本試劑盒只能用于科學研究，不得用于醫學診斷

人（Human）風疹病毒IGM抗體（RV-IgM）

ELISA檢測試劑盒

使用說明書

檢測原理

試劑盒采用雙抗體一步間接法酶聯免疫吸附試驗（ELISA）。往預先包被中風疹病毒抗原的包被微孔中，依次加入標本、HRP標記的檢測抗體，經過溫育并*洗滌。用底物TMB顯色，TMB在過氧化物酶的催化下轉化成藍色，并在酸的作用下轉化成最終的黃色。用酶標儀在450nm波長下測定吸光度（OD 值），與CUTOFF值相比較，從而判定標本中風疹病毒IGM抗體（RV-IgM）的存在與否。

樣品收集、處理及保存方法

1.  血清：使用不含熱原和內毒素的試管，操作過程中避免任何細胞刺激，收集血液后，3000轉離心10分鐘將血清和紅細胞迅速小心地分離。

2.  血漿：EDTA、檸檬酸鹽或肝素抗凝。3000轉離心30分鐘取上清。

3.  細胞上清液：3000轉離心10分鐘去除顆粒和聚合物。

4.  組織勻漿：將組織加入適量生理鹽水搗碎。3000轉離心10分鐘取上清。

5.  保存：如果樣本收集后不及時檢測，請按一次用量分裝，凍存于-20℃，避免反復凍融，在室溫下解凍并確保樣品均勻地充分解凍。

自備物品

• 酶標儀（450nm）

• 高精度加樣器及槍頭：0.5-10uL、2-20uL、20-200uL、200-1000uL

• 37℃恒溫箱

操作注意事項

1.  試劑盒保存在2-8℃，使用前室溫平衡20分鐘。從冰箱取出的濃縮洗滌液會有結晶，這屬于正常現象，水浴加熱使結晶*溶解后再使用。

2.  實驗中不用的板條應立即放回自封袋中，密封（低溫干燥）保存。

3.  預處理后的樣本請按照操作步驟用樣本稀釋液適當稀釋以達到試劑盒的的*檢測效果。

4.  嚴格按照說明書中標明的時間、加液量及順序進行溫育操作。

5.  所有液體組分使用前充分搖勻。

試劑盒組成

試劑的準備

20×洗滌緩沖液的稀釋：蒸餾水按1：20稀釋，即1份的20×洗滌緩沖液加19份的蒸餾水。

洗板方法

1.  手工洗板：甩盡孔內液體，每孔加滿洗滌液，靜置1min后甩盡孔內液體，在吸水紙上拍干，如此洗板5次。

2.  自動洗板機：每孔注入洗液350μL，浸泡1min，洗板5次。

操作步驟

1.  從室溫平衡20min后的鋁箔袋中取出所需板條，剩余板條用自封袋密封放回4℃。

2.  設置陰、陽性對照孔和樣本孔，陰、陽性對照孔中加入陰性對照、陽性對照各50μL；

3.  待測樣本孔先加待測樣本10μL，再加樣本稀釋液40μL；

4.  隨后陰、陽性對照孔和樣本孔中每孔加入辣根過氧化物酶（HRP）標記的檢測抗體100μL，用封板膜封住反應孔，37℃水浴鍋或恒溫箱溫育60min。

5.  棄去液體，吸水紙上拍干，每孔加滿洗滌液，靜置1min，甩去洗滌液，吸水紙上拍干，如此重復洗板5次（也可用洗板機洗板）。

6.  每孔加入底物A、B各50μL，37℃避光孵育15min。

7.  每孔加入終止液50μL，15min內，在450nm波長處測定各孔的OD值。

結果判斷

1.  試驗有效性：陽性對照孔OD值平均值≥1.00；

               陰性對照孔OD值平均值≤0.15。

2.  臨界值（Cut off）計算：臨界值=陰性對照孔平均值+0.15

3.  陰性判斷：樣品OD值＜臨界值（Cut off），樣品為陰性

4.  陽性判斷：樣品OD值＞臨界值（Cut off），樣品為陽性

試劑盒性能

• 準確性：陽性對照孔OD值平均值≥1.00；陰性對照孔OD值平均值≤0.15，說明試驗結果有效。

• 特異性：不與其它可溶性結構類似物交叉反應。

• 重復性：板內、板間變異系數均小于15%。

• 貯藏：2-8℃，避光防潮保存。

• 有效期：6個月

免責聲明

•  試劑盒僅供研究使用，不得用于臨床實驗或人體實驗，否則所產生的一切后果，由實驗者承擔，本公司概不負責。

•  嚴格按照說明書操作，實驗者違反說明書操作，后果由實驗者承擔。

FOR RESEARCH USE ONLY.

NOT FOR USE IN DIAGNOSTIC PROCEDURES.

Human Rubella virus IgM (RV-IgM) ELISA Kit instruction

Intended use

This RV-IgM 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 RV-IgM in the sample, this RV-IgM 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 cutoff value. The existence or not of RV-IgM in the samples is then determined by comparing the O.D. of the samples to the CUT OFF.

Sample collection and storages

Serum - Use a serum separator tube and allow samples to clot for 30 minutes before centrifugation for 10 minutes at approximately 3000×g. Remove serum and assay immediately or aliquot and store samples at -20℃ or -80℃.Avoid repeated freeze-thaw cycles

Plasma - Collect plasma using EDTA or heparin as an anticoagulant. Centrifuge samples for 30 minutes at 3000×g at 2-8℃ within 30 minutes of collection. Store samples at -20℃or -80℃. Avoid repeated freeze-thaw cycles.

Cell culture supernates and other biological fluids - Remove particulates by centrifugation and assay immediately or aliquot and store samples at -20℃or -80℃. 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.  Standard microplate reader(450nm)

2.  Precision pipettes and Disposable pipette tips.

3.  37 ℃ incubator

Precautions

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

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

3. Mix all reagents before using.

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

Materials supplied

Reagent preparation

20×wash solution:Dilute with Distilled or deionized water 1:20.

Assay procedure

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

2.  Separately add Positive control and Negative control 50μl to the Positive and Negative well; Add testing sample 10μl then add Sample Diluent 40μl to testing sample well.

3.  Add 100μl of HRP-conjugate reagent to each well, cover with an adhesive strip and incubate for 60 minutes at 37°C.

4. Aspirate each well and wash, repeating the process four times for a total of five washes. Wash by filling each well with Wash Solution (400μl) using a squirt bottle, manifold dispenser or autowasher. Complete removal of liquid at each step is essential to good performance. After the last wash, remove any remaining Wash Solution by aspirating or decanting. Invert the plate and blot it against clean paper towels.

5. Add chromogen solution A 50μl and chromogen solution 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.

Determine the result

1.  Test validity: the average of Positive control well≥1.00; the average of Negative control well ≤0.15.

2.  Calculate Critical (CUT OFF): Critical= the average of Negative control well + 0.15.

Negative Result: sample OD< Calculate Critical (CUT OFF) is Negative.

Positive Result: sample OD≥ Calculate Critical (CUT OFF) is Positive.

Storage and validity

Storage：  2-8℃.

validity： six months.

FOR RESEARCH USE ONLY;

NOT FOR THERAPEUTIC OR DIAGNOSTIC APPLICATIONS!

PLEASE READ THROUGH ENTIRE PROCEDURE BEFORE