Human β2-microglobulin（β2-MG） ELISA Kit

（96 tests）

This immunoassay kit allows for the in vitro rapid detection of human β2-MG concentrations in serum, plasma.

Expiration date six months from the date of manufacture

 

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This assay employs the competitive inhibition enzyme immunoassay technique. An antibody specific to β2-MG has been pre-coated onto a microplate. Standards or samples are added to the appropriate microtiter plate wells with HRP-conjugated β2-MG and incubated. A competitive inhibition reaction is launched between β2-MG （Standards or samples） and HRP-conjugated β2-MG with the pre-coated antibody specific for β2-MG. The more amount of β2-MG in samples, the less antibody bound by HRP-conjugated β2-MG. Then the substrate solutions are added to the wells, respectively. And the color develops in opposite to the amount of β2-MG in the sample. The color development is stopped and the intensity of the color is measured.

The standard curve concentrations used for the ELISA’s were 10μg/ml, 2.5μg/ml, 0.5μg/ml, 0.1μg/ml, 0.025μg/ml.

This assay recognizes human β2-MG. No significant cross-reactivity or interference was observed.

The minimum detectable dose of human β2-MG is typically less than 0.01 μg/ml. The sensitivity of this assay, or Lower Limit of Detection （LLD） was defined as the lowest protein concentration that could be differentiated from zero.

 

1.    Unopened test kits should be stored at 2-8?C upon receipt and the microtiter plate should be kept in a sealed bag. The test kit may be used throughout the expiration date of the kit, provided it is stored as prescribed above. Refer to the package label for the expiration date.

2.    Opened test plate should be stored at 2-8?C in the aluminum foil bag with desiccants to minimize exposure to damp air. The kits will remain stable until the expiring date shown, provided it is stored as prescribed above.

3.    A microtiter plate reader with a bandwidth of 10 nm or less and an optical density range of 0-3 OD or greater at 450nm wavelength is acceptable for use in absorbance measurement.

 

1. Bring all reagents and plate to room temperature for at least 30 minutes before use. Unused wells need store at 2-8℃and avoid sunlight.

2. Wash Buffer If crystals have formed in the concentrate, warm to room temperature and mix gently until the crystals have compley dissolved. Dilute 15 ml of Wash Buffer Concentrate into deionized or distilled water to prepare 300 ml of Wash Buffer.

3. To avoid cross-contamination, change pipette tips between additions of each standard level, between sample additions, and between reagent additions. Also, use separate reservoirs for each reagent.

4. When using an automated plate washer, adding a 30 second soak period following the addition of wash buffer, and/or rotating the plate 180 degrees between wash steps may improve assay precision.

5. Substrate Solution should remain colorless or light blue until added to the plate. Keep Substrate Solution protected from light. Substrate Solution should change from colorless or light blue to gradations of blue.

6. Stop Solution should be added to the plate in the same order as the Substrate Solution. The color developed in the wells will turn from blue to yellow upon addition of the Stop Solution. Wells that are green in color indicate that the Stop Solution has not mixed thoroughly with the Substrate Solution.

 

 

1          Microplate reader capable of measuring absorbance at 450 nm, with the correction wavelength set at 540 nm or 570 nm.

2          Pipettes and pipette tips.

3          Deionized or distilled water.

4          Squirt bottle, manifold dispenser, or automated microplate washer.

5          An incubator which can provide stable incubation conditions up to 37°C±0.5°C.

 

Serum Use a serum separator tube （SST） and allow samples to clot for 30 minutes before centrifugation for 15 minutes at 1000 x g. Remove serum and assay immediay or aliquot and store samples at -20°C. Centrifuge the sample again after thawing before the assay. Avoid repeated freeze-thaw cycles.

Plasma Collect plasma using citrate, EDTA, or heparin as an anticoagulant. Centrifuge for 15 minutes at 1000 x g within 30 minutes of collection. Assay immediay or aliquot and

 

1 Set a Blank well without any solution. Add 50μl of Standard or Sample per well. Standard need test in duplicate.

2 Add 50μl of HRP-conjugate to each well （not to Blank well）, Mix well and then incubate for 1 hour at 37°C.

3 Fill each well with Wash Buffer （about 200μl）, stay for 10 seconds and Spinning. Repeat the process for a total of three washes. Complete removal of liquid at each step is essential to good performance. After the last wash, remove any remaining Wash Buffer by aspirating or decanting. Invert the plate and blot it against clean paper towels.

4 Add 50μl of Substrate A and Substrate B to each well, mix well. Incubate for 15 minutes at 37°C. Keeping the plate away from drafts and other temperature fluctuations in the dark.

wells containing the highest concentration of standards

develop obvious blue color. If color change does not appear

uniform, gently tap the plate to ensure thorough mixing. 6 Determine the optical density of each well within 10 minutes,

using a microplate reader set to 450 nm.

Average the duplicate readings for each standard, Blank, and sample and subtract the optical density of Blank. Create a standard curve by reducing the data using computer software capable of generating a four parameter logistic （4-PL） curve-fit. As an alternative, construct a standard curve by plotting the mean absorbance for each standard on the x-axis against the concentration on the y-axis and draw a best fit curve through the points on the graph. The data may be linearized by plotting the log of the β2-MG concentrations versus the log of the O.D. and the best fit line can be determined by regression analysis. This procedure will produce an adequate but less precise fit of the

1          The kit should not be used beyond the expiration date on the kit label.

2          Do not mix or substitute reagents with those from other lots or sources.

3          Any variation in operator, pipetting technique, washing technique, incubation time or temperature, and kit age can cause variation in binding.

4          This assay is designed to eliminate interference by soluble receptors, binding proteins, and other factors present in biological samples. Until all factors have been tested in the Immunoassay, the possibility of interference cannot be excluded.