人β2糖蛋白1抗體（β2-GP1-Ab）ELISA檢測(cè)試劑盒.

【資料簡(jiǎn)介】

檢測(cè)原理

試劑盒采用間接法酶聯(lián)免疫吸附試驗(yàn)（ELISA）。往預(yù)先包被人β2糖蛋白1抗體（β2-GP1-Ab）捕獲抗原的包被微孔中，依次加入標(biāo)本、標(biāo)準(zhǔn)品、HRP標(biāo)記的檢測(cè)抗體，經(jīng)過(guò)溫育并*洗滌。用底物TMB顯色，TMB在過(guò)氧化物酶的催化下轉(zhuǎn)化成藍(lán)色，并在酸的作用下轉(zhuǎn)化成最終的黃色。顏色的深淺和樣品中的人β2糖蛋白1抗體（β2-GP1-Ab）呈正相關(guān)。用酶標(biāo)儀在450nm 波長(zhǎng)下測(cè)定吸光度（OD 值），判斷樣品是否含有人β2糖蛋白1抗體（β2-GP1-Ab）。

樣品收集、處理及保存方法

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

2.  血漿：EDTA、檸檬酸鹽或肝素抗凝。3000轉(zhuǎn)離心30分鐘取上清。

3.  細(xì)胞上清液：3000轉(zhuǎn)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(zhuǎn)離心10分鐘取上清。

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

自備物品

1. 酶標(biāo)儀（450nm）

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

3. 37℃恒溫箱

操作注意事項(xiàng)

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(huì)有結(jié)晶，這屬于正常現(xiàn)象，水浴加熱使結(jié)晶*溶解后再使用。

2.  實(shí)驗(yàn)中不用的板條應(yīng)立即放回自封袋中，密封（低溫干燥）保存。

3.  預(yù)處理后的樣本無(wú)需稀釋?zhuān)苯尤?/span>10μL加樣即可。

4.  嚴(yán)格按照說(shuō)明書(shū)中標(biāo)明的時(shí)間、加液量及順序進(jìn)行溫育操作。

5.  所有液體組分使用前充分搖勻。

試劑盒組成

名稱(chēng)	96孔配置	48孔配置	備注
微孔酶標(biāo)板	96孔	48孔	無(wú)
陰性對(duì)照	0.3mL	0.3mL	無(wú)
陽(yáng)性對(duì)照	0.3mL	0.3mL	無(wú)
樣本稀釋液	6mL	3mL	無(wú)
檢測(cè)抗體-HRP	10mL	5mL	無(wú)
20×洗滌緩沖液	25mL	15mL	按說(shuō)明書(shū)進(jìn)行稀釋
底物A	6mL	3mL	無(wú)
底物B	6mL	3mL	無(wú)
終止液	6mL	3mL	無(wú)
封板膜	2張	2張	無(wú)
說(shuō)明書(shū)	1份	1份	無(wú)
自封袋	1個(gè)	1個(gè)	無(wú)

試劑的準(zhǔn)備

20×洗滌緩沖液的稀釋?zhuān)赫麴s水按1：20稀釋?zhuān)?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(nèi)液體，每孔加滿洗滌液，靜置1min后甩盡孔內(nèi)液體，在吸水紙上拍干，如此洗板5次。

2.  自動(dòng)洗板機(jī)：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(shè)置陰、陽(yáng)性對(duì)照孔和樣本孔，陰、陽(yáng)性對(duì)照孔中加入陰性對(duì)照、陽(yáng)性對(duì)照各50μL；

3. 待測(cè)樣本孔先加待測(cè)樣本10μL，再加樣本稀釋液40μL；

4. 隨后陰、陽(yáng)性對(duì)照孔和樣本孔中每孔加入辣根過(guò)氧化物酶（HRP）標(biāo)記的檢測(cè)抗體100μL，用封板膜封住反應(yīng)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(fù)洗板5次（也可用洗板機(jī)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(nèi)，在450nm波長(zhǎng)處測(cè)定各孔的OD值。

結(jié)果判斷

1.  試驗(yàn)有效性：陽(yáng)性對(duì)照孔OD值平均值≥1.00；

              陰性對(duì)照孔OD值平均值≤0.15。

2.  臨界值（Cut off）計(jì)算：臨界值=陰性對(duì)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(yáng)性判斷：樣品OD值＞臨界值（Cut off），樣品為陽(yáng)性

試劑盒性能

1. 準(zhǔn)確性：陽(yáng)性對(duì)照孔OD值平均值≥1.00；陰性對(duì)照孔OD值平均值≤0.15，說(shuō)明試驗(yàn)結(jié)果有效。

2. 特異性：不與其它可溶性結(jié)構(gòu)類(lèi)似物交叉反應(yīng)。

3. 重復(fù)性：板內(nèi)、板間變異系數(shù)均小于15%。

4. 貯藏：2-8℃，避光防潮保存。

5. 有效期：6個(gè)月

免責(zé)聲明

1.  試劑盒僅供研究使用，不得用于臨床實(shí)驗(yàn)或人體實(shí)驗(yàn)，否則所產(chǎn)生的一切后果，由實(shí)驗(yàn)者承擔(dān)，本公司概不負(fù)責(zé)。

2.  嚴(yán)格按照說(shuō)明書(shū)操作，實(shí)驗(yàn)者違反說(shuō)明書(shū)操作，后果由實(shí)驗(yàn)者承擔(dān)。

FOR RESEARCH USE ONLY.

NOT FOR USE IN DIAGNOSTIC PROCEDURES.

Human β2-Glycoprotein 1 antibody (β2-GP1-Ab) ELISA Kit instruction

Intended use

This β2-GP1-Ab ELISA kit is intended Laboratory for Research use only and is not for use in diagnostic or therapeutic procedures. In order to determine whether contains β2-GP1-Ab in the sample, this β2-GP1-Ab ELISA Kit includes Negative control and Positive control. The Stop Solution changes the color from blue to yellow and the intensity of the color is measured at 450 nm using a spectrophotometer. The color depth was positively correlated with the β2-GP1-Ab in the sample .

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 should be centrifugated adequately 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

Name	96 determinations	48 determinations
Microelisa stripplate	96 strips	48 strips
Negative control	0.3ml	0.3ml
Positive control	0.3ml	0.3ml
Sample diluent	6.0ml	3.0ml
HRP-Conjugate reagent	10.0ml	5.0ml
20X Wash solution	25ml	15ml
Chromogen Solution A	6.0ml	3.0ml
Chromogen Solution B	6.0ml	3.0ml
Stop Solution	6.0ml	3.0ml
Closure plate membrane	2	2
User manual	1	1
Sealed bags	1	1

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; Blank well doesn’t add anyting.

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 BEGINNING!