Neuron-specific enolase calibration product and preparation method thereof
An enolase-specific technology, which is applied in the field of neuron-specific enolase calibrator and its preparation, can solve the problems of unstandardized production, large batch-to-batch variation, and high cost of calibrator, and achieve easy standardized production and long-term validity Long-lasting, low-cost effects
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[0026] A preparation method of a neuron-specific enolase calibrator of the present invention specifically comprises the following steps:
[0027] (a) prepare buffer solution;
[0028] (b) adding a protective agent and different concentrations of neuron-specific enolase to the buffer obtained in step (a);
[0029] (c) freeze-drying the buffer mixture obtained in step (b) to obtain a neuron-specific enolase calibrator.
[0030] Preferably, the buffer is one or more of MOPSO, Tris, borate buffer; more preferably, the buffer is MOPSO or Tris or a mixture of MOPSO and Tris.
[0031] Preferably, the pH of the buffer is 7.0-7.5; more preferably, the pH of the buffer is 7.2-7.4.
[0032] Preferably, the concentration of the buffer is 10-30 mM; more preferably, the concentration of the buffer is 10-20 mM.
[0033] Preferably, the protective agent is a mixture of proteins, sugars, antioxidants and bacteriostatic agents; wherein, the proteins are preferably ovalbumin or human serum al...
Embodiment 1
[0040] Example 1 Preparation of neuron-specific enolase calibrator
[0041] Prepare 100 mL of MOPSO buffer solution with a pH of 7.0 and a concentration of 10 mM, add 0.5 g of human serum albumin, 4 g of trehalose, 1 g of sodium thiosulfate and 0.05 g of sodium azide, and filter through a 0.22 μm filter membrane; NSE was added to the matrix of the calibration substance; the prepared neuron-specific enolase calibration substance was weighed 1g ± 0.005g / bottle, put into a freeze dryer, and freeze-dried; the prepared neuron-specific enolase Add 1g ± 0.005g of purified water to the lyophilized powder of the calibration product, redissolve at room temperature for 15 minutes, and perform the test. According to the NSE concentration and the corresponding light value, a dose-response curve is drawn.
Embodiment 2
[0042] Example 2 Preparation of Neuron-specific Enolase Calibrator
[0043] Prepare 100 mL of Tris buffer solution with a pH of 7.4 and a concentration of 20 mM, add 0.5 g of ovalbumin, 4 g of trehalose, 1 g of sodium thiosulfate and 0.05 g of sodium azide to it, and filter through a 0.22 μm filter membrane; Add NSE to the prepared calibrator matrix; weigh the prepared neuron-specific enolase calibrator 1g ± 0.005g / bottle, put it into a freeze dryer, and freeze-dry; add the prepared neuron-specific enolase Add 1g±0.005g of purified water to the freeze-dried powder of the alcoholase calibrator, redissolve at room temperature for 15 minutes, and conduct the test. According to the NSE concentration and the corresponding light value, draw a dose-response curve, such as figure 1 shown.
[0044] The pH buffers, proteins, sugars, antioxidants and preservatives used in the above examples can also be replaced by any one or a combination of the aforementioned definitions, and the prepa...
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