Work with LifeSpan to design a custom immunohistochemistry to address your specific biological question. Outsource the entire localization process without having to
worry about finding and characterizing target specific antibodies, sourcing and validating difficult-to-find tissues, and having the ability to interpret the resulting
immunostaining in relation to complex human pathologies.
TCR Screening Services
Test your therapeutic antibodies in immunohistochemistry against a broad panel of normal frozen human tissue types in order to determine potential unintended binding.
Our non-GLP TCR services are designed on the FDA recommendation outlined in their "Points to Consider in the Manufacture and Testing of Monoclonal Antibody Products for Human Use".
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Rabbit Polyclonal (IgG) to Human GAA / Alpha-Glucosidase, Acid
Human, Mouse
Western blot
HRP Conjugated
Rabbit Polyclonal (IgG) to Human GAA / Alpha-Glucosidase, Acid
Human
Western blot (applications tested for the base form of this product only)
Unconjugated
Details
Human GAA / Alpha-Glucosidase, Acid
Rabbit
Human (tested or 100% immunogen sequence identity)
IgG Polyclonal
Unconjugated.
Also available conjugated with Biotin, FITC.
Antigen-specific affinity chromatography followed by Protein A affinity chromatography
Unmodified
Applications
Western blot (1:100 - 1:400)
(applications tested for the base form of this product only)
Specificity and Use
Recombinant GaA (Ala761-Asn919) expressed in E. coli.
aa761-919
The antibody is a rabbit polyclonal antibody raised against GaA. It has been selected for its ability to recognize GaA in immunohistochemical staining and western blotting.
ELISA 1:100-1:5000; ICC 1:50-500; WB 1:50-400;
Packaging
PBS, pH 7.4, 0.02% sodium azide, 50% glycerol.
Store at 4°C for frequent use. Aliquot and store at -20°C for up to 1 year. Avoid freeze/thaw cycles
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.