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GSDME
Gasdermin EDFNA5, ICERE-1
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]
Top validated antibodies |
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| Proteintech Group |  13075-1-AP |
34 references | Polyclonal |
WB
EL
IHC
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| Atlas Antibodies | HPA011326 |
2 references | Polyclonal |
WB
ICC
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| LSBio | LS-C167375 |
Polyclonal |
WB
IHC
|
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| Invitrogen Antibodies | MA5-36092 |
Monoclonal |
WB
ICC
IHC
FC
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| Novus Biologicals | 28490002 |
2 references | Polyclonal |
WB
EL
IHC
|
|
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