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WASF1 Antibody (Center) Blocking peptide

Synthetic peptide

Product Information
Primary Accession Q92558
Clone Names 100430290
Peptide ID 100430290
Additional Information
Gene ID 8936
Other Names Wiskott-Aldrich syndrome protein family member 1, WASP family protein member 1, Protein WAVE-1, Verprolin homology domain-containing protein 1, WASF1, KIAA0269, SCAR1, WAVE1
Target/Specificity The synthetic peptide sequence used to generate the antibody AP14110c was selected from the Center region of WASF1. A 10 to 100 fold molar excess to antibody is recommended. Precise conditions should be optimized for a particular assay.
Format Synthetic peptide was lyophilized with 100% acetonitrile and is supplied as a powder. Reconstitute with 0.1 ml DI water for a final concentration of 1 mg/ml.
StorageMaintain refrigerated at 2-8°C for up to 6 months. For long term storage store at -20°C.
PrecautionsThis product is for research use only. Not for use in diagnostic or therapeutic procedures.
Protein Information
Name WASF1
Synonyms KIAA0269, SCAR1, WAVE1
Function Downstream effector molecule involved in the transmission of signals from tyrosine kinase receptors and small GTPases to the actin cytoskeleton. Promotes formation of actin filaments. Part of the WAVE complex that regulates lamellipodia formation. The WAVE complex regulates actin filament reorganization via its interaction with the Arp2/3 complex.
Cellular Location Cytoplasm, cytoskeleton. Cell junction, synapse. Note=Dot-like pattern in the cytoplasm Concentrated in Rac-regulated membrane-ruffling areas
Tissue Location Highly expressed in brain. Lowly expressed in testis, ovary, colon, kidney, pancreas, thymus, small intestine and peripheral blood
Research Areas
Citations (0)

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The protein encoded by this gene, a member of theWiskott-Aldrich syndrome protein (WASP)-family, plays a criticalrole downstream of Rac, a Rho-family small GTPase, in regulatingthe actin cytoskeleton required for membrane ruffling. It has beenshown to associate with an actin nucleation core Arp2/3 complexwhile enhancing actin polymerization in vitro. Wiskott-Aldrichsyndrome is a disease of the immune system, likely due to defectsin regulation of actin cytoskeleton. Multiple alternatively splicedtranscript variants encoding the same protein have been found forthis gene.


Namekata, K., et al. Proc. Natl. Acad. Sci. U.S.A. 107(16):7586-7591(2010)Roignot, J., et al. Cancer Lett. 288(1):116-123(2010)Kang, R., et al. Leukemia 24(1):177-186(2010)Takata, K., et al. Am. J. Pathol. 175(1):17-24(2009)He, Y.L., et al. Zhongguo Dang Dai Er Ke Za Zhi 11(2):88-92(2009)

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$ 80.00
Cat# BP14110c
(40 western blots)
Availability: In Stock
Bulk Size
Seasonal Special on Bulk Order
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