SOD1/Superoxide Dismutase Monoclonal Antibody (AN200019P)
For research use only.
| Verified Samples |
Verified Samples in WB: Jurkat, Hela, HepG2 Verified Samples in FCM: HeLa |
| Dilution | WB 1:500-1:1000, FCM 1:100-1:500, IP 0.2-1 μL/mg of lysate |
| Isotype | IgG2b |
| Host | Mouse |
| Reactivity | Human |
| Applications | WB, FCM, IP |
| Clonality | Monoclonal |
| Immunogen | Recombinant Human SOD1 / Superoxide Dismutase protein |
| Abbre | SOD1 |
| Synonyms | hSod, HEL-S, SOD1, ALS, ALS1, HEL-S-44, IPOA, SOD, hSod1, homodimer, Superoxide dismutase [Cu-Zn], Amyotrophic lateral sclerosis 1 adult, Cu/Zn SOD, Cu/Zn superoxide dismutase, Epididymis secretory protein Li 44, HEL S 44, Indophenoloxidase A, Mn superoxide dismutase, SOD soluble, SOD2, SODC, Superoxide dismutase 1, Superoxide dismutase 1 soluble, Superoxide dismutase Cu Zn, Superoxide dismutase cystolic |
| Swissprot | |
| Calculated MW | 16 kDa |
| Observed MW |
20 kDa
The actual band is not consistent with the expectation.
Western blotting is a method for detecting a certain protein in a complex sample based on the specific binding of antigen and antibody. Different proteins can be divided into bands based on different mobility rates. The mobility is affected by many factors, which may cause the observed band size to be inconsistent with the expected size. The common factors include: 1. Post-translational modifications: For example, modifications such as glycosylation, phosphorylation, methylation, and acetylation will increase the molecular weight of the protein. 2. Splicing variants: Different expression patterns of various mRNA splicing bodies may produce proteins of different sizes. 3. Post-translational cleavage: Many proteins are first synthesized into precursor proteins and then cleaved to form active forms, such as COL1A1. 4. Relative charge: the composition of amino acids (the proportion of charged amino acids and uncharged amino acids). 5. Formation of multimers: For example, in protein dimer, strong interactions between proteins can cause the bands to be larger. However, the use of reducing conditions can usually avoid the formation of multimers. If a protein in a sample has different modified forms at the same time, multiple bands may be detected on the membrane. |
| Cellular Localization | Cytoplasm, Mitochondrion, Nucleus. |
| Concentration | 1 mg/mL |
| Buffer | 0.2 μm filtered solution in PBS |
| Purification Method | Protein A |
| Research Areas | Signal Transduction, Cell Biology, Cancer, Metabolism |
| Clone No. | 8D9 |
| Conjugation | Unconjugated |
| Storage | This antibody can be stored at 2℃-8℃ for one month without detectable loss of activity. Antibody products are stable for twelve months from date of receipt when stored at -20℃ to -80℃. Preservative-Free. Avoid repeated freeze-thaw cycles. |
| Shipping | Ice bag |
| background | 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. |
Other Clones
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Unconjugated
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