This nuclear gene encodes a multi-pass membrane protein that is targeted to the mitochondrial inner membrane. The encoded protein is an ATP-dependent transporter that may mediate the passage of organic and inorganic molecules out of the mitochondria. Loss of function of the related gene in mouse results in a disruption of iron homeostasis between the mitochondria and cytosol. Alternative splicing results in multiple transcript variants.
ABC transporter 8; ABCB8; ATP-binding cassette sub-family B member 8, mitochondrial; ATP-binding cassette, sub-family B (MDR/TAP), member 8; ATP-binding cassette, sub-family B, member 8; M-ABC1; MABC1 M-ABC1 EST328128; mitochondrial ABC protein; Mitochondrial ATP-binding cassette 1; Mitochondrial potassium channel ATP-binding subunit; Mitochondrial sulfonylurea-receptor; MITOSUR
Cat # 15952665
100 µL
Cat # 15887653
100 µL
Cat # 15758761
100 µL
Cat # 15683625
100 µL
Cat # 16670085
100 µL
Cat # 16034767
100 uL
Cat # 16049456
100 ug
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