TMPRSS3 DNAxPab
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More Files
- More Functions
Western Blot (Transfected lysate)
Western Blot analysis of TMPRSS3 expression in transfected 293T cell line by TMPRSS3 DNAxPab polyclonal antibody.
Lane 1: TMPRSS3 transfected lysate(51.37 KDa).
Lane 2: Non-transfected lysate.
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Specification
Product Description
Rabbit polyclonal antibody raised against a partial-length human TMPRSS3 DNA using DNAx™ Immune technology.
Technology
Immunogen
TMPRSS3 (NP_115781.1, 70 a.a. ~ 344 a.a) partial-length human DNA
Sequence
HFDCSGKYRCRSSFKCIELIARCDGVSDCKDGEDEYRCVRVGGQNAVLQVFTAASWKTMCSDDWKGHYANVACAQLGFPSYVSSDNLRVSSLEGQFREEFVSIDHLLPDDKVTALHHSVYVREGCASGHVVTLQCTACGHRRGYSSRIVGGNMSLLSQWPWQASLQFQGYHLCGGSVITPLWIITAAHCVYDLYLPKSWTIQVGLVSLLDNPAPSHLVEKIVYHSKYKPKRLGNDIALMKLAGPLTFNGTSGSLCGSAALPLFQEDLQLLIEAFL
Host
Rabbit
Reactivity
Human
Purification
Protein A
Quality Control Testing
Antibody reactive against mammalian transfected lysate.
Storage Buffer
In 1x PBS, pH 7.4
Storage Instruction
Store at -20°C or lower. Aliquot to avoid repeated freezing and thawing.
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Applications
Western Blot (Transfected lysate)
Western Blot analysis of TMPRSS3 expression in transfected 293T cell line by TMPRSS3 DNAxPab polyclonal antibody.
Lane 1: TMPRSS3 transfected lysate(51.37 KDa).
Lane 2: Non-transfected lysate.
Immunofluorescence (Transfected cell)
Flow Cytometry (Transfected cell)
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Gene Info — TMPRSS3
Entrez GeneID
64699GeneBank Accession#
NM_032405.1Protein Accession#
NP_115781.1Gene Name
TMPRSS3
Gene Alias
DFNB10, DFNB8, ECHOS1, TADG12
Gene Description
transmembrane protease, serine 3
Gene Ontology
HyperlinkGene Summary
This gene encodes a protein that belongs to the serine protease family. The encoded protein contains a serine protease domain, a transmembrane domain, a 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. [provided by RefSeq
Other Designations
OTTHUMP00000109345|serine protease TADG12
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Interactome
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Disease
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