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猪细小病毒(PV )试剂盒(ELISA)

Porcine PV   ELISAKit

Forthe qualitative in vitro dAdobe Systemsetermination of Porcine parvovirus   concentrations in

serum - plasma - tissue homogenates - otherbiological fluids

FOR LABORATORY RESEARCH USE ONLY。

NOT FOR USE IN DIAGNOSTIC PROCEDURES。

This package insert must be read in itsentirety before using this product.

ELISA

ENZYME LINKED IMMUNOSORBENT ASSAY


INTENDEDUSE ANDTEST PRINCIPLE

This PV   ELISA kit is intended Laboratory for Researchuse only and is not for use in diagnostic or therapeutic procedures。 In orderto determine whether contains PV   in thesample, this PV   ELISA Kit includesNegative control and Positive control。 The Stop Solution changes the color fromblue to yellow and the intensity of the color is measured at 450 nm using aspectrophotometer。 The color depth was positively correlated with the PV   in the sample 。

SAMPLECOLLECTION AND STORAGES

Serum- Use a serum separator tube and allow samples to clot for two hours at roomtemperature or overnight at 4 beforecentrifugation for 20 minutes at approximately 1000×g. Assay freshly preparedserum immediately or sAdobe Systemstoresamples in aliquot at -20 or -80for later use. Avoid repeated freeze/thaw cycles.

Plasma- Collect plasma using EDTA or heparin as an anticoagulant. Centrifuge samplesfor 15 minutes at 1000×g at 2-8 within 30minutes of collection。 Remove plasma and assay immediately or store samples inaliquot at -20 or -80for later use. Avoid repeated freeze/thaw cycles.

Tissuehomogenates - For general information, hemolysis blood may affectthe result, so you should rinse the tissues with ice-cold PBS (0.01M, pH=7.4)to remove excess blood thoroughly. Tissue pieces should be weighed and thenminced to small pieces which will be homogenized in PBS (the volume depends onthe weight of the tissue. 9mL PBS would be appropriate to 1 gram tissue pieces.Some protease inhibitor is recommended to add into the PBS.) with a glasshomogenizer on ice. To further break the cells, you can sonicate the suspensionwith an ultrasonic cell disrupter or subject it to freeze-thaw cycles. Thehomogenates are then centrifugated for 5minutes at 5000×g to get the supernate.

Cellculture supernates and other biological fluids - Centrifugesamples for 20 minutes at 1000×g. Remove particulates and assay immediately orstore samples in aliquot at -20or -80for later use. Avoid repeated freeze/thaw cycles.

 Note:   The samples shoule be centrifugated dequately and no hemolysis or granulewas allowed。

MATERIALSREQUIRED BUT NOT SUPPLIED

1.   37 ℃ incubator

2.   Standard microplate reader capable of measuringabsorbanceat450nm

3.   Precision pipettes, disposable pipette tipsand Absorbent paper

4.   Distilledor deionized water

REAGENTS PROVIDED

All reagents provided are stored at 2-8°C。 Refer to theexpiration date on the label。

Adobe SystemsAdobe Systems

Name

96determinations

48 determinations

MICROTITER PLATE

96 strips

48 strips

Negative control

0.3ml/vial

0.3ml/vial

Positive control

0.3ml/vial

0.3ml/vial

Sample diluent

6.0ml

3.0ml

ENZYME CONJUGATE

10。0ml

5。0ml

WASH SOLUTION

25ml

15ml

SUBSTRATE A

6.0ml

3.0ml

SUBSTRATE B

6.0ml

3。0ml

STOP SOLUTION

6。0ml

3.0ml

Closure plate membrane

2

2

User manual

1

1

Sealed bags

1

1

PRECAUTIONS

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

2.       Allow kit reagents and materials to reach roomtemperature (20-25°C) before use. Do not use water baths to thaw samples orreagents.

3.       Do not use kit components beyond their expiration date.

4.       Use only deionized or distilled water to dilute reagents。

5.       Do not remove microtiter plate from the storage bag untilneeded. Unused strips should be stored at 2-8°C in their pouch with thedesiccant provided.

6.       Use fresh disposable pipette tips for each transfer toavoid contamination.

7.       Do not mix acid and sodium hypochlorite solutions。

8.       Serum and plasma should be handled as potentiallyhazardous and capable of transmitting disease. Disposable gloves must be wornduring the assay procedure, since no known test method can offer completeassurance that products derived from Rat blood will not transmit infectiousagents. Therefore, all blood derivatives should be considered potentiallyinfectious and good laboratory practices should be followed.

9.       All samples should be disposedAdobe Systems of in a manner that will inactivate viruses.

10.   Liquid Waste: Add sodium hypochlorite to a finalconcentration of 1.0%. The waste should be allowed to stand for a minimum of 30minutes to inactivate the viruses before disposal.

11.   Substrate Solution is easily contaminated. If bluishprior to use, do not use。

12.   Substrate B contain 20% acetone, keep this reagent awayfrom sources of heat or flame。

13.   Remove all kit reagents from refrigerator and allow themto reach room temperature ( 20-25°C).

REAGENT PREPARATION AND STORAGE

Wash Solution (1X) - Dilute 1 volume of Wash solution (20X)with 19 volumes of deionized or distilled water。 Wash Solution is stable for 1month at 2-8°C。

ASSAY PROCEDURE

1. Prepare all reagents beforestarting assay procedure. It is recommended that all Standards and Samples beadded in duplicate to the Microtiter plate.

2.   Add 50μl of NegativecontrolPositive control and test sample to the appropriate wells。 Blankwell doesn’t add anyting.

3.   Add10lofEnzymeconjugate to standard wells and sample wells exceptthe blank well, coverwith an adhesive stripandincubatefor 60 minutes at37°C.

4。   Wash the Microtiter Plate 4 times。

Manual Washing- Remove incubation mixture by aspirating contents of theplate into a sink or proper waste container. Using a squirt bottle, fill eachwell completely with Wash Solution (1X), then aspirate contents of the plateinto a sink or proper waste container. Repeat this procedure for a total of fourtimes. After final wash, invert plate, and blot dry by hitting plate ontoabsorbent paper or paper towels until no moisture appears. Note: Hold the sidesof the plate frame firmly when washing the plate to assure that all stripsremain securely in frame.

Automated Washing - Aspirate allwells, then wash plates four times using Wash Buffer (1X). Always adjust yourwasher to aspirate as much liquid as possible and set fill volume at350μL/well/wash. After final wash, invert plate, and blot dry by hitting plateonto absorbent paper or paper towels until no moisture appears.

5.   Add Substrate A 50μl and SubstrateB 50μl to each well. Gently mix andincubate for 15 minutes at 37°C.Protect from light.

6.   Add 50μl Stop Solution to each well. The colorin the wells should change from blue toyellow。 If the color in the wells is greenor the color change does notappear uniform,gently tap the plate to ensure thorough mixing.

7.   ReadtheOpticalDensity(O.D.)at450Adobe Systems nmusingamicrotiterplatereaderwithin15 minutes.

Adobe Systems

DETERMINE THE RESULT

1.       Test validity: the average of Positive control well≥0.8;the average of Negative control well ≤0.2.

2.       Calculate Critical (CUT OFF): Critical= the average ofNegative control well + 0。15。

3.       Negative Result: sample OD< Calculate Critical (CUTOFF) is Negative。

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

CALCULATION OF RESULTS

1.       This standard curve is used to determine the amount in anunknown sample. The standard curve is generated by plotting the average O.D.(450 nm) obtained for each of the six standard concentrations on the vertical (X)axis versus the corresponding concentration on the horizontal (Y) axis.

2.       First, calculate the mean O.D. value for each standardand sample. All O.D. Values are subtracted by the mean value of the balnk wellbefore result interpretation. Construct the standard curve using graph paper orstatistical software.

3.       To determine the amount in each sample, first locate theO。D。 value on the Y-axis and extend a horizontal line to the standard curve。 Atthe point of intersection, draw a vertical line to the X-axis and read thecorresponding concentration。

4.       Any variation in operator, pipetting and washingtechnique, incubation time or temperature, and kit age can cause variation in result.Each user should obtain their own standard curve.

5.       Intra-assay CV(%) and Inter-assayAdobe Systems CV(%)are less than 15%.

6.       Cross-reactivity: No significant cross-reactivity orinterference was observed.

7.       Storage: 2-8℃ (Use frequently); six months (-20℃)

FOR RESEARCH USE ONLY;NOT FOR THERAPEUTIC OR DIAGNOSTIC APPLICATIONS!PLEASE READ THROUGHENTIRE PROCEDURE BEFORE BEGINNING!
猪细小病毒(PV )试剂盒(ELISA)

使用说明书

l   本试剂盒用于体外定性检测血清、血浆、组织匀浆及相关液体样本中猪细小病毒(PV )Adobe Systems

l   有效期:6个月

l 保存条件:2-8℃

l   本试剂盒仅供科研使用,不得用于临床诊断

实验原理

试剂盒采用双抗体夹心法酶联免疫吸附试验(ELISA)。往预先包被猪细小病毒(PV )捕获抗体的包被微孔中,依次加入标本、阴性和阳性对照、HRP标记的检测抗体,经过温育并彻底洗涤。用底物TMB显色,TMB在过氧化物酶的催化下转化成蓝色,并在酸的作用下转化成最终的黄色。颜色的深浅和样品中的猪细小病毒(PV )呈正相关。用酶标仪在450nm 波长下测定吸光度(OD 值),判定阴阳性。

样本处理及要求

1.   血清将收集于血清分离管的全血标本在室温放置2小时或4过夜,然后1000×g离心20分钟,取上清即可,或将上清置于-20-80保存,但应避免反复冻融。
2.  
血浆EDTA或肝素作为抗凝剂采集标本,并将标本在采集后的30分钟内于2-8 1000×g离心15分钟,取上清即可检测,或将上清置于-20-80保存,但应避免反复冻融。
3.
组织匀浆:用预冷的PBS(0.01M, pH=7.4)冲洗组织,去除残留血液(匀浆中裂解的红细胞会影响测量结果),称重后将组织剪碎。将剪碎的组织与对应体积的PBS(一般按1:9的重量体积比,比如1g的组织样品对应9mLPBS,具体体积可根据实验需要适当调整,并做好记录。推荐在PBS中加入蛋白酶抑制剂)加入玻璃匀浆器中,于冰上充分研磨。为了进一步裂解组织细胞,可以对匀浆液进行超声破碎,或反复冻融。最后将匀浆液于5000×g离心5~10分钟,取上清检测。

4。   细胞培养物上清或其它生物标本:1000×g离心20分钟,取上清即可检测,或将上清置于-20℃或-80℃保存,但应避免反复冻融。

注:标本溶血会影响最后检测结果,因此溶血标本不宜进行此项检测。

需要而未提供的试剂和器材Adobe Systems

1.       酶标仪(450nm

2.       高精度加样器及枪头:0.5-10uL2-20uL20-200uL200-1000uL

3.       37℃恒温箱

4.   蒸馏水或去离子水

试剂盒组成

名称

96孔配置

48孔配置

备注

微孔酶标板

96

48

阴性对照

0。3mL

0.3mL

阳性对照

0.3mL

0.3mL

样本稀释液

6mL

3mL

检测抗体-HRP

10mL

5mL

20×洗涤缓冲液

25mL

15mL

按说明书进行稀释

底物A

6mL

3mL

底物B

6mL

3mL

终止液

6mL

3mL

封板膜

2

2

说明书

1

1

自封袋

1

1

注意事项

1.       严格按照规定的时间和温度进行温育以保证准确结果。所有试剂都必须在使用前达到室温20-25℃。使用后立即冷藏保存试剂。

2.       洗板不正确可以导致不准确的结果。在加入底物前确保尽量吸干孔内液体。温育过程中不要让微孔干燥掉。

3.       消除板底残留的液体和手指印,否则影响OD值。

4.       底物显色液应呈无色或很浅的颜色,已经变蓝的底物液不能使用。

5.       避免试剂和标本的交叉污染以免造成错误结果。

6.       在储存和温育时避免强光直接照射。

7.       平衡至室温后再打开密封袋以防水滴凝聚在冷板条上。

8.       任何反应试剂不能接触漂白溶剂或漂白溶剂所散发的强烈气体。任何漂白成分都会破坏试剂盒中反应试剂的生物活性。

9.       不能使用过期产品。

10.   如果可能传播疾病,所有的样品都应管理好,按照规定的程序处理样品和检测装置。

试剂准备

试剂盒从冷藏环境中取出应在室温平衡后方可使用。

2洗涤缓冲液的稀释:蒸馏水按120稀释,即120×洗涤缓冲液加19份蒸馏水。

Adobe Systems

操作步骤

1.   从室温平衡20min后的铝箔袋中取出所需板条,剩余板条用自封袋密封放回4℃

2.   设置阴性对照孔、阳性对照孔和样本孔,阴性、阳新对照孔各加50μL对照品;

3.   样本孔中加入待测样本50μL;空白孔不加。

4. 除空白孔外,标准品孔和样本孔中每孔加入辣根过氧化物酶(HRP)标记的检测抗体100μL,用封板膜封住反应孔,37℃水浴锅或恒温箱温育60min。

5.   弃去液体,吸水纸上拍干,每孔加满洗涤液(350μL),静置1min,甩去洗涤液,吸水纸上拍干,如此重复洗板5次(也可用洗板机洗板)。

6。   每孔加入底物AB50μL37℃避光孵育15min

7。   每孔加入终止液50μL,15min内,在450nm波长处测定各孔的OD值。

实验结果计算

1。 阴性对照OD值:小于0.2。

2。 阳性对照OD值:大于0.8。

3、阳性判断(Cut-Off值):阴性对照OD+0.15,样本OD值大于阈值,判定为阳性,反之,为阴性。


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