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Download PDF DatasheetCatalogue No : BS3587
| Host | Reactivity | Size | Application | stock | price | cart |
| BS3587 | H,M,R | 100μg | WB IHC IF | ![]() |
258.00 | ![]() |
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Email:shdiahds@163.com Click here for qusetions for this product! |
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1 mg/ml in Phosphate buffered saline (PBS) with 15 mM sodium azide, approx. pH 7.2.
The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen and the purity is > 95% (by SDS-PAGE).
VASP (A232) antibody detects endogenous levels of VASP protein.
WB: 1:500~1:1000 IHC: 1:50~1:200 IF:1:50~1:200

Immunohistochemistry (IHC) analyzes of VASP (A232) antibody in paraffin-embedded human tonsil tissue.
Store at 4°C short term. Aliquot and store at -20°C long term. Avoid freeze-thaw cycles.
The Wiskott-Aldrich syndrome (WAS) is characterized by thrombocytopeni,a eczem,a defects in cell-mediated and humoral immunity and a propensity for lymphoproliferative diseases. The syndrome is the result of a mutation in the gene encoding a proline-rich protein termed WASP. WASP has been identified as a downstream effector of Cdc42 and has been implicated in Actin polymerization and cytoskeletal organization. A distantly related protein, VASP (vasodilator-stimulated phosphoprotein), is involved in the maintenance of cytoarchitecture by interacting with Actin-like filaments. VASP shares a limited degree of homology with the amino terminus of WASP, which is frequently mutated in WAS patients. An established substrate of cAMP and cGMP dependent kinases, VASP is phosphorylated on a regulatory serine residue 157 and localizes to focal adhesions, microfilaments and highly active regions of the plasma membrane. VASP is highly expressed in human platelets and, like WASP, may play a role in cytoskeletal organization.