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Invitrogen™ alpha Galactosidase Polyclonal Antibody
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Catalog No. PIPA5119890
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100 μL
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PIPA5119890 100 μL
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Catalog No. PIPA5119890 Supplier Invitrogen™ Supplier No. PA5119890
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Description

Rabbit Polyclonal Antibody

Positive Control: 293T cell lysate, MCF-7 cell lysate, Hela, human breast tissue, human endometrium tissue, human kidney tissue. Subcellular Location: Lysosome.

This gene encodes a homodimeric glycoprotein that hydrolyses the terminal alpha-galactosyl moieties from glycolipids and glycoproteins. This enzyme predominantly hydrolyzes ceramide trihexoside, and it can catalyze the hydrolysis of melibiose into galactose and glucose. A variety of mutations in this gene affect the synthesis, processing, and stability of this enzyme, which causes Fabry disease, a rare lysosomal storage disorder that results from a failure to catabolize alpha-D-galactosyl glycolipid moieties.
TRUSTED_SUSTAINABILITY

Specifications

Antigen alpha Galactosidase
Applications Immunohistochemistry (Paraffin), Western Blot, Immunocytochemistry
Classification Polyclonal
Concentration 1 mg/mL
Conjugate Unconjugated
Formulation PBS with 0.05% BSA, 40% glycerol and 0.05% sodium azide; pH 7.4
Gene GLA
Gene Accession No. P06280
Gene Alias Agalsidase; agalsidase alfa; Ags; Alpha-D-galactosidase A; alpha-D-galactoside galactohydrolase; alpha-D-galactoside galactohydrolase 1; alpha-gal A; alpha-galactosidase A; GALA; galactosidase alpha; galactosidase, alpha; GLA; Melibiase
Gene Symbols GLA
Host Species Rabbit
Immunogen Recombinant protein within human Galactosidase alpha aa 81-280.
Purification Method Antigen affinity chromatography
Quantity 100 μL
Regulatory Status RUO
Primary or Secondary Primary
Gene ID (Entrez) 2717
Target Species Human
Content And Storage Store at 4°C short term. For long term storage, store at -20°C, avoiding freeze/thaw cycles.
Product Type Antibody
Form Liquid
Isotype IgG
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Safety and Handling

WARNING: Cancer - www.P65Warnings.ca.gov
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