兔二胺氧化酶（DAO）试剂盒（ELISA）说明书仅供参考，详情请咨询我司的销售人员。
Rabbit DAO ELISA Kit
For the quantitative in vitro determination of Rabbit diamine oxidase concentrations in
serum - plasma - celiac fluid - tissue homogenate - body fluid
FOR LABORATORY RESEARCH USE ONLY.
NOT FOR USE IN DIAGNOSTIC PROCEDURES.
This package insert must be read in its entirety before using this product.
ELISA
ENZYME LINKED IMMUNOSORBENT ASSAY
INTENDED USE AND TEST PRINCIPLE
This DAO 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 DAO in the sample, this DAO 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 DAO concentration. The concentration of DAO 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 approximately 2000×g. Remove serum and assay immediately or aliquot and store samples at -20℃. Avoid repeated freeze-thaw cycles
Plasma - Collect plasma using heparin as an anticoagulant. Centrifuge samples for 30 minutes at 2000×g at 2-8℃ within 30 minutes of collection. Store samples at -20℃. Avoid repeated freeze-thaw cycles.
Cell culture supernates, tissue homogenate and other biological fluids - Remove particulates by centrifugation and assay immediately or aliquot and store samples at -20℃. Avoid repeated freeze-thaw cycles.
Note: The samples shoule be centrifugated dequately and no hemolysis or granule was allowed.
MATERIALS REQUIRED BUT NOT SUPPLIED
1. 37 ℃ incubator
2. Standard microplate reader capable of measuring absorbance at 450 nm
3. Precision pipettes, disposable pipette tips and Absorbent paper
4. Distilled or deionized water
REAGENTS PROVIDED
All reagents provided are stored at 2-8°C. Refer to the expiration date on the label.
Name96 determinations48 determinations
MICROTITER PLATE8*12strips8*6strips
STANDARD（6 vial）0.3ml/vial0.3ml/vial
SAMPLE DILUENT6.0ml3.0ml
ENZYME CONJUGATE10.0ml5.0ml
WASH SOLUTION25ml15ml
SUBSTRATE A6.0ml3.0ml
SUBSTRATE B6.0ml3.0ml
STOP SOLUTION6.0ml3.0ml
Closure plate membrane22
User manual11
Sealed bags11
Note:
1. Standard concentration was followed by: 800, 400, 200, 100, 50, 0 U/L.
2. If samples generate values higher than the highest standard, please dilute the samples with Sample Diluent and repeat the assay.
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.
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 19 volumes of deionized or distilled water. Wash Solution is 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 well doesn’t add anyting.
3. Add 100μl of Enzymeconjugate to standard wells and sample wells except the blank well, cover with an adhesive strip and 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 completely 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 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 Substrate A 50μl and Substrate B 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 to yellow. If the color in the wells is green or the color change does not appear 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(%) is less than 10% and Inter-assay CV(%) is less than 15%.
6.Assay range: 25 U/L – 800 U/L.
7. Sensitivity: The minimum detectable dose of Rabbit DAO is typically less than 1.0 U/L.
8. Cross-reactivity: This assay recognizes recombinant and natural Rabbit DAO. No significant cross-reactivity or interference was observed.
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!
兔二胺氧化酶（DAO）试剂盒（ELISA）使用说明书
本试剂盒用于体外定量检测血清、血浆、组织、细胞上清及相关液体样本中兔二胺氧化酶（DAO）的含量。
有效期：6个月
保存条件：2-8℃
实验原理
试剂盒采用双抗体一步夹心法酶联免疫吸附试验（ELISA）。往预先包被兔二胺氧化酶（DAO）捕获抗体的包被微孔中，依次加入标本、标准品、HRP标记的检测抗体，经过温育并彻底洗涤。用底物TMB显色，TMB在过氧化物酶的催化下转化成蓝色，并在酸的作用下转化成最终的黄色。颜色的深浅和样品中的兔二胺氧化酶（DAO）呈正相关。用酶标仪在450nm 波长下测定吸光度（OD 值），计算样品浓度。
样本处理及要求
1. 血清：全血标本请于室温放置2小时或4℃过夜后于1000g离心20分钟，取上清即可检测，或将标本放于-20℃或-80℃保存，但应避免反复冻融。
2. 血浆：可用EDTA或肝素作为抗凝剂，标本采集后30分钟内于2 - 8°C 1000g离心20分钟，或将标本放于-20℃或-80℃保存，但应避免反复冻融。
3. 细胞培
