Instruction manual of porcine von Willebrand factor (vWF) ELISA kit

This kit is for research use only

Intended application

Quantitative determination of VWF content in pig serum, plasma or other related fluids by ELISA.

product description

VonWillebrandFactor is a polyglycan protein, which is combined with coagulation factor VIII in a non-covalent manner to form a complex and is present in plasma. During normal hemostasis, vWF in the form of high molecular weight polymers can act as a molecular bridge to mediate the adhesion reaction of platelet globulin IB and subendothelial collagen. Congenital VWF abnormalities can cause moderate to severe bleeding tendencies-this is VonWillebrand disease (VWD).

Experimental principle

This kit uses double antibody sandwich enzyme-labeled immunoassay to determine the vWF level in the specimen. The microtiter plate is coated with purified antibody to make a solid-phase antibody, and vWF antigen, biotinylated anti-vWF antibody, and HRP-labeled avidin are added to the monoclonal antibody-coated microwells in sequence, and washed thoroughly before use TMB color development. TMB 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 vWF in the sample. The absorbance (OD value) was measured with a microplate reader at a wavelength of 450 nm, and the sample concentration was calculated.

Kit composition and reagent preparation

1. ELISA plate: one piece (96 wells) 2. Standard product (lyophilized product): 2 bottles, each bottle is diluted with sample diluent to 1ml before use, and after being capped, it is allowed to stand for more than 10 minutes, then repeated Rubbing to help dissolve, its concentration is 50ng / mL, after serial dilution, it is diluted to 50ng / mL, 25ng / mL, 12.5ng / mL, 6.25ng / mL, 3.12ng / mL, 1.56ng / mL , 0.78ng / mL, the original solution is directly used as the highest standard concentration, and the sample dilution is directly used as the standard concentration of 0ng / mL, prepared within 15 minutes before use.

For example, to prepare a 25ng / mL standard: take 0.5ml of 50ng / mL of the above standard and add it to an Eppendorf tube containing 0.5ml of sample diluent, mix well, and the rest of the concentration can be deduced by analogy.

3. Sample diluent: 1 × 20ml / bottle. 4. Test the diluent A: 1 × 10ml / bottle. 5. Test diluent B: 1 × 10ml / bottle. 6. Detection solution A: 1 × 120ul / bottle (1: 100), diluted with detection diluent A1: 100 before use, prepared according to the pre-calculated total amount required for each experiment (100ul per well) before dilution, In actual preparation, more 0.1-0.2ml should be prepared. For example, 1ul detection solution A plus 99ul detection dilution A is prepared in proportion, mix gently and prepare within one hour before use. 7. Detection solution B: 1 × 120ul / bottle (1: 100) is diluted with detection diluent B1: 100 before use. The dilution method is the same as that of Test Solution A. 8. Substrate solution: 1 × 10ml / bottle. 9. Concentrated washing solution: 1 × 30ml / bottle, each bottle is diluted 25 times with distilled water. 10. Stop solution: 1 × 10ml / bottle (2NH2SO4).

Collection and preservation of specimens

1. Serum: Please leave the specimen at room temperature for 2 hours or overnight at 4 ° C and centrifuge at 1000xg for 20 minutes. Take the supernatant for testing, or store the specimen at -20 ° C, but avoid repeated freezing and thawing.

2. Plasma: EDTA or heparin can be used as anticoagulant. Centrifuge the sample at 2-8 ° C and 1000xg for 15 minutes within 30 minutes after collection, or store the specimen at -20 ° C, but avoid repeated freezing and thawing.

Note: Hemolysis of specimens will affect the final test results, so hemolysis specimens should not be tested.

Steps

Each reagent is equilibrated to room temperature before use. Before starting the experiment, please configure all reagents in advance. When the reagents or samples are diluted, they should be mixed well. Try to avoid foaming when mixing. A standard curve should be made for each test. If the sample concentration is too high, the sample should be diluted with the sample diluent in the test tube to make the sample meet the detection range of the kit.

1. Add sample: set blank hole, standard hole and sample hole to be tested respectively. Add 100ul of sample diluent to the blank well, and 100ul of the standard or the sample to be tested in the remaining well. Be careful not to have air bubbles. Add the sample to the bottom of the well of the microtiter plate. The target plate is covered with a cover or film and reacted at 37 ° C for 120 minutes.

To ensure the validity of the experimental results, please use a new standard solution for each experiment.

2. Discard the liquid and spin dry without washing. Add 100ul of detection solution A working solution to each well (take 1ul of detection solution A plus 99ul of detection dilution A to prepare, mix gently and prepare within one hour before use), 37 ℃, 60 minutes. 3. After incubating for 60 minutes, discard the liquid in the hole, spin dry, wash the plate 3 times, soak for 1-2 minutes each time, 350ul / per hole, spin dry (you can also pat the liquid in the hole to pat dry). 4. Add 100ul of testing solution B working fluid (same as testing A working fluid) to each well at 37 ℃ for 60 minutes. 5. After incubating for 60 minutes, discard the liquid in the hole, spin dry, wash the plate 5 times, soak for 1-2 minutes each time, 350ul / per hole, spin dry (you can also pat the liquid in the hole to pat dry). 6. Add 90ul of substrate solution to each well in sequence, and develop color at 37 ° C in the dark (within 30 minutes) (at this time, the first 3-4 wells of the standard product have a clear blue color in the front, and the gradient of the back 3-4 wells is not. obvious). 7. Add 50ul of stop solution to each well in sequence to stop the reaction (in this case, the blue color turns to yellow). The order of adding the stop solution should be the same as that of the substrate solution. In order to ensure the accuracy of the experimental results, the termination solution should be added as soon as possible after the substrate reaction time expires. 8. Measure the optical density (OD value) of each well in sequence using an enzyme-linked instrument at a wavelength of 450 nm. Test within 15 minutes after adding stop solution.

Note:

1. One hole is left for each experiment as a blank zero-adjusting hole. No reagents are added to this hole, only the substrate solution and 2NH2SO4 are added at the end. Use this hole to adjust the OD value to zero when measuring.

2. In order to prevent the sample from evaporating, the reaction plate is placed in a closed box covered with a damp cloth during the test, and the enzyme plate is covered with a cover or film.

3. Store unused microplates or reagents at 2-8 ° C. Standard products, working solution A, and working solution B should be configured and used according to the required amount, do not run out at once. Do not reuse the diluted standard, test solution A working solution or test solution B working solution.

4. It is recommended to set a double-hole test when testing samples to ensure the accuracy of the test results.

Plate washing method Manual plate washing method: absorb (not to touch the wall) or shake off the liquid in the enzyme plate; place a few layers of water on the experimental table

Paper, with the microtiter plate down and vigorously pat several times; inject at least 0.3ml of the recommended wash buffer into the well and soak for 1-2 minutes, as needed

Yes, repeat this process several times.
Automatic plate washing: If there is an automatic plate washing machine, it should be used in the formal experiment process after being used skillfully.

Specificity

The kit can detect recombinant or natural porcine vWF at the same time, and has no cross-reactivity with other related proteins.

Calculation

Taking the concentration of the standard as the abscissa (logarithmic coordinate) and the OD value as the ordinate (ordinary coordinate), draw a standard curve on semi-logarithmic coordinate paper, and find the corresponding concentration from the standard curve according to the OD value of the sample; Multiply by the dilution factor; or use the standard concentration and OD value to calculate the linear regression equation of the standard curve, substitute the OD value of the sample into the equation, calculate the sample concentration, and multiply by the dilution factor to obtain the actual concentration of the sample.

Precautions

1. The washing process is very important, inadequate washing is easy to cause false positives. 2. It is best to control the sampling time within 5 minutes. If there are many specimens, it is recommended to use a volley gun to add samples. 3. Please make a standard curve at the same time of each measurement, it is best to make a double hole. 4. If the content of the substance to be tested in the specimen is too high, please dilute it and then determine it. When calculating, please multiply by the dilution factor.

5. When preparing the standard and the working solution of the test solution, please prepare it with the corresponding diluent, not to be confused.

6. Please keep the substrate away from light.

examination range:

0.78ng / mL-50ng / mL

Explanation

1. Kit storage: -20 ℃ (when not in use for a long time); 2-8 ℃ (when used frequently).

2. Validity: 6 months

3. The concentrated washing liquid will have salt precipitation, and it can be heated and dissolved in the water bath when diluted.

4. The well of the ELISA plate just opened may contain a little water-like substance. This is normal and will not have any impact on the experimental results.

5. There may be inconsistencies between the Chinese and English instructions. Please refer to the English instructions.

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