OPA1 Polyclonal Antibody
Sizes: 50µl, 100µl
Catalogue Numbers: BS90986-50, BS90986-100
Product: Rabbit IgG, 1mg/ml in PBS with 0.02% sodium azide, 50% glycerol, pH7.2
Swiss-Prot: O60313(Human) P58281(Mouse) Q2TA68(Rat)
Host: Rabbit
Reactivity: Human, Mouse, Rat
Applications: WB, ICC/IF, IHC, FC
All Applications: WB:1:500-1:1,000
ICC:1:50-1:200
IHC:1:50-1:200
FC:1:50-1:100
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.
Purification and Purity: Store at +4°C after thawing. Aliquot store at -20°C or -198°C. Avoid repeated freeze / thaw cycles.
Storage and Stability: Store at +4°C after thawing. Aliquot store at -20°C or -80°C. Avoid repeated freeze / thaw cycles.
Specificity: OPA1 polyclonal antibody detects endogenous levels of OPA1 protein.
Bioworld Molecular Weight: 85 kDa
Note: For research use only, not for use in diagnostic procedure.
Extra Notes: Western blot analysis of OPA1 on mouse brain tissue(1) and A431 cell(2) lysate using anti-OPA1 antibody at 1/1,000 dilution., ICC staining OPA1 in Hela cells (green). The nuclear counter stain is DAPI (blue). Cells were fixed in paraformaldehyde, permeabilised with 0.25% Triton X100/PBS.
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,
Immunogen: Recombinant protein
Conjugate: Unconjugated
Modification: Unmodified