Human MIG ELISA Kit

For the quantitative in vitro determination of Human monokine induced by interferon-gamma concentrations in

serum - plasma - celiac fluid - tissue homogenate - body fluid

Catalogue Number: SU-B10060

FOR LABORATORY RESEARCH USE ONLY.

NOT FOR USE IN DIAGNOSTIC PROCEDURES.

This package insert must be read in its entirety before using thisproduct.

ELISA

ENZYME LINKED IMMUNOSORBENT ASSAY

INTENDED USE AND TEST PRINCIPLE

This MIG ELISA kit is intended Laboratory for Research use only and is not for use in diagnostic or therapeutic procedures. The Stop Solution changes the color from blue to yellow and the intensity of the color is measured at 450 nm using a spectrophotometer. In order to measure the concentration of MIG in the sample, this MIG ELISA Kit includes a set of calibration standards. The calibration standards are assayed at the same time as the samples and allow the operator to produce a standard curve of Optical Density versus MIG concentration. The concentration of MIG in the samples is then determined by comparing the O.D. of the samples to the standard curve.

SAMPLE COLLECTION AND STORAGES

Serum-Use a serum separator tube and allow samples to clot for 2 hours at room temperature or overnight at 4℃before centrifugation for 20 minutes at approximay 2000×g. Remove serum and assay immediay or aliquot and store samples at -20℃.Avoid repeated freeze-thaw cycles

Plasma-Collect plasma using heparin as an anticoagulant. Centrifuge samples for 30minutes at 2000×g at 2-8℃ within 30 minutes of collection. Store samples at -20℃. Avoid repeated freeze-thaw cycles.

Cell culture supernates, tissue homogenateand other biological fluids -Remove particulates by centrifugation and assay immediay or aliquot and store samples at -20℃. Avoid repeated freeze-thaw cycles.

Note: The samples shoule be centrifugated dequay and no hemolysis or granule was allowed.

MATERIALS REQUIRED BUT NOT SUPPLIED

1.  37 ℃ incubator

2.  Standard microplate readercapable of measuring absorbance at 450 nm

3.  Precision pipettes, disposable pipette tipsand Absorbent paper

4. Distilled or deionized water

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REAGENTS PROVIDED

Note:

1.  Standard concentrationwas followed by:2400,1200,600,300,150,75pg/mL.

2. Ifsamplesgeneratevalueshigherthanthehigheststandard, pleasedilutethesampleswithSampleDiluentandrepeattheassay.

PRECAUTIONS

1. Do not substitute reagents from one kit lot to another. Standard, conjugate and microtiter plates are matched for optimal performance. Use only the reagents supplied by manufacturer.

2. Allow kit reagents and materials to reach room temperature (20-25°C) before use. Do not use water baths to thaw samples or reagents.

3. Do not use kit components beyond their expiration date.

4. Use only deionized or distilled water to dilute reagents.

5. Do not remove microtiter plate from the storage bag until needed. Unused strips should be stored at 2-8°C in their pouch with the desiccant provided.

6. Use fresh disposable pipette tips for each transfer to avoid contamination.

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7. Do not mix acid and sodium hypochlorite solutions.

8. Serum and plasma should be handled as potentially hazardous and capable of transmitting disease. Disposable gloves must be worn during the assay procedure, since no known test method can offer complete assurance that products derived from Rat blood will not transmit infectious agents. Therefore, all blood derivatives should be considered potentially infectious and good laboratory practices should be followed.

9. All samples should be disposed of in a manner that will inactivate viruses.

10. Liquid Waste: Add sodium hypochlorite to a final concentration of 1.0%. The waste should be allowed to stand for a minimum of 30 minutes to inactivate the viruses before disposal.

11. Substrate Solution is easily contaminated. If bluish prior to use, do not use.

12. Substrate B contain 20% acetone, keep this reagent away from sources of heat or flame.

13. Remove all kit reagents from refrigerator and allow them to reach room temperature ( 20-25°C).

REAGENT PREPARATION AND STORAGE

Wash Solution(1X) -Dilute 1 volume of Wash solution(20X) with 19volumes of deionized or distilled water. Wash Solutionis stable for 1 month at 2-8°C.

ASSAY PROCEDURE

1. Prepare all reagents before starting assay procedure. It is recommended that all Standards and Samples be added in duplicate to the Microtiter plate.

2. Add 50μl of Standard or Sample to the appropriate wells. Blank welldoesn’t add anyting.

3. Add 100μl of Enzymeconjugate to standard wellsand sample wells except the blank well, cover with anadhesive stripand incubate for 60 minutes at 37°C.

4. Wash the Microtiter Plate 4 times.

Manual Washing - Remove incubation mixture by aspirating contents of the plate into a sink or proper waste container. Using a squirt bottle, fill each well compley with Wash Solution (1X), then aspirate contents of the plate into a sink or proper waste container. Repeat this procedure for a total of four times. After final wash, invert plate, and blot dry by hitting plate onto absorbent paper or paper towels until no moisture appears. Note: Hold the sides of the plate frame firmly when 5

washing the plate to assure that all strips remain securely in frame.

Automated Washing - Aspirate all wells, then wash plates four times using Wash Buffer (1X). Always adjust your washer to aspirate as much liquid as possible and set fill volume at 350μL/well/wash. After final wash, invert plate, and blot dry by hitting plate onto absorbent paper or paper towels until no moisture appears.

5. Add SubstrateA 50μl and SubstrateB 50μl to each well.Gently mix and incubate for 15 minutes at 37°C. Protect from light.

6. Add 50μl Stop Solution to each well. The color in the wells should change from blue toyellow. If the color in the wells is green or the color change does notappear uniform,gently tap the plate to ensure thorough mixing.

7. Read the Optical Density (O.D.) at 450 nm using a microtiter plate reader within 15 minutes.

CALCULATION OF RESULTS

1. This standard curve is used to determine the amount in an unknown sample. The standard curve is generated by plotting the average O.D. (450 nm) obtained for each of the six standard concentrations on the vertical (X) axis versus the corresponding concentration on the horizontal (Y) axis.

2. First, calculate the mean O.D. value for each standard and sample. All O.D. Values are subtracted by the mean value of the balnk well before result interpretation. Construct the standard curve using graph paper or statistical software.

3. To determine the amount in each sample, first locate the O.D. value on the Y-axis and extend a horizontal line to the standard curve. At the point of intersection, draw a vertical line to the X-axis and read the corresponding concentration.

4. Any variation in operator, pipetting and washing technique, incubation time or temperature, and kit age can cause variation in result. Each user should obtain their own standard curve.

5. Intra-assay CV(%) and Inter-assay CV（％）are less than 15%.

6. Assay range: 75 pg/mL– 2400 pg/mL.

7. Sensitivity: The minimum detectable dose of Human MIG is typically less than 10 pg/mL.

8. Cross-reactivity: This assay recognizes recombinant and natural Human MIG. No significant cross-reactivity or interference was observed. 6

9. Storage: 2-8℃ (Use frequently); six months (-20℃)。

10.Standard curve

FOR RESEARCH USE ONLY; NOT FOR THERAPEUTIC OR DIAGNOSTIC APPLICATIONS!PLEASE READ THROUGH ENTIRE PROCEDURE BEFORE BEGINNING!