Abcc2 (NM_013806) Mouse Tagged ORF Clone Lentiviral Particle
CAT#: MR227613L4V
- LentiORF®
Lenti ORF particles, Abcc2 (GFP-tagged) - Mouse ATP-binding cassette, sub-family C (CFTR/MRP), member 2 (Abcc2), 200ul, >10^7 TU/mL
Lentiviral Particles: DDK w/ Puro
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USD 365.00
Specifications
Product Data | |
Type | Mouse Tagged ORF Clone |
Tag | mGFP |
Symbol | Abcc2 |
Synonyms | Abc30; AI173996; Cmoat; cMRP; Mrp2 |
Mammalian Cell Selection | Puromycin |
Vector | pLenti-C-mGFP-P2A-Puro |
ACCN | NM_013806 |
ORF Size | 4629 bp |
Sequence Data |
The ORF insert of this clone is exactly the same as(MR227613).
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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_013806.2, NP_038834.2 |
RefSeq Size | 5389 bp |
RefSeq ORF | 4632 bp |
Locus ID | 12780 |
UniProt ID | Q8VI47 |
Cytogenetics | 19 36.67 cM |
Gene Summary | The membrane-associated protein encoded by this gene is a member of the superfamily of ATP-binding cassette (ABC) transporters. ABC proteins transport various molecules across extra- and intra-cellular membranes. ABC genes are divided into seven distinct subfamilies (ABC1, MDR/TAP, MRP, ALD, OABP, GCN20, White). This protein is a member of the MRP subfamily which is involved in multi-drug resistance. This protein functions in the canalicular surface of the hepatocyte and in biliary transport, and appears to contribute to drug resistance in mammalian cells. Several different mutations in the human gene have been observed in patients with Dubin-Johnson syndrome (DJS), an autosomal recessive disorder characterized by conjugated hyperbilirubinemia. Alternative splice variants have been observed for this gene; however, they have not been fully described. [provided by RefSeq, Jul 2008] |
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