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ACP2, 31-380aa, Human, His tag, E.coli

Product Description

ACP2 also known as Lysosomal acid phosphatase isoform 1. ACP2 is composed of two subunits, alpha and beta, and is chemically and genetically distinct from red cell acid phosphatase. it is a member of a family of distinct isoenzymes which hydrolyze orthophosphoric monoesters to alcohol and phosphate. Acid phosphatase deficiency is caused by mutations in the ACP2 (beta subunit) and ACP3 (alpha subunit) genes. Recombinant human ACP2, fused to His-tag at N-terminus, was expressed in E.coli.
List Price: $371.00
QTY
SKU:
IBATGP2959

Product Description

ACP2 also known as Lysosomal acid phosphatase isoform 1. ACP2 is composed of two subunits, alpha and beta, and is chemically and genetically distinct from red cell acid phosphatase. it is a member of a family of distinct isoenzymes which hydrolyze orthophosphoric monoesters to alcohol and phosphate. Acid phosphatase deficiency is caused by mutations in the ACP2 (beta subunit) and ACP3 (alpha subunit) genes. Recombinant human ACP2, fused to His-tag at N-terminus, was expressed in E.coli.

Other Details

Catalog number:
IBATGP2959
concentration:
1mg/ml (determined by Bradford assay)
Datasheet:
formulation:
Liquid, In 20mM Tris-HCl (pH8.0) containing 10% glycerol
molecular_weight:
42.9kDa (373aa)
notes:
For research use only, not for use in diagnostic procedures.
The datasheet for this product (see above) is intended to serve as an example only. Please refer to the datasheet provided with the protein for precise details.
Other names:
Lysosomal acid phosphatase isoform 1, LAP
purity:
> 85% by SDS - PAGE
size:
100 µg
storage:
Can be stored at +4C short term (1-2 weeks). For long term storage, aliquot and store at -20C or -70C. Avoid repeated freezing and thawing cycles.

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