DFNA5 Proteine
(Deafness, Autosomal Dominant 5 (DFNA5))
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].
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DFNA5
Spezies: Human
Wirt: Escherichia coli (E. coli)
Recombinant
Greater than 95 % by SDS-PAGE gel analyses
ELISA, WB
1 image
DFNA5
Spezies: Human
Wirt: Wheat germ
Recombinant
ELISA, WB, AA, AP
1 image
DFNA5
Spezies: Human
Wirt: Wheat germ
Recombinant
ELISA, WB, AA, AP
1 image
DFNA5
Spezies: Human
Wirt: HEK-293 Cells
Recombinant
> 80 % as determined by SDS-PAGE and Coomassie blue staining
AbP, STD
1 image
Aliase für DFNA5 Proteine
gasdermin E (Gsdme) Proteinegasdermin Eb (gsdmeb) Proteine
DFNA5, deafness associated tumor suppressor (DFNA5) Proteine
gasdermin E L homeolog (gsdme.L) Proteine
gasdermin E (GSDME) Proteine
2310037D07Rik Proteine
4932441K13Rik Proteine
Dfna5h Proteine
EG14210 Proteine
Fin15 Proteine
fk59f08 Proteine
ICERE-1 Proteine
MGC83660 Proteine
wu:fc41e05 Proteine
wu:fk59f08 Proteine
zgc:91916 Proteine
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