DFNA5/GSDME Polyclonal antibody, PBS Only

DFNA5/GSDME Polyclonal Antibody for WB, IHC, IF/ICC, IP, Indirect ELISA
Cat No. 31363-1-PBS

Host / Isotype

Rabbit / IgG

Reactivity

human, mouse

Applications

WB, IHC, IF/ICC, IP, Indirect ELISA

DFNA5, Gasdermin E, Gasdermin-E, GSDME, deafness, autosomal dominant 5

Formulation:  PBS Only
Conjugate:  Unconjugated
Size/Concentration: 

-/ -

Freight/Packing: -

Quantity

Please visit your regions distributor:


Product Information

31363-1-PBS targets DFNA5/GSDME in WB, IHC, IF/ICC, IP, Indirect ELISA applications and shows reactivity with human, mouse samples.

Tested Reactivity human, mouse
Host / Isotype Rabbit / IgG
Class Polyclonal
Type Antibody
Immunogen

CatNo: Ag35186

Product name: Recombinant human DFNA5 protein

Source: e coli.-derived, PGEX-4T

Tag: GST

Domain: 90-190 aa of BC019689

Sequence: NVTKDSNVVLEIPAATTIAYGVIELYVKLDGQFEFCLLRGKQGGFENKKRIDSVYLDPLVFREFAFIDMPDAAHGISSQDGPLSVLKQATLLLERNFHPFA

Predict reactive species
Full Name deafness, autosomal dominant 5
Calculated Molecular Weight 496 aa, 55 kDa
Observed Molecular Weight55 kDa, 35 kDa, 25 kDa
GenBank Accession NumberBC019689
Gene Symbol DFNA5
Gene ID (NCBI) 1687
Conjugate Unconjugated
FormLiquid
Purification MethodAntigen affinity Purification
UNIPROT IDO60443
Storage Buffer PBS only, pH 7.3.
Storage ConditionsStore at -80°C.

Background Information

DFNA5 (deafness, autosomal dominant 5), also known as GSDME or ICERE-1, is a 496 amino acid protein that is expressed in cochlea tissue, as well as in placenta, brain, heart, liver, lung and pancreas. Defects in the gene encoding DFNA5 are the cause of non-syndromic sensorineural deafness autosomal dominant type 5 (DFNA5), a form of sensorineural hearing loss that results from damage to one of various structures that receive sound information in the brain. GSDME produced two GSDME fragments with MW of 35 kDa and 25 kDa.

Loading...
||
New chat

Able

正在加载,请稍候...