"SOD1" Related Products

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Recombinant Human SOD1

Cat.No.: SOD1-30341TH
Product Overview: Recombinant full length Human Superoxide Dismutase 1 with N-terminal proprietary tag; amino acids 1-54, MW 45kDa.
Description: The protein encoded by this gene binds copper and zinc ions and is one of two isozymes responsible for destroying free superoxide radicals in the body. The encoded isozyme is a soluble cytoplasmic protein, acting as a homodimer to convert naturally-occuring but harmful superoxide radicals to molecular oxygen and hydrogen peroxide. The other isozyme is a mitochondrial protein. Mutations in this gene have been implicated as causes of familial amyotrophic lateral sclerosis. Rare transcript variants have been reported for this gene.
Source: E. coli
Form: Liquid
Storage buffer: Preservative: NoneConstituents: 25% Glycerol, 50mM Tris HCl, 150mM Sodium chloride, 0.25mM DTT, 0.1mM PMSF, pH 7.5
Storage: Shipped on dry ice. Upon delivery aliquot and store at -80oC. Avoid freeze / thaw cycles.
Sequence Similarities: Belongs to the Cu-Zn superoxide dismutase family.
Gene Name: SOD1 superoxide dismutase 1, soluble [ Homo sapiens ]
Official Symbol: SOD1
Synonyms: SOD1; superoxide dismutase 1, soluble; ALS, ALS1, amyotrophic lateral sclerosis 1 (adult); superoxide dismutase [Cu-Zn]; IPOA;
Gene ID: 6647
mRNA Refseq: NM_000454
Protein Refseq: NP_000445
MIM: 147450
Uniprot ID: P00441
Chromosome Location: 21q22.11
Pathway: Amyotrophic lateral sclerosis (ALS), organism-specific biosystem; Amyotrophic lateral sclerosis (ALS), conserved biosystem; FOXA1 transcription factor network, organism-specific biosystem; Folate Metabolism, organism-specific biosystem; Hemostasis, organism-specific biosystem;
Function: chaperone binding; copper ion binding; metal ion binding; oxidoreductase activity; protein binding;

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