GSDME Rabbit Polyclonal Antibody
Catalog #:EAB11100
Host / Isotype Clonality Applications MW (kDa) Reactivity
Rabbit IgG Polyclonal WB, ELISA 55 Human, Rat
Applications Dilutions
The application notes include recommended starting dilutions;optimal dilutions/concentrations should be detemined by the end user.
WB=1:500-2000
Application Key

WB-Western Blot IP-Immunoprecipitation IHC-Immunohistochemistry IHC-P-Immunohistochemistry-Paraffin
IF
-Immunofluorescence ICC-Immunocytochemistry FC-Flow Cytometry

Reactivity Key

H-Human M-Mouse R-Rat Mk-Monkey B-Bovine Pg-Pig Hm-Hamster Dg-Dog C-Chicken X-Xenopus Z-Zebrafish
Hr
-Horse All-All Species Expected

Product Information
Conjugate Unconjugate
Specificity GSDME Rabbit Polyclonal Antibody detects endogenous levels of GSDME protein.
Purification Affinity purification
Concentration 1mg/ml
Format Liquid
Formulation In PBS, pH 7.4, containing 0.02% sodium azide,0.5% BSA and 50% glycerol.
Shipping Gel Pack
Storage Store at -20°C least 1 year from the date of shipment. avoid repeated freeze/thaw cycles. Aliquots may be stored at +4°C for 1-2 weeks.
UniProt ID

O60443

Entrez Gene ID

1687

Product Description

GSDME(Gasdermin E) also known as DFNA5 is a 496 amino acid protein that is expressed in cochlea tissue, as well as in placenta, brain, heart, liver, lung and pancreas. GSDME plays a crucial role in auditory function; mutations in the gene encoding GSDME are associated with non-syndromic sensorineural deafness autosomal dominant type 5, a condition that leads to hearing loss due to damage in the auditory pathways of the brain. GSDME is located on human chromosome 7, which contains over 1,000 genes and accounts for nearly 5% of the human genome. Notably, defects in other genes on chromosome 7 have been implicated in various genetic disorders, including Osteogenesis imperfecta and Williams-Beuren syndrome, highlighting the critical nature of this chromosomal region in human health.

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For Research Use Only, Not For Diagnostic Or Therapeutic Procedures.
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