Gene: OTOF
Official Full Name: otoferlinprovided by HGNC
Gene Summary: 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]
| Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
|---|---|---|---|---|---|---|
| KOA12251 | OTOF Knockout cell line (AC16) | Human | OTOF | 1:3-1:4 | negative | Online Inquiry |
| KOA27697 | OTOF Knockout cell line (BEAS-2B) | Human | OTOF | 1:3~1:4 | negative | Online Inquiry |
| KOA43133 | OTOF Knockout cell line (U-2932) | Human | OTOF | 1:2-1:4 | negative | Online Inquiry |
| KOA58510 | OTOF Knockout cell line (TPC-1) | Human | OTOF | 1:5-1:8 | negative | Online Inquiry |
| KOA73936 | OTOF Knockout cell line (NCM460) | Human | OTOF | 1:2~1:3 | negative | Online Inquiry |
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