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Recombinant human OPA3 protein

Cat:P08296

Summary:

【Derived From】: E.coli
【Endotoxin】: Not measured
【Amino Acid】: 1-180AA
【Purity】: ≥85% by SDS-PAGE.
【Name】: OPA3
【Full Name】: optic atrophy 3 (autosomal recessive,with chorea and spastic paraplegia)
【Uniprot】: Q9H6K4
【Gene ID】: 80207
【Species Reactivity】: Human Mouse (Bovine )
【Mol Mass】: 20kDa
【Application】: Immunology research
【Purification】: NI-NTA affinity purification
【Bioactive】: N0
【Tag】: With a 6×His tag at the N/C-terminus.
【Concentration】: 1mg/ml by SDS-PAGE.

Store:

【Reconstitution】: Reconstituted protein solution can be diluted with distilled water. Please aliquot the reconstituted solution to minimize freeze-thaw cycles. (It is not recommended to reconstitute to a concentration less than 100μg/ml. Dissolve the lyophilized protein in distilled water.)
【Storage】: Reconstituted protein solution can be stored at 4-7℃ for 1-2 weeks, stored at < -20℃ for 1 year.
【Formulation】: Powder: Lyophilized from a 0.2 μm filtered solution of 2-8M Urea, 20mM Tris-HCl, 150mM NaCl, 1mM DTT, PH7.2-8.0.

Background:

The mouse ortholog of this protein co-purifies with the mitochondrial inner membrane. Mutations in this gene have been shown to result in 3-methylglutaconic aciduria type III and autosomal dominant optic atrophy and cataract. Multiple transcript variants encoding different isoforms have been found for this gene.

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