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MCP4 (CCL13) (NM_005408) Human Tagged ORF Clone Lentiviral Particle
CAT＃: RC203789L3V
- LentiORF®
-
Lenti ORF particles, CCL13 (Myc-DDK tagged) - Human chemokine (C-C motif) ligand 13 (CCL13), 200ul, >10^7 TU/mL
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CNY 7,410.00
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Specifications
| Product Data | |
| Product Name | MCP4 (CCL13) (NM_005408) Human Tagged ORF Clone Lentiviral Particle |
| Synonyms | CKb10; MCP-4; NCC-1; NCC1; SCYA13; SCYL1 |
| Vector | pLenti-C-Myc-DDK-P2A-Puro |
| ACCN | NM_005408 |
| ORF Size | 294 bp |
| Sequence Data |
The ORF insert of this clone is exactly the same as(RC203789).
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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_005408.2 |
| RefSeq Size | 861 bp |
| RefSeq ORF | 297 bp |
| Locus ID | 6357 |
| Protein Families | Druggable Genome, Secreted Protein |
| Protein Pathways | Chemokine signaling pathway, Cytokine-cytokine receptor interaction, NOD-like receptor signaling pathway |
| MW | 11 kDa |
| Gene Summary | This antimicrobial gene is one of several Cys-Cys (CC) cytokine genes clustered on the q-arm of chromosome 17. Cytokines are a family of secreted proteins involved in immunoregulatory and inflammatory processes. The CC cytokines are proteins characterized by two adjacent cysteines. The cytokine encoded by this gene displays chemotactic activity for monocytes, lymphocytes, basophils and eosinophils, but not neutrophils. This chemokine plays a role in accumulation of leukocytes during inflammation. It may also be involved in the recruitment of monocytes into the arterial wall during artherosclerosis. [provided by RefSeq, Sep 2014] |
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