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Product Name
Alpha galactosidase A antibody
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Description
Alpha galactosidase A Rabbit Polyclonal antibody. Positive IHC detected in human liver tissue, human liver cancer tissue, mouse liver tissue. Positive WB detected in HeLa cells, HEK-293 cells. Positive IP detected in HEK-293 cells. Observed molecular weight by Western-blot: 49 kDa
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Tested applications
ELISA, IHC, IP, WB
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Species reactivity
Human,Mouse,Rat; other species not tested.
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Alternative names
Alpha galactosidase A antibody; galactosidase antibody; alpha antibody
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Isotype
Rabbit IgG
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Preparation
This antibody was obtained by immunization of Alpha galactosidase A recombinant protein (Accession Number: NM_000169). Purification method: Antigen affinity purified.
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Clonality
Polyclonal
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Formulation
PBS with 0.02% sodium azide and 50% glycerol pH 7.3.
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Storage instructions
Store at -20℃. DO NOT ALIQUOT
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Applications
Recommended Dilution:
WB: 1:500-1:5000
IP: 1:500-1:5000
IHC: 1:20-1:200
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Validations
HeLa cells were subjected to SDS PAGE followed by western blot with Catalog No:107870(GLA antibody) at dilution of 1:1000
Immunohistochemical of paraffin-embedded human liver using Catalog No:107870(GLA antibody) at dilution of 1:50 (under 10x lens)
Immunohistochemical of paraffin-embedded human liver using Catalog No:107870(GLA antibody) at dilution of 1:50 (under 40x lens)
IP Result of anti-GLA (IP:Catalog No:107870, 3ug; Detection:Catalog No:107870 1:1000) with HEK-293 cells lysate 1800ug.
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Background
GLA, also named as Melibiase, Agalsidas and Alpha-galactosidase A, Belongs to the glycosyl hydrolase 27 family. It hydrolysis of terminal, non-reducing alpha-D-galactose residues in alpha-D-galactosides, including galactose oligosaccharides, galactomannans and galactolipids. Fabry disease is an X-linked lysosomal storage disorder resulting from the deficient activity of GLA. Enzyme replacement therapy (ERT) with GLA is currently the most effective therapeutic strategy for patients with Fabry disease, a lysosomal storage disease.
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