 أو الفرشاة الجميلة ، واختيار اللون الرمادي لdarkish الرمادي الأجنة وترتيبها في خط على مربع من الورق Whatman 3MM المنقوع بالماء. يجب أن تكون جميع الأجنة في الاتجاه نفسه ، وكما يجب أن يكون الحقن في القطب الخلفي. نهاية الأمامي من الجنين هو أوسع قليلا من الخلفية. الجافة ورقة الترشيح مع الأجنة عن طريق الضغط على ورق الترشيح جافة لأنها (أشياء الرطب ولن تلتزم الشريط). لنقل البيض ، وعكس الشريحة التي تحتوي على الشريط على الوجهين ، ثم اضغط بلطف ضد البيض. نهاية الخلفي من البيض يجب أن تكون قريبة جدا من حافة الشريط جانب ومزدوجة. </li><li style=";text-align:right;direction:rtl"> تجفيف الأجنة حوالي 1 دقيقة. في درجة حرارة الغرفة. أنها بداية لرصعة قليلا لأنها جافة. </li><li style=";text-align:right;direction:rtl"> تغطي الأجنة المجفف مع النفط لمنع جفاف الهالوكربون أخرى. </li></ol> Microinjection للأجنة <ol style=";text-align:right;direction:rtl"><li style=";text-align:right;direction:rtl"> وأهم جانب من جوانب جيدة الحقن هي نوعية الإبرة (انظر المواد). </li><li style=";text-align:right;direction:rtl"> شغل الإبرة مع الحل القائم على الحمض النووي ليتم حقنها باستخدام microloader. مطلوب حل القليل جدا الحقن : 1 الى 2 ميكرولتر. </li><li style=";text-align:right;direction:rtl"> الاتصال الإبرة إلى Transjector ، التي تسيطر على الوقت الحقن (مانو) وضغط (600) ، والضغط الخلفي (250). يتم تنفيذ Microinjection باستخدام المجهر مع مرحلة الانتقال (لايكا) في التكبير 10 x و micromanipulator. إذا لزم الأمر ، قد أثار المجهر مرحلة التحضير التي تكون التراص الشرائح المجهر 4-5. ضع الغطاء زلة تحمل أجنة على المرحلة التي أثيرت. حقن الأجنة أفقيا لمنع تمزق من باطنة المشيماء ؛ اختراق ينبغي أن يكون في القطب الخلفي. عن طريق الحقن ، وأظل الإبرة ثابتة وتحريك مرحلة من مراحل المجهر. </li><li style=";text-align:right;direction:rtl"> حقن 0،2-0،5 NL الحل الموافق حوالي 1-5 ٪ من حجم الجنين. السيطرة على حجم الحقن عن طريق ضبط ضغط الحقن والوقت. ينبغي أن انحنى قليلا ، والأجنة المجفف في أعقاب استعادة مظهر متورم الحقن. </li><li style=";text-align:right;direction:rtl"> اختيار الأجنة من زلة تغطية باستخدام الملقط الغرامة أو فرشاة غرامة ، ووضعها في كوب من البلاستيك مع القطن الرطب ورقة الترشيح الرطب. تغطي الدورق مع المناديل الورقية. تبقي في مكان مع شريط مطاطي حول الحافة والعودة إلى الظروف insectary لمدة 4 أيام. </li></ol> بعد الحقن <ol style=";text-align:right;direction:rtl"><li style=";text-align:right;direction:rtl"> بعد أربعة أيام ، ورقة الجنين بدقة مكان ، جنين ، الجانب السلبي ، على الماء في علبة بلاستيكية كبيرة مع كمية صغيرة من الطعام. أجنة يفقس على مدى فترة طويلة جدا : لا تخلص من ثقافة على الأقل حتى 4-5 أسابيع بعد الحقن. </li></ol> تلاحظ الحمض النووي للحقن تم عزل الحمض النووي البلازميد حل للحقن باستخدام طقم البلازميد EndoFree. وعجلت بناء مزيج مساعد البلازميد معا في تركيز الحق ، مع izopropanol. وكان بيليه تغسل مع الايثانول 70 ٪ قبل إعادة التعليق في المخزن الحقن. قبل الحقن ، باستخدام الحمض النووي نظيفة Millex GV - العمود.

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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>1x Injection solution</td>
<td>Buffer</td>
<td>&nbsp;</td>
<td>&nbsp;</td>
<td>5mM KCl, 0.1mM sodium phosphate, ph 6. 8</td>
</tr>
<tr>
<td>Construct plasmid</td>
<td>DNA</td>
<td>&nbsp;</td>
<td>&nbsp;</td>
<td>0.5 mg/ml. </td>
</tr>
<tr>
<td>Helper plasmid</td>
<td>DNA</td>
<td>&nbsp;</td>
<td>&nbsp;</td>
<td>0.3 mg/ml </td>
</tr>
<tr>
<td>EndoFree Plasmid kit</td>
<td>Kit</td>
<td>Qiagen</td>
<td>&nbsp;</td>
<td>&nbsp;</td>
<tr>
<td>Millex-GV column</td>
<td>&nbsp;</td>
<td>&nbsp;</td>
<td>SLGV RO4 NL</td>
<td>To clean DNA.</td>
</tr>
<tr>
<td>Glass puller</td>
<td>Instrument</td>
<td>Sutter Instrument Co</td>
<td>Model P-87</td>
<td>Heat-815, Pull-10, Vel-10, Time-100.
Heat-700, Pull-30, Vel-36, Time-50
</td>
</tr>
<tr>
<td>Quartz puller</td>
<td>Instrument</td>
<td>Sutter Instrument Co</td>
<td>Model P-2000</td>
<td>Heat-275, Fil-3, Vel-38, Del-250, Pull-141</td>
</tr>
<tr>
<td>Injection glass needles</td>
<td>&nbsp;</td>
<td>&nbsp;</td>
<td>&nbsp;</td>
<td>Prepared by drawing capillary tubing into a fine 3-8 um with a shaft of approximately 100-300 um micropipette puller. When the needle is new, the tip is sealed and usually breaks in the first or second injection or the glass needle tip can be beveled using a Brown type micro-pipette beveller (Sutter Instrument).</td>
</tr>
<tr>
<td>Aedes aegypti</td>
<td>Animal</td>
<td>&nbsp;</td>
<td>&nbsp;</td>
<td>Male and female mosquitos, to obtain embryos.</td>
</tr>
<tr>
<td>Drosophila culture vial</td>
<td>&nbsp;</td>
<td>&nbsp;</td>
<td>&nbsp;</td>
<td>For mosquito egg-laying.</td>
</tr>
<tr>
<td>Halocarbon oil</td>
<td>Reagent</td>
<td>&nbsp;</td>
<td>&nbsp;</td>
<td>Oil for desiccation: Halocarbon oil 700:Halocarbon oil 27(1:1)</td>
</tr>
<tr>
<td>Forceps No5</td>
<td>Tool</td>
<td>&nbsp;</td>
<td>&nbsp;</td>
<td>&nbsp;</td>
<tr>
<td>Fine paintbrush</td>
<td>&nbsp;</td>
<td>Sable</td>
<td>No. 0000</td>
<td>&nbsp;</td>
<tr>
<td>Whatman paper</td>
<td>Tool</td>
<td>&nbsp;</td>
<td>&nbsp;</td>
<td>&nbsp;</td>
<tr>
<td>Microloader</td>
<td>Tool</td>
<td>Eppendorf</td>
<td>5242 956.003</td>
<td>&nbsp;</td>
<tr>
<td>Transjector</td>
<td>Tool</td>
<td>Eppendorf</td>
<td>&nbsp;</td>
<td>&nbsp;</td>
<tr>
<td>Microscope</td>
<td>&nbsp;</td>
<td>Leica</td>
<td>&nbsp;</td>
<td>With moving stage and micromanipulator.</td>
</tr>
<tr>
<td>3MM Whatman paper</td>
<td>&nbsp;</td>
<td>&nbsp;</td>
<td>&nbsp;</td>
<td>&nbsp;</td>
<tr>
<td>double sided tape</td>
<td>&nbsp;</td>
<td>&nbsp;</td>
<td>&nbsp;</td>
<td>&nbsp;</td>		</tbody>
		</table>
		</div>
			<div>
					</div>

microinjection of a. aegypti embryos to obtain transgenic mosquitoes

في هذا الفيديو ، Nijole Jasinskiene يوضح المنهجية المستخدمة لتوليد البعوض المعدلة وراثيا الزاعجة المصرية ، والتي هي نواقل حمى الضنك. وأظهرت أساليب إعداد صحيح microinjection الإبر ، dessicating الأجنة ، وأداء microinjection.

Watch this Scientific Journal Video about Microinjection of A. aegypti Embryos to Obtain Transgenic Mosquitoes at JoVE.com

Microinjection of A. aegypti Embryos to Obtain Transgenic Mosquitoes

Microinjection الجنين بعوض ألف الحصول على البعوض المعدلة وراثيا

In this video, Nijole Jasinskiene demonstrates the methodology employed to generate transgenic Aedes aegypti mosquitoes, which are vectors for dengue ...

microinjection-of-a-aegypti-embryos-to-obtain-transgenic-mosquitoes

Research

JoVE Journal

Biology

15.1K Views.  University of California, Irvine (UCI). في هذا الفيديو ، Nijole Jasinskiene يوضح المنهجية المستخدمة لتوليد البعوض المعدلة وراثيا الزاعجة المصرية ، والتي هي نواقل حمى الضنك. وأظهرت أساليب إعداد صحيح microinjection الإبر ، dessicating الأجنة ، وأداء microinjection.

Video: Microinjection of A. aegypti Embryos to Obtain Transgenic Mosquitoes

Injection of An. stephensi Embryos to Generate Malaria-resistant Mosquitoes

The introduction of exogenous genes into the genomes of mosquitoes requires microinjection techniques tailored to the specific species of interest. This video protocol demonstrates a method used by the James laboratory to microinject DNA constructs into Anopheles stephensi embryos for the generation of transformed mosquitoes. Techniques for preparing microinjection needles, collecting and preparing embryos and performing the microinjection are illustrated.

Anopheles stephensi mosquitoes are vectors for malaria inhabiting India and throughout Asia. This video demonstrates the technique for performing microinjections of this species with transgenes that will confer resistance to the malaria to the mosquito. Much of the methodology demonstrated in this video is applicable to microinjection techniques of other mosquito species.

حقن آن. stephensi الجنين لتوليد الملاريا مقاومة البعوض

The introduction of exogenous genes into the genomes of mosquitoes requires microinjection techniques tailored to the specific species of interest. This ...

Protocol for Dengue Infections in Mosquitoes (A. aegypti) and Infection Phenotype Determination

The purpose of this procedure is to infect the Aedes mosquito with dengue virus in a laboratory condition and examine the infection level and dynamic of the virus in the mosquito tissues. This protocol is routinely used for studying mosquito-virus interactions, especially for identification of novel host factors that are able to determine vector competence. The entire experiment must be conducted in a BSL2 laboratory. Similar to Plasmodium falciparum infections, proper attire including gloves and lab coat must be worn at all times. After the experiment, all the materials that came in contact with the virus need to be treated with 75% ethanol and bleached before proceeding with normal washing. All other materials need to be autoclaved before discarding them.

Protocol for Dengue Infections in Mosquitoes A. aegypti and Infection Phenotype Determination

Once a gene is identified as potentially refractory for the dengue virus, it must be evaluated for it's role in preventing viral infections within the mosquito. This protocol illustrates how the extent of dengue infections of mosquitoes can be assayed. The techniques for growing up the virus in culture, membrane feeding mosquitoes human blood, and assaying viral titers in the mosquito midgut are demonstrated.

بروتوكول للعدوى حمى الضنك في البعوض (بعوض ألف) ، وتحديد النمط الظاهري العدوى

The purpose of this procedure is to infect the Aedes mosquito with dengue virus in a laboratory condition and examine the infection level and dynamic of ...

Dissection of Midgut and Salivary Glands from Ae. aegypti Mosquitoes

The mosquito midgut and salivary glands are key entry and exit points for pathogens such as Plasmodium parasites and Dengue viruses. This video protocol demonstrates dissection techniques for removal of the midgut and salivary glands from Aedes aegypti mosquitoes. 



The mosquito midgut and salivary glands are key entry and exit points for vector pathogens like Plasmodium falciparum and the dengue virus. This video demonstrates the dissection techniques for removing the midgut and salivary glands from Aedes aegypti mosquitoes.

تشريح الغدد اللعابية والمعي المتوسط ​​من AE. بعوض البعوض

The mosquito midgut and salivary glands are key entry and exit points for pathogens such as Plasmodium parasites and Dengue viruses. This video protocol ...

Building a Better Mosquito: Identifying the Genes Enabling Malaria and Dengue Fever Resistance in A. gambiae and A. aegypti Mosquitoes

In this interview, George Dimopoulos focuses on the physiological mechanisms used by mosquitoes to combat Plasmodium falciparum and dengue virus infections.   Explanation is given for how key refractory genes, those genes conferring resistance to vector pathogens, are identified in the mosquito and how this knowledge can be used to generate transgenic mosquitoes that are unable to carry the malaria parasite or dengue virus.

In this interview, George Dimopoulos focuses on the physiological mechanisms used by mosquitoes to combat Plasmodium falciparum and dengue virus infections. Explanation is given for how key refractory genes, those genes conferring resistance to vector pathogens, are identified in the mosquito and how this knowledge can be used to generate transgenic mosquitoes that are unable to carry the malaria parasite or dengue virus.

بناء عالم أفضل البعوض : تحديد الجينات تمكين الملاريا وحمى الضنك حمى المقاومة في الغامبية ألف وألف البعوض بعوض

In this interview, George Dimopoulos focuses on the physiological mechanisms used by mosquitoes to combat Plasmodium falciparum and dengue virus ...

Generation of Stable Transgenic C. elegans Using Microinjection

Transgenic Caenorhabditis elegans can be readily created via microinjection of a DNA plasmid solution into the gonad 1. The plasmid DNA rearranges to form extrachromosomal concatamers that are stably inherited, though not with the same efficiency as actual chromosomes 2. A gene of interest is co-injected with an obvious phenotypic marker, such as rol-6 or GFP, to allow selection of transgenic animals under a dissecting microscope. The exogenous gene may be expressed from its native promoter for cellular localization studies. Alternatively, the transgene can be driven by a different tissue-specific promoter to assess the role of the gene product in that particular cell or tissue. This technique efficiently drives gene expression in all tissues of C. elegans except for the germline or early embryo 3. Creation of transgenic animals is widely utilized for a range of experimental paradigms. This video demonstrates the microinjection procedure to generate transgenic worms. Furthermore, selection and maintenance of stable transgenic C. elegans lines is described.

This video demonstrates the technique of microinjection into the gonad of C. elegans to create transgenic animals.

توليد مستقرة ايليجانس جيم المعدلة وراثيا عن طريق Microinjection

Transgenic Caenorhabditis elegans can be readily created via microinjection of a DNA plasmid solution into the gonad 1.  The plasmid DNA rearranges to ...

Microinjection of Zebrafish Embryos to Analyze Gene Function

One of the advantages of studying zebrafish is the ease and speed of manipulating protein levels in the embryo.  Morpholinos, which are synthetic oligonucleotides with antisense complementarity to target RNAs, can be added to the embryo to reduce the expression of a particular gene product.  Conversely, processed mRNA can be added to the embryo to increase levels of a gene product.  The vehicle for adding either mRNA or morpholino to an embryo is microinjection.  Microinjection is efficient and rapid, allowing for the injection of hundreds of embryos per hour.  This video shows all the steps involved in microinjection.  Briefly, eggs are collected immediately after being laid and lined up against a microscope slide in a Petri dish.  Next, a fine-tipped needle loaded with injection material is connected to a microinjector and an air source, and the microinjector controls are adjusted to produce a desirable injection volume.  Finally, the needle is plunged into the embryo's yolk and the morpholino or mRNA is expelled.

This video shows how morpholino or mRNA can be injected into zebrafish embryos at the one-cell stage to decrease or increase the level of specific gene products during subsequent development.

Microinjection الجنين اسماك الزرد إلى تحليل وظائف الجينات

One of the advantages of studying zebrafish is the ease and speed of manipulating protein levels in the embryo.  Morpholinos, which are synthetic ...

Microinjection of Medaka Embryos for use as a Model Genetic Organism

In this video, we demonstrate the technique of microinjection into one-cell stage medaka embryos. Medaka is a small egg-laying freshwater fish that allows both genetic and embryological analyses and is one of the vertebrate model organisms in which genome-wide phenotype-driven mutant screens were carried out 1, as in zebrafish and the mouse. Divergence of functional overlap of related genes between medaka and zebrafish allows identification of novel phenotypes that are unidentifiable in a single species 2, thus medaka and zebrafish are complementary for genetic dissection of vertebrate genome functions.
To take advantage of medaka fish whose embryos are transparent and develop externally, microinjection is an essential technique to inject cell-tracers for labeling cells, mRNAs or anti-sense oligonucleotides for over-expressing and knocking-down genes of interest, and DNAs for making transgenic lines.

Medaka and zebrafish are complementary for genetic dissection of vertebrate genome functions. This protocol highlights the key points for successful microinjection into medaka embryos, an important technique for embryological and genetic analysis using medaka and zebrafish in a laboratory.

Microinjection الجنين الميداكا لاستخدامها بوصفها كائنا النموذجي الوراثية

In this video, we demonstrate the technique of microinjection into one-cell stage medaka embryos. Medaka is a small egg-laying freshwater fish that allows ...

RNAi-mediated Gene Knockdown and In Vivo Diuresis Assay in Adult Female Aedes aegypti Mosquitoes

This video protocol demonstrates an effective technique to knockdown a particular gene in an insect and conduct a novel bioassay to measure excretion rate. This method can be used to obtain a better understanding of the process of diuresis in insects and is especially useful in the study of diuresis in blood-feeding arthropods that are able to take up huge amounts of liquid in a single blood meal. 
This RNAi-mediated gene knockdown combined with an in vivo diuresis assay was developed by the Hansen lab to study the effects of RNAi-mediated knockdown of aquaporin genes on Aedes aegypti mosquito diuresis1. 
The protocol is setup in two parts: the first demonstration illustrates how to construct a simple mosquito injection device and how to prepare and inject dsRNA into the thorax of mosquitoes for RNAi-mediated gene knockdown. The second demonstration illustrates how to determine excretion rates in mosquitoes using an in vivo bioassay.

RNAi-mediated Gene Knockdown and In Vivo Diuresis Assay in Adult Female Aedes aegypti Mosquitoes

In this protocol we combine RNAi-mediated gene silencing with an in vivo diuresis assay to study the effects knockdown of genes of interest has on mosquito fluid excretion.

رني ضربة قاضية بوساطة الجينات و<em&gt; في الجسم الحي</em&gt; فحص إدرار البول في الإناث البالغات<em&gt; الزاعجة المصرية</em&gt; البعوض

This video protocol demonstrates an effective technique to knockdown a particular gene in an insect and conduct a novel bioassay to measure excretion ...

Generation of Transgenic Hydra by Embryo Microinjection

As a member of the phylum Cnidaria, the sister group to all bilaterians, Hydra can shed light on fundamental biological processes shared among multicellular animals. Hydra is used as a model for the study of regeneration, pattern formation, and stem cells. However, research efforts have been hampered by lack of a reliable method for gene perturbations to study molecular function. The development of transgenic methods has revitalized the study of Hydra biology1. Transgenic Hydra allow for the tracking of live cells, sorting to yield pure cell populations for biochemical analysis, manipulation of gene function by knockdown and over-expression, and analysis of promoter function. Plasmid DNA injected into early stage embryos randomly integrates into the genome early in development. This results in hatchlings that express transgenes in patches of tissue in one or more of the three lineages (ectodermal epithelial, endodermal epithelial, or interstitial). The success rate of obtaining a hatchling with transgenic tissue is between 10% and 20%. Asexual propagation of the transgenic hatchling is used to establish a uniformly transgenic line in a particular lineage. Generating transgenic Hydra is surprisingly simple and robust, and here we describe a protocol that can be easily implemented at low cost.

Generation of Transgenic Hydra by Embryo Microinjection

Stably transgenic Hydra are made by microinjection of plasmid DNA into embryos followed by random genomic integration and asexual propagation to establish a uniform line. Transgenic Hydra are used to track cell movements, overexpress genes, study promoter function, or knock down gene expression using RNAi.

جيل المعدلة وراثيا<em&gt; حيدرة</em&gt; من جانب الأجنة حقن مكروي

As a member of the phylum Cnidaria, the sister group to all bilaterians, Hydra can shed light on fundamental biological processes shared among ...

Maintaining Aedes aegypti Mosquitoes Infected with Wolbachia

Aedes aegypti mosquitoes experimentally infected with Wolbachia are being utilized in programs to control the spread of arboviruses such as dengue, chikungunya and Zika. Wolbachia-infected mosquitoes can be released into the field to either reduce population sizes through incompatible matings or to transform populations with mosquitoes that are refractory to virus transmission. For these strategies to succeed, the mosquitoes released into the field from the laboratory must be competitive with native mosquitoes. However, maintaining mosquitoes in the laboratory can result in inbreeding, genetic drift and laboratory adaptation which can reduce their fitness in the field and may confound the results of experiments. To test the suitability of different Wolbachia infections for deployment in the field, it is necessary to maintain mosquitoes in a controlled laboratory environment across multiple generations. We describe a simple protocol for maintaining Ae. aegypti mosquitoes in the laboratory, which is suitable for both Wolbachia-infected and wild-type mosquitoes. The methods minimize laboratory adaptation and implement outcrossing to increase the relevance of experiments to field mosquitoes. Additionally, colonies are maintained under optimal conditions to maximize their fitness for open field releases.

Maintaining Aedes aegypti Mosquitoes Infected with Wolbachia

Aedes aegypti mosquitoes infected with Wolbachia are being released into natural populations to suppress the transmission of arboviruses. We describe methods to rear Ae. aegypti with Wolbachia infections in the laboratory for experiments and field release, taking precautions to minimize laboratory adaptation and selection.

الحفاظ على بعوض الزاعجة المصرية "البعوض مصابة" ولبخيه

Aedes aegypti mosquitoes experimentally infected with Wolbachia are being utilized in programs to control the spread of arboviruses such as dengue, ...