Anti-Adeno-associated virus (AAV), VP 1

Category: Anti-AAV Products
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03-61056
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Product Name Anti-Adeno-associated virus (AAV), VP 1
Description Adeno-associated virus (AAV) is a small virus which infects humans and some other primate species. AAV is not currently known to cause disease and consequently the virus causes a very mild immune response. Gene therapy vectors using AAV can infect both dividing and quiescent cells and persist in an extrachromosomal state without integrating into the genome of the host cell. These features make AAV a very attractive candidate for creating viral vectors for gene therapy, and for the creation of isogenic human disease models. Mouse Monoclonal Antibody to Adeno-associated virus (AAV), VP 1. A1 reacts with VP1 of adeno-associated virus. A1 reacts with VP1 of AAV-2; weak cross-reaction with serotypes 1, 3, 4, 5, 6. In immunoprecipitation, an occasional reaction with a non-AAV-derived protein is found.
Synonyms AAV2
Clone A1
Immunogen Adeno-associated virus capsid proteins and virus particles
Isotype IgG2a
Specificity Epitope mapping experiments (Wobus et al., see below) identified aa123 to aa131 of VP1 capsid protein as the specific binding region. In immunoprecipitation, an occasional reaction with a non-AAV-derived protein is found
Reactivity Human, Primate
Applications ELISA, IF, IHC, IP, WB
Form Purified (Protein A), in PBS containing 1% BSA and 0.1% sodium-azide
Storage 2-8C for immediate use, or at -2°C (aliquot)
References Wistuba, A. et al.(1997) J. of Virology 71: 1341-1352Wobus,CE. et al. (2000) J. Virol 74 (19): 9281-9292
Background Adeno-associated virus (AAV) is a small virus which infects humans and some other primate species. AAV is not currently known to cause disease and consequently the virus causes a very mild immune response. Gene therapy vectors using AAV can infect both dividing and quiescent cells and persist in an extrachromosomal state without integrating into the genome of the host cell. These features make AAV a very attractive candidate for creating viral vectors for gene therapy, and for the creation of isogenic human disease models
Supplier ARP

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