DFNA5/GSDME Polyklonaler Antikörper

DFNA5/GSDME Polyklonal Antikörper für WB, IHC, IF/ICC, IP, Indirect ELISA

Wirt / Isotyp

Kaninchen / IgG

Getestete Reaktivität

human, Maus

Anwendung

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

Konjugation

Unkonjugiert

Kat-Nr. : 31363-1-PBS

Synonyme

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



Geprüfte Anwendungen

Produktinformation

31363-1-PBS bindet in WB, IHC, IF/ICC, IP, Indirect ELISA DFNA5/GSDME und zeigt Reaktivität mit human, Maus

Getestete Reaktivität human, Maus
Wirt / Isotyp Kaninchen / IgG
Klonalität Polyklonal
Typ Antikörper
Immunogen DFNA5/GSDME fusion protein Ag35186
Vollständiger Name deafness, autosomal dominant 5
Berechnetes Molekulargewicht 496 aa, 55 kDa
Beobachtetes Molekulargewicht55 kDa, 35 kDa, 25 kDa
GenBank-ZugangsnummerBC019689
Gene symbol DFNA5
Gene ID (NCBI) 1687
Konjugation Unkonjugiert
Form Liquid
Reinigungsmethode Antigen-Affinitätsreinigung
Lagerungspuffer PBS only
LagerungsbedingungenStore at -80°C. 20ul Größen enthalten 0,1% BSA.

Hintergrundinformationen

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.