OPA1 polyclonal, anti-human, mouse, rat

Background:
OPA1 is a cause of optic atrophy type 1. OPA1 is mostly expressed in the mitochondrial biogenesis. OPA1 is a cause of optic atrophy type 1. OPA1 is mostly expressed In retina but can also be expressed in brain, testis, heart and skeletal muscles.

Alternative Name:
ProA affinity purified, Dynamin like 120 kDa protein, Dynamin like 120 kDa protein, mitochondrial, Dynamin-like 120 kDa protein, form S1, FLJ12460, Juvenile kjer type optic atrophy, KIAA0567, KJER type, Large GTP binding protein, largeG, MGM1, Mitochondrial dynamin like 120 kDa protein, Mitochondrial dynamin like GTPase, NPG, NTG, OAK, OPA 1, opa1, OPA1 gene, OPA1, Optic atrophy 1 (autosomal dominant), OPTIC ATROPHY 1, Optic atrophy 1 gene protein, Optic atrophy 1 homolog (human), Optic atrophy protein 1, Optic atrophy protein 1 homolog,

Application Dilution:
WB:1:500-1:1,000
ICC:1:50-1:200
IHC:1:50-1:200
FC:1:50-1:100

Specificity: OPA1 polyclonal antibody detects endogenous levels of OPA1 protein.

Immunogen:
Recombinant protein

MW: 85 kDa

Swiss-Prot: O60313(Human) P58281(Mouse) Q2TA68(Rat)

Purification & Purity:
Store at +4°C after thawing. Aliquot store at -20°C or -198°C. Avoid repeated freeze / thaw cycles.

Format:
Rabbit IgG, 1mg/ml in PBS with 0.02% sodium azide, 50% glycerol, pH7.2

Storage:
Store at +4°C after thawing. Aliquot store at -20°C or -80°C. Avoid repeated freeze / thaw cycles.

For research use only, not for use in diagnostic procedure.