CXCR4 (NM_001008540) Human Tagged ORF Clone Lentiviral Particle
CAT#: RC214548L4V
- LentiORF®
Lenti ORF particles, CXCR4 (mGFP-tagged) - Human chemokine (C-X-C motif) receptor 4 (CXCR4), transcript variant 1, 200ul, >10^7 TU/mL
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CNY 8,835.00
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Specifications
Product Data | |
Product Name | CXCR4 (NM_001008540) Human Tagged ORF Clone Lentiviral Particle |
Synonyms | CD184; D2S201E; FB22; HM89; HSY3RR; LAP-3; LAP3; LCR1; LESTR; NPY3R; NPYR; NPYRL; NPYY3R; WHIM; WHIMS |
Vector | pLenti-C-mGFP-P2A-Puro |
ACCN | NM_001008540 |
ORF Size | 1068 bp |
Sequence Data |
The ORF insert of this clone is exactly the same as(RC214548).
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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_001008540.1 |
RefSeq Size | 1912 bp |
RefSeq ORF | 1071 bp |
Locus ID | 7852 |
Protein Families | Druggable Genome, ES Cell Differentiation/IPS, GPCR, Transmembrane |
Protein Pathways | Axon guidance, Chemokine signaling pathway, Cytokine-cytokine receptor interaction, Endocytosis, Leukocyte transendothelial migration |
MW | 40 kDa |
Gene Summary | This gene encodes a CXC chemokine receptor specific for stromal cell-derived factor-1. The protein has 7 transmembrane regions and is located on the cell surface. It acts with the CD4 protein to support HIV entry into cells and is also highly expressed in breast cancer cells. Mutations in this gene have been associated with WHIM (warts, hypogammaglobulinemia, infections, and myelokathexis) syndrome. Alternate transcriptional splice variants, encoding different isoforms, have been characterized. [provided by RefSeq, Jul 2008] |
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