CD35 (CR1) (NM_000573) Human Tagged ORF Clone Lentiviral Particle
CAT#: RC216533L1V
- LentiORF®
Lenti ORF particles, CR1 (Myc-DDK tagged) - Human complement component (3b/4b) receptor 1 (Knops blood group) (CR1), transcript variant F, 200ul, >10^7 TU/mL
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USD 365.00
Specifications
Product Data | |
Type | Human Tagged ORF Clone Lentiviral Particle |
Tag | Myc-DDK |
Symbol | CR1 |
Synonyms | C3BR; C4BR; CD35; KN |
Mammalian Cell Selection | None |
Vector | pLenti-C-Myc-DDK |
ACCN | NM_000573 |
ORF Size | 6117 bp |
Sequence Data |
The ORF insert of this clone is exactly the same as(RC216533).
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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_000573.3 |
RefSeq Size | 8629 bp |
RefSeq ORF | 6120 bp |
Locus ID | 1378 |
UniProt ID | P17927 |
Cytogenetics | 1q32.2 |
Protein Families | Druggable Genome, Transmembrane |
Protein Pathways | Complement and coagulation cascades, Hematopoietic cell lineage |
MW | 223.7 kDa |
Gene Summary | This gene is a member of the receptors of complement activation (RCA) family and is located in the 'cluster RCA' region of chromosome 1. The genome is polymorphic at this locus with allele-specific splice variants encoding different isoforms, based on the presence/absence of long homologous repeats (LHRs). The gene encodes a monomeric single-pass type I membrane glycoprotein found on erythrocytes, leukocytes, glomerular podocytes, and splenic follicular dendritic cells. The Knops blood group system is a system of antigens located on this protein. The protein mediates cellular binding to particles and immune complexes that have activated complement. Decreases in expression of this protein and/or mutations in this gene have been associated with gallbladder carcinomas, mesangiocapillary glomerulonephritis, systemic lupus erythematosus, sarcoidosis and Alzheimer's disease. Mutations in this gene have also been associated with a reduction in Plasmodium falciparum rosetting, conferring protection against severe malaria. [provided by RefSeq, May 2020] |
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