Superoxide Dismutase 1 (SOD1) (Center) Rabbit Polyclonal Antibody
CAT#: AP18205PU-N
Superoxide Dismutase 1 (SOD1) (Center) rabbit polyclonal antibody
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CNY 6314.00
货期*
2周
规格
| Cited in 1 publication. |
Specifications
| Product Data | |
| Applications | WB |
| Recommend Dilution | ELISA: 1/1,000. Western blot: 1/100 - 1/500. |
| Reactivity | Human |
| Host | Rabbit |
| Clonality | Polyclonal |
| Immunogen | KLH conjugated synthetic peptide selected from the Center region of human SOD1 |
| Specificity | This antibody reacts to Superoxide Dismutase 1 (SOD1). |
| Formulation | PBS with 0.09% (W/V) sodium azide State: Liquid purified Ig |
| Concentration | lot specific |
| Purification | Affinity chromatography on Protein A |
| Conjugation | Unconjugated |
| Storage Condition | Store the antibody undiluted at 2-8°C for one month or (in aliquots) at -20°C for longer. Avoid repeated freezing and thawing. |
| Gene Name | superoxide dismutase 1, soluble |
| Database Link | |
| Background | SOD1 binds copper and zinc ions and is one of two isozymes responsible for destroying free superoxide radicals in the body. This 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. |
| Synonyms | SOD-1, CuZn-SOD, CuZnSOD, IPOA, ALS1 |
| Reference Data | |
| Protein Families | Druggable Genome |
| Protein Pathways | Amyotrophic lateral sclerosis (ALS), Huntington's disease, Prion diseases |
Citations (1)
| The use of this Antibodies has been cited in the following citations: |
|---|
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Defective activation of the MAPK/ERK pathway, leading to PARP1 and DNMT1 dysregulation, is a common defect in IgA nephropathy and Henoch-Schönlein purpura.
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Journal of nephrology
,PubMed ID 29497996
[SOD1]
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