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CheKine™ Mirco Glycogen Phosphorylase a (GPa) Activity Assay Kit

CheKine™ Mirco Glycogen Phosphorylase a (GPa) Activity Assay Kit

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Specification

Product name CheKine™ Mirco Glycogen Phosphorylase a (GPa) Activity Assay Kit
SampleType Animal tissues, Cells or Bacteria, Plasma, Serum or other Liquid samples
Alternative GPa

Product Properties

Kit components •Extraction Buffer
•Reagent I
•Reagent Ⅱ
•Reagent Ⅲ
•Reagent Ⅳ
Features & Benefits The verified samples are complete in type and easy to operate.
Usage notes • If not assayed immediately, samples can be stored at -80°C for one month.• It is recommended to perform several dilutions of your sample to ensure the readings are within the standard value range.• Fresh samples are necessary for good results. If don't perform the assay at the same time, it's better to complete the Sample Preparation step before storing the samples.
Storage instructions Storage at -20°C and Keep from light immediately upon receipt. Kit has a storage time of 6 months from receipt. Refer to list of materials supplied for storage conditions of individual components.
Shipping Gel pack with blue ice.
Precautions The product listed herein is for research use only and is not intended for use in human or clinical diagnosis. Suggested applications of our products are not recommendations to use our products in violation of any patent or as a license. We cannot be responsible for patent infringements or other violations that may occur with the use of this product.

Additional Information

Background Glycogen phosphorylase is divided into active glycogen phosphorylase a (Glycogen phosphorylase a, GPa) and inactive glycogen phosphorylase b (Glycogen phosphorylase b, GPb) two forms. The decomposition of glycogen is mainly carried out under the catalysis of glycogen phosphorylase a. CheKine™ Micro Glycogen Phosphorylase a (GPa) Activity Assay Kit can detect animal tissues, cells or bacteria, plasma, serum or other liquid samples. In this kit, when no activator is added, GPa catalyzes the production of glucose residues from glycogen and inorganic phosphorus to glycogen and glucose 1-phosphate. Under the action of phosphoglucose mutase and 6-phosphate glucose dehydrogenase, it further catalyzes the reduction of NADP to NADPH. Measuring the rate of increase of NADPH at 340 nm can reflect the activity of GPa.
Alternative GPa

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