豬口蹄疫病毒（FMDV）ELISA檢測(cè)試劑
本試劑盒只能用于科學(xué)研究，不得用于醫(yī)學(xué)診斷
豬口蹄疫病毒（fmdv）elisa檢測(cè)試劑盒
使用說明書
檢測(cè)原理
試劑盒采用雙抗體夾心法酶聯(lián)免疫吸附試驗(yàn)（elisa）。往預(yù)先包被豬口蹄疫病毒（fmdv）捕獲抗體的包被微孔中，依次加入陰性對(duì)照、陽性對(duì)照、樣本、hrp標(biāo)記的檢測(cè)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(zhuǎn)化成藍(lán)色，并在酸的作用下轉(zhuǎn)化成終的黃色。顏色的深淺和樣品中的豬口蹄疫病毒（fmdv）呈正相關(guān)。用酶標(biāo)儀在450nm 波長(zhǎng)下測(cè)定吸光度（od 值），判斷樣品是否含有豬口蹄疫病毒（fmdv）。
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
酶標(biāo)儀（450nm）高精度加樣器及槍頭：0.5-10ul、2-20ul、20-200ul、200-1000ul37℃恒溫箱操作注意事項(xiàng)
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。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。預(yù)處理后的樣本無需稀釋，直接取10μl加樣即可。嚴(yán)格按照說明書中標(biāo)明的時(shí)間、加液量及順序進(jìn)行溫育操作。所有液體組分使用前充分搖勻。試劑盒組成
名稱
96孔配置
48孔配置
備注
微孔酶標(biāo)板
96孔
48孔
無
陰性對(duì)照
0.3ml
0.3ml
無
陽性對(duì)照
0.3ml
0.3ml
無
*
6ml
3ml
無
檢測(cè)抗體-hrp
10ml
5ml
無
20×洗滌緩沖液
25ml
15ml
按說明書進(jìn)行稀釋
底物a
6ml
3ml
無
底物b
6ml
3ml
無
終止液
6ml
3ml
無
封板膜
2張
2張
無
說明書
1份
1份
無
自封袋
1個(gè)
1個(gè)
無
試劑的準(zhǔn)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(dòng)洗板機(jī)：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(shè)置陰、陽性對(duì)照孔和樣本孔，陰、陽性對(duì)照孔中加入陰性對(duì)照、陽性對(duì)照各50μl；待測(cè)樣本孔先加待測(cè)樣本10μl，再加*40μl；隨后陰、陽性對(duì)照孔和樣本孔中每孔加入辣根過氧化物酶（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。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）。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(zhǎng)處測(cè)定各孔的od值。結(jié)果判斷
1. 試驗(yàn)有效性：陽性對(duì)照孔o(hù)d值平均值≥1.00；
陰性對(duì)照孔o(hù)d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. 陽性判斷：樣品od值＞臨界值（cut off），樣品為陽性
試劑盒性能
準(zhǔn)確性：陽性對(duì)照孔o(hù)d值平均值≥1.00；陰性對(duì)照孔o(hù)d值平均值≤0.15，說明試驗(yàn)結(jié)果有效。特異性：不與其它可溶性結(jié)構(gòu)類似物交叉反應(yīng)。重復(fù)性：板內(nèi)、板間變異系數(shù)均小于15%。貯藏：2-8℃，避光防潮保存。有效期：6個(gè)月免責(zé)聲明
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)。嚴(yán)格按照說明書操作，實(shí)驗(yàn)者違反說明書操作，后果由實(shí)驗(yàn)者承擔(dān)。
for research use only.
not for use in diagnostic procedures.
porcinefoot-and-mouth disease virus antigen(fmdv) elisa kit instruction
intended use
this fmdvelisa kit is intended laboratory for research use only and is not for use in diagnostic or therapeutic procedures.in order to determine whether contains fmdv in the sample, this fmdv elisa kit includes negative controlandpositive 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 fmdv in the sample .
samplecollection 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 30minutes 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 shouldbe 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. donotsubstitutereagentsfromone kitto another.standard, conjugateandmicroplates are matchedfor optimal performance.useonly thereagentssuppliedby manufacturer.
2. donotremovemicroplatefromthe storage baguntilneeded.unusedstripsshouldbe stored at2-8°cin their pouchwiththe desiccantprovided.
3. mix all reagents before using.
remove allkitreagentsfromrefrigerator and allowthemto reachroomtemperature( 20-25°c)
materials supplied
name
96determinations
48determinations
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 water1:20.
assay procedure
1. prepare allreagentsbeforestartingassayprocedure.itisrecommendedthatallstandardsand samplesbe addedin duplicateto the microelisastripplate.
2.separately add positive control and negative control 50μl to the positive and negative well, add testing sample10μl then add sample diluent 40μl to testing sample well; blank welldoesn’t add anyting.
3. add100μlofhrp-conjugate reagentto each well,cover with anadhesive stripandincubatefor60 minutesat37°c.
4. aspirate each well and wash, repeating the process fourtimes for a total of five washes.wash by filling each well with wash solution(400μl) using a squirt bottle, manifolddispenseror autowasher. complete removal of liquid at each step is essential to good performance. after the last wash, remove any remaining wash solutionby aspirating ordecanting. 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 toyellow. 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. readtheopticaldensity(o.d.)at450nmusinga microtiterplatereaderwithin15minutes.
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 controlwell + 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!
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豬口蹄疫病毒（fmdv）elisa檢測(cè)試劑盒
使用說明書
檢測(cè)原理
試劑盒采用雙抗體夾心法酶聯(lián)免疫吸附試驗(yàn)（elisa）。往預(yù)先包被豬口蹄疫病毒（fmdv）捕獲抗體的包被微孔中，依次加入陰性對(duì)照、陽性對(duì)照、樣本、hrp標(biāo)記的檢測(cè)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(zhuǎn)化成藍(lán)色，并在酸的作用下轉(zhuǎn)化成終的黃色。顏色的深淺和樣品中的豬口蹄疫病毒（fmdv）呈正相關(guān)。用酶標(biāo)儀在450nm 波長(zhǎng)下測(cè)定吸光度（od 值），判斷樣品是否含有豬口蹄疫病毒（fmdv）。
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
酶標(biāo)儀（450nm）高精度加樣器及槍頭：0.5-10ul、2-20ul、20-200ul、200-1000ul37℃恒溫箱操作注意事項(xiàng)
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。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。預(yù)處理后的樣本無需稀釋，直接取10μl加樣即可。嚴(yán)格按照說明書中標(biāo)明的時(shí)間、加液量及順序進(jìn)行溫育操作。所有液體組分使用前充分搖勻。試劑盒組成
名稱
96孔配置
48孔配置
備注
微孔酶標(biāo)板
96孔
48孔
無
陰性對(duì)照
0.3ml
0.3ml
無
陽性對(duì)照
0.3ml
0.3ml
無
*
6ml
3ml
無
檢測(cè)抗體-hrp
10ml
5ml
無
20×洗滌緩沖液
25ml
15ml
按說明書進(jìn)行稀釋
底物a
6ml
3ml
無
底物b
6ml
3ml
無
終止液
6ml
3ml
無
封板膜
2張
2張
無
說明書
1份
1份
無
自封袋
1個(gè)
1個(gè)
無
試劑的準(zhǔn)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(dòng)洗板機(jī)：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(shè)置陰、陽性對(duì)照孔和樣本孔，陰、陽性對(duì)照孔中加入陰性對(duì)照、陽性對(duì)照各50μl；待測(cè)樣本孔先加待測(cè)樣本10μl，再加*40μl；隨后陰、陽性對(duì)照孔和樣本孔中每孔加入辣根過氧化物酶（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。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）。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(zhǎng)處測(cè)定各孔的od值。結(jié)果判斷
1. 試驗(yàn)有效性：陽性對(duì)照孔o(hù)d值平均值≥1.00；
陰性對(duì)照孔o(hù)d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. 陽性判斷：樣品od值＞臨界值（cut off），樣品為陽性
試劑盒性能
準(zhǔn)確性：陽性對(duì)照孔o(hù)d值平均值≥1.00；陰性對(duì)照孔o(hù)d值平均值≤0.15，說明試驗(yàn)結(jié)果有效。特異性：不與其它可溶性結(jié)構(gòu)類似物交叉反應(yīng)。重復(fù)性：板內(nèi)、板間變異系數(shù)均小于15%。貯藏：2-8℃，避光防潮保存。有效期：6個(gè)月免責(zé)聲明
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)。嚴(yán)格按照說明書操作，實(shí)驗(yàn)者違反說明書操作，后果由實(shí)驗(yàn)者承擔(dān)。
for research use only.
not for use in diagnostic procedures.
porcinefoot-and-mouth disease virus antigen(fmdv) elisa kit instruction
intended use
this fmdvelisa kit is intended laboratory for research use only and is not for use in diagnostic or therapeutic procedures.in order to determine whether contains fmdv in the sample, this fmdv elisa kit includes negative controlandpositive 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 fmdv in the sample .
samplecollection 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 30minutes 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 shouldbe 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. donotsubstitutereagentsfromone kitto another.standard, conjugateandmicroplates are matchedfor optimal performance.useonly thereagentssuppliedby manufacturer.
2. donotremovemicroplatefromthe storage baguntilneeded.unusedstripsshouldbe stored at2-8°cin their pouchwiththe desiccantprovided.
3. mix all reagents before using.
remove allkitreagentsfromrefrigerator and allowthemto reachroomtemperature( 20-25°c)
materials supplied
name
96determinations
48determinations
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 water1:20.
assay procedure
1. prepare allreagentsbeforestartingassayprocedure.itisrecommendedthatallstandardsand samplesbe addedin duplicateto the microelisastripplate.
2.separately add positive control and negative control 50μl to the positive and negative well, add testing sample10μl then add sample diluent 40μl to testing sample well; blank welldoesn’t add anyting.
3. add100μlofhrp-conjugate reagentto each well,cover with anadhesive stripandincubatefor60 minutesat37°c.
4. aspirate each well and wash, repeating the process fourtimes for a total of five washes.wash by filling each well with wash solution(400μl) using a squirt bottle, manifolddispenseror autowasher. complete removal of liquid at each step is essential to good performance. after the last wash, remove any remaining wash solutionby aspirating ordecanting. 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 toyellow. 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. readtheopticaldensity(o.d.)at450nmusinga microtiterplatereaderwithin15minutes.
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 controlwell + 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!
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