Method for extracting and detecting biotin of bird nest
A detection method, biotin technology, applied in the direction of measurement device, test sample preparation, color/spectral characteristic measurement, etc., can solve the problems of large investment in high-efficiency liquid phase methods, troublesome operation of microbial methods, and large amount of solvents, etc., to achieve Overcoming cumbersome detection steps, simple detection methods, and the effect of overcoming cumbersome steps
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Embodiment 1
[0030] Weigh 1 gram of bird's nest powder that has been removed from impurities, add 40ml of dimethylformamide, Stir and extract in a water bath for 1 h. The extract was centrifuged with a high-speed centrifuge (10,000rpm) for 10min. Remove the supernatant and add an equal amount of ethanol, at 65 Concentrate by rotary evaporation. Spot 15 μl of the concentrated extract (i.e. sample solution) on a silica gel 60 F254 high-efficiency thin-layer plate (10cm×10cm), and use the external standard one-point method to spot the biotin standard at 1 l (1.48mg / ml). The developer is chloroform (v): acetone (v): methanol (v): glacial acetic acid (v) = 2.5: 1.5: 2: 0.01, unfolded in a 10cm × 12cm × 15cm expansion cylinder, the expansion distance is 6cm, and the development time is 20min. After unfolding, the plate was dried first, and then stained with 0.05% potassium permanganate staining solution. Put the dyed board into 100 After drying in an oven for 12 minutes, the Rf value ...
Embodiment 2
[0032] Weigh 1 gram of bird's nest powder that has been removed from impurities, add 25ml of dimethylformamide, The water bath was stirred and extracted for 2h. The extract was centrifuged with a high-speed centrifuge (10,000rpm) for 10min. Remove the supernatant and add an equal amount of ethanol at 50 Concentrate by rotary evaporation. Spot 15 μl of the concentrated extract (i.e. sample solution) on a silica gel 60 F254 high-efficiency thin-layer plate (10cm×10cm), and use the external standard one-point method to spot the biotin standard at 1 I (1.48 mg / ml). The developing agent is chloroform (v): acetone (v): methanol (v): glacial acetic acid (v) = 1.5: 2.5: 1: 0.1, unfolded in a 10cm×12cm×15cm developing cylinder, the spreading distance is 6cm, and the developing time is 20min. After unfolding, the plate was dried first, and then stained with 0.05% potassium permanganate staining solution. Put the dyed plate into 120 Dry in an oven for 8 minutes, and the Rf val...
Embodiment 3
[0034] Weigh 1 gram of bird's nest powder that has been removed from impurities, add 30ml of dimethylformamide, Stir and extract in a water bath for 1.5 hours. The extract was centrifuged with a high-speed centrifuge (10,000rpm) for 10min. Remove the supernatant and add an equal amount of ethanol, at 60 Concentrate by rotary evaporation. Spot 15 μl of the concentrated extract (i.e. sample solution) on a silica gel 60 F254 high-efficiency thin-layer plate (10cm×10cm), and use the external standard one-point method to spot the biotin standard at 1 l (1.48mg / ml). The developer is chloroform (v): acetone (v): methanol (v): glacial acetic acid (v) = 2.0: 2.0: 1.5: 0.05, and it is developed in a 10cm × 12cm × 15cm expansion cylinder, the expansion distance is 6cm, and the development time for 20min. After unfolding, the plate was dried first, and then stained with 0.05% potassium permanganate staining solution. Put the dyed plate into 110 After drying in an oven for 10 min...
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