ST14 (NM_021978) Human Tagged ORF Clone Lentiviral Particle
CAT#: RC207136L3V
- LentiORF®
Lenti ORF particles, ST14 (Myc-DDK tagged) - Human suppression of tumorigenicity 14 (colon carcinoma) (ST14), 200ul, >10^7 TU/mL
Lentiviral Particles: DDK mGFP mGFP w/ Puro
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USD 365.00
Specifications
Product Data | |
Type | Human Tagged ORF Clone Lentiviral Particle |
Tag | Myc-DDK |
Symbol | ST14 |
Synonyms | ARCI11; CAP3; HAI; MT-SP1; MTSP1; PRSS14; SNC19; TADG15; TMPRSS14 |
Mammalian Cell Selection | Puromycin |
Vector | pLenti-C-Myc-DDK-P2A-Puro |
ACCN | NM_021978 |
ORF Size | 2565 bp |
Sequence Data |
The ORF insert of this clone is exactly the same as(RC207136).
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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_021978.3 |
RefSeq Size | 3319 bp |
RefSeq ORF | 2568 bp |
Locus ID | 6768 |
UniProt ID | Q9Y5Y6 |
Cytogenetics | 11q24.3 |
Domains | CUB, Tryp_SPc, ldl_recept_a |
Protein Families | Druggable Genome, Protease, Transmembrane |
MW | 94.6 kDa |
Gene Summary | The protein encoded by this gene is an epithelial-derived, integral membrane serine protease. This protease forms a complex with the Kunitz-type serine protease inhibitor, HAI-1, and is found to be activated by sphingosine 1-phosphate. This protease has been shown to cleave and activate hepatocyte growth factor/scattering factor, and urokinase plasminogen activator, which suggest the function of this protease as an epithelial membrane activator for other proteases and latent growth factors. The expression of this protease has been associated with breast, colon, prostate, and ovarian tumors, which implicates its role in cancer invasion, and metastasis. [provided by RefSeq, Jul 2008] |
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