VAV1 Antibody (Center)
Affinity Purified Rabbit Polyclonal Antibody (Pab)
- SPECIFICATION
- CITATIONS
- PROTOCOLS
- BACKGROUND
Application
| WB, E |
---|---|
Primary Accession | P15498 |
Other Accession | NP_005419.2 |
Reactivity | Human |
Host | Rabbit |
Clonality | Polyclonal |
Isotype | Rabbit IgG |
Calculated MW | 98314 Da |
Antigen Region | 437-466 aa |
Gene ID | 7409 |
---|---|
Other Names | Proto-oncogene vav, VAV1, VAV |
Target/Specificity | This VAV1 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 437-466 amino acids from the Central region of human VAV1. |
Dilution | WB~~1:1000 |
Format | Purified polyclonal antibody supplied in PBS with 0.09% (W/V) sodium azide. This antibody is purified through a protein A column, followed by peptide affinity purification. |
Storage | Maintain refrigerated at 2-8°C for up to 2 weeks. For long term storage store at -20°C in small aliquots to prevent freeze-thaw cycles. |
Precautions | VAV1 Antibody (Center) is for research use only and not for use in diagnostic or therapeutic procedures. |
Name | VAV1 |
---|---|
Synonyms | VAV |
Function | Couples tyrosine kinase signals with the activation of the Rho/Rac GTPases, thus leading to cell differentiation and/or proliferation. |
Tissue Location | Widely expressed in hematopoietic cells but not in other cell types |
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Provided below are standard protocols that you may find useful for product applications.
Background
The protein encoded by this proto-oncogene is a member of the Dbl family of guanine nucleotide exchange factors (GEF) for the Rho family of GTP binding proteins. The protein is important in hematopoiesis, playing a role in T-cell and B-cell development and activation. This particular GEF has been identified as the specific binding partner of Nef proteins from HIV-1. Coexpression and binding of these partners initiates profound morphological changes, cytoskeletal rearrangements and the JNK/SAPK signaling cascade, leading to increased levels of viral transcription and replication.
References
Bailey, S.D., et al. Diabetes Care 33(10):2250-2253(2010)
Hollmann, A., et al. Hematol Oncol 28(3):142-150(2010)
Barda-Saad, M., et al. EMBO J. 29(14):2315-2328(2010)
Davila, S., et al. Genes Immun. 11(3):232-238(2010)
Kim, H.S., et al. Immunity 32(2):175-186(2010)
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