VSX1抗体应用：WB 1:500-2000 ELISA 1:5000-20000visual system homeobox 1(VSX1) Homo sapiens The protein encoded by this gene contains a paired-like homeodomain and binds to the core of the locus control region of the red/green visual pigment gene cluster. The encoded protein may regulate expression of the cone opsin genes early in development. Mutations in this gene can cause posterior polymorphous corneal dystrophy and keratoconus. Alternatively spliced transcript variants encoding different isoforms have been described. [provided by RefSeq, Jul 2008],

VSX2 抗体应用：WB 1:500-2000 ELISA 1:5000-20000visual system homeobox 2(VSX2) Homo sapiens This gene encodes a homeobox protein originally described as a retina-specific transcription factor. Mutations in this gene are associated with microphthalmia, cataracts and iris abnormalities. [provided by RefSeq, Oct 2009],

VTA1抗体应用：WB 1:500-2000 C6ORF55 encodes a protein involved in trafficking of the multivesicular body, an endosomal compartment involved in sorting membrane proteins for degradation in lysosomes (Ward et al., 2005 [PubMed 15644320]).[supplied by OMIM, Mar 2008],

VTM2A抗体应用：WB 1:500-2000 ELISA 1:5000-20000

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