PCSK9 Knockout cell line (AC16)
Catalog Number: KOA03598
Price: Online Inquiry
Catalog Number: KOA03598
Price: Online Inquiry
| Product Information | |
|---|---|
| Product Name | PCSK9 Knockout cell line (AC16) |
| specification | 1*10^6 |
| Storage and transportation | Shipped on dry ice; Store in liquid nitrogen |
| Cell morphology | Fibroblast-like, adherent |
| Passage ratio | 1:3-1:4 |
| species | Human |
| Gene | PCSK9 |
| Gene ID | 255738 |
| Build method | Electroporation/Lentivirus |
| Mycoplasma testing | negative |
| Cultivation system | 90% DMEM/F12+10% FBS |
| Parental Cell Line | AC16 |
| Quality Control | Genotype: PCSK9 Knockout cell line (AC16)>95% viability before freezing. All cells were tested and found to be free of bacterial, viruses,mycoplasma and other toxins. |
| Gene Information | |
|---|---|
| Gene Official Full Name | proprotein convertase subtilisin/kexin type 9provided by HGNC |
| Also known as | FH3; PC9; FHCL3; NARC1; LDLCQ1; NARC-1; HCHOLA3 |
| Gene Description | This gene encodes a member of the subtilisin-like proprotein convertase family, which includes proteases that process protein and peptide precursors trafficking through regulated or constitutive branches of the secretory pathway. The encoded protein undergoes an autocatalytic processing event with its prosegment in the ER and is constitutively secreted as an inactive protease into the extracellular matrix and trans-Golgi network. It is expressed in liver, intestine and kidney tissues and escorts specific receptors for lysosomal degradation. It plays a role in cholesterol and fatty acid metabolism. Mutations in this gene have been associated with autosomal dominant familial hypercholesterolemia. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Feb 2014] |
| Expression | Biased expression in lung (RPKM 5.3), liver (RPKM 3.3) and 9 other tissues See more |
Please note that all services are for research use only. Not intended for any clinical use.
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