Human Colony Stimulating Factor 2 Receptor Beta (CSF2Rb) Elisa Kit
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Human Colony Stimulating Factor 2 Receptor Beta (CSF2Rb) Elisa Kit is for research use only. Human Colony Stimulating Factor 2 Receptor Beta (CSF2Rb) Elisa Kit Instructions for Use Detection range: 96T 15 ng / L-400ng / L Experimental principle: this The kit used double antibody sandwich method to determine the level of human colony stimulating factor 2 receptor β (CSF2Rb) in the specimen. Microporous plates were coated with purified human colony stimulating factor 2 receptor β (CSF2Rb) antibody to prepare solid-phase antibodies, and colony stimulating factor 2 receptor β (CSF2Rb) was added to the microwells coated with mAb in turn The HRP-labeled colony-stimulating factor 2 receptor β (CSF2Rb) antibody binds to form an antibody-antigen-enzyme-labeled antibody complex, which is washed and washed with a substrate TMB for color development. TMB is converted into blue under the catalysis of HRP enzyme, and into the final yellow under the action of acid. The color depth is positively correlated with the colony stimulating factor 2 receptor β (CSF2Rb) in the sample. The absorbance (OD value) was measured with a microplate reader at a wavelength of 450 nm, and the concentration of human colony stimulating factor 2 receptor β (CSF2Rb) in the sample was calculated by a standard curve. Purpose: This kit is used to determine the content of colony stimulating factor 2 receptor β (CSF2Rb) in human serum, plasma and related liquid samples. Human colony stimulating factor 2 receptor β (CSF2Rb) Elisa kit composition: 1.30 times concentrated washing solution 20ml × 1 bottle 7 stop solution 6ml × 1 bottle 2. enzyme label reagent 6ml × 1 bottle 8 standard (800ng / L) 0.5 ml × 1 bottle 3. Enzyme label coating plate 12 wells × 8 strips 9 standard dilution 1.5ml × 1 bottle 4. sample dilution 6ml × 1 bottle 10 instructions 1 copy 5. developer A solution 6ml × 1 bottle 11 Sealing film 2 sheets 6. Chromogen B solution 6ml × 1 / bottle 12 Sealed bag 1 specimen requirement: 1. Cannot detect samples containing NaN3, because NaN3 inhibits the activity of horseradish peroxidase (HRP). 2. The specimens should be extracted as soon as possible after collection. The extraction should be carried out according to 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. Operation steps: 1. Dilution of standard product: This kit provides one original standard product. The user can perform dilution in a small test tube according to the following chart. 400ng / L No. 5 standard 150μl original standard added 150μl standard dilution 200ng / L No. 4 standard 150μl No. 5 standard added 150μl standard dilution 100ng / L No. 3 standard 150μl No. 4 standard Add 150μl standard dilution 50ng / L No. 2 standard 150μl No. 3 standard add 150μl standard dilution 25ng / L No. 1 standard 150μl No. 2 standard add 150μl standard dilution 2. Add samples: Separately set blank wells (the blank control wells do not add samples and enzyme-labeled reagents, the rest of the steps are the same), standard wells, sample wells to be tested. Accurately add 50μl of standard on the enzyme-coated plate, add 40μl of sample diluent to the sample well, and then add 10μl of sample to be tested (the final dilution of the sample is 5 times) Add the sample and add the sample to the bottom of the well of the microplate, try not to touch the wall of the well, shake gently to mix. 3. Incubation: seal the plate with a sealing film and incubate at 37 ° C for 30 minutes. 4. Mixing solution: Dilute 30 times concentrated washing solution with distilled water 30 times before use. 5. Washing: Carefully remove the sealing film, discard the liquid, spin dry, fill each well with washing solution, let it stand for 30 seconds and then discard , Repeat this 5 times, pat dry. 6. Add enzyme: add 50μl of enzyme label reagent to each well, except blank well. 7. Incubation: The operation is the same as 3. 8. Washing: The operation is the same as 5. 9. Color development: add 50μl of developer A to each well, then add 50μl of developer B, mix gently, and develop color at 37 ℃ in the dark 15 minutes. 10. Stop: add 50 μl of stop solution to each well to stop the reaction (at this time, the blue turns to yellow). 11. Determination: Measure the absorbance (OD value) of each well in sequence with the blank air conditioner at zero and 450 nm wavelength. The measurement should be carried out within 15 minutes after adding the stop solution. Summary of operation procedures: calculation, taking the concentration of the standard as the abscissa and the OD value as the ordinate, draw a standard curve on the coordinate paper, and find out the corresponding concentration from the standard curve according to the OD value of the sample; 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 then multiply it by the dilution factor to obtain the actual concentration of the sample. Note: 1. The kit should be taken out of the refrigerated environment and should be equilibrated at room temperature for 15-30 minutes before use. If the enzyme label coated plate is not used up after opening, the strip should be stored in a sealed bag. 2. Crystals may be precipitated in the concentrated washing liquid, which can be heated and dissolved in the water bath during dilution, and the results will not be affected during washing. 3. The sample adder should be used in each step of sample addition, and its accuracy should be regularly checked to avoid test errors. 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. 4. Please make a standard curve at the same time of each measurement, it is best to 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 greater than the OD value of the first well of the standard well), please dilute it with a certain multiple of the sample diluent (n times) before measuring, and finally multiply the total dilution when calculating Multiple (× n × 5). 5. The sealing film is limited to one-time use to avoid cross contamination. 6. Please keep the substrate away from light. 7. Strictly follow the instructions, and the test results must be determined based on the reading of the microplate reader. 8. All samples, washing liquid and various wastes should be treated as infectious agents. 9. The components of different batches of this reagent shall not be mixed. 10. If there is any difference with the English manual, the English manual shall prevail. Storage conditions and expiration date: 1. Kit storage: 2-8 ℃. 2. Validity: 6 months