This kit can only be used for scientific research, not for medical diagnosis
Rat N-acetyl-Î²-D-glucosaminidase (NAG) ELISA detection kit
The kit uses double antibody one-step sandwich enzyme-linked immunosorbent assay (ELISA). To the coated microwells pre-coated with rat N-acetyl-Î²-D-glucosaminidase (NAG) capture antibody, add specimen, standard, and HRP-labeled detection antibody in sequence, incubate and wash thoroughly. The color is developed with the substrate TMB, which is converted into blue under the catalysis of peroxidase and into the final yellow under the action of acid. The color depth is positively correlated with the rat N-acetyl-Î²-D-glucosaminidase (NAG) in the sample. Measure the absorbance (OD value) at 450nm with a microplate reader to calculate the sample concentration.
Sample collection, processing and storage methods
1. Serum: Use a test tube that does not contain pyrogens and endotoxins. Avoid any cell stimulation during the operation. After collecting blood, centrifuge at 3000 rpm for 10 minutes to quickly and carefully separate serum and red blood cells.
2. Plasma: EDTA, citrate or heparin anticoagulation. Take the supernatant by centrifugation at 3000 rpm for 30 minutes.
3. Cell supernatant: centrifuge at 3000 rpm for 10 minutes to remove particles and polymers.
4. Tissue homogenate: Add tissue to the right amount of saline and mash. Take the supernatant by centrifugation at 3000 rpm for 10 minutes.
5. Preservation: If the sample is not tested in time after collection, please aliquot it in one dose and freeze it at -20 â„ƒ to avoid repeated freezing and thawing. Thaw at room temperature and ensure that the sample is thawed evenly and fully.
Bring your own items
1. Microplate reader (450nm)
2. High-precision sampler and tip: 0.5-10uL, 2-20uL, 20-200uL, 200-1000uL
3. 37 â„ƒ thermostat
1. Store the kit at 2-8 Â° C and equilibrate at room temperature for 20 minutes before use. The concentrated washing liquid taken out of the refrigerator will have crystals, which is a normal phenomenon. The water bath is heated to completely dissolve the crystals before use.
2. The slats not used in the experiment should be immediately returned to the ziplock bag, sealed (dry at low temperature) and stored.
3. The standard dilution can be regarded as a negative control or blank; the sample after pretreatment does not need to be diluted, just take 10Î¼L and add it.
4. Perform the incubation operation strictly in accordance with the time, amount of liquid and sequence indicated in the manual.
5. Shake all liquid components thoroughly before use.
48 hole configuration
12 holes Ã— 8
12 holes Ã— 4 strips
Standard product (160 U / L)
Dilute according to the instructions
20 Ã— washing buffer
Dilute according to the instructions
Note: The standard product is diluted with standard product diluent in order: 160, 80, 40, 20, 10, 5 U / L
Dilution of 20 Ã— washing buffer: 1:20 dilution of distilled water, ie 1 part of 20 Ã— washing buffer plus 19 parts of distilled water
1. Manually wash the plate: throw away all the liquid in the hole, fill each hole with the washing liquid, leave the liquid in the hole after standing for 1 min, pat dry on the absorbent paper, and wash the plate 5 times in this way.
2. Automatic plate washing machine: Inject 350Î¼L of washing liquid into each well, soak for 1min, and wash the plate 5 times.
1. Take out the required slats from the aluminum foil bag after equilibrating at room temperature for 20 min. The remaining slats are sealed with a ziplock bag and put back at 4 Â° C.
2. Set up standard wells and sample wells, add 50Î¼L of standard products of different concentrations to the standard wells;
3. Add 10Î¼L of the sample to be tested first, and then add 40Î¼L of the sample diluent;
4. Then add 100 Î¼L of detection antibody labeled with horseradish peroxidase (HRP) to each well of the standard and sample wells, seal the reaction well with a sealing plate, and incubate for 60 min in a 37 Â° C water bath or incubator.
5. Discard the liquid, pat dry on the absorbent paper, fill each well with the washing solution, let stand for 1min, shake off the washing solution, pat dry on the absorbent paper, and repeat washing the plate 5 times (you can also wash the plate with a washing machine)
6. Add 50 Î¼L of substrate A and B to each well, and incubate at 37 Â° C in the dark for 15 minutes.
7. Add 50Î¼L of stop solution to each well, and measure the OD value of each well at 450nm wavelength within 15min.
Draw standard curve: In the Excel worksheet, the standard product concentration is used as the abscissa, and the corresponding OD value is used as the ordinate.
1. Accuracy: The correlation coefficient R between the linear regression of the standard product and the expected concentration is greater than or equal to 0.9900.
2. Sensitivity: The minimum detection concentration is less than 1.0 U / L.
3. Specificity: Does not cross-react with other soluble structural analogs.
4. Repeatability: The coefficients of variation within and between panels are less than 15%.
5. Storage: 2-8 â„ƒ, protected from light and moisture.
6. Validity: 6 months
1. The kit is for research use only, and should not be used for clinical or human experiments, otherwise all the consequences will be borne by the experimenter, and the company will not be responsible.
2. Strictly follow the instructions, and the experimenter violates the instructions, and the consequences will be borne by the experimenter.
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