小鼠晚期糖基化终末产物AGEs酶联免疫分析ELISA.docx

1、小鼠晚期糖基化终末产物AGEs酶联免疫分析ELISA小鼠晚期糖基化终末产物 (AGEs)酶联免疫分析（ELISA）试剂盒利用说明书本试剂仅供研究利用 目的：本试剂盒用于测定小鼠血清，血浆及相关液体样本中晚期糖基化终末产物 (AGEs)含量。实验原理： 本试剂盒应用双抗体夹心法测定标本中小鼠晚期糖基化终末产物 (AGEs)水平。用纯化的小鼠晚期糖基化终末产物 (AGEs)抗体包被微孔板，制成固相抗体，往包被单抗的微孔中依次加入晚期糖基化终末产物 (AGEs)，再与HRP标记的晚期糖基化终末产物 (AGEs)抗体结合，形成抗体-抗原-酶标抗体复合物，通过完全洗涤后加底物TMB显色。TMB在HRP酶

2、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晚期糖基化终末产物 (AGEs)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小鼠晚期糖基化终末产物 (AGEs)浓度。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（48）2片（96）密封袋1个1个酶标包被板1481962-8保存标准品：720ng/L1瓶1瓶2-8保存标准品稀释液1瓶1瓶2-8保存酶标试剂3 ml1瓶6 ml1瓶2-8保存样品稀释液3 ml1瓶6 ml1瓶2-8保存显色剂A液3 ml1瓶6 ml1瓶2-8保存显色剂B液3 ml1瓶6 ml1瓶2-

3、8保存终止液3ml1瓶6ml1瓶2-8保存20倍浓缩洗涤液20ml1瓶30ml1瓶2-8保存样本处置及要求：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）。认真搜集上清，保留进程中如显现沉淀，应再次离心。2. 血浆：应依照标本的要求选择EDTA、柠檬酸钠或肝素作为抗凝剂，混合10-20分钟后，离心20分钟左右（2000-3000转/分）。认真搜集上清，保留进程中如有沉淀形成，应该再次离心。3. 尿液：用无菌管搜集，离心20分钟左右（2000-3000转/分）。认真搜集上清，保留进程中如有沉淀形成，应再次离心。胸腹水、脑脊液参如实行。4. 细胞培育上清：

4、检测分泌性的成份时，用无菌管搜集。离心20分钟左右（2000-3000转/分）。认真搜集上清。检测细胞内的成份时，用PBS（）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）。认真搜集上清。保留进程中如有沉淀形成，应再次离心。5. 组织标本：切割标本后，称取重量。加入必然量的PBS，。用液氮迅速冷冻保留备用。标本融化后仍然维持2-8的温度。加入必然量的PBS（），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）。认真搜集上清。分装后一份待检测，其余冷冻备用。6. 标本搜集后及早进行提

5、取，提取按相关文献进行，提取后应尽快进行实验。假设不能马上进行实验，可将标本放于-20保留，但应幸免反复冻融.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1.标准品的稀释与加样：在酶标包被板上设标准品孔10孔，在第一、第二孔中别离加标准品100l，然后在第一、第二孔中加标准品稀释液50l，混匀；然后从第一孔、第二孔中各取100l别离加到第三孔和第四孔，再在第三、第四孔别离加标准品稀释液50l，混匀；然后在第三孔和第四孔中先各取50l弃掉，再各取50l别离加到第五、第六孔中，再在第五、第六孔中别离加标准品稀释液50ul，混匀；混匀后从第五、第六孔中各取5

6、0l别离加到第七、第八孔中，再在第七、第八孔中别离加标准品稀释液50l，混匀后从第七、第八孔中别离取50l加到第九、第十孔中，再在第九第十孔别离加标准品稀释液50l，混匀后从第九第十孔中各取50l弃掉。（稀释后各孔加样量都为50l，浓度别离为480ng/L，320ng/L ，160ng/L，80ng/L， 40ng/L）。2.加样：别离设空白孔（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40l，然后再加待测样品10l（样品最终稀释度为5倍）。加样将样品加于酶标板孔底部，尽可能不触及孔壁，轻轻晃动混匀。3.温育：用封板膜封板后置37温育

7、30分钟。4.配液：将20倍浓缩洗涤液用蒸馏水20倍稀释后备用。5.洗涤：警惕揭掉封板膜，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。6.加酶：每孔加入酶标试剂50l，空白孔除外。7.温育：操作同3。8.洗涤：操作同5。9.显色：每孔先加入显色剂A50l，再加入显色剂B50l，轻轻震荡混匀，37避光显色15分钟. 10.终止：每孔加终止液50l，终止反映（现在蓝色立转黄色）。11.测定：以空白空调零，450nm波长依序测量各孔的吸光度（OD值）。 测定应在加终止液后15分钟之内进行。注意事项：1试剂盒从冷藏环境中掏出应在室温平稳15-30分钟后方可利用，酶标包被板开封

8、后如未用完，板条应装入密封袋中保留。2浓洗涤液可能会有结晶析出，稀释时可在水浴中加温助溶，洗涤时不阻碍结果。3各步加样均应利用加样器，并常常校对其准确性，以幸免实验误差。一次加样时刻最好操纵在5分钟内，如标本数量多，推荐利用排枪加样。4请每次测定的同时做标准曲线，最好做复孔。如标本中待测物质含量太高（样本OD值大于标准品孔第一孔的OD值），请先用样品稀释液稀释必然倍数（n倍）后再测定，计算时请最后乘以总稀释倍数（n5）。5封板膜只限一次性利用，以幸免交叉污染。6底物请避光保留。7严格依照说明书的操作进行，实验结果判定必需以酶标仪读数为准.8所有样品，洗涤液和各类废弃物都应按传染物处置。9本试剂

9、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，依照样品的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值为以上。2.批内与批见应别离小于9%和11%检测范围： 20ng/L -500ng/L 保留条件及有效期：1.试剂盒保留：；2-8。2有效期：6个月Mouse advanced glycat

10、ion end productsFOR RESEARCH USE ONLYDrug NamesGeneric Name：Mouse advanced glycation end products (AGEs) ELISA Kit.PurposeThis kit allows for the determination of AGEs concentrations in Mouse serum, blood plasma, and other biological fluids.Principle of the assayThe kit assay Mouse AGEs level in the

11、 sample，use Purified Mouse AGEs antibody to coat microtiter plate wells, make solid-phase antibody, then add AGEs to wells, Combined AGEs antibody which With HRP labeled , become antibody - antigen - enzyme-antibody complex, after washing Completely, Add TMB substrate solution,TMB substrate becomes

12、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. The concentration of AGEs in the samples is then determined by comparing the . of the samples to the standard cur

13、ve.Materials provided with the kitMaterials provided with the kit48determinations96 determinationsStorageUser manual11Closure plate membrane22Sealed bags11Microelisa stripplate112-8Standard：720ng/L1 bottle1 bottle2-8Standard diluent1 bottle1 bottle2-8HRP-Conjugate reagent3ml1 bottle6ml1 bottle2-8Sam

14、ple diluent3ml1 bottle6ml1 bottle2-8Chromogen Solution A3ml1 bottle6ml1 bottle2-8Chromogen Solution B3ml1 bottle6ml1 bottle2-8Stop Solution3ml1 bottle6ml1 bottle2-8wash solution20ml1 bottle30ml1 bottle2-8Specimen requirements1.serum- coagulation at room temperature 10-20 mins，centrifugation 20-min a

15、t the speed of 2000-3000 remove supernatant, If precipitation appeared, Centrifugal again.2.plasma-use suited EDTA, citrate or heparinized plasma as an anticoagulant,mix 10-20 mins ,centrifugation 20-min at the speed of 2000-3000 remove supernatant, If precipitation appeared, Centrifugal again.3.Uri

16、ne-collect sue a sterile container, centrifugation 20-min at the speed of 2000-3000 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 con

17、tainer, centrifugation 20-min at the speed of 2000-3000 remove supernatant,detect the composition of cells, Dilut cell suspension with PBS（）, Cell concentration reached 1 million / ml, repeated freeze-thaw cycles, damage cells and release of intracellular components, centrifugation 20-min at the spe

18、ed of 2000-3000 remove supernatant, If precipitation appeared, Centrifugal again.5.Tissue samples- After cutting samples, check the weight,add PBS（）, Rapidly frozen with liquid nitrogen, maintain samples at 2-8 after melting,add PBS（）, Homogenized by hand or Grinders, centrifugation 20-min at the sp

19、eed of 2000-3000 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 cant, specimen can be kept in -20 to preserve, Avoid repeated freeze-thaw cycles.7.Cant detec

20、t the sample which contain NaN3, because NaN3 inhibits HRP active.Assay procedure and add sample to Standard: set 10 Standard wells on the ELISA plates coated, add Standard 100l to the first and the second well, then add Standard dilution 50l to the first and the second well, mix; take out 100l form

21、 the first and the second well then add it to the third and the forth well separately. then add Standard dilution 50l to the third and the forth well ,mix ; then take out 50l from the third and the forth well discard, add 50l to the fifth and the sixth well ,then add Standard dilution 50l to the fif

22、th and the sixth well, mix ; take out 50l from the fifth and the sixth well and add to the seventh and the eighth well, then add Standard dilution 50l to the seventh and the eighth well ,mix ; take out 50l from the seventh and the eighth well and add to the ninth and the tenth well, add Standard dil

23、ution 50l to the ninth and the tenth well, mix , take out 50l from the ninth and the tenth well discard(add Sample 50l to each well after Diluting ,(density: 480ng/L，320ng/L ，160ng/L，80ng/L， 40ng/L) sample：Set blank wells separately (blank comparison wells dont add sample and HRP-Conjugate reagent,

24、other each step operation is same). testing sample well. add Sample dilution 40l to testing sample well, then add testing sample 10l (sample final dilution is 5-fold), add sample to wells , dont touch the well wall as far as possible, and Gently mix.: After closing plate with Closure plate membrane

25、,incubate for 30 min at 37. liquid: wash solution diluted 20-fold with distilled water and reserve.：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. enzyme：Add HRP-Conjugate reagent 50l to each well,

26、 except blank well. ：Operation with 3.：Operation with 5.：Add Chromogen Solution A 50ul and Chromogen Solution B to each well, evade the light preservation for 15 min at 37 the reaction：Add Stop Solution50l to each well, Stop the reaction(the blue color change to yellow color).：take blank well as zer

27、o , Read absorbance at 450nm after Adding Stop Solution and within 15min.Important notes1.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.2.wash

28、ing buffer will Crystallization separation, it can be heated the water helps dissolve when dilute . Washing does not affect the result.3.add Sample with sampler Each step, And proofread its accuracy frequently, avoids the experimental error. add sample within 5 min, if the number of sample is much ,

29、 recommend to use Volley .4.if the testing material content is excessively higher (The sample OD is bigger than the first standard well ),please dilute Sample (n-fold), Please diluente and multiplied by the dilution factor.（n5）.5.Closure plate membrane only limits the disposable use, to avoid cross-

30、contamination.6.The substrate evade the light preservation.7.Please according to use instruction strictly, The test result determination must take the microtiter plate reader as a standard.8.All samples, washing buffer and each kind of reject should according to infective material process.9.Do not mix reagents with those from other lots.Calculate Assay range20ng/L -500ng/LStorage and validity1Storage： 2-8.2validity： six months.