PC1/3 (PCSK1) (NM_000439) Human Tagged ORF Clone Lentiviral Particle
CAT#: RC221711L1V
- LentiORF®
-
Lenti ORF particles, PCSK1 (Myc-DDK tagged) - Human proprotein convertase subtilisin/kexin type 1 (PCSK1), transcript variant 1, 200ul, >10^7 TU/mL
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CNY 8,930.00
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规格
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Specifications
Product Data | |
Product Name | PC1/3 (PCSK1) (NM_000439) Human Tagged ORF Clone Lentiviral Particle |
Synonyms | BMIQ12; NEC1; PC1; PC3; SPC3 |
Vector | pLenti-C-Myc-DDK |
ACCN | NM_000439 |
ORF Size | 2259 bp |
Sequence Data |
The ORF insert of this clone is exactly the same as(RC221711).
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OTI Disclaimer | The molecular sequence of this clone aligns with the gene accession number as a point of reference only. However, individual transcript sequences of the same gene can differ through naturally occurring variations (e.g. polymorphisms), each with its own valid existence. This clone is substantially in agreement with the reference, but a complete review of all prevailing variants is recommended prior to use. More info |
OTI Annotation | This clone was engineered to express the complete ORF with an expression tag. Expression varies depending on the nature of the gene. |
Reference Data | |
RefSeq | NM_000439.3 |
RefSeq Size | 5054 bp |
RefSeq ORF | 2262 bp |
Locus ID | 5122 |
Domains | Peptidase_S8, P |
Protein Families | Druggable Genome, Protease, Secreted Protein |
MW | 84.15 kDa |
Gene Summary | 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 initial autocatalytic processing event in the ER to generate a heterodimer which exits the ER and sorts to subcellular compartments where a second autocatalytic even takes place and the catalytic activity is acquired. The protease is packaged into and activated in dense core secretory granules and expressed in the neuroendocrine system and brain. This gene encodes one of the seven basic amino acid-specific members which cleave their substrates at single or paired basic residues. It functions in the proteolytic activation of polypeptide hormones and neuropeptides precursors. Mutations in this gene have been associated with susceptibility to obesity and proprotein convertase 1/3 deficiency. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene [provided by RefSeq, Jan 2014] |
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