Dry chemical reagent tablet for high-density lipoprotein cholesterol and preparation method of dry chemical reagent tablet
A high-density lipoprotein and cholesterol technology, which is applied in material analysis by observing the effect on chemical indicators, analysis by chemical reaction of materials, color/spectral property measurement, etc., can solve the problem of insufficient sensitivity of hydrogen peroxide. , to increase stability, improve accuracy and precision, and reduce interference
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Embodiment 1
[0047] The prepared reaction reagent 1 was coated on a highly asymmetric polysulfone (BTS) membrane using a coating machine, and was vacuum dried at 30-50 °C for 2 h. Use the prepared reagents 2 and 3 to soak the polyethersulfone (PES) membrane and the blood filtration membrane for 5 minutes, respectively, and vacuum dry at 30-50°C for 2 hours. The highly asymmetric polysulfone (BTS) membrane, polyethersulfone (PES) membrane, blood filtration membrane and nylon membrane were cut into rectangular pieces of 8.3mm*4.4mm size using a microcomputer rapid cutter in turn, and assembled in sequence Put it into the card case, and put it in an opaque bottle containing a desiccant and store it away from light.
[0048] Reagent 1:
[0049] Phosphate buffer (pH=6.8) 100mM Hydroxypropylmethylcellulose 25g / L cholesterol esterase 35U / mL cholesterol oxidase 22U / mL peroxidase 800U / mL trehalose 0.1% BSA 0.2% Chromogen 0.25% methanol...
Embodiment 2
[0056] The prepared reaction reagent 1 was coated on a highly asymmetric polysulfone (BTS) membrane using a coating machine, and was vacuum dried at 30-50 °C for 2 h. Use the prepared reagents 2 and 3 to soak the polyethersulfone (PES) membrane and the blood filtration membrane for 5 minutes, respectively, and vacuum dry at 30-50°C for 2 hours. The highly asymmetric polysulfone (BTS) membrane, polyethersulfone (PES) membrane, blood filtration membrane and nylon membrane were cut into rectangular pieces of 8.3mm*4.4mm size using a microcomputer rapid cutter in turn, and assembled in sequence Put it into the card case, and put it in an opaque bottle containing a desiccant and store it away from light.
[0057] Reagent 1:
[0058] Phosphate buffer (pH=6.8) 100mM Hydroxypropylmethylcellulose 25g / L cholesterol esterase 35U / mL cholesterol oxidase 22U / mL peroxidase 800U / mL trehalose 0.1% BSA 0.2% Chromogen 0.25% methanol...
Embodiment 3
[0065] The prepared reaction reagent 1 was coated on a highly asymmetric polysulfone (BTS) membrane using a coating machine, and was vacuum dried at 30-50 °C for 2 h. Use the prepared reagents 2 and 3 to soak the polyethersulfone (PES) membrane and the blood filtration membrane for 5 minutes, respectively, and vacuum dry at 30-50°C for 2 hours. The highly asymmetric polysulfone (BTS) membrane, polyethersulfone (PES) membrane, blood filtration membrane and nylon membrane were cut into rectangular pieces of 8.3mm*4.4mm size using a microcomputer rapid cutter in turn, and assembled in sequence Put it into the card case, and put it in an opaque bottle containing a desiccant and store it away from light.
[0066] Reagent 1:
[0067] Phosphate buffer (pH=6.8) 100mM Hydroxypropylmethylcellulose 25g / L cholesterol esterase 25U / mL cholesterol oxidase 14U / mL peroxidase 500U / mL trehalose 0.1% BSA 0.2% Chromogen 0.25% methanol...
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