catalog number :
MBS7243020
products type :
ELISA Kit
products full name :
Rat ATP-binding cassette sub-family B member 6, mitochondrial (ABCB6) ELISA Kit
products short name :
ATP-binding cassette sub-family B member 6, mitochondrial (ABCB6)
other names :
ATP-binding cassette sub-family B member 6, mitochondrial; ATP-binding cassette sub-family B member 6, mitochondrial; ATP-binding cassette sub-family B member 6, mitochondrial; mt-ABC transporter 3; P-glycoprotein-related protein; mitochondrial ABC transporter 3; ATP-binding cassette half-transporter; ubiquitously-expressed mammalian ABC half transporter; ATP-binding cassette, sub-family B (MDR/TAP), member 6 (Langereis blood group); Mitochondrial ABC transporter 3; Mt-ABC transporter 3; P-glycoprotein-related protein; Ubiquitously-expressed mammalian ABC half transporter
products gene name :
ABCB6
other gene names :
ABCB6; ABCB6; ABC; LAN; PRP; DUH3; umat; ABC14; MTABC3; MCOPCB7; MTABC3; PRP; UMAT; Mt-ABC transporter 3
uniprot entry name :
ABCB6_HUMAN
storage stability :
Store all reagents at 2-8 degree C.
products categories :
Signal Transduction
ncbi acc num :
NP_005680.1
ncbi gb acc num :
NM_005689.2
ncbi mol weight :
88,600 Da
ncbi pathways :
ABC Transporters Pathway 83035!!ABC Transporters Pathway 436!!ABC-family Proteins Mediated Transport Pathway 106573!!Mitochondrial ABC Transporters Pathway 477113!!Transmembrane Transport Of Small Molecules Pathway 106572
ncbi 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 MDR/TAP subfamily. Members of the MDR/TAP subfamily are involved in multidrug resistance as well as antigen presentation. This half-transporter likely plays a role in mitochondrial function. Localized to 2q26, this gene is considered a candidate gene for lethal neonatal metabolic syndrome, a disorder of mitochondrial function. [provided by RefSeq, Jul 2008]