绵羊雌二醇（e2）酶联免疫分析(elisa)
试剂盒使用说明书
本试剂仅供研究使用目的：本试剂盒用于测定绵羊血清、血浆、组织匀浆及相关液体样本中雌二醇（e2）的含量。
实验原理：
本试剂盒应用双抗体夹心法测定标本中绵羊雌二醇（e2）水平。用纯化的绵羊雌二醇（e2）捕获抗体包被微孔板，制成固相抗体，往包被的微孔中依次加入绵羊雌二醇（e2），再与hrp标记的检测抗体结合，形成抗体-抗原-酶标抗体复合物，经过*洗涤后加底物tmb显色。tmb在hrp酶的催化下转化成蓝色，并在酸的作用下转化成终的黄色。颜色的深浅和样品中的绵羊雌二醇（e2）呈正相关。用酶标仪在450nm波长下测定吸光度（od值），通过标准曲线计算样品中绵羊雌二醇（e2）含量。
试剂盒组成：
试剂盒组成
48孔配置
96孔配置
保存
说明书
1份
1份
封板膜
2片
2片
密封袋
1个
1个
酶标包被板
1×48
1×96
2-8℃保存
标准品
0.3ml×6管
0.3ml×6管
2-8℃保存
酶标试剂
5 ml×1瓶
10 ml×1瓶
2-8℃保存
样品稀释液
3 ml×1瓶
6 ml×1瓶
2-8℃保存
显色剂a液
3 ml×1瓶
6 ml×1瓶
2-8℃保存
显色剂b液
3 ml×1瓶
6 ml×1瓶
2-8℃保存
终止液
3 ml×1瓶
6 ml×1瓶
2-8℃保存
20×浓缩洗涤液
15ml×1瓶
25ml×1瓶
2-8℃保存
注：标准品浓度依次为：200、100、50、25、12.5、0 pg/ml.
样本处理及要求：
1. 血清：室温血液自然凝固10-20分钟，离心20分钟左右（2000-3000转/分）。仔细收集上清，保存过程中如出现沉淀，应再次离心。
2. 血浆：应根据标本的要求选择edta或柠檬酸钠作为抗凝剂，混合10-20分钟后，离心20分钟左右（2000-3000转/分）。仔细收集上清，保存过程中如有沉淀形成，应该再次离心。
3. 尿液：用无菌管收集，离心20分钟左右（2000-3000转/分）。仔细收集上清，保存过程中如有沉淀形成，应再次离心。胸腹水、脑脊液参照实行。
4. 细胞培养上清：检测分泌性的成份时，用无菌管收集。离心20分钟左右（2000-3000转/分）。仔细收集上清。检测细胞内的成份时，用pbs（ph7.2-7.4）稀释细胞悬液，细胞浓度达到100万/ml左右。通过反复冻融，以使细胞破坏并放出细胞内成份。离心20分钟左右（2000-3000转/分）。仔细收集上清。保存过程中如有沉淀形成，应再次离心。
5. 组织标本：切割标本后，称取重量。加入一定量的pbs，ph7.4。用液氮迅速冷冻保存备用。标本融化后仍然保持2-8℃的温度。加入一定量的pbs（ph7.4），用手工或匀浆器将标本匀浆充分。离心20分钟左右（2000-3000转/分）。仔细收集上清。分装后一份待检测，其余冷冻备用。
6. 标本采集后尽早进行提取，提取按相关文献进行，提取后应尽快进行实验。若不能马上进行试验，可将标本放于-20℃保存，但应避免反复冻融.
7. 不能检测含nan3的样品，因nan3抑制辣根过氧化物酶的（hrp）活性。
操作步骤
标准品的加样：设置标准品孔和样本孔，标准品孔各加不同浓度的标准品50μl；。加样：分别设空白孔（空白对照孔不加样品及酶标试剂，其余各步操作相同）、待测样品孔。在酶标包被板上待测样品孔中先加样品稀释液40μl，然后再加待测样品10μl（样品终稀释度为5倍）。加样将样品加于酶标板孔底部，尽量不触及孔壁，轻轻晃动混匀。加酶：每孔加入酶标试剂100μl，空白孔除外。温育：用封板膜封板后置37℃温育60分钟。配液：将20倍浓缩洗涤液用蒸馏水20倍稀释后备用。洗涤：小心揭掉封板膜，弃去液体，甩干，每孔加满洗涤液，静置30秒后弃去，如此重复5次，拍干。显色：每孔先加入显色剂a50μl，再加入显色剂b50μl，轻轻震荡混匀，37℃避光显色15分钟.终止：每孔加终止液50μl，终止反应（此时蓝色立转黄色）。测定：以空白孔调零，450nm波长依序测量各孔的吸光度（od值）。测定应在加终止液后15分钟以内进行。
注意事项：
试剂盒从冷藏环境中取出应在室温平衡15-30分钟后方可使用，酶标包被板开封后如未用完，板条应装入密封袋中保存。浓洗涤液可能会有结晶析出，稀释时可在水浴中加温助溶，洗涤时不影响结果。各步加样均应使用加样器，并经常校对其准确性，以避免试验误差。一次加样时间控制在5分钟内，如标本数量多，*使用排枪加样。请每次测定的同时做标准曲线，做复孔。如标本中待测物质含量过高（样本od值大于标准品孔孔的od值），请先用样品稀释液稀释一定倍数（n倍）后再测定，计算时请后乘以总稀释倍数（×n×5）。封板膜只限一次性使用，以避免交叉污染。底物请避光保存。严格按照说明书的操作进行，试验结果判定必须以酶标仪读数为准.所有样品，洗涤液和各种废弃物都应按传染物处理。本试剂不同批号组分不得混用。10. 如与英文说明书有异，以英文说明书为准。
计算：
以标准物的浓度为横坐标，od值为纵坐标，
在坐标纸上绘出标准曲线，根据样品的od
值由标准曲线查出相应的浓度；再乘以稀释
倍数；或用标准物的浓度与od值计算出标
准曲线的直线回归方程式，将样品的od值
代入方程式，计算出样品浓度，再乘以稀释
倍数，即为样品的实际浓度。
（此图仅供参考）
试剂盒性能：
1.样品线性回归与预期浓度相关系数r值为0.95以上。
2.批内变异系数与批间变异系数应分别小于10%和15% 。
检测范围：
6.25 pg/ml-200 pg/ml
灵敏度：
低检测浓度小于1.0 pg/ml
保存条件及有效期：
1.试剂盒保存：2-8℃。
2．有效期： 6个月
sheep estradiol
for research use only
drug names
generic name：sheep estradiol (e2)elisa kit.
purpose
this kit allows for the determination ofe2 concentrationsin sheepserum, plasma, tissue homogenates and other biological fluids.
principle of the assay
the kitassay sheep e2 level in the sample, use purified sheep e2antibody to coat microtiter plate wells, make solid-phase antibody,thenadde2to the wells,combinedantibody which with hrplabeled, becomeantibody-antigen-enzyme-antibody complex, after washing completely,add tmb substrate solution,tmb substrate becomes blue color at hrp enzyme-catalyzed, reaction is terminated by the addition of a sulphuricacidsolution and the color change is measured spectrophotometrically at a wavelength of 450 nm.the concentration ofe2in the samples is then determined by comparing the o.d. of the samples to the standard curve.
materials provided with the kit
materials provided with the kit
48determinations
96determinations
storage
user manual
1
1
closure plate membrane
2
2
sealed bags
1
1
microelisa stripplate
1
1
2-8℃
standard
0.3ml×6bottle
0.3ml×6bottle
2-8℃
hrp-conjugate reagent
5ml×1 bottle
10ml×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℃
20×washsolution
15ml×1 bottle
25ml×1 bottle
2-8℃
note:standard concentration was followed by:
200、100、50、25、12.5、0 pg/ml.
specimen requirements
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.plasma-use suited edta or citrate plasmaas 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.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.cell culture supernatant-detect secretory components,collect sue a sterile container,centrifugation 20-min at the speed of 2000-3000 r.p.m. 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.tissue samples-after cutting samples, check the weight,add pbs（ph7.2-7.4）,rapidly frozen with liquid nitrogen,maintainsamples at2-8℃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.extractas 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.can’t detect the sample which contain nan3, becausenan3inhibits hrp active.assay procedure
1.add standard: set standard wells, testing sample wells. add standard 50μl to standard well.
2.add sample：set blank wells separately (blank comparison wells don’t add sample and hrp-conjugate reagent, other each step operation is same). testing sample well. add sample dilution 40μl to testing sample well, then add testing sample 10μl (sample final dilutionis 5-fold),add sample to wells,don’t touch the well wall as far as possible, and gently mix.
3.add enzyme：addhrp-conjugate reagent 100μl to each well, exceptblank well.
4.incubate: after closing plate with closure plate membrane ,incubate for 60 min at 37℃.
5.configurate liquid:20-foldwash solution diluted20-foldwith distilled water and reserve.
6.washing：uncover closure plate membrane, discardliquid, dry by swing, add washing buffer to every well, still for 30s then drain,repeat 5 times, dry by pat.
7.color：addchromogen solution a50ul andchromogen solution b to each well,evade the light preservationfor 15 min at 37℃
8.stop the reaction：add stop solution50μlto each well, stop the reaction(the blue color change to yellow color).
9.assay：take blank well as zero ,read absorbance at 450nm after adding stop solution and within 15min.
important notes
the kit takes out from the refrigeration environment should be balanced 15-30 minutes in the room temperature,elisa plates coated if has not use up after opened, the plate should be stored in sealed bag.washing buffer will crystallization separation, it can be heated the water helps dissolve when dilute . washing does not affect the result.add sample with sampler each step, and proofread its accuracy frequently, avoids the experimental error. add sample within 5 mins, if the number of sample is much , recommend to use volley .if the testing material content is excessively higher(the sample od is bigger than the first standard well ),please dilute sample (n-fold), please diluenteandmultiplied by the dilution factor.（×n×5）.closure plate membraneonly limits the disposable use, to avoid cross-contamination.the substrate evade the light preservation.please according to use instruction strictly, the test result determination must take themicrotiter plate readeras a standard.all samples, washing buffer and each kind of reject should according to infective material process.do not mix reagents with those from other lots.
calculate
assay range
6.25 pg/ml - 200 pg/ml
sensitivity
the minimum detectable dose is typically less than 1.0 pg/ml
storage and validity
1．storage： 2-8℃.
2．validity： six months.