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Human PCSK9/FH3/HCHOLA3 ORF/cDNA clone-Lentivirus plasmid (NM_174936.3)
SKU: pGMLV000015
Size: 10 µg
Concentration: generally 0.5ug/ul, usually not less than 0.3ug/ul
Leading Time: 3-7 working days
Pre-made Human PCSK9/FH3/HCHOLA3 Lentiviral expression plasmid for PCSK9 lentivirus packaging, PCSK9 lentivirus production, overexpression stable cell line development, cell transient transfection and gene delivery targeting T/B/NK cells, macrophages, cardiomyocytes, hepatocytes, and neurons.
Our GM-Lentiviral vector is seamlessly integrated with the GM lentivirus packaging system. Discover more about the GM lentivirus packaging system.
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Product Description
| Catalog ID | pGMLV000015 |
| Gene Name | PCSK9 |
| Accession Number | NM_174936.3 |
| Gene ID | 255738 |
| Species | Human |
| Product Type | Lentivirus plasmid (overexpression) |
| Insert Length | 2079 bp |
| Gene Alias | FH3,HCHOLA3,LDLCQ1,NARC-1,NARC1,PC9 |
| Fluorescent Reporter | ZsGreen |
| Mammalian Cell Selection | Puromyocin |
| Fusion Tag | 3xflag (C-Terminal) |
| Promoter | CMV |
| Resistance | Amplicin |
Reference
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Associated products
Target information
| Target ID | GM-T62206 |
| Target Name | PCSK9 |
| Gene ID | 255738, 100102, 717147, 298296, 102152231, 100147049 |
| Gene Symbol and Synonyms | FH3,FHCL3,HCHOLA3,LDLCQ1,NARC-1,NARC1,PC9,PCSK9 |
| Uniprot Accession | Q8NBP7 |
| Uniprot Entry Name | PCSK9_HUMAN |
| Protein Sub-location | Transmembrane Protein |
| Category | Therapeutics Target, INN Index |
| Disease | Ovary Cancer |
| Gene Ensembl | ENSG00000169174 |
| Target Classification | Not Available |
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]
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