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Hexokinase(HK) is an allosteric enzyme, hexokinase dont has a strong specificity, hexokinase is easy to be suppressed with glucose-6-phosphate and ADP. Hexokinase affinity is very strong. Hexokinase has four different types, these types of differences are derived from alternative splicing of the same gene, which is the gene exons (separated by a portion of the intron) reassembled. In different types of cells, there are many functions and structure similar enzyme hexokinase, including hexokinase I, hexokinase II, hexokinase III, and the hexokinase IV (also known as glucokinase). Such enzymes called isozymes, they have the same effect, but it is manufactured by a different gene. dscujbsdjvb
Hexokinase method is recognized as the reference method for measuring blood glucose hexokinase method is applicable to automatic analyzers. Mild hemolysis, lipemia, jaundice, vitamin C, sodium fluoride, liver Beijing, EDTA and oxalate hexokinase method does not interfere with the measurement results. Because red blood cells released from the organic phosphate and some of the enzymes can be consumed NADP, they may interfere with the hexokinase method for the measurement results.
The principle of hexokinase tnf elisa kit is that glucose and ATP in HK of the catalyst, generating glucose 6 - phosphate and ADP; 6 - phosphate glucose and NADP in G6PDH of the catalyst, yields 6 - phosphate gluconic acid lactone and NADPH. NADP and G6PDH in adequate conditions, using glucose 6 - phosphate dehydrogenase (G6PDH) the coupling reaction, NADPH and content changes of glucose 6 - phosphate content change is proportional to 340 nm is detected by the NADPH content changes, the amount of increase in absorbance is reflected in the size of the HK vitality.

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