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TMPRSS3 encodes a protein that belongs to the serine protease family. Additionally we are shipping TMPRSS3 Proteins (4) and TMPRSS3 Kits (2) and many more products for this protein.
Showing 10 out of 69 products:
Human Monoclonal TMPRSS3 Primary Antibody for ELISA, WB - ABIN566271
Guerrero, Wang, Bachvarova, Gregoire, Renaud, Plante, Bachvarov: A novel genome-based approach correlates TMPRSS3 overexpression in ovarian cancer with DNA hypomethylation. in Gynecologic oncology 2012
Human Polyclonal TMPRSS3 Primary Antibody for ELISA, WB - ABIN238616
Lee, Park, Kim, Park: Pathogenic mutations but not polymorphisms in congenital and childhood onset autosomal recessive deafness disrupt the proteolytic activity of TMPRSS3. in Journal of medical genetics 2003
Human Polyclonal TMPRSS3 Primary Antibody for EIA, IHC (fro) - ABIN1109275
Guipponi, Vuagniaux, Wattenhofer, Shibuya, Vazquez, Dougherty, Scamuffa, Guida, Okui, Rossier, Hancock, Buchet, Reymond, Hummler, Marzella, Kudoh, Shimizu, Scott, Antonarakis, Rossier: The transmembrane serine protease (TMPRSS3) mutated in deafness DFNB8/10 activates the epithelial sodium channel (ENaC) in vitro. in Human molecular genetics 2002
Human Polyclonal TMPRSS3 Primary Antibody for IF, WB - ABIN390923
Elbracht, Senderek, Eggermann, Thürmer, Park, Westhofen, Zerres: Autosomal recessive postlingual hearing loss (DFNB8): compound heterozygosity for two novel TMPRSS3 mutations in German siblings. in Journal of medical genetics 2007
TMPRSS3 (show TMPRSS4 Antibodies) expression is an independent prognostic factor for breast cancer patients. Bioinformatic analysis of potential TMPRSS3 (show TMPRSS4 Antibodies) binding proteins revealed that TMPRSS3 (show TMPRSS4 Antibodies) could be a key regulator of cancer pathways.
Low expression levels of hepsin (show HPN Antibodies) and TMPRSS3 (show TMPRSS4 Antibodies) are associated with poor breast cancer survival
Single nucleotide polymorphisms in TMPRSS3 (show TMPRSS4 Antibodies) (rs3814903 and rs11203200) are significantly associated with breast cancer risk.
homozygous mutation TMPRSS3 (show TMPRSS4 Antibodies): c.535G>A causes prelingual hearing loss in this Tibetan family
The prevalence of TMPRSS3 (show TMPRSS4 Antibodies) mutations among Korean postlingual hearing loss is 8.3 %. The p.A306T variant of TMPRSS3 (show TMPRSS4 Antibodies) is the common founder allele in Koreans. A novel variant, p.T248M of TMPRSS3 (show TMPRSS4 Antibodies), was predicted to have milder pathogenicity.
Description of the spectrum of mutations in TMPRSS3 (show TMPRSS4 Antibodies) in 374 families with autosomal recessive, non-syndromic hearing loss from India.
Association between TMPRSS3 (show TMPRSS4 Antibodies) genotypes and phenotype variants in autosomal recessive nonsyndromic hearing loss.
Six TMPRSS3 (show TMPRSS4 Antibodies) variants were found to cosegregate in 10 consanguineous Pakistani families with autosomal recessive non-syndromic hearing impairment.
Data imply that TMPRSS3 (show TMPRSS4 Antibodies)-A/D overexpression in EOC is probably due to hypomethylation of their control region.
TMPRSS3 (show TMPRSS4 Antibodies) gene is not a major contributor to non-syndromic deafness in the Moroccan population.
miR (show MLXIP Antibodies)-204 has a role in suppressing cochlear spiral ganglion neuron survival in vitro by targeting TMPRSS3
Lack of Tmprss3 leads to a decrease in Kcnma1 (show KCNMA1 Antibodies) potassium channels expression in cochlear inner hair cells.
The distribution of TMPRSS3 was observed in many regions of the mouse cochlea, but mainly in the spiral ganglion neurons.
Tmprss3 acts as a permissive factor for cochlear hair cells survival and activation at the onset of hearing and is required for saccular hair cell survival
This gene encodes a protein that belongs to the serine protease family. The encoded protein contains a serine protease domain, a transmembrane domain, an LDL receptor-like domain, and a scavenger receptor cysteine-rich domain. Serine proteases are known to be involved in a variety of biological processes, whose malfunction often leads to human diseases and disorders. This gene was identified by its association with both congenital and childhood onset autosomal recessive deafness. This gene is expressed in fetal cochlea and many other tissues, and is thought to be involved in the development and maintenance of the inner ear or the contents of the perilymph and endolymph. This gene was also identified as a tumor-associated gene that is overexpressed in ovarian tumors. Alternatively spliced transcript variants have been described.
transmembrane protease, serine 3
, transmembrane protease serine 3-like
, serine protease TADG-12
, transmembrane protease serine 3
, tumor-associated differentially-expressed gene 12 protein
, transmembrane proteinase serine 3