OPA1 蛋白
(Optic Atrophy 1 (Autosomal Dominant) (OPA1))
This gene product is a nuclear-encoded mitochondrial protein with similarity to dynamin-related GTPases. It is a component of the mitochondrial network. Mutations in this gene have been associated with optic atrophy type 1, which is a dominantly inherited optic neuropathy resulting in progressive loss of visual acuity, leading in many cases to legal blindness. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Mar 2009].
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6 results :
OPA1
宿主: 人
宿主: 大肠杆菌（E. Coli）
Recombinant
> 90 %
WB, SDS, Imm, PC
OPA1
宿主: 人
宿主: HEK-293 Cells
Recombinant
> 80 % as determined by SDS-PAGE and Coomassie blue staining
AbP, STD
1 image
Aliases for OPA1 蛋白
OPA1, mitochondrial dynamin like GTPase (Opa1) 蛋白OPA1, mitochondrial dynamin like GTPase (OPA1) 蛋白
optic atrophy 1 (autosomal dominant) (opa1) 蛋白
1200011N24Rik 蛋白
AI225888 蛋白
AI847218 蛋白
fk62d06 蛋白
largeG 蛋白
lilr3 蛋白
MGM1 蛋白
mKIAA0567 蛋白
NPG 蛋白
NTG 蛋白
wu:fb77a10 蛋白
wu:fk62d06 蛋白
zgc:92092 蛋白
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