本試劑盒只能用于科學研究，不得用于醫(yī)學診斷

大鼠過氧亞硝基陰離子（ONOO-）ELISA 檢測試劑盒

使用說明書

檢測原理

試劑盒采用雙抗體夾心法酶聯(lián)免疫吸附試驗（ELISA）。往預先

包被大鼠過氧亞硝基陰離子（ONOO-）捕獲抗體的包被微孔中，依次

加入標本、標準品、HRP標記的檢測抗體，經(jīng)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

用下轉化成終的黃色。顏色的深淺和樣品中的大鼠過氧亞硝基陰

離子（ONOO-）呈正相關。用酶標儀在450nm 波長下測定吸光度（OD

值），計算樣品濃度。

樣品收集、處理及保存方法

• 血清：使用不含熱原和內(nèi)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。

• 血漿：EDTA、檸檬酸鹽或肝素抗凝。3000 轉離心 30 分鐘取上清。

• 細胞上清液：3000 轉離心 10 分鐘去除顆粒和聚合物。

• 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

• 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(xiàn)象，水浴加熱使結晶*溶解后再使用。

• 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。

• 預處理后的樣本無需稀釋，直接取 10μL 加樣即可。

• 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。

• 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

• 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。

• 自動洗板機：每孔注入洗液 350μL，浸泡 1min，洗板 5 次。

操作步驟

• 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℃。

• 設置標準品孔和樣本孔，標準品孔各加不同濃度的標準品 50μ

L；

• 待測樣本孔先加待測樣本 10μL，再加* 40μL；

• 隨后標準品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。

• 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）。

• 每孔加入底物 A、B 各 50μL，37℃避光孵育 15min。

• 每孔加入終止液 50μL，15min 內(nèi)，在 450nm 波長處測定各孔的

OD 值。

結果判斷

繪制標準曲線：在 Excel 工作表中，以標準品濃度作橫坐標，對應

試劑盒性能

• 準確性：標準品線性回歸與預期濃度相關系數(shù) R 值，大于等于

0.9900。

• 靈敏度：低檢測濃度小于 0.1 μmol/L。

• 特異性：不與其它可溶性結構類似物交叉反應。

• 重復性：板內(nèi)變異系數(shù)小于 10%、板間變異系數(shù)小于 15%。

FOR RESEARCH USE ONLY.

NOT FOR USE IN DIAGNOSTIC PROCEDURES.

Rat ONOO- (ONOO-) ELISA Kit instruction

Intended use

This ONOO- 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 ONOO- in the sample, this ONOO- 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 ONOO- concentration. The concentration of ONOO- 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 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

• Standard microplate reader(450nm)

• Precision pipettes and Disposable pipette tips.

• 37 ℃ incubator

Precautions

• 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.

• 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.

• Mix all reagents before using.

Remove all kit reagents from refrigerator and allow them to reach room temperature

( 20-25°C)

Materials supplied

Note: Standard concentration was followed by: 120、60、30、15、7.5、0 μmol/L.

Reagent preparation

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

Assay procedure

1. Prepare all r e a g e n t s before starting assay procedure. It is recommended that all Standards and Samples be added in duplicate to the Microelisa Stripplate.

• Add standard: Set Standard wells, testing sample wells. Add standard 50μl to standard well.
• Add Sample: Add testing sample 10μl Then add sample diluent 40μl to testing sample well; Blank well doesn’t add anyting.
• Add 100μl of HRP-conjugate reagent to each well, cover with an adhesive strip and incubate for 60 minutes at 37°C.
• 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.
• 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.
• 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.