Gene: IFITM5
Official Full Name: interferon induced transmembrane protein 5provided by HGNC
Gene Summary: This gene encodes a membrane protein thought to play a role in bone mineralization. This gene is located on chromosome 11 in a cluster of related genes which are induced by interferon, however, this gene has not been shown to be interferon inducible. A similar gene, located in a gene cluster on mouse chromosome 7, is a member of the interferon-inducible fragilis gene family. The mouse gene encodes a transmembrane protein described as participating in germ cell competence. A mutation in the 5' UTR of this gene has been associated with osteogenesis imperfecta type V (PMID: 22863190, 22863195). [provided by RefSeq, Aug 2012]
| Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
|---|---|---|---|---|---|---|
| KOA02706 | IFITM5 Knockout cell line (AC16) | Human | IFITM5 | 1:3-1:4 | negative | Online Inquiry |
| KOA18152 | IFITM5 Knockout cell line (BEAS-2B) | Human | IFITM5 | 1:3~1:4 | negative | Online Inquiry |
| KOA33602 | IFITM5 Knockout cell line (U-2932) | Human | IFITM5 | 1:2-1:4 | negative | Online Inquiry |
| KOA49008 | IFITM5 Knockout cell line (TPC-1) | Human | IFITM5 | 1:5-1:8 | negative | Online Inquiry |
| KOA64408 | IFITM5 Knockout cell line (NCM460) | Human | IFITM5 | 1:2~1:3 | negative | Online Inquiry |
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