Tissue expression
Cell line expression
Protein structure
OTOF
OtoferlinDFNB6, DFNB9, FER1L2
Mutations in this gene are a cause of neurosensory nonsyndromic recessive deafness, DFNB9. The short form of the encoded protein has 3 C2 domains, a single carboxy-terminal transmembrane domain found also in the C. elegans spermatogenesis factor FER-1 and human dysferlin, while the long form has 6 C2 domains. The homology suggests that this protein may be involved in vesicle membrane fusion. Several transcript variants encoding multiple isoforms have been found for this gene. [provided by RefSeq, Jul 2008]
Top validated antibodies |
|||||
antibodies-online | ABIN346891 | 2 references | Monoclonal |
WB
EL
IP
IHC |
|
LSBio | LS-C407830 | Polyclonal |
WB
IHC |
||
Invitrogen Antibodies | PA5-79776 | Polyclonal |
WB
IHC |
||
NSJ Bioreagents | R32323 | Polyclonal |
WB
IHC |
||
GeneTex | GTX85796 | Polyclonal |
EL
IHC |
All Antibodies
Filters
Enhanced validation
Supportive data in Antibodypedia
Data presented on provider website
Data in Antibodypedia (inconclusive)
Recommended by provider
Supportive data in Antibodypedia
Data presented on provider website
Data in Antibodypedia (inconclusive)
Recommended by provider