Guinea pig (Guinea) substance P (SP) ELISA detection kit This reagent is for research use only. Test principle: The SP kit is a solid-phase sandwich enzyme-linked immunosorbent assay (ELISA). Standards with known SP concentrations, unknown concentrations The sample is added to the microplate for detection. Incubate the SP and biotin-labeled antibody first. After washing, HRP labeled with avidin was added. After incubation and washing, the unbound enzyme conjugate is removed, and then substrates A and B are added to act simultaneously with the enzyme conjugate. Produce colors. The color depth is proportional to the concentration of SP in the sample. Kit contents and preparation: kit components 96 well configuration 48 well configuration 96/48 servings enzyme label plate 1 plate (96T) half plate (48T) plastic membrane plate cover 1 half plate standard: 100pg / ml 1 bottle (1.0ml) 1 bottle (0.5ml) blank control 1 bottle (1.0ml) 1 bottle (0.5ml) standard dilution buffer 1 bottle (8.0ml) 1 bottle (4.0ml) biotin-labeled anti-SP antibody 1 bottle (8.0ml) 1 bottle (4.0ml) Avidin-HRP 1 bottle (12ml) 1 bottle (5ml) wash buffer 1 bottle (20ml) 1 bottle (10ml) Substrate A 1 bottle (6.0ml ) 1 bottle (3.0ml) of substrate B 1 bottle (6.0ml) 1 bottle (3.0ml) stop solution 1 bottle (6.0ml) 1 bottle (3.0ml) Self-provided materials: 1. Distilled water. 2. Sampler: 5ul, 10ul, 50ul, 100ul, 200ul, 500ul, 1000ul. 3. Oscillator and magnetic stirrer, etc. 4. Sample collection, processing and storage methods: 1. Serum ... Avoid any cell stimulation during the operation. Use test tubes free of pyrogens and endotoxins. After collecting blood, centrifuge at 1000 × g for 10 minutes to quickly and carefully separate the red blood cells. 2. Plasma ... EDTA, citrate and heparin plasma can be used for detection. Centrifuge at 1000 × g for 30 minutes to remove particles. 3. Cell supernatant ... centrifuge at 1000 × g for 10 minutes to remove particles and polymer. 4. Tissue homogenate ... Mash the tissue with appropriate amount of saline. Centrifuge at 1000 × g for 10 minutes, and take the supernatant. 5. Storage ... If the sample is not used immediately, it should be divided into small parts -70 ℃ to avoid repeated freezing. If possible, do not use hemolysis or hyperlipidemia. If there are a large number of particles in the serum, centrifuge or filter before testing. Do not thaw at 37 ° C or higher. Thaw at room temperature and ensure that the sample is thawed evenly and adequately. Handling precautions: ◠Reagents should be stored according to the label instructions and returned to room temperature before use. The sparse standards should be discarded and cannot be stored. ◠Slats not used in the experiment should be immediately returned to the packaging bag, sealed and stored to avoid deterioration. ◠Any unused reagents should be packed or covered. Do not mix reagents of different batches. Use before warranty. ◠Use a disposable pipette tip to avoid cross-contamination, and avoid using a sampler with a metal part when drawing the stop solution and the substrates A and B. ◠Use a clean plastic container to prepare the washing solution. Mix all components and samples in the kit thoroughly before use. ◠Substrate A should evaporate to avoid opening the lid for a long time. Substrate B is sensitive to light and avoid prolonged exposure to light. Avoid contact with hands, it is toxic. The OD value should be read immediately after the experiment is completed. ◠The order of adding reagents should be consistent to ensure the same incubation time of all reaction wells. ◠Perform the incubation operation in accordance with the time, amount and sequence of the liquid indicated in the manual. Safety: 1. Avoid direct contact with the termination liquid and substrates A and B. Once contact with these liquids, please rinse with water as soon as possible. 2. Don't eat, drink, smoke or use cosmetics in real difficulties. 3. Do not use your mouth to absorb any components in the kit. Preparation of reagents: 1. Standards: Serial dilutions of standards should be prepared during the experiment and cannot be stored. Before dilution, the standard was mixed by shaking. The dilution ratio is as follows: 100pg / ml (No. 6 standard) The original concentration is added without dilution 50ul 50pg / ml (No. 5 standard) 100ul of the original standard is added 100ul of the standard dilution 25pg / ml ( Standard No. 4) 100ul No. 5 standard added 100ul standard dilution 12.5pg / ml (No. 3 standard) 100ul No. 4 standard added 100ul standard dilution 6.25pg / ml (No. 2 standard ) 100ul No. 3 standard is added 100ul standard dilution 3.15pg / ml (No. 1 standard) 100ul No. 2 standard is added 100ul standard dilution 0pg / ml (blank control) The original concentration is not directly diluted Add 50ul2. Dilution of washing buffer (50 ×): 50 times dilution with distilled water. Kit performance: 1. Sensitivity: The smallest detection concentration is less than No. 1 standard. Linearity of dilution. The correlation coefficient between the linear regression of the sample and the expected concentration is 0.990. 2. Specificity: Does not react with other cytokines. 3. Repeatability: The coefficients of variation within and between plates are less than 10%. Operation steps: 1. Before use, mix all reagents thoroughly. Don't make the liquid generate a lot of foam, so as to avoid adding a large number of bubbles during sample addition, which will cause errors in sample addition. 2. Determine the number of slats required based on the number of samples to be tested plus the number of standard products. It is recommended to make multiple holes for each standard and blank hole. Each sample is determined according to its own quantity, and those that can use multiple holes can be used as much as possible. 3. Add 50ul of the diluted standard to the reaction well and 50ul of the sample to be tested in the reaction well. Immediately add 50ul of biotin-labeled antibody. Cover the membrane plate, mix gently by shaking, and incubate at 37 ° C for 45 minutes. 4. Shake off the liquid in the hole, fill the hole with washing liquid, shake for 30 seconds, shake off the washing liquid, pat dry with absorbent paper. Repeat this operation 4 times. If washing with a plate washer, the number of washes is increased once. 5. Add 100ul of streptavidin-HRP to each well, gently shake and mix, and incubate at 37 ° C for 30 minutes. 6. Shake off the liquid in the hole, fill each hole with washing liquid, shake for 30 seconds, shake off the washing liquid, pat dry with absorbent paper. Repeat this operation 4 times. If washing with a plate washer, the number of washes is increased once. 7. Add 50ul of substrate A and B to each well, gently shake and mix, and incubate at 37 ° C for 5 minutes. Avoid light. 8. Remove the enzyme labeling plate and quickly add 50ul of stop solution. After adding the stop solution, the results should be measured immediately. 9. Measure the OD value of each well at 450nm wavelength. Judgment and analysis of results: 1. Instrument value: read the OD value of each well on a microplate reader with a wavelength of 450 nm. 2. Take the absorbance OD value as the ordinate (Y), and the corresponding SP standard concentration as the abscissa (X) , To make the corresponding curve, the SP content of the sample can be converted from the standard curve to the corresponding concentration according to its OD value, and then multiplied by the dilution factor; or the standard equation concentration and OD value to calculate the regression equation of the standard curve, the sample The OD value of is substituted into the equation to calculate the sample concentration, and then multiplied by the dilution factor, which is the actual concentration of the sample. 3. Range of detection value: 0-100pg / ml4, Sensitivity: 0.1pg / ml
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