추천 제품
생물학적 소스
rabbit
Quality Level
결합
unconjugated
항체 형태
affinity isolated antibody
항체 생산 유형
primary antibodies
클론
polyclonal
양식
buffered aqueous solution
분자량
antigen ~50 kDa
종 반응성
rat, human, mouse, dog
농도
~1.0 mg/mL
기술
indirect immunofluorescence: 1-2 μg/mL using MDCK cells
western blot: 1-2 μg/mL using HEK-293T, NIH-3T3 and Rat2 cell extracts
UniProt 수납 번호
배송 상태
dry ice
저장 온도
−20°C
타겟 번역 후 변형
phosphorylation (pSer239)
유전자 정보
human ... VASP(7408)
mouse ... Vasp(22323)
rat ... Vasp(361517)
일반 설명
Monoclonal Anti-WASH1 (mouse IgG1 isotype) is derived from the hybridoma WASH1-27 produced by the fusion of mouse myeloma cells and splenocytes from BALB/c mice immunized with a synthetic peptide corresponding to an internal region of human WASH1. VASP (vasodilator-stimulated phosphoprotein) belongs to the family of Ena/VASP actin-regulatory proteins. VASP is localized at highly dynamic membrane regions, focal adhesion sites, lamellipodia protrusions, filopodia tips and along stress fibers.
면역원
synthetic peptide containing phosphorylated Ser239 of human VASP conjugated to KLH. The corresponding sequence is identical in mouse and rat VASP.
애플리케이션
Anti-phospho-VASP [pSer239] antibody produced in rabbit has been used in:
- immunoblotting
- immunoprecipitation
- immunofluorescence
생화학적/생리학적 작용
VASP (vasodilator-stimulated phosphoprotein) is implicated in cell motility and adhesion. VASP is localized at cell matrix and cell-cell contacts and plays an important role in adherens junction formation and stabilization in epithelial cells. VASP is a substrate for cAMP- and cGMP-dependent protein kinases. It is phosphorylated at multiple sites including Ser157, Ser239 and Thr278. cGMP-dependent protein kinase I (cGKI) phosphorylates VASP in a variety of cells, including platelets, fibroblasts and endothelial cells. In platelets, cGMP-mediated phosphorylation of VASP correlates with inhibition of agonist-induced platelet aggregation. Ena/VASP proteins are required for neurite initiation and extension in the developing cortex. VASP has been shown to be required for endothelial barrier function in vivo. Knockout of Ena/VASP proteins in mice leads to increased endothelial permeability causing fatal vascular leakage and haemorrhaging during late embryonic development. In contrast, overexpression of VASP enhances barrier function of endothelial cells in vitro and increases their force generation.
물리적 형태
Solution in 0.01 M phosphate buffered saline, pH 7.4, containing 15 mM sodium azide.
면책조항
Unless otherwise stated in our catalog or other company documentation accompanying the product(s), our products are intended for research use only and are not to be used for any other purpose, which includes but is not limited to, unauthorized commercial uses, in vitro diagnostic uses, ex vivo or in vivo therapeutic uses or any type of consumption or application to humans or animals.
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Storage Class Code
10 - Combustible liquids
Flash Point (°F)
Not applicable
Flash Point (°C)
Not applicable
가장 최신 버전 중 하나를 선택하세요:
Ena/VASP is required for endothelial barrier function in vivo
The Journal of Cell Biology, 179(4), 761-775 (2007)
Ena/VASP proteins: regulators of the actin cytoskeleton and cell migration
Annual Review of Cell and Developmental Biology, 19(1), 541-564 (2003)
Ena/VASP Is Required for neuritogenesis in the developing cortex
Neuron, 56(3), 441-455 (2007)
Relaxing the actin cytoskeleton for adhesion and movement with Ena/VASP
The Journal of Cell Biology, 181(1), 19-25 (2008)
The vasodilator-stimulated phosphoprotein is regulated by cyclic GMP-dependent protein kinase during neutrophil spreading
Journal of Immunology, 166(9), 5550-5556 (2001)
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