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WB analysis of various sample lysates using GTX66293 WISP3 antibody. Dilution : 1:1000 Loading : 25microg per lane
WB analysis of various sample lysates using GTX66293 WISP3 antibody. Dilution : 1:1000 Loading : 25microg per lane
WB analysis of various sample lysates using GTX66293 WISP3 antibody. Dilution : 1:1000 Loading : 25microg per lane

WISP3 antibody

GTX66293
GeneTex
ApplicationsWestern Blot
Product group Antibodies
TargetCCN6
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Overview

  • Supplier
    GeneTex
  • Product Name
    WISP3 antibody
  • Delivery Days Customer
    9
  • Application Supplier Note
    WB: 1:500 - 1:2000. *Optimal dilutions/concentrations should be determined by the researcher.Not tested in other applications.
  • Applications
    Western Blot
  • Certification
    Research Use Only
  • Clonality
    Polyclonal
  • Conjugate
    Unconjugated
  • Gene ID8838
  • Target name
    CCN6
  • Target description
    cellular communication network factor 6
  • Target synonyms
    CCN family member 6; cellular communication network factor 6; epididymis secretory sperm binding protein; LIBC; PPAC; PPD; PPRD; WISP3; WISP-3; WNT1 inducible signaling pathway protein 3
  • Host
    Rabbit
  • Isotype
    IgG
  • Protein IDO95389
  • Protein Name
    WNT1-inducible-signaling pathway protein 3
  • Scientific Description
    This gene encodes a member of the WNT1 inducible signaling pathway (WISP) protein subfamily, which belongs to the connective tissue growth factor (CTGF) family. WNT1 is a member of a family of cysteine-rich, glycosylated signaling proteins that mediate diverse developmental processes. The CTGF family members are characterized by four conserved cysteine-rich domains: insulin-like growth factor-binding domain, von Willebrand factor type C module, thrombospondin domain and C-terminal cystine knot-like domain. This gene is overexpressed in colon tumors. It may be downstream in the WNT1 signaling pathway that is relevant to malignant transformation. Mutations of this gene are associated with progressive pseudorheumatoid dysplasia, an autosomal recessive skeletal disorder, indicating that the gene is essential for normal postnatal skeletal growth and cartilage homeostasis. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]
  • Storage Instruction
    -20°C or -80°C,2°C to 8°C
  • UNSPSC
    12352203

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