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NNT1 (CLCF1) (NM_013246) Human Tagged ORF Clone Lentiviral Particle
CAT＃: RC204427L2V
- LentiORF®
-
Lenti ORF particles, CLCF1 (mGFP-tagged) - Human cardiotrophin-like cytokine factor 1 (CLCF1), transcript variant 1, 200ul, >10^7 TU/mL
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CNY 8,360.00
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Specifications
| Product Data | |
| Product Name | NNT1 (CLCF1) (NM_013246) Human Tagged ORF Clone Lentiviral Particle |
| Synonyms | BSF-3; BSF3; CISS2; CLC; NNT-1; NNT1; NR6 |
| Vector | pLenti-C-mGFP |
| ACCN | NM_013246 |
| ORF Size | 675 bp |
| Sequence Data |
The ORF insert of this clone is exactly the same as(RC204427).
|
| 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_013246.2 |
| RefSeq Size | 1860 bp |
| RefSeq ORF | 678 bp |
| Locus ID | 23529 |
| Protein Families | Druggable Genome, Secreted Protein |
| Protein Pathways | Cytokine-cytokine receptor interaction, Jak-STAT signaling pathway |
| MW | 25.2 kDa |
| Gene Summary | This gene is a member of the glycoprotein (gp)130 cytokine family and encodes cardiotrophin-like cytokine factor 1 (CLCF1). CLCF1 forms a heterodimer complex with cytokine receptor-like factor 1 (CRLF1). This dimer competes with ciliary neurotrophic factor (CNTF) for binding to the ciliary neurotrophic factor receptor (CNTFR) complex, and activates the Jak-STAT signaling cascade. CLCF1 can be actively secreted from cells by forming a complex with soluble type I CRLF1 or soluble CNTFR. CLCF1 is a potent neurotrophic factor, B-cell stimulatory agent and neuroendocrine modulator of pituitary corticotroph function. Defects in CLCF1 cause cold-induced sweating syndrome 2 (CISS2). This syndrome is characterized by a profuse sweating after exposure to cold as well as congenital physical abnormalities of the head and spine. Alternative splicing results in multiple transcript variants encoding distinct isoforms.[provided by RefSeq, Oct 2009] |
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