GAA Peptide (AAP44226)

Data Sheet
 
Sku AAP44226
Old sku AAPP25606
Price $99.00
Name GAA Peptide (AAP44226)
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Size 100 ug
Gene GAA
Alias symbols LYAG
Gene id 2548
Description of target GAA 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. This gene encodes 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.
Swissprot id P10253
Protein accession num NP_000143
Nucleotide accession num NM_000152
Protein size 952 amino acids
Molecular weight 98kDa
Application IHC, WB
Partner proteins NCF1
Quality control The peptide is characterized by mass spectroscopy
Key reference Wan,L., (er) J. Neurol. (2008) In press
Description This is a synthetic peptide designed for use in combination with anti-GAA antibody (Catalog #: ARP44226_P050) made by Aviva Systems Biology. It may block above mentioned antibody from binding to its target protein in western blot and/or immunohistochecmistry under proper experimental settings. There is no guarantee for its use in other applications. Please inquire for more details.
Product format Lyophilized powder
Reconstitution and storage Add 100ul of sterile PBS. Final peptide concentration is 1 mg/ml in PBS. For longer periods of storage, store at -20C. Avoid repeat freeze-thaw cycles.
Lead time Domestic: within 24 hours delivery  International: 3-5 business days
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