DFNA5/GSDME Polyclonal antibody proteintech 13075-1-AP

$449.00
In stock
SKU
13075-1-AP

 

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

Host / Isotype: Rabbit / IgG Class: Polyclonal
Reactivity: Human, Mouse And More (1) Immunogen: CatNo: Ag3746 Product name: Recombinant human DFNA5 protein Source: e coli.-derived, PGEX-4T Tag: GST Domain: 111-460 aa of BC019689 Sequence: SQSSFGTLRKQEVDLQQLIRDSAERTINLRNPVLQQVLEGRNEVLCVLTQKITTMQKCVISEHMQVEEKCGGIVGIQTKTVQVSATEDGNVTKDSNVVLEIPAATTIAYGVIELYVKLDGQFEFCLLRGKQGGFENKKRIDSVYLDPLVFREFAFIDMPDAAHGISSQDGPLSVLKQATLLLERNFHPFAELPEPQQTALSDIFQAVLFDDELLMVLEPVCDDLVSGLSPTVAVLGELKPRQQQDLVAFLQLVGCSLQGGCPGPEDAGSKQLFMTAYFLVSALAEMPDSAAALLGTCCKLQIIPTLCHLLRALSDDGVSDLEDPTLTPLKDTERFGIVQRLFASADISL Predict reactive species
 Applications: WB, IHC, IF, FC (Intra), IP, CoIP, ELISA Observed Molecular Weight: 496 aa, 55 kDa
Formulation: PBS, Azide, Glycerol GenBank Accession Number: BC019689
Conjugate: Unconjugated Gene Symbol: DFNA5
Tested Applications: Positive WB detected in Gene ID (NCBI): 1687
Application: Western Blot (WB) RRID: AB_2093053
Dilution: WB : 1:1000-1:8000 Conjugate: Unconjugated
Tested Reactivity: Human, Mouse Form: Liquid
Host / Isotype: Rabbit / IgG 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.

 

 

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