Glycogen Phosphorylase b (Gpb) Activity Assay Kit
Cat.No:BC3355 Solarbio
Detection Method:Spectrophotometer/Microplate Reader
Storage:Store at -20℃,6 months
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Glycogen Phosphorylase b (Gpb) Activity Assay KitDetection Method:Spectrophotometer/Microplate Reader
Storage:Store at -20℃,6 months
Qty:
Size:
Name | Glycogen Phosphorylase b (Gpb) Activity Assay Kit |
Detection Method | Spectrophotometer/Microplate Reader |
Storage | Store at -20℃,6 months |
Recommend | If 96-well plate is used for determination, 96-well UV plate should be used, recommended item numberYA0602 |
Unit | Kit |
Specification | 100T/48S |
Determination of Significance:
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. When no activator is added, glycogen phosphorylase a 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 340nm can reflect the activity of glycogen phosphorylase a. The activity of GP (GPa and GPb) is measured by adding an activator, and GPa activity is measured when no activator is added. GPb activity can be obtained by subtracting GPa activity from GP activity.
Measurement Principle:
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. When no activator is added, glycogen phosphorylase a 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 340nm can reflect the activity of glycogen phosphorylase a. The activity of GP (GPa and GPb) is measured by adding an activator, and GPa activity is measured when no activator is added. GPb activity can be obtained by subtracting GPa activity from GP activity.
Self Provided:
Ultraviolet spectrophotometer/microplate reader, low temperature centrifuge, constant temperature incubator/water bath, adjustable pipette, mortar/homogenizer, micro quartz cuvette/96 well UV flat -bottom plate, ice and distilled water.
Note:Product information may be optimized and upgraded. Please refer to the actual label information for accuracy.
Remark:These protocols are for reference only. Solarbio does not independently validate these methods.
Note:
1. The products are all for scientific research use only. Do not use it for medical, clinical diagnosis or treatment, food and cosmetics, etc. Do not store them in ordinary residential areas.
2. For your safety and health, please wear laboratory clothes, disposable gloves and masks.
3. The experimental results may be affected by many factors, after-sale service is limited to the product itself and does not involve other compensation.
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