Rat α1 acid glycoprotein (α1-AGP) elisa detection kit instructions

Rat α1 acid glycoprotein ( α1-AGP ) elisa detection kit instructions, elisa kit technology

Rat ( α1-AGP ) ELISA kit, ELISA kit technology

This reagent is for research use only. Specimen: serum or plasma

Shanghai Yuanmu Biological Professional Supply

Test principle:

The α1-AGP kit is a solid phase sandwich enzyme-linked immunosorbent assay (ELISA). Standards with unknown concentrations of α1-AGP and samples of unknown concentration are added to the microplates for detection. The α1-AGP and biotinylated antibodies were first incubated simultaneously. After washing, avidin-labeled HRP was added. After incubation and washing, the unbound enzyme conjugate is removed, then the substrates A, B, and the enzyme conjugate are added simultaneously. Produce color. The depth of the color is proportional to the concentration of α1-AGP in the sample.

α1-AGP kit is an enzyme linked immunosorbent assay (ELISA), which is known to be the standard sample of α1-AGP concentration and the unknown concentration of the sample. At the same time, the α1-AGP and biotin labeled antibodies were incubated After washing, add the HRP labeled with affinity. After warming and washing, the removal of non binding enzyme binding, and then join the substrate A, B, and enzyme binding at the same time. Produce color. Of color and the concentration of α1-AGP in the sample is proportional to the relationship.

Kit content and its preparation

Self-contained materials

1. Distilled water.

2. Sampler: 5ul, 10ul, 50ul, 100ul, 200ul, 500ul, 1000ul.

3. Oscillators and magnetic stirrers, etc.

safety

1. Avoid direct contact with the stop solution and substrates A, B. Once exposed to these liquids, rinse with water as soon as possible.

2. Do not eat, drink, smoke or use cosmetics during the experiment.

3. Do not use your mouth to take any ingredients from the kit.

[ α1 Acid Glycoprotein ( α1-AGP ) ELISA Kit] Handling Precautions

1. Reagents should be stored according to the label instructions and returned to room temperature before use. Standards after dilution should be discarded and cannot be stored.

2. The slats not used in the experiment should be immediately put back into the bag and sealed to prevent deterioration.

3. Other reagents not used should be packaged or covered. Do not mix reagents of different batches. Use before warranty.

4. Use a disposable tip to avoid cross-contamination. Avoid pipettes with metal parts when drawing stop solution and substrate A and B.

5. Use a clean plastic container to configure the wash solution. Mix all the ingredients and samples in the kit thoroughly before use.

6. Wash the enzyme plate should be fully patted dry, do not put the absorbent paper directly into the enzyme standard reaction well to absorb water.

7. Substrate A should be volatilized to avoid opening the lid for extended periods of time. Substrate B is sensitive to light and avoids prolonged exposure to light. Avoid contact with hands and be toxic. The OD value should be read immediately after the experiment is completed.

8. The order of addition of reagents should be consistent to ensure that all wells are incubated for the same time.

9. The incubation was carried out according to the time indicated in the instructions, the amount of addition and the order.

Sample collection, processing and storage methods

1. Serum ---- Avoid any cell irritation during the procedure. A test tube containing no pyrogen and alpha 1 acid glycoprotein was used. After collecting the blood, the serum and red blood cells were quickly and carefully separated by centrifugation at 1000 x g for 10 minutes.

2, plasma ----- EDTA, citrate, heparin plasma can be used for testing. The pellet was removed by centrifugation at 1000 x g for 30 minutes.

3. Cell supernatant - 1000 x g was centrifuged for 10 minutes to remove particles and polymer.

4, tissue homogenate ----- the tissue is added to the appropriate amount of physiological saline mash. Centrifuge at 1000 × g for 10 minutes, take the supernatant

5. Storage ------If the sample is not used immediately, it should be divided into small parts - 70 °C to avoid repeated freezing. Do not use hemolysis or hyperlipemia as much as possible. If there are large amounts of particles in the serum, centrifuge or filter before testing. Do not heat thaw at 37 ° C or higher. It should be thawed at room temperature and ensure that the sample is fully thawed evenly.

Reagent preparation

1. Standard: The serial dilution of the standard should be prepared during the experiment and cannot be stored. Mix the standard shakes before dilution. The dilution ratio is as follows:

2. Dilution of wash buffer (50 x): 50-fold dilution of distilled water.

Steps

1. Mix all reagents thoroughly before use. Do not allow the liquid to generate a large amount of foam, so as to avoid adding a large amount of air bubbles during the loading, resulting in errors in the loading.

2. The number of slats required is determined by the number of samples to be tested plus the number of standards. Multiple holes are recommended for each standard and blank hole. Each sample is determined according to its own quantity, and it is possible to use the double hole as much as possible to make a double hole. The specimen was diluted 1:1 with the specimen dilution and 50 ul was added to the reaction well.

3. 50 ul of the diluted standard was added to the reaction well, and 50 ul of the sample to be tested was added to the reaction well. Immediately add 50 ul of biotinylated antibody. Cover the membrane, mix gently by shaking, and incubate for 1 hour at 37 °C.

4. Remove the liquid from the well, fill each well with the washing solution, shake for 30 seconds, remove the washing solution, and pat dry with absorbent paper. Repeat this operation 3 times. If washing with a washer, the number of washings is increased once.

5. 80 ul of affinity streptavidin-HRP was added to each well, and the mixture was gently shaken and incubated at 37 ° C for 30 minutes.

6. Remove the liquid from the well, fill each well with the washing solution, shake for 30 seconds, remove the washing solution, and pat dry with absorbent paper. Repeat this operation 3 times. If washing with a washer, the number of washings is increased once.

7. Add 50 μl of each of the substrates A and B to each well, mix gently by shaking, and incubate at 37 ° C for 10 minutes. Avoid lighting.

8. Remove the microplate and quickly add 50 ul of stop solution. Immediately after adding the stop solution, the results should be determined.

9. The OD value of each well was measured at a wavelength of 450 nm.

[ α1 acid glycoprotein ( α1-AGP ) ELISA kit] recommended experimental protocol

Limit

The results above the No. 6 standard are non-linear and no accurate results can be obtained from this standard curve.

Α1 acid glycoprotein ( α1-AGP ) ELISA kit performance

1. Sensitivity: The minimum detection concentration is less than the No. 1 standard. The linearity of the dilution. The linear regression coefficient of the sample and the expected concentration correlation coefficient R value was 0.990.

2. Specificity: Does not react with other cytokines.

3. Repeatability: The coefficient of variation between the plate and the plate is less than 10%.

Result judgment and analysis

1. Instrument value: read the OD value of each hole on a microplate reader with a wavelength of 450 nm.

2. The absorbance OD value is the ordinate (Y), and the corresponding α1-AGP standard concentration is the abscissa (X), and the corresponding curve is obtained. The α1-AGP content of the sample can be converted from the standard curve according to the OD value. The corresponding concentration.

3. Detection range: 0-80ng/ml

4. Sensitivity: 0.1 ng/ml

The performance of kit:

1 sensitivity: minimum dα1-AGPection concentration is less than 1 standard. Linearity of dilution. Sample linear regression and the expected concentration correlation coefficient R value is 0.990.

2: no specific reaction with other cytokines.

3 repeatability: plate, plate bα1-AGPween the coefficients of variation were less than 10%.

CHADD

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