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The protein encoded by TSPAN12 is a member of the transmembrane 4 superfamily, also known as the tetraspanin family. Additionally we are shipping TSPAN12 Proteins (3) and many more products for this protein.
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Human Polyclonal TSPAN12 Primary Antibody for EIA, WB - ABIN453861
Berditchevski: Complexes of tetraspanins with integrins: more than meets the eye. in Journal of cell science 2001
Show all 2 references for ABIN453861
Chicken Polyclonal TSPAN12 Primary Antibody for WB - ABIN2782782
Scherer, Cheung, MacDonald, Osborne, Nakabayashi, Herbrick, Carson, Parker-Katiraee, Skaug, Khaja, Zhang, Hudek, Li, Haddad, Duggan, Fernandez, Kanematsu, Gentles, Christopoulos, Choufani, Kwasnicka et al.: Human chromosome 7: DNA sequence and biology. ... in Science (New York, N.Y.) 2003
Several novel mutations (missense, non-stop (show USP22 Antibodies) and insertion) were detected in the coding regions of FZD4 (show FZD4 Antibodies), TSPAN12 and ZNF408 (show ZNF408 Antibodies) genes among the unrelated vitreoretinopathy probands.The mutations in FZD4 (show FZD4 Antibodies) and TSPAN12 were involved in autosomal dominant and autosomal recessive families and further validates the involvement of these gene in familial exudative vitreoretinopathy development.
The authors report a case of familial exudative vitreoretinopathy in the spectrum of osteoporosis pseudoglioma syndrome associated with novel mutations of the LRP5 (show LRP5 Antibodies) and TSPAN12 genes that resulted in a phenotype similar to bilateral persistent fetal vasculature.
Among the patients with pathogenic mutations detected, FZD4 (show FZD4 Antibodies) mutations accounted for the largest proportion of autosomal inheritance FEVR (show NDP Antibodies) cases (13/18 patients, 72.2%), followed by LRP5 (show LRP5 Antibodies) (4/18 patients, 22.2%) and TSPAN12 (1/18 patients, 5.6%).
Here we describe a case of a female infant affected by cystic fibrosis (show S100A8 Antibodies) and by a severe form of exudative vitreoretinopathy. In particular, we have detected the homozygous missense mutation c.668 T > C in TSPAN12.
Novel mutation in TSPAN12 leads to autosomal recessive inheritance of congenital vitreoretinal disease with intra-familial phenotypic variability.
Novel mutations have been described in the TSPAN12 gene in Chinese patients with familial exudative vitreoretinopathy.
These results suggest that stroma-derived p53 (show TP53 Antibodies) plays a pivotal role in epithelial cancer progression and that TSPAN12 and CXCL6 are potential targets for lung cancer therapy.
TSPAN12 plays a role in supporting primary tumor growth and suppressing metastasis.
This study is the first report of recessive mutations in TSPAN12 and shows that patients with two mutant alleles have a severe form of FEVR (show NDP Antibodies) or retinal dysplasia, whereas heterozygous family members have mild familial exudative vitreoretinopathy phenotypes
The largest miRNA-146a-TSPAN12 response to stress of amyloidbeta peptide + tumor necrosis factoralpha is found in human neuronal glial cells from Alzheimer brain.
Data indicate that Norrin (show NDP Antibodies) multimers and TSPAN12 cooperatively promote multimerization of FZD4 (show FZD4 Antibodies) and its associated proteins to elicit physiological levels of signaling.
The protein encoded by this gene is a member of the transmembrane 4 superfamily, also known as the tetraspanin family. Most of these members are cell-surface proteins that are characterized by the presence of four hydrophobic domains. The proteins mediate signal transduction events that play a role in the regulation of cell development, activation, growth and motility.
, transmembrane 4 superfamily member 12
, tetraspan NET-2