Creatine kinase isoenzyme detection kit
A technology for detecting kits and creatine kinase, which is applied in measuring devices, instruments, and biological material analysis, etc., can solve the problems such as the kit detection linear range is not wide, the reagent storage is unstable, and the anti-interference ability is poor, so as to avoid defects Influence, improve the detection range, avoid the effect of interference
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Embodiment 1
[0043] The creatine kinase isoenzyme detection kit provided in this embodiment includes reagent R1 and reagent R2, and the composition of the reagent R1 and reagent R2 is as follows:
[0044] Reagent R1:
[0045]
[0046]
[0047] In the table: the mass ratio of TritonX-100 and styrene polyoxyethylene ether is 3.2:1.
[0048] Preparation of reagent R1: according to the components and content of reagent R1 in the above table, take the components of reagent R1, add them into purified water, mix well, adjust the pH value to 7.0, filter through a filter membrane, and constant volume to obtain reagent R1 .
[0049] Reagent R2:
[0050]
[0051] In the table: the mass ratio of triethanolamine, glycine and casein is 0.5:1:2.5.
[0052] Preparation of reagent R2:
[0053] ①Microsphere activation: Add polystyrene latex microspheres with a diameter of 300nm and surface-modified carboxyl groups to the MOPS buffer with a pH of 7.2, and add 1-ethyl-(3-dimethylaminopropyl) carb...
Embodiment 2
[0059] The creatine kinase isoenzyme detection kit provided in this embodiment includes reagent R1 and reagent R2, and the composition of the reagent R1 and reagent R2 is as follows:
[0060] Reagent R1:
[0061]
[0062] In the table: the mass ratio of TritonX-100 and styrene polyoxyethylene ether is 2.5:1.
[0063] Preparation of reagent R1: According to the components and contents of reagent R1 in the above table, take each component of reagent R1, add them into purified water, mix well, adjust the pH value to 6.5, filter through a filter membrane, and constant volume to obtain reagent R1 .
[0064] Reagent R2:
[0065]
[0066] In the table: the mass ratio of triethanolamine, glycine and casein is 1:1:3.
[0067] Preparation of reagent R2:
[0068] ①Microsphere activation: Add polystyrene latex microspheres with a diameter of 400nm and surface-modified amino groups to the HEPES buffer with a pH of 6.0, and add mercaptonicotinamide, react at 30°C for 35min, and re...
Embodiment 3
[0074] The creatine kinase isoenzyme detection kit provided in this embodiment includes reagent R1 and reagent R2, and the composition of the reagent R1 and reagent R2 is as follows:
[0075] Reagent R1:
[0076]
[0077] In the table: the mass ratio of TritonX-100 and styrene polyoxyethylene ether is 4.5:1.
[0078] Preparation of reagent R1: According to the components and content of reagent R1 in the above table, take each component of reagent R1, add them into purified water, mix well, adjust the pH value to 8.0, filter through a filter membrane, and constant volume to obtain reagent R1 .
[0079] Reagent R2:
[0080]
[0081]
[0082] In the table: the mass ratio of triethanolamine, glycine and casein is 2:1:4.
[0083] Preparation of reagent R2:
[0084] ①Microsphere activation: Add polystyrene latex microspheres with a diameter of 250nm and surface-modified hydroxyl groups to the MOPSO buffer with a pH of 7.5, and add isocyanate, react at 25°C for 40min, re...
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