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Anti-GAA / Alpha-Glucosidase, Acid Antibody (clone 43G7) IHC-plus™ LS-B7964

Note: This antibody replaces LS-C150491


Wt. Vol. Conc. Price
- 100 µl - Unavailable

Most Popular GAA / Alpha-Glucosidase, Acid Antibodies

Anti-GAA / Alpha-Glucosidase, Acid Antibody (aa218-267) LS-C80648
Rabbit Polyclonal (IgG) to Human GAA / Alpha-Glucosidase, Acid
Human, Monkey, Mouse, Rat, Bovine, Dog, Guinea pig, Hamster, Pig, Zebrafish
Western blot
Western blot Image
Anti-GAA / Alpha-Glucosidase, Acid Antibody (clone 43G7) IHC-plus™ LS-B7964
Mouse-Balb/c Monoclonal [clone 43G7] (IgG1) to Human GAA / Alpha-Glucosidase, Acid
IHC - Paraffin, Western blot
Immunohistochemistry Image
Anti-GAA / Alpha-Glucosidase, Acid Antibody (aa174-203) IHC-plus™ LS-B10678
Rabbit Polyclonal to Human GAA / Alpha-Glucosidase, Acid
IHC - Paraffin, Western blot
Immunohistochemistry Image

100% Guaranteed 100% Guaranteed
Mouse-Balb/c Monoclonal [clone 43G7] (IgG1) to Human GAA / Alpha-Glucosidase, Acid
IHC - Paraffin, Western blot


Human GAA / Alpha-Glucosidase, Acid
Human (tested or 100% immunogen sequence identity)
IgG1 Monoclonal [43G7]
Tissue culture supernatant


  • IHC - Paraffin (1:50)
  • Western blot

Specificity and Use

GAA / Alpha-Glucosidase, Acid antibody was raised against purified acid alpha-glucosidase from human placenta
Reacts with the two major bands with apparent molecular weights of 76 000 and 70 000, theband with a molecular weight of about 94000 and minor bands with apparent molecular weightsof less than 67 000, when analyzing alpha-glucosidase isolated from placenta by polyacrylamide gelelectrophoresis in the presence of SDS and a reducing agent.


0.09% sodium azide
Short term 4°C, long term aliquot and store at -20°C, avoid freeze thaw cycles.
For research use only.

About GAA / Alpha-Glucosidase, Acid

P10253 NM_000152 NP_000143.2

GAA Antibody, Acid maltase Antibody, Aglucosidase alfa Antibody, Glucosidase, alpha Antibody, Lysosomal alpha-glucosidase Antibody, Glucosidase, alpha acid Antibody, LYAG Antibody

GAA / Alpha-Glucosidase, Acid is acid alpha-glucosidase, which is essential for the degradation of glycogen to glucose in lysosomes. Different forms of acid alpha-glucosidase are obtained by proteolytic processing. Defects in this gene are the cause of glycogen storage disease II, also known as Pompe's disease, which is an autosomal recessive disorder with a broad clinical spectrum. Three transcript variants encoding the same protein have been found for this gene.


Immunohistochemistry on paraffin-embedded sections of human placenta.


Anti-GAA antibody IHC of human liver. Immunohistochemistry of formalin-fixed, paraffin-embedded tissue after heat-induced antigen retrieval. Antibody LS-B7964 dilution 1:50.

Requested From: 
Date Requested: 3/25/2017

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