Technical data of human 25-hydroxyvitamin D3 (25(OH)D3/25HVD3) kit
1. This kit is for research use only.
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Storage conditions and expiration date:
1. Kit storage: 2-8 ° C.
2. Validity: 6 months
Detection range: 48T 25 ng/L -800 ng/L
purpose of usage:
This kit is used to determine the content of 25-hydroxyvitamin D3 (25(OH)D3/25HVD3) in human serum, plasma and related liquid samples.
Experimental principle
This kit uses the double antibody sandwich method to determine the level of human 25-hydroxyvitamin D3 (25(OH)D3/25HVD3) in the specimen. The microporous plate was coated with purified human 25-hydroxyvitamin D3 (25(OH)D3/25HVD3) antibody to prepare a solid phase antibody, and 25-hydroxyvitamin D3 (25 (OH) was sequentially added to the microcapsule of the coated monoclonal antibody. D3/25HVD3), and then combined with HRP-labeled 25-hydroxyvitamin D3 (25(OH)D3/25HVD3) antibody to form an antibody-antigen-enzyme-labeled antibody complex, which was thoroughly washed and then added with substrate TMB. TMB is converted to blue under the catalysis of HRP enzyme and converted to the final yellow color by the action of an acid. The color depth is positively correlated with the 25-hydroxyvitamin D3 class (25(OH)D3/25HVD3) in the sample. The absorbance (OD value) was measured with a microplate reader at a wavelength of 450 nm, and the concentration of human 25-hydroxyvitamin D3 (25(OH)D3/25HVD3) in the sample was calculated from a standard curve.
Kit composition
1 20 times concentrated washing solution 20ml × 1 bottle 7 Stop solution 3ml × 1 bottle
2 enzyme standard reagent 3ml × 1 bottle 8 standard (1600ng / L) 0.5ml × 1 bottle
3 Enzyme label coating plate 12 holes × 4 strips 9 standard dilution solution 1.5ml × 1 bottle
4 sample dilution 3ml × 1 bottle 10 instructions 1 copy
5 developer A liquid 3ml × 1 bottle 11 sealing film 2 sheets
6 developer B solution 3ml × 1 bottle 12 sealed bag 1
Specimen requirements
1. The specimens should be extracted as soon as possible after collection, and the extraction should be carried out according to the relevant literature. The experiment should be carried out as soon as possible after extraction. If the test cannot be performed immediately, the specimen can be stored at -20 °C, but repeated freezing and thawing should be avoided.
2. Samples containing NaN3 could not be detected because NaN3 inhibited horseradish peroxidase (HRP) activity.
Steps
1. Dilution of standard: This kit provides one original standard, which can be diluted in a small tube according to the following chart.
800 ng/L No. 5 Standard 150 μl of the original standard was added to 150 μl of the standard dilution.
400 ng/L No. 4 Standard 150 μl of No. 5 Standard Add 150 μl Standard Diluent
200 ng/L l No. 3 Standard 150 μl of Standard No. 4 Add 150 μl of Standard Diluent
100 ng/L No. 2 Standard 150 μl of No. 3 Standard Add 150 μl Standard Diluent
50 ng/L No. 1 Standard 150 μl of No. 2 Standard Add 150 μl Standard Diluent
2. Adding samples: set blank holes separately (the blank control wells are not added with the sample and the enzyme standard reagent, the other steps are the same), the standard holes, and the sample holes to be tested. Accurately load 50 μl of the standard on the enzyme-labeled plate, add 40 μl of the sample dilution to the well to be tested, and then add 10 μl of the sample to be tested (the final dilution of the sample is 5 times). Add the sample to the bottom of the well of the microplate, try not to touch the wall of the well, and shake gently to mix.
3. Incubation: The plate was sealed with a sealing film and incubated at 37 ° C for 30 minutes.
4. Dosing: 20 times concentrated washing solution diluted with distilled water 20 times and used
5. Washing: Carefully remove the sealing film, discard the liquid, dry it, fill each well with the washing liquid, let stand for 30 seconds, then discard it, repeat 5 times, and pat dry.
6. Add enzyme: 50 μl of enzyme labeling reagent was added to each well, except for blank wells.
7. Incubation: The operation is the same as 3.
8. Washing: The operation is the same as 5.
9. Color development: Add 50 μl of the developer to each well, then add 50 μl of the developer, gently shake and mix, and color at 37 ° C for 15 minutes.
10. Termination: 50 μl of stop solution was added to each well to terminate the reaction (when the blue color turned yellow).
11. Measurement: The absorbance (OD value) of each well was measured sequentially with a blank air conditioner of zero and a wavelength of 450 nm. The measurement should be carried out within 15 minutes after the addition of the stop solution.
Precautions:
1. The kit should be taken out from the refrigerated environment and should be used at room temperature for 15-30 minutes before use. If the enzyme label is unsealed after opening, the slats should be stored in a sealed bag.
2. Concentrated washing liquid may crystallize out. When diluted, it can be heated and dissolved in a water bath. The washing will not affect the result.
3. The sampler should be used for each step, and the accuracy should be corrected frequently to avoid test errors. The loading time is controlled within 5 minutes. If the number of specimens is large, it is recommended to use a gun.
4. Please make a standard curve at the same time for each measurement and make a double hole. If the content of the substance to be tested in the specimen is too high (the OD value of the sample is larger than the OD value of the standard pore), please first dilute the sample dilution with a certain multiple (n times) and then measure it. When calculating, multiply the total dilution factor ( ×n×5).
5. The sealing film is intended for single use only to avoid cross-contamination.
6. Please keep the substrate away from light.
7. Strictly follow the instructions of the manual, the test results must be based on the microplate reader reading.
8. All samples, washings and various wastes should be treated as infectious materials.
9. The different batch components of this reagent must not be mixed.
10. In the case of an English manual, the English manual shall prevail.
Storage conditions and expiration date
1. The kit is stored at: 2-8 °C.
2. Validity: 6 months
Antimalarial:
Antimalarial medications, also known as antimalarials, are designed to prevent or cure malaria. Such drugs may be used for some or all of the following:
Treatment of malaria in individuals with suspected or confirmed infection
Prevention of infection in individuals visiting a malaria-endemic region who have no immunity (Malaria prophylaxis)
Routine intermittent treatment of certain groups in endemic regions (Intermittent preventive therapy)
Some antimalarial agents, particularly chloroquine and hydroxychloroquine, are also used in the treatment of rheumatoid arthritis and lupus-associated arthritis.
Current practice in treating cases of malaria is based on the concept of combination therapy, since this offers several advantages, including reduced risk of treatment failure, reduced risk of developing resistance, enhanced convenience, and reduced side-effects. Prompt parasitological confirmation by microscopy, or alternatively by rapid diagnostic tests, is recommended in all patients suspected of malaria before treatment is started. Treatment solely on the basis of clinical suspicion should only be considered when a parasitological diagnosis is not accessible.
Antiparasitic:
Antiparasitics are a class of medications which are indicated for the treatment of parasitic diseases, such as those caused by helminths,amoeba, ectoparasites, parasitic fungi, and protozoa, among others. Antiparasitics target the parasitic agents of the infections by destroying them or inhibiting their growth;[4] they are usually effective against a limited number of parasites within a particular class. Antiparasitics are one of the antimicrobial drugs which include antibiotics that target bacteria, and antifungals that target fungi. They may be administered orally, intravenously or topically.
Broad-spectrum antiparasitics, analogous to broad-spectrum antibiotics for bacteria, are antiparasitic drugs with efficacy in treating a wide range of parasitic infections caused by parasites from different classes.
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