TMPRSS3 rabbit pAb

TMPRSS3 rabbit pAb

AO-06-ES3619-100

TMPRSS3 rabbit pAb 100μL

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Antibody Product Overview

ELK.NoES3619
Product nameTMPRSS3 rabbit pAb
ReactivityHuman;Mouse
ApplicationsWB;IHC;IF;ELISA
Other nameTMPRSS3; ECHOS1; TADG12; Transmembrane protease serine 3; Serine protease TADG-12; Tumor-associated differentially-expressed gene 12 protein
Size100μL
Unit price ($)248
Human gene ID64699
Human Swiss-ProtP57727
SourceRabbit
IsotypeIgG
TargetTMPRSS3
Fields
Gene nameTMPRSS3
Protein nameTransmembrane protease serine 3
Human gene linkView Human Gene
Human Swiss linkView Human Swiss-Prot
Mouse gene ID140765
Mouse gene linkView Mouse Gene
Mouse Swiss-ProtQ8K1T0
Mouse Swiss linkView Mouse Swiss-Prot
Rat gene ID
Rat gene link
Rat Swiss-Prot
Rat Swiss link
ImmunogenThe antiserum was produced against synthesized peptide derived from human TMPRSS3. AA range:405-454
SpecificityTMPRSS3 Polyclonal Antibody detects endogenous levels of TMPRSS3 protein.
FormulationLiquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
ClonalityPolyclonal
DilutionWestern Blot: 1/500 - 1/2000. Immunohistochemistry: 1/100 - 1/300. Immunofluorescence: 1/200 - 1/1000. ELISA: 1/10000. Not yet tested in other applications.
PurificationThe antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
Concentration1 mg/ml
Storage stability-20°C/1 year
Molecular Weight (Da)
Observed band (KD)49kD
BackgroundThis 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. [provided by RefSeq, Jan 2012],
Functiondisease:Defects in TMPRSS3 are a cause of non-syndromic sensorineural deafness autosomal recessive type 10 (DFNB10) [MIM:605316].,disease:Defects in TMPRSS3 are the cause of non-syndromic sensorineural deafness autosomal recessive type 8 (DFNB8) [MIM:601072]. DFNA8 is a form of sensorineural hearing loss. Sensorineural deafness results from damage to the neural receptors of the inner ear, the nerve pathways to the brain, or the area of the brain that receives sound information.,function:Probable protease. Seems to be capable of activating ENaC.,PTM:Undergoes autoproteolytic activation.,similarity:Belongs to the peptidase S1 family.,similarity:Contains 1 LDL-receptor class A domain.,similarity:Contains 1 peptidase S1 domain.,similarity:Contains 1 SRCR domain.,tissue specificity:Expressed in many tissues including fetal cochlea. Isoform T is found at increased levels in some carcinomas.,
Subcellular locationEndoplasmic reticulum membrane ; Single-pass type II membrane protein .
ExpressionExpressed in many tissues including fetal cochlea. Isoform T is found at increased levels in some carcinomas.

Additional Images

Image 1
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Western Blot analysis of various cells using TMPRSS3 Polyclonal Antibody. Secondary antibody(catalog#:RS0002) was diluted at 1:20000
Image 2
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Immunofluorescence analysis of HeLa cells, using TMPRSS3 Antibody. The picture on the right is blocked with the synthesized peptide.
Image 3
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Western blot analysis of lysates from HUVEC cells, using TMPRSS3 Antibody. The lane on the right is blocked with the synthesized peptide.
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Western blot analysis of the lysates from HT-29 cells using TMPRSS3 antibody.
: AO-06-ES3619-100
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Hurry! only 10 items left in stock.

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