primary rabbit monoclonal antibodies against v5 (ABclonal Biotechnology)
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90
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ABclonal Biotechnology
primary rabbit monoclonal antibodies against v5
Primary Rabbit Monoclonal Antibodies Against V5, supplied by ABclonal Biotechnology, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/primary+rabbit+antibodies+against+v5/primary+rabbit+monoclonal+antibodies+against+v5/pm38411032-196-23-30
Average 90 stars, based on 1 article reviews
Primary Rabbit Monoclonal Antibodies Against V5, supplied by ABclonal Biotechnology, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/primary+rabbit+antibodies+against+v5/primary+rabbit+monoclonal+antibodies+against+v5/pm38411032-196-23-30
Average 90 stars, based on 1 article reviews
primary rabbit monoclonal antibodies against v5 - by Bioz Stars,
2026-09
90/100 stars
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Incubation:Article Title: Distribution analysis of TRH in Bactrocera dorsalis using a CRISPR/Cas9-mediated reporter knock-in strain. Article Snippet: Associate Editor: Shahid Karim Abstract Although the study of many genes and their protein products is limited by the availability of high-quality antibodies, this problem could be solved by fusing a tag/reporter to an endogenous gene using a gene-editing approach.. The type II bacterial CRISPR/Cas system has been demonstrated to be an efficient gene-targeting technology for many insects, including the oriental fruit fly Bactrocera dorsalis.. However, knocking in, an important editing method of the CRISPR/Cas9 system, has lagged in its application in insects. Blocking Assay:Article Title: Distribution analysis of TRH in Bactrocera dorsalis using a CRISPR/Cas9-mediated reporter knock-in strain. Article Snippet: Associate Editor: Shahid Karim Abstract Although the study of many genes and their protein products is limited by the availability of high-quality antibodies, this problem could be solved by fusing a tag/reporter to an endogenous gene using a gene-editing approach.. The type II bacterial CRISPR/Cas system has been demonstrated to be an efficient gene-targeting technology for many insects, including the oriental fruit fly Bactrocera dorsalis.. However, knocking in, an important editing method of the CRISPR/Cas9 system, has lagged in its application in insects. |