Gene: CERKL
Official Full Name: CERK like autophagy regulatorprovided by HGNC
Gene Summary: This gene was initially identified as a locus (RP26) associated with an autosomal recessive form of retinitis pigmentosa (arRP) disease. This gene encodes a protein with ceramide kinase-like domains, however, the protein does not phosphorylate ceramide and its target substrate is currently unknown. This protein may be a negative regulator of apoptosis in photoreceptor cells. Mutations in this gene cause a form of retinitis pigmentosa characterized by autosomal recessive cone and rod dystrophy (arCRD). Alternative splicing of this gene results in multiple transcript variants encoding different isoforms and non-coding transcripts.[provided by RefSeq, May 2010]
| Catalog Number | Product Name | Species | Gene | Passage ratio | Mycoplasma testing | Price |
|---|---|---|---|---|---|---|
| KOA02771 | CERKL Knockout cell line (AC16) | Human | CERKL | 1:3-1:4 | negative | Online Inquiry |
| KOA18217 | CERKL Knockout cell line (BEAS-2B) | Human | CERKL | 1:3~1:4 | negative | Online Inquiry |
| KOA33667 | CERKL Knockout cell line (U-2932) | Human | CERKL | 1:2-1:4 | negative | Online Inquiry |
| KOA49073 | CERKL Knockout cell line (TPC-1) | Human | CERKL | 1:5-1:8 | negative | Online Inquiry |
| KOA64473 | CERKL Knockout cell line (NCM460) | Human | CERKL | 1:2~1:3 | negative | Online Inquiry |
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