DFNA5 rabbit pAb
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DFNA5 rabbit pAb
Background :
Hearing impairment is a heterogeneous condition with over 40 loci described. The protein encoded by this gene is expressed in fetal cochlea, however, its function is not known. Nonsyndromic hearing impairment is associated with a mutation in this gene. Three transcript variants encoding two different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]Description :
Hearing impairment is a heterogeneous condition with over 40 loci described. The protein encoded by this gene is expressed in fetal cochlea, however, its function is not known. Nonsyndromic hearing impairment is associated with a mutation in this gene. Three transcript variants encoding two different isoforms have been found for this gene. [provided by RefSeq, Jul 2008],UniProt :
O60443Swiss Prot :
O60443Reactivity :
Human; RatImmunogen :
Synthesized peptide derived from DFNA5 . at AA range: 200-280Clonality :
PolyclonalSource :
RabbitApplications :
WB; ELISAConcentration :
1 mg/mlDilution :
Western Blot: 1/500 - 1/2000. ELISA: 1/40000. Not yet tested in other applications.Molecular Weight :
54kDStorage Conditions :
-20°C/1 yearObserved Molecular Weight :
54kDFragment :
IgGSubcellular Location :
[Gasdermin-E, N-terminal]: Cell membrane ; Multi-pass membrane protein .; [Gasdermin-E]: Cytoplasm, cytosol .Other Product Names :
DFNA5; ICERE1; Non-syndromic hearing impairment protein 5; Inversely correlated with estrogen receptor expression 1; ICERE-1Gene ID (Human) :
1687

