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ALAS2 Protein

ALAS2 Origin: Human Host: Escherichia coli (E. coli) Recombinant > 85 % as determined by reducing SDS-PAGE.
Catalog No. ABIN7319672
  • Target See all ALAS2 Proteins
    ALAS2 (Aminolevulinate, delta-, Synthase 2 (ALAS2))
    Protein Type
    Recombinant
    Origin
    • 5
    • 2
    • 1
    Human
    Source
    • 2
    • 2
    • 2
    • 1
    • 1
    Escherichia coli (E. coli)
    Purpose
    Recombinant Human Catalase/CAT Protein
    Sequence
    Ala2-Leu527
    Characteristics
    Recombinant Human Catalase is produced by our E.coli expression system and the target gene encoding Ala2-Leu527 is expressed.
    Purity
    > 85 % as determined by reducing SDS-PAGE.
    Endotoxin Level
    < 1.0 EU per μg as determined by the LAL method.
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    Discover our top product ALAS2 Protein
  • Restrictions
    For Research Use only
  • Format
    Frozen, Liquid
    Buffer
    Supplied as a 0.2 μm filtered solution of 20 mM PB,150 mM NaCl, pH 7.4.
    Storage
    -20 °C
    Storage Comment
    Store at < -20°C, stable for 6 months. Please minimize freeze-thaw cycles.
  • Target
    ALAS2 (Aminolevulinate, delta-, Synthase 2 (ALAS2))
    Alternative Name
    alase (ALAS2 Products)
    Synonyms
    anh1 Protein, asb Protein, xlsa Protein, ALAS-E Protein, ALASE Protein, ANH1 Protein, ASB Protein, XLDPP Protein, XLEPP Protein, XLSA Protein, alas-e Protein, cb1063 Protein, sau Protein, sauternes Protein, ALAS Protein, Alas-2 Protein, 5'-aminolevulinate synthase 2 Protein, aminolevulinate, delta-, synthase 2 Protein, aminolevulinic acid synthase 2, erythroid Protein, alas2 Protein, ALAS2 Protein, Alas2 Protein, alas2.L Protein
    Background

    Background: Catalase (CAT) is a member of the catalase family. It exists as a homotetramer that occurs in almost all aerobically respiring organisms and serves to protect cells from the toxic effects of hydrogen peroxide. Catalase is localized in the peroxisome. Catalase promotes growth of cells including T-cells, B-cells, myeloid leukemia cells, melanoma cells, mastocytoma cells, and normal and transformed fibroblast cells. Defects in CAT are the cause of acatalasemia which is characterized by absence of catalase activity in red cells and is associated with ulcerating oral lesions.

    Synonym: MGC138422,MGC138424

    Molecular Weight
    59.7 kDa
    UniProt
    P04040
    Pathways
    Transition Metal Ion Homeostasis
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