VWA1抗体应用：WB 1:500-2000 ELISA 1:5000-20000von Willebrand factor A domain containing 1(VWA1) Homo sapiens VWA1 belongs to the von Willebrand factor (VWF; MIM 613160) A (VWFA) domain superfamily of extracellular matrix proteins and appears to play a role in cartilage structure and function (Fitzgerald et al., 2002 [PubMed 12062410]).[supplied by OMIM, Nov 2010],

VWA3A抗体应用：WB 1:500-2000 ELISA 1:5000-20000similarity:Contains 2 VWFA domains.,

VWCE抗体应用：WB 1:500-2000 ELISA 1:5000-20000function:May be a regulatory element in the beta-catenin signaling pathway and a target for chemoprevention of hapatocellular carcinoma.,induction:By HBxAg.,similarity:Contains 4 EGF-like domains.,similarity:Contains 6 VWFC domains.,subcellular location:According to PubMed:16496348 is localized in the cytoplasm.,tissue specificity:Expressed in liver.,

VWF抗体应用：IHC-p 1:50-300von Willebrand factor(VWF) Homo sapiens This gene encodes a glycoprotein involved in hemostasis. The encoded preproprotein is proteolytically processed following assembly into large multimeric complexes. These complexes function in the adhesion of platelets to sites of vascular injury and the transport of various proteins in the blood. Mutations in this gene result in von Willebrand disease, an inherited bleeding disorder. An unprocessed pseudogene has been found on chromosome 22. [provided by RefSeq, Oct 2015],

WASH1抗体应用：WB 1:500-2000

WASH6抗体应用：WB 1:500-2000

WASL抗体应用：WB 1:500-2000 ELISA 1:5000-20000Wiskott-Aldrich syndrome like(WASL) Homo sapiens This gene encodes a member of the Wiskott-Aldrich syndrome (WAS) protein family. Wiskott-Aldrich syndrome proteins share similar domain structure, and associate with a variety of signaling molecules to alter the actin cytoskeleton. The encoded protein is highly expressed in neural tissues, and interacts with several proteins involved in cytoskeletal organization, including cell division control protein 42 (CDC42) and the actin-related protein-2/3 (ARP2/3) complex. The encoded protein may be involved in the formation of long actin microspikes, and in neurite extension. [provided by RefSeq, Jul 2013],

WBS22抗体应用：WB 1:500-2000 This gene encodes a protein containing a nuclear localization signal and an S-adenosyl-L-methionine binding motif typical of methyltransferases, suggesting that the encoded protein may act on DNA methylation. This gene is deleted in Williams syndrome, a multisystem developmental disorder caused by the deletion of contiguous genes at 7q11.23. Alternatively spliced transcript variants have been found. [provided by RefSeq, Feb 2011],

WDFY1抗体应用：WB 1:500-2000 ELISA 1:5000-20000WD repeat and FYVE domain containing 1(WDFY1) Homo sapiens The protein encoded by this gene is a phosphatidylinositol 3-phosphate binding protein, which contains a FYVE zinc finger domain and multiple WD-40 repeat domains. When exogenously expressed, it localizes to early endosomes. Mutagenesis analysis demonstrates that this endosomal localization is mediated by the FYVE domain. [provided by RefSeq, Jan 2015],

WDFY2抗体应用：WB 1:500-2000This gene encodes a protein that contains two WD domains and an FYVE zinc finger region. The function of this gene is unknown. An alternatively spliced transcript variant of this gene may exist. [provided by RefSeq, Jul 2008],