ALAS2 Protein
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- Target See all ALAS2 Proteins
- ALAS2 (Aminolevulinate, delta-, Synthase 2 (ALAS2))
- Protein Type
- Recombinant
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Origin
- Human
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Source
- 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.
- Top Product
- Discover our top product ALAS2 Protein
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Aminolevulinate, delta-, Synthase 2 (ALAS2) (AA 1-100) protein (GST tag)
ALAS2 Origin: Human Host: Wheat germ Recombinant WB, ELISA, AA, AP
Aminolevulinate, delta-, Synthase 2 (ALAS2) (AA 1-587) protein (GST tag)ALAS2 Origin: Human Host: Wheat germ Recombinant WB, ELISA, AA, AP
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- Restrictions
- For Research Use only
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- 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.
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- 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
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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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