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Hprae_1093 assay kit :: General Alpha-Glucosidase Assay Kit

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Catalog # MBS8243263
Unit / Price
  100 Assays  /  $370 +1 FREE 8GB USB
Typical Testing Data/Standard Curve (for reference only)
Product Name

Alpha-Glucosidase (Hprae_1093), Assay Kit

Popular Item
Also Known As

Alpha-Glucosidase Microplate Assay Kit

Product Synonym Names
EC; Alpha-glucosidase; Acid maltase; Glucoinvertase; Glucosidosucrase; Lysosomal alpha-glucosidase; Maltase; Maltase-glucoamylase
Research Use Only
For Research Use Only. Not for use in diagnostic procedures.
Request for Current Manual Insert
Sequence Length
Species Reactivity
Tissue extracts, Cell lysate, Cell culture media and Other biological fluids Samples
Detection Range
1 umol/L - 250 umol/L
Preparation and Storage
Shipped and store at 4 degree C for 6 months.
Product Note
Our Assay Kit assays are dynamic research tools and sometimes they may be updated and improved. If the format of this assay is important to you then please request the current manual or contact our technical support team with a presales inquiry before placing an order. We will confirm the current details of the assay. We cannot guarantee the sample manual posted online is the most current manual.
Other Notes
Small volumes of Hprae_1093 assay kit vial(s) may occasionally become entrapped in the seal of the product vial during shipment and storage. If necessary, briefly centrifuge the vial on a tabletop centrifuge to dislodge any liquid in the container`s cap. Certain products may require to ship with dry ice and additional dry ice fee may apply.
Related Product Information for
Hprae_1093 assay kit
Background: ?-Glucosidase breaks down ?-1,4 linked polysaccharides to glucose, which can be utilized as a source of energy. In the biotechnology industry, ?-glucosidase is used to produce glucose from intermediate breakdown products of starch hydrolysis generated by enzymes such as amylase. Pompe disease, one of the 12 known glycogen storage diseases, is an autosomal recessive metabolic disorder attributed to ?-glucosidase deficiency. In this disease, glycogen accumulates in the lysosomes, resulting in progressive muscle weakness, heart failure and other neurological symptoms. The assay is initiated with the enzymatic hydrolysis of the glucoside by ?-Glucosidase. The enzyme catalysed reaction products p-nitrophenol, can be measured at a colorimetric readout at 400 nm.
Applications Tested/Suitable for Hprae_1093 assay kit
Functional Assay

Typical Testing Data/Standard Curve (for reference only) of Hprae_1093 assay kit
Hprae_1093 assay kit Typical Testing Data/Standard Curve (for reference only) image
Sample Manual Insert of MBS8243263. Click to request current manual
NCBI/Uniprot data below describe general gene information for Hprae_1093. It may not necessarily be applicable to this product.
NCBI Accession #
Molecular Weight
93,827 Da[Similar Products]
NCBI Official Full Name
UniProt Protein Name
UniProt Synonym Protein Names
Protein Family
UniProt Gene Name
Hprae_1093  [Similar Products]
UniProt Entry Name
All of MyBioSource's Products are for scientific laboratory research purposes and are not for diagnostic, therapeutics, prophylactic or in vivo use. Through your purchase, you expressly represent and warrant to MyBioSource that you will properly test and use any Products purchased from MyBioSource in accordance with industry standards. MyBioSource and its authorized distributors reserve the right to refuse to process any order where we reasonably believe that the intended use will fall outside of our acceptable guidelines.
While every efforts were made to ensure the accuracy of the information provided in this datasheet, MyBioSource will not be liable for any omissions or errors contained herein. MyBioSource reserves the right to make changes to this datasheet at any time without prior notice.

It is the responsibility of the customer to report product performance issues to MyBioSource within 30 days of receipt of the product. Please visit our Terms & Conditions page for more information.
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