Shanghai Xitang Biotechnology Co., Ltd. 021-55229872, 65333639
D- dimer (D-Dimer) ELISA kit instructions for use rat
 ( for serum, plasma, cell culture supernatants and biological fluids )
principle
This experiment used double antibody sandwich ABC-ELISA. The anti-rat D-Dimer monoclonal antibody was coated on the plate, the D-Dimer in the standard and the sample was combined with the monoclonal antibody, and the biotinylated anti-rat D-Dimer was added to form an immune complex attached to the plate. On the horseradish peroxidase-labeled Streptavidin combined with biotin, the substrate working solution is blue, and finally the stop solution sulfuric acid is added, and the OD value is measured at 450 nm. The D-Dimer concentration is proportional to the OD value, and can be passed. Draw a standard curve to determine the D-Dimer concentration in the specimen.
Kit composition ( 2-8 ° C preservation)
Coated Wells | 96 holes | Enzyme Conjugate | 12ml |
10× specimen dilution (Sample Buffer) | 12ml | 20×Wash Buffer | 50ml |
Standards: 600ng/bottle | 2 bottles | Substrate working fluid (TMB Solution) | 12ml |
Primary antibody working solution (Biotinylated Antibody) | 12ml | Stop Solution | 12ml |
Prepare reagents and collect blood samples
1. Collection of specimens: serum, plasma (EDTA, citrate, heparin anticoagulation), cell culture supernatant, tissue homogenate, etc., as early as possible, stored at 2-8 ° C for 48 hours; longer time must be frozen (-20 °C or -70 °C) Save to avoid repeated freezing and thawing. All specimens should be diluted with the specimen dilution at least 1 : 100 (take 10 ul, add 990 ul of the dilution, and dilute 100 times).
2. Standard solution preparation: Add 0.3 ml of distilled water before use and mix to form a 2000 ng/ml solution. Set 8 tubes of standard tube, and add 200 ul of standard dilution solution to each tube. Add 200 ul of 2000 ng/ml standard solution to the first tube, mix and aspirate 200 ul with the sampler, and transfer to the second tube. Repeat the dilution as described above, and aspirate 200 ul from the seventh tube and discard it. The eighth tube is a blank control.
3. The 10× specimen dilution was diluted 1:10 with distilled water (example: 1 ml concentrated dilution + 9 ml distilled water).
4. Washing solution: diluted 1:20 with distilled water (example: 1 ml concentrated washing solution added to 19 ml of distilled water)
Test procedure
1. Loading: Add 100 ul of standard or sample to be tested in each well. Mix the reaction plate thoroughly and let it stand at 37 °C for 120 minutes.
2. Wash the plate: Wash the plate thoroughly with washing solution 4-6 times, and dry it on the filter paper.
3. Add 100 ul of the first antibody working solution to each well. The reaction plate was thoroughly mixed and placed at 37 ° C for 60 minutes.
4. Wash the board: the same as before.
5. Add 100 ul of enzyme-labeled antibody working solution per well. The reaction plate was placed at 37 ° C for 30 minutes.
6. Wash the board: same as before.
7. Add 100 ul of substrate working solution per well, set 37 The reaction was carried out in the dark at °C for 15 minutes.
8. Add 100 ul of stop solution to each well and mix.
9. Measure the absorbance at 450 nm using a microplate reader within 30 minutes.
Result calculation and judgment
1. All OD values ​​should be subtracted from the blank value before calculation.
2. Take the standard 1000, 500, 250, 125, 62.5, 31.2, 15.6, 0 ng/ml as the abscissa and OD as the ordinate. Draw on the coordinate paper and draw the standard curve.
3. Find the corresponding D-Dimer content on the graph based on the OD value of the sample, and multiply by the dilution factor.
Kit performance
1. Sensitivity: The minimum D-Dimer detection concentration is less than 8 ng/ml.
2. Specificity: Recombinant or natural rat D-Dimer can be detected simultaneously. Does not cross-react with other cytokines in rats.
3. Repeatability: The coefficient of variation in the plate and plate is less than 9%.
Precautions
1. It is recommended to make double holes for the above standard holes and samples to be tested. The standard curve should be made at the same time for each measurement.
2. The washing process is critical. Insufficient washing will result in an accuracy error and an erroneous rise in the OD value.
3. After the slats are opened, the remaining slats should be sealed again to keep the slats dry .
4. This kit should be stored in a 4 o C refrigerator.
5. This kit is for scientific research only and cannot be used for clinical diagnosis!
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