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Recombinant Superoxide Dismutase 1 Monoclonal Antibody (E-AB-81608)

AllSizePriceQty
100μL $ 260.00
50μL $ 160.00
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For research use only.

Verified Samples Verified Samples in WB: A549, HL-60, C6
Verified Samples in IHC: Human breast cancer
Dilution WB 1:500-1:1000,  IHC 1:50-1:100
Isotype IgG
Host Rabbit
Reactivity Human,  Rat
Applications WB,  IHC-P
ClonalityRabbit Monoclonal
ImmunogenA synthetic peptide of human Superoxide Dismutase 1
AbbreSuperoxide Dismutase 1
SynonymsALS,  ALS1,  Amyotrophic lateral sclerosis 1 adult,  Cu/Zn SOD,  Cu/Zn superoxide dismutase,  Epididymis secretory protein Li 44,  HEL S 44,  Homodimer,  IPOA,  Indophenoloxidase A,  Mn superoxide dismutase,  SOD,  SOD soluble,  SOD1,  SOD2,  SODC,  Superoxide dismutase [Cu-Z,  hSod1
Swissprot
Calculated MW16 kDa
Observed MW 16 kDa

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 LocalizationCytoplasm. The pathogenic variants ALS1 Arg-86 and Ala-94 gradually aggregates and accumulates in mitochondria.
Concentration300 μg/mL
Buffer50mM Tris-Glycine(pH 7.4), 0.15M NaCl, 40% Glycerol, 0.05% stabilizer and 0.05% protective protein.
Purification MethodAffinity Purified
Research AreasCancer,  Cell Biology,  Metabolism,  Signal Transduction
Clone No.R08-5A5
ConjugationUnconjugated
Storage Store at -20°C Valid for 12 months. Avoid freeze / thaw cycles.
ShippingThe product is shipped with ice pack,upon receipt,store it immediately at the temperature recommended.
backgroundThe 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

1 Results

    Other Formats

    1 Results

    Unconjugated

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