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Wnt1 Inducible Signaling Pathway Protein 3 (WISP3) ELISA Kits

WISP3 encodes a member of the WNT1 inducible signaling pathway (WISP) protein subfamily, which belongs to the connective tissue growth factor (CTGF) family. Additionally we are shipping Wnt1 Inducible Signaling Pathway Protein 3 Antibodies (40) and Wnt1 Inducible Signaling Pathway Protein 3 Proteins (7) and many more products for this protein.

list all ELISA KIts Gene Name GeneID UniProt
WISP3 8838 O95389
Anti-Mouse WISP3 WISP3 327743 D3Z5L9
Anti-Rat WISP3 WISP3 499461  
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Top Wnt1 Inducible Signaling Pathway Protein 3 ELISA Kits at antibodies-online.com

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Catalog No. Reactivity Sensitivity Range Quantity Supplier Delivery Price Details
Human 0.058 ng/ml 0.235-15 ng/mL 96 Tests Log in to see 11 to 13 Days
$910.56
Details

More ELISA Kits for Wnt1 Inducible Signaling Pathway Protein 3 Interaction Partners

Zebrafish Wnt1 Inducible Signaling Pathway Protein 3 (WISP3) interaction partners

  1. One paralog of mammalian wisp3 was found in zebrafish.

  2. Overexpression of zebrafish Wisp3 protein inhibited bone morphogenetic protein (BMP) and Wnt signaling in developing zebrafish.

Human Wnt1 Inducible Signaling Pathway Protein 3 (WISP3) interaction partners

  1. Studies indicate that the CYR61 (show CYR61 ELISA Kits) CTGF (show CTGF ELISA Kits) NOV (show NOV ELISA Kits) matricellular proteins (CCN family of proteins) comprises the members CCN1 (show CCNA2 ELISA Kits), CCN2 (show CTGF ELISA Kits), CCN3 (show NOV ELISA Kits), CCN4 (show WISP1 ELISA Kits), CCN5 (show WISP2 ELISA Kits) and CCN6 and have been identified in various types of cancer.

  2. WISP3 harbored not only frameshift mutation but also mutational intratumoral heterogeneity and loss of expression, which together might play a role in tumorigenesis of GC and CRC (show CALR ELISA Kits) with MSI (show MSI1 ELISA Kits)-H by inhibiting tumor suppressor functions of WISP3.

  3. WISP3 variant leads to the diagnosis of SEDT (show TRAPPC2 ELISA Kits)-PA.

  4. Novel and recurrent mutations in WISP3 and an atypical phenotype have been described in Indian families with progressive pseudorheumatoid dysplasia.

  5. A novel mutation c.667T>G (p.Cys223Gly) and the c.857C>G (p.Ser286*) mutation were detected in three Chinese patients with PPD (show HPD ELISA Kits).

  6. This study identified 3 different WISP3 mutations in 2 unrelated Chinese families with spondyloepiphyseal dysplasia tarda with progressive arthropathy.

  7. Suggest WISP3-Wnt (show WNT2 ELISA Kits)/beta-catenin (show CTNNB1 ELISA Kits) axis may have role in regulating gastric cancer cell proliferation and metastasis.

  8. Novel C223G and C252X mutations in exon 4 of the WISP3 gene are responsible for progressive pseudorheumatoid dysplasia in Chinese patients.

  9. Results are indicative of an operational WISP3-IGF1 (show IGF1 ELISA Kits) regulatory loop whereby WISP3 preserves cartilage integrity by restricting IGF1 (show IGF1 ELISA Kits)-mediated hypertrophic changes in chondrocytes, at least partly, upon interaction with IGF1 (show IGF1 ELISA Kits).

  10. A report on 11 different homozygous mutations and one instance of compound heterozygosity in the WISP3 gene in patients with progressive pseudorheumatoid dysplasia.

Mouse (Murine) Wnt1 Inducible Signaling Pathway Protein 3 (WISP3) interaction partners

  1. demonstrated that CCN6 induced the proliferation of lung fibroblasts by binding to integrin beta1, leading to the phosphorylation of FAK (show PTK2 ELISA Kits)(Y397).

  2. the WISP3 gene is essential to skeletal growth or homeostasis in humans but not in mice [WISP3]

Wnt1 Inducible Signaling Pathway Protein 3 (WISP3) Antigen Profile

Antigen Summary

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.

Gene names and symbols associated with WISP3

  • WNT1 inducible signaling pathway protein 3 (wisp3) antibody
  • WNT1 inducible signaling pathway protein 3 (WISP3) antibody
  • WNT1 inducible signaling pathway protein 3 (Wisp3) antibody
  • CCN6 antibody
  • ENSMUSG00000062074 antibody
  • Gm735 antibody
  • LIBC antibody
  • PPAC antibody
  • PPD antibody
  • RGD1564120 antibody
  • si:dkey-119m7.6 antibody
  • WISP-3 antibody
  • WISP3 antibody

Protein level used designations for WISP3

WNT1 inducible signaling pathway protein 3 , WNT1-inducible-signaling pathway protein 3 , WNT1-inducible-signaling pathway protein 3-like , CCN family member 6 , WISP-3

GENE ID SPECIES
566864 Danio rerio
695430 Macaca mulatta
741440 Pan troglodytes
770827 Gallus gallus
784564 Bos taurus
794092 Danio rerio
100072430 Equus caballus
100124323 Xenopus (Silurana) tropicalis
100440568 Pongo abelii
8838 Homo sapiens
327743 Mus musculus
499461 Rattus norvegicus
100686448 Canis lupus familiaris
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