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.

Specificity:

OPA1 polyclonal antibody detects endogenous levels of OPA1 protein.

Alternative names:

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,

Species reactivity:

Human, Mouse, Rat

Host:

Rabbit

Ig type:

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

Immunogen:

Recombinant protein

Purification & Purity:

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

Molecular weight:

85 kDa

Applications:

WB ICC/IF IHC FC

Usage:

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

Storage:

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

Precautions:

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

More info:

Email: info@sobekbio.com

Orders:

Email: orders@sobekbio.com