Anti-RDL and Anti-mGlutR1 Receptors Antibody Testing in Honeybee Brain Sections using CRISPR-Cas9
Cluster Regularly Interspaced Short Palindromic Repeats (CRISPR)/CRISPR-associated protein 9 (Cas9) is a gene editing technique widely used in studies of gene function. We use this method in this study to check for the specificity of antibodies developed against the insect GABAA receptor subunit Res...
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creator | Sinakevitch, Irina Kurtzman, Zev Choi, Hyun G. Ruiz Pardo, David Arturo Dahan, Romain A. Klein, Nathaniel Bugarija, Branimir Wendlandt, Erik Smith, Brian H. |
description | Cluster Regularly Interspaced Short Palindromic Repeats (CRISPR)/CRISPR-associated protein 9 (Cas9) is a gene editing technique widely used in studies of gene function. We use this method in this study to check for the specificity of antibodies developed against the insect GABAA receptor subunit Resistance to Dieldrin (RDL) and a metabotropic glutamate receptor mGlutR1 (mGluRA). The antibodies were generated in rabbits against the conjugated peptides specific to fruit flies (Drosophila melanogaster) as well to honeybees (Apis mellifera). We used these antibodies in honeybee brain sections to study the distribution of the receptors in honeybee brains. The antibodies were affinity purified against the peptide and tested with immunoblotting and the classical method of preadsorption with peptide conjugates to show that the antibodies are specific to the corresponding peptide conjugates against which they were raised. Here we developed the CRISPR-Cas9 technique to test for the reduction of protein targets in the brain 48 h after CRISPR-Cas9 injection with guide RNAs designed for the corresponding receptor. The CRISPR-Cas9 method can also be used in behavioral analyses in the adult bees when one or multiple genes need to be modified. |
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We use this method in this study to check for the specificity of antibodies developed against the insect GABAA receptor subunit Resistance to Dieldrin (RDL) and a metabotropic glutamate receptor mGlutR1 (mGluRA). The antibodies were generated in rabbits against the conjugated peptides specific to fruit flies (Drosophila melanogaster) as well to honeybees (Apis mellifera). We used these antibodies in honeybee brain sections to study the distribution of the receptors in honeybee brains. The antibodies were affinity purified against the peptide and tested with immunoblotting and the classical method of preadsorption with peptide conjugates to show that the antibodies are specific to the corresponding peptide conjugates against which they were raised. Here we developed the CRISPR-Cas9 technique to test for the reduction of protein targets in the brain 48 h after CRISPR-Cas9 injection with guide RNAs designed for the corresponding receptor. The CRISPR-Cas9 method can also be used in behavioral analyses in the adult bees when one or multiple genes need to be modified.</description><identifier>ISSN: 1940-087X</identifier><identifier>EISSN: 1940-087X</identifier><identifier>DOI: 10.3791/59993</identifier><identifier>PMID: 32065127</identifier><language>eng</language><publisher>United States: MyJove Corporation</publisher><subject>Animals ; Antibodies - metabolism ; Bees - metabolism ; Brain - metabolism ; CRISPR-Cas Systems - genetics ; Dieldrin - metabolism ; Drosophila melanogaster - genetics ; Neuroscience ; Rabbits ; Receptors, Metabotropic Glutamate - metabolism ; RNA, Guide, CRISPR-Cas Systems - genetics ; RNA, Messenger - genetics ; RNA, Messenger - metabolism</subject><ispartof>Journal of Visualized Experiments, 2020-01 (155)</ispartof><rights>Copyright © 2020, Journal of Visualized Experiments</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c327t-ecb144d0fc3994c8d612764fee7386589cece5a01f3d2e9c882c6206a320e7583</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Uhttps://www.jove.com/files/email_thumbs/59993.png</thumbnail><link.rule.ids>314,780,784,3843,27924,27925</link.rule.ids><linktorsrc>$$Uhttp://dx.doi.org/10.3791/59993$$EView_record_in_Journal_of_Visualized_Experiments$$FView_record_in_$$GJournal_of_Visualized_Experiments</linktorsrc><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/32065127$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Sinakevitch, Irina</creatorcontrib><creatorcontrib>Kurtzman, Zev</creatorcontrib><creatorcontrib>Choi, Hyun G.</creatorcontrib><creatorcontrib>Ruiz Pardo, David Arturo</creatorcontrib><creatorcontrib>Dahan, Romain A.</creatorcontrib><creatorcontrib>Klein, Nathaniel</creatorcontrib><creatorcontrib>Bugarija, Branimir</creatorcontrib><creatorcontrib>Wendlandt, Erik</creatorcontrib><creatorcontrib>Smith, Brian H.</creatorcontrib><title>Anti-RDL and Anti-mGlutR1 Receptors Antibody Testing in Honeybee Brain Sections using CRISPR-Cas9</title><title>Journal of Visualized Experiments</title><addtitle>J Vis Exp</addtitle><description>Cluster Regularly Interspaced Short Palindromic Repeats (CRISPR)/CRISPR-associated protein 9 (Cas9) is a gene editing technique widely used in studies of gene function. We use this method in this study to check for the specificity of antibodies developed against the insect GABAA receptor subunit Resistance to Dieldrin (RDL) and a metabotropic glutamate receptor mGlutR1 (mGluRA). The antibodies were generated in rabbits against the conjugated peptides specific to fruit flies (Drosophila melanogaster) as well to honeybees (Apis mellifera). We used these antibodies in honeybee brain sections to study the distribution of the receptors in honeybee brains. The antibodies were affinity purified against the peptide and tested with immunoblotting and the classical method of preadsorption with peptide conjugates to show that the antibodies are specific to the corresponding peptide conjugates against which they were raised. Here we developed the CRISPR-Cas9 technique to test for the reduction of protein targets in the brain 48 h after CRISPR-Cas9 injection with guide RNAs designed for the corresponding receptor. 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We use this method in this study to check for the specificity of antibodies developed against the insect GABAA receptor subunit Resistance to Dieldrin (RDL) and a metabotropic glutamate receptor mGlutR1 (mGluRA). The antibodies were generated in rabbits against the conjugated peptides specific to fruit flies (Drosophila melanogaster) as well to honeybees (Apis mellifera). We used these antibodies in honeybee brain sections to study the distribution of the receptors in honeybee brains. The antibodies were affinity purified against the peptide and tested with immunoblotting and the classical method of preadsorption with peptide conjugates to show that the antibodies are specific to the corresponding peptide conjugates against which they were raised. Here we developed the CRISPR-Cas9 technique to test for the reduction of protein targets in the brain 48 h after CRISPR-Cas9 injection with guide RNAs designed for the corresponding receptor. 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subjects | Animals Antibodies - metabolism Bees - metabolism Brain - metabolism CRISPR-Cas Systems - genetics Dieldrin - metabolism Drosophila melanogaster - genetics Neuroscience Rabbits Receptors, Metabotropic Glutamate - metabolism RNA, Guide, CRISPR-Cas Systems - genetics RNA, Messenger - genetics RNA, Messenger - metabolism |
title | Anti-RDL and Anti-mGlutR1 Receptors Antibody Testing in Honeybee Brain Sections using CRISPR-Cas9 |
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