By in Product release

New Arrivals:Five kinds of biochemical kits meet your needs!

 

Last week, we have published a popular science knowledge about depression|hemolytic anemia|cancer treatment|energy transmission, in which several related detection indexes mentioned in the article, such as G6PDH, NADK, ATPase, MAO, etc., quickly attracted the attention of many customers, and they left messages to express their expectation for further understanding.

Now the opportunity has come,our company has launched five kinds of biochemical kits, corresponding to the above-mentioned detection indexes. In order to let everyone understand the characteristics of the new product in more detail,this paper will analyze from the principle and advantages.

 

New product list

CheKine™ Cell Metabolism Assay Kit (High Sensitivity & Stability)

Product Name Description Cat. No. Size
CheKine™ Glucose-6-Phosphate Dehydrogenase (G6PDH) Activity Colorimetric Assay Kit Determination of G6PDH activity KTB1011 48/96T
CheKine™ NAD+ kinase (NADK) Activity Colorimetric Assay Kit Determination of NADK activity KTB1022 48/96T
CheKine™ Monoamine Oxidase (MAO) Activity Colorimetric Assay Kit Determination of MAO activity KTB1900 48/96T
CheKine™ Na⁺/K⁺-ATPase Activity Colorimetric Assay Kit Determination of Na⁺/K⁺-ATPase activity KTB1800 48/96T
CheKine™ Ca2⁺/Mg2⁺-ATPase Activity Colorimetric Assay Kit Determination of Ca2⁺/Mg2⁺-ATPase activity KTB1810 48/96T

 

CheKine™ Glucose-6-Phosphate Dehydrogenase (G6PDH) Activity Colorimetric Assay Kit

Assay Principle:

The kit provides a simple method for detecting glucose-6-phosphate dehydrogenase (G6PDH) activity in a variety of biological samples such as serum, plasma, tissues, cells,plants and bacteria. In the assay, G6PDH present in the sample converts NADP+ to NADPH, which has an absorbance at 340 nm. The absorbance of NADPH is proportional to the G6PDH activity present in the sample.

 

CheKine™ NAD+ kinase (NADK) Activity Colorimetric Assay Kit

Assay Principle:

The kit provides a simple method for detecting NADK activity in a variety of biological samples such as serum, plasma, tissues, cells, plants and bacteria. In the assay, NADK catalyzes the phosphorylation of NAD+ to produce NADP+; NADP+ can be reduced to NADPH by glucose-6-phosphate dehydrogenase. NADPH has a characteristic absorption peak at 340 nm. The rate of NADPH increase at 340 nm can reflect NADK activity.

 

CheKine™ Monoamine Oxidase (MAO) Activity Colorimetric Assay Kit

Assay Principle:

The kit provides a simple method for detecting MAO activity in a variety of biological samples such as serum, plasma, tissues, cells, plants, bacteria and Fungi. In the assay, MAO catalyzes the deamination of monoamine substrates to the corresponding aldehydes, which are further oxidized to acid. The substrate has a characteristic absorption peak at 360 nm. The rate of monoamine substrates decrease at 360 nm can reflect MAO activity.

 

CheKine™ Na⁺/K⁺-ATPase Activity Colorimetric As-say Kit

Assay Principle:

The kit provides a simple method for detecting Na⁺/K⁺-ATPase activity in a variety of biological samples such as serum, plasma, tissues, cells, plants and bacteria. In the assay, Na⁺/K⁺-ATPase catalyzes ATP hydrolysis to produce ADP and inorganic phosphorus. The content of inorganic phosphorus can reflect the activity of ATPase.

 

CheKine™ Ca2⁺/Mg2⁺-ATPase Activity Colorimetric Assay Kit

Assay Principle:

The kit provides a simple method for detecting Ca2/Mg2-ATPase activity in a variety of biological samples such as serum, plasma, tissues, cells, plants and bacteria. In the assay, Ca2/Mg2-ATPase catalyzes ATP hydrolysis to produce ADP and inorganic phosphorus. The content of inorganic phosphorus can reflect the activity of ATPase.

 

The common advantages of these five biochemical kits are as follows:

  • A wide range of applicable samples: serum, plasma, tissue, cells, bacteria, plants.
  • Simple operation steps:The sample can be directly tested after processing, and the operation time is short, and the fastest one takes only 3 minutes.
  • Plasma and serum samples can be detected directly without processing.
  • Detailed sample preparation and result calculation methods are provided.