BD-PT4364

SOD-1 Rabbit Polyclonal Antibody

SOD1; Superoxide dismutase [Cu-Zn]; Superoxide dismutase 1; hSod1

常规抗体

SOD1

Superoxide dismutase [Cu-Zn]

WB

Human,Mouse,Rat

1 mg/ml

Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% New type preservative N.

6647

http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=6647

P00441

http://www.uniprot.org/uniprotkb/P00441/entry

20655

http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=20655

P08228

http://www.uniprot.org/uniprot/P08228

24786

http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=24786

P07632

http://www.uniprot.org/uniprot/P07632

The antiserum was produced against synthesized peptide derived from human SOD-1. AA range:36-85

SOD-1 Polyclonal Antibody detects endogenous levels of SOD-1 protein.

WB 1:500 - 1:2000. ELISA: 1:10000. Not yet tested in other applications.

18kD

-20°C/1 year

Polyclonal, Rabbit,IgG

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. [provided by RefSeq, Jul 2008],

Colon,Fetal brain cortex,Placenta,

Cytoplasm . Mitochondrion . Nucleus . Predominantly cytoplasmic; the pathogenic variants ALS1 Arg-86 and Ala-94 gradually aggregates and accumulates in mitochondria. .

Amyotrophic lateral sclerosis (ALS);Huntington's disease;Prion diseases;

catalytic activity:2 superoxide + 2 H(+) = O(2) + H(2)O(2).,cofactor:Binds 1 copper ion per subunit.,cofactor:Binds 1 zinc ion per subunit.,disease:Defects in SOD1 are the cause of amyotrophic lateral sclerosis type 1 (ALS1) [MIM:105400]. ALS1 is a familial form of amyotrophic lateral sclerosis, a neurodegenerative disorder affecting upper and lower motor neurons and resulting in fatal paralysis. Sensory abnormalities are absent. Death usually occurs within 2 to 5 years. The etiology of amyotrophic lateral sclerosis is likely to be multifactorial, involving both genetic and environmental factors. The disease is inherited in 5-10% of cases leading to familial forms.,function:Destroys radicals which are normally produced within the cells and which are toxic to biological systems.,miscellaneous:The protein (both wild-type and ALS1 variants) has a tendency to form fibrillar aggregates in the absence of the intramolecular disulfide bond or of bound zinc ions. These aggregates may have cytotoxic effects. Zinc binding promotes dimerization and stabilizes the native form.,online information:ALS genetic mutations db,online information:Superoxide dismutase entry,PTM:Unlike wild-type protein, the pathogenics variants ALS1 Arg-38, Arg-47, Arg-86 and Ala-94 are polyubiquitinated by RNF19A; which leads to their proteasomal degradation.,similarity:Belongs to the Cu-Zn superoxide dismutase family.,subunit:Homodimer. The pathogenics variants ALS1 Arg-38, Arg-47, Arg-86 and Ala-94 interact with RNF19A, whereas wild-type protein does not.,

现货

The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.