"OPA1" Related Products

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Recombinant Human OPA1 cell lysate

Cat.No.: OPA1-1251HCL
Description: 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.
Species: Human
Size: 100 ul
Storage Buffer: 1X Sample Buffer (50 mM Tris-HCl, 2% SDS, 10% glycerol, 300 mM 2-mercaptoethanol, 0.01% Bromophenol blue)
Applications: Western Blot;
Gene Name: OPA1 optic atrophy 1 (autosomal dominant) [ Homo sapiens ]
Official Symbol: OPA1
Synonyms: OPA1; optic atrophy 1 (autosomal dominant); dynamin-like 120 kDa protein, mitochondrial; dynamin like guanosine triphosphatase; FLJ12460; KIAA0567; MGM1; mitochondrial dynamin like GTPase; NPG; NTG; optic atrophy protein 1; mitochondrial dynamin-like GTPase; dynamin-like guanosine triphosphatase; mitochondrial dynamin-like 120 kDa protein; largeG;
Gene ID: 4976
mRNA Refseq: NM_015560
Protein Refseq: NP_056375
MIM: 605290
UniProt ID: O60313
Chromosome Location: 3q28-q29
Function: GTP binding; GTPase activity; magnesium ion binding; nucleotide binding; protein binding;

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