Gene: SYT14
Official Full Name: synaptotagmin 14provided by HGNC
Gene Summary: This gene is a member of the synaptotagmin gene family and encodes a protein similar to other family members that mediate membrane trafficking in synaptic transmission. The encoded protein is a calcium-independent synaptotagmin. Mutations in this gene are a cause of autosomal recessive spinocerebellar ataxia-11 (SCAR11), and a t(1;3) translocation of this gene has been associated with neurodevelopmental abnormalities. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene, and a pseudogene of this gene is located on the long arm of chromosome 4. [provided by RefSeq, Dec 2011]
| Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
|---|---|---|---|---|---|---|
| KOA03589 | SYT14 Knockout cell line (AC16) | Human | SYT14 | 1:3-1:4 | negative | Online Inquiry |
| KOA19036 | SYT14 Knockout cell line (BEAS-2B) | Human | SYT14 | 1:3~1:4 | negative | Online Inquiry |
| KOA34486 | SYT14 Knockout cell line (U-2932) | Human | SYT14 | 1:2-1:4 | negative | Online Inquiry |
| KOA49889 | SYT14 Knockout cell line (TPC-1) | Human | SYT14 | 1:5-1:8 | negative | Online Inquiry |
| KOA65295 | SYT14 Knockout cell line (NCM460) | Human | SYT14 | 1:2~1:3 | negative | Online Inquiry |
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