豬藍(lán)耳病抗體（PRRS-Ab）ELISA試劑盒說(shuō)明書(shū)

【資料簡(jiǎn)介】

1
豬藍(lán)耳病抗體（PRRS-Ab）酶聯(lián)免疫分析（ELISA）
試劑盒使用說(shuō)明書(shū)
本試劑僅供研究使用 目的：本試劑盒用于測(cè)定豬血清，血漿及相關(guān)
液體樣本中藍(lán)耳病抗體（PRRS-Ab）水平。
實(shí)驗(yàn)原理：
本試劑盒采用雙抗原夾心酶聯(lián)免疫法（ELISA）測(cè)定標(biāo)本中豬藍(lán)耳病抗體（PRRS-Ab） 。
用純化的藍(lán)耳病抗體（PRRS-Ab）抗原包被微孔板，制成固相抗原，可與樣品中藍(lán)耳病抗體
（PRRS-Ab）相結(jié)合，經(jīng)洗滌除去未結(jié)合的抗體和其他成分后再與 HRP 標(biāo)記的藍(lán)耳病抗體
（PRRS-Ab）抗原結(jié)合，形成抗原-抗體-酶標(biāo)抗原復(fù)合物，經(jīng)過(guò)*洗滌后加底物 TMB 顯
色。TMB 在 HRP 酶的催化下轉(zhuǎn)化成藍(lán)色，并在酸的作用下轉(zhuǎn)化成zui終的黃色。用酶標(biāo)儀在
450nm 波長(zhǎng)下測(cè)定吸光度（OD 值） ，與 CUTOFF 值相比較，從而判定標(biāo)本中藍(lán)耳病抗體
（PRRS-Ab）的存在與否。
試劑盒組成：
試劑盒組成 48孔配置 96孔配置 保存
說(shuō)明書(shū) 1 份 1份
封板膜 2片（48） 2片（96）
密封袋 1 個(gè) 1個(gè)
酶標(biāo)包被板 1×48 1×96 2-8℃保存
陰性對(duì)照 0.5ml×1 瓶 0.5ml×1瓶 2-8℃保存
陽(yáng)性對(duì)照 0.5ml×1 瓶 0.5ml×1瓶 2-8℃保存
酶標(biāo)試劑 3 ml×1 瓶 6 ml×1瓶 2-8℃保存
樣品稀釋液 3 ml×1 瓶 6 ml×1瓶 2-8℃保存
顯色劑 A 液 3 ml×1 瓶 6 ml×1瓶 2-8℃保存
顯色劑 B 液 3 ml×1 瓶 6 ml×1瓶 2-8℃保存
終止液 3ml×1 瓶 6ml×1 瓶 2-8℃保存
濃縮洗滌液 （20ml×20倍）×1瓶 （20ml×30 倍）×1瓶 2-8℃保存
樣本處理及要求：
1. 血清：室溫血液自然凝固 10-20 分鐘，離心 20分鐘左右（2000-3000 轉(zhuǎn)/分） 。仔細(xì)收集上
清，保存過(guò)程中如出現(xiàn)沉淀，應(yīng)再次離心。
2. 血漿：應(yīng)根據(jù)標(biāo)本的要求選擇 EDTA或檸檬酸鈉作為抗凝劑，混合 10-20 分鐘后，離心
20 分鐘左右（2000-3000 轉(zhuǎn)/分） 。仔細(xì)收集上清，保存過(guò)程中如有沉淀形成，應(yīng)該再次
離心。
3. 尿液：用無(wú)菌管收集，離心 20 分鐘左右（2000-3000 轉(zhuǎn)/分） 。仔細(xì)收集上清，保存過(guò)程
中如有沉淀形成，應(yīng)再次離心。胸腹水、腦脊液參照實(shí)行。
4. 細(xì)胞培養(yǎng)上清：檢測(cè)分泌性的成份時(shí)，用無(wú)菌管收集。離心 20分鐘左右（2000-3000 轉(zhuǎn)/
分） 。仔細(xì)收集上清。檢測(cè)細(xì)胞內(nèi)的成份時(shí)，用 PBS（PH7.2-7.4）稀釋細(xì)胞懸液，細(xì)胞2
濃度達(dá)到 100萬(wàn)/ml 左右。通過(guò)反復(fù)凍融，以使細(xì)胞破壞并放出細(xì)胞內(nèi)成份。離心 20 分
鐘左右（2000-3000轉(zhuǎn)/分） 。仔細(xì)收集上清。保存過(guò)程中如有沉淀形成，應(yīng)再次離心。
5. 組織標(biāo)本：切割標(biāo)本后，稱取重量。加入一定量的 PBS，PH7.4。用液氮迅速冷凍保存?zhèn)?br />用。標(biāo)本融化后仍然保持 2-8℃的溫度。加入一定量的 PBS（PH7.4） ，用手工或勻漿器
將標(biāo)本勻漿充分。離心 20 分鐘左右（2000-3000 轉(zhuǎn)/分） 。仔細(xì)收集上清。分裝后一份待
檢測(cè)，其余冷凍備用。
6. 標(biāo)本采集后盡早進(jìn)行提取，提取按相關(guān)文獻(xiàn)進(jìn)行，提取后應(yīng)盡快進(jìn)行實(shí)驗(yàn)。若不能馬上
進(jìn)行試驗(yàn)，可將標(biāo)本放于-20℃保存，但應(yīng)避免反復(fù)凍融.
7. 不能檢測(cè)含 NaN3的樣品，因 NaN3 抑制辣根過(guò)氧化物酶的（HRP）活性。
操作步驟：
1. 編號(hào)：將樣品對(duì)應(yīng)微孔按序編號(hào)，每板應(yīng)設(shè)陰性對(duì)照 2孔、陽(yáng)性對(duì)照 2 孔、空白對(duì)照 1
孔（空白對(duì)照孔不加樣品及酶標(biāo)試劑，其余各步操作相同）
2. 加樣：分別在陰、陽(yáng)性對(duì)照孔中加入陰性對(duì)照、陽(yáng)性對(duì)照 50μl。然后在待測(cè)樣品孔先
加樣品稀釋液 40μl，然后再加待測(cè)樣品 10μl。加樣將樣品加于酶標(biāo)板孔底部，盡量不
觸及孔壁，輕輕晃動(dòng)混勻，
3. 溫育：用封板膜封板后置 37℃溫育 30分鐘。
4. 配液：將 30（48T 的 20倍）倍濃縮洗滌液加蒸餾水至 600ml 后備用
5. 洗滌：小心揭掉封板膜，棄去液體，甩干，每孔加滿洗滌液，靜置 30 秒后棄去，如此
重復(fù) 5次，拍干。
6. 加酶：每孔加入酶標(biāo)試劑 50μl，空白孔除外。
7. 溫育：操作同 3。
8. 洗滌：操作同 5。
9. 顯色：每孔先加入顯色劑 A 50μl，再加入顯色劑 B 50μl，輕輕震蕩混勻，37℃避光顯色
15分鐘
10. 終止：每孔加終止液 50μl，終止反應(yīng)（此時(shí)藍(lán)色立轉(zhuǎn)黃色） 。
11. 測(cè)定：以空白空調(diào)零，450nm波長(zhǎng)依序測(cè)量各孔的吸光度（OD 值） 。 測(cè)定應(yīng)在加終止
液后 15分鐘以內(nèi)進(jìn)行。
結(jié)果判定：
試驗(yàn)有效性：陽(yáng)性對(duì)照孔平均值≥1.00; 陰性對(duì)照平均值≤0.10
臨界值（CUT OFF）計(jì)算：臨界值=陰性對(duì)照孔平均值+0.15
陰性判定：樣品 OD 值< 臨界值（CUT OFF）者為藍(lán)耳病抗體（PRRS-Ab）陰性
陽(yáng)性判定：樣品 OD 值≥ 臨界值（CUT OFF）者為藍(lán)耳病抗體（PRRS-Ab）陽(yáng)性
注意事項(xiàng)
1．操作嚴(yán)格按照說(shuō)明書(shū)進(jìn)行，本試劑不同批號(hào)組分不得混用。
2．試劑盒從冷藏環(huán)境中取出應(yīng)在室溫平衡 15-30 分鐘后方可使用，酶標(biāo)包被板開(kāi)封后如未
用完，板條應(yīng)裝入密封袋中保存。
3．濃洗滌液可能會(huì)有結(jié)晶析出，稀釋時(shí)可在水浴中加溫助溶，洗滌時(shí)不影響結(jié)果。
4．封板膜只限一次性使用，以避免交叉污染。
5．底物請(qǐng)避光保存。
6．試驗(yàn)結(jié)果判定必須以酶標(biāo)儀讀數(shù)為準(zhǔn)，使用雙波長(zhǎng)檢測(cè)時(shí)，參考波長(zhǎng)為 630nm
7．所有樣品，洗滌液和各種廢棄物都應(yīng)按傳染物處理。終止液為 2M的硫酸，使用時(shí)必須
注意安全。3
保存條件及有效期
1．試劑盒保存： ；2-8℃。
2．有效期：6 個(gè)月4
FOR RESEARCH USE ONLY
PRRS Ab
Drug Names
Generic Name：PRRS Ab ELISA Kit.
Purpose
This kit allows for the determination of PRRS Ab in Porcine serum, and
other biological fluids.
Principle of the assay
The kit assay PRRS Ab level in the sample，use Purified PRRS antigen to
coat microtiter plate wells, make solid-phase antigen, then add PRRS Ab to
wells, Combined With PRRS Ab, after washing and removing non-combinative
and other components ,then Combined PRRS which with HRP labeled
become antigen - antibody - enzyme- antigen complex, after washing
Compley, Add TMB substrate solution,, TMB substrate becomes blue color
At HRP enzyme-catalyzed, reaction is terminated by the addition of a sulphuric
acid solution and the color change is measured spectrophotometrically at a
wavelength of 450 nm. Compared with the CUTOFF value, according to this to
judge PRRS Ab exist in the sample or not.5
Materials provided with the kit
Materials provided
with the kit
48determinations 96 determinations
Stora
ge
User manual 1 1
Closure plate
membrane
2 2
Sealed bags 1 1
Microelisa stripplate 1 1 2-8℃
Negative control 0.5ml×1 bottle 0.5ml×1 bottle 2-8℃
Positive control 0.5ml×1 bottle 0.5ml×1 bottle 2-8℃
HRP-Conjugate
reagent
3ml×1 bottle 6ml×1 bottle 2-8℃
Sample diluent 3ml×1 bottle 6ml×1 bottle 2-8℃
Chromogen Solution
A 3ml×1 bottle 6ml×1 bottle 2-8℃
Chromogen Solution
B 3ml×1 bottle 6ml×1 bottle 2-8℃
Stop Solution 3ml×1 bottle 6ml×1 bottle 2-8℃
wash solution
（20ml×20 fold）
×1bottle
（20ml×30 fold）
×1bottle
2-8℃
Specimen requirements
1. serum- coagulation at room temperature 10-20 mins， centrifugation 20-min
at the speed of 2000-3000 r.p.m. remove supernatant, If precipitation
appeared, Centrifugal again.
2. plasma-use suited EDTA or citrate plasma as an anticoagulant,mix 10-20
mins ,centrifugation 20-min at the speed of 2000-3000 r.p.m. remove
supernatant, If precipitation appeared, Centrifugal again.
3. Urine-collect sue a sterile container, centrifugation 20-min at the speed of
2000-3000 r.p.m. remove supernatant, If precipitation appeared,
Centrifugal again. The Operation of Hydrothorax and cerebrospinal fluid
Reference to it.
4. cell culture supernatant-detect secretory components, collect sue a
sterile container, centrifugation 20-min at the speed of 2000-3000 r.p.m.6
remove supernatant,detect the composition of cells, Dilut cell suspension
with PBS（PH7.2-7.4）, Cell concentration reached 1 million / ml, repeated
freeze-thaw cycles, damage cells and release of intracellular components,
centrifugation 20-min at the speed of 2000-3000 r.p.m. remove supernatant,
If precipitation appeared, Centrifugal again.
5. Tissue samples- After cutting samples, check the weight,add PBS
（PH7.2-7.4）, Rapidly frozen with liquid nitrogen, maintain samples at
2-8℃ after melting,add PBS（PH7.4）, Homogenized by hand or Grinders,
centrifugation 20-min at the speed of 2000-3000 r.p.m. remove
supernatant.
6. extract as soon as possible after Specimen collection,and according to the
relevant literature, and should be experiment as soon as possible after the
extraction. If it can’t, specimen can be kept in -20 ℃ to preserve, Avoid
repeated freeze-thaw cycles.
7. Can’t detect the sample which contain NaN3, because NaN3 inhibits HRP
active.
Assay procedure
1.Number: to sample correspond microtitration well and Number Sequence,
each plate should be set feminine comparison 2 wells, masculine comparison
2 wells, blank comparison 1 well(don’t add sample and HRP-Conjugate
reagent to blank comparison well, other each step the operation are same).
2.add sample：separay add Positive control and Negative control 50μl to the
Positive and Negative well . add Sample dilution 40μl to testing sample well,
then add testing sample 10μl. add sample to the bottom of ELISA plates
coated well , don’t touch the well wall as far as possible, and Gently mix.
3.Incubate: After closing plate with Closure plate membrane ,incubate for 30
min at 37℃.
4.Configurate liquid: 30-fold (or 20-fold)wash solution diluted until 600ml,and7
reserve.
5.washing：Uncover Closure plate membrane, discard Liquid, dry by swing,
add washing buffer to every well, still for 30s then drain, repeat 5 times, dry by
pat.
6.add enzyme： Add HRP-Conjugate reagent 50μlto each well, except the blank
well.
7.incubate：Operation with 3.
8.washing：Operation with 5.
9.color：Add Chromogen Solution A 50ul and Chromogen Solution B to each
well, evade the light preservation for 15 min at 37℃
10.Stop the reaction： Add Stop Solution50μl to each well, Stop the reaction(the
blue color change to yellow color).
11. assay：take blank well as zero , Read absorbance at 450nm after Adding
Stop Solution and within 15min.
Determine the result
Test validity: the average of Positive control well≥1.00; the average of
Negative control well ≤0.10.
Calculate Critical(CUT OFF) : Critical= the average of Negative control well
+ 0.15.
Negative control: sample OD< Calculate Critical(CUT OFF) is PRRS Ab
Negative control.
Positive control: ample OD≥ Calculate Critical(CUT OFF) is PRRS Ab
Positive control.
Important notes8
1.Please according to use instruction strictly, Do not mix reagents with those
from other lots.
2.The kit takes out from the refrigeration environment should be balanced
15-30 minutes in the room temperature then use, ELISA plates coated if
has not use up after opened, the plate should be stored in Sealed bag.
3.washing buffer will Crystallization separation, it can be heated the water
helps dissolve when dilute . Washing does not affect the result.
4.Closure plate membrane only limits the disposable use, in order to avoid
the overlapping pollution
5.The substrate please evade the light preservation.
6.The test result determination must take the microtiter plate reader as a
standard, when use dual-wavelength to assay, Reference wavelength is
630nm.
7.All samples, washing buffer and each kind of reject should according to
infective material process. Stopp Solution is 2M sulphuric acid. You must pay
attention to safe when use .
Storage and validity
1．Storage： 2-8℃.
2．validity： six months.