大鼠d二聚體d2d酶聯(lián)免疫分析

1、<p>　　大鼠D二聚體 (D2D)酶聯(lián)免疫分析</p><p><b>　　試劑盒使用說明書</b></p><p>　　本試劑僅供研究使用 目的：本試劑盒用于測定大鼠血清，血漿及相關(guān)液體樣本中D二聚體 (D2D)的含量。</p><p><b>　　實驗原理：</b></p><

2、;p>　　本試劑盒應(yīng)用雙抗體夾心法測定標(biāo)本中大鼠D二聚體 (D2D)水平。用純化的大鼠D二聚體 (D2D)抗體包被微孔板，制成固相抗體，往包被單抗的微孔中依次加入D二聚體 (D2D)，再與HRP標(biāo)記的羊抗人抗體結(jié)合，形成抗體-抗原-酶標(biāo)抗體復(fù)合物，經(jīng)過徹底洗滌后加底物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)化成最終的黃色。顏色的深淺和樣品中的D二聚體 (D2D)呈正相關(guān)。用酶標(biāo)儀在450nm波長下測定吸光度

3、（OD值），通過標(biāo)準(zhǔn)曲線計算樣品中大鼠D二聚體 (D2D)濃度。</p><p><b>　　試劑盒組成：</b></p><p><b>　　樣本處理及要求：</b></p><p>　　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，保存過程中如出現(xiàn)沉淀，應(yīng)再次離

4、心。</p><p>　　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，保存過程中如有沉淀形成，應(yīng)該再次離心。</p><p>　　3. 尿液：用無菌管收集，離心20分鐘左右（2000-3000轉(zhuǎn)/分）。仔細(xì)收集上清，保存過程中如有沉淀形成，應(yīng)再次離心。胸腹水、腦脊液參照實行。</p&g

5、t;<p>　　4. 細(xì)胞培養(yǎng)上清：檢測分泌性的成份時，用無菌管收集。離心20分鐘左右（2000-3000轉(zhuǎn)/分）。仔細(xì)收集上清。檢測細(xì)胞內(nèi)的成份時，用PBS（PH7.2-7.4）稀釋細(xì)胞懸液，細(xì)胞濃度達(dá)到100萬/ml左右。通過反復(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。保存過程中如有沉淀形成，應(yīng)再次離心。</p><p>　　5. 組織標(biāo)本

6、：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)溆?。?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，其余冷凍備用。</p><p>　　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)行實驗。若不能馬上進(jìn)行試驗，可將標(biāo)本放于-20℃保存，但應(yīng)避

7、免反復(fù)凍融.</p><p>　　7. 不能檢測含NaN3的樣品，因NaN3抑制辣根過氧化物酶的（HRP）活性。</p><p><b>　　操作步驟：</b></p><p>　　標(biāo)準(zhǔn)品的稀釋與加樣：在酶標(biāo)包被板上設(shè)標(biāo)準(zhǔn)品孔10孔，在第一、第二孔中分別加標(biāo)準(zhǔn)品100μl，然后在第一、第二孔中加標(biāo)準(zhǔn)品稀釋液50μl，混勻；然后從第一孔、第二孔中

8、各取100μl分別加到第三孔和第四孔，再在第三、第四孔分別加標(biāo)準(zhǔn)品稀釋液50μl，混勻；然后在第三孔和第四孔中先各取50μl棄掉，再各取50μl分別加到第五、第六孔中，再在第五、第六孔中分別加標(biāo)準(zhǔn)品稀釋液50ul，混勻；混勻后從第五、第六孔中各取50μl分別加到第七、第八孔中，再在第七、第八孔中分別加標(biāo)準(zhǔn)品稀釋液50μl，混勻后從第七、第八孔中分別取50μl加到第九、第十孔中，再在第九第十孔分別加標(biāo)準(zhǔn)品稀釋液50μl，混勻后從第九第十孔

9、中各取50μl棄掉。（稀釋后各孔加樣量都為50μl，濃度分別為3600pg/ml ，2400pg/ml，1200pg/ml，600pg/ml，300pg/ml）。</p><p>　　加樣：分別設(shè)空白孔（空白對照孔不加樣品及酶標(biāo)試劑，其余各步操作相同）、待測樣品孔。在酶標(biāo)包被板上待測樣品孔中先加樣品稀釋液40μl，然后再加待測樣品10μl（樣品最終稀釋度為5倍）。加樣將樣品加于酶標(biāo)板孔底部，盡量不觸及孔壁，輕輕晃

10、動混勻。</p><p>　　溫育：用封板膜封板后置37℃溫育30分鐘。</p><p>　　配液：將30（48T的20倍）倍濃縮洗滌液用蒸餾水30（48T的20倍）倍稀釋后備用。</p><p>　　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。</p><p>　　加酶：每孔加入酶標(biāo)試劑50μ

11、l，空白孔除外。</p><p><b>　　溫育：操作同3。</b></p><p><b>　　洗滌：操作同5。</b></p><p>　　顯色：每孔先加入顯色劑A50μl，再加入顯色劑B50μl，輕輕震蕩混勻，37℃避光顯色15分鐘. </p><p>　　終止：每孔加終止液50μl，終止反

12、應(yīng)（此時藍(lán)色立轉(zhuǎn)黃色）。</p><p>　　測定：以空白空調(diào)零，450nm波長依序測量各孔的吸光度（OD值）。 測定應(yīng)在加終止液后15分鐘以內(nèi)進(jìn)行。</p><p><b>　　注意事項：</b></p><p>　　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)包被板開封后如未用完，板條應(yīng)裝入密封袋中保存。</p&g

13、t;<p>　　濃洗滌液可能會有結(jié)晶析出，稀釋時可在水浴中加溫助溶，洗滌時不影響結(jié)果。</p><p>　　各步加樣均應(yīng)使用加樣器，并經(jīng)常校對其準(zhǔn)確性，以避免試驗誤差。一次加樣時間最好控制在5分鐘內(nèi)，如標(biāo)本數(shù)量多，推薦使用排槍加樣。</p><p>　　請每次測定的同時做標(biāo)準(zhǔn)曲線，最好做復(fù)孔。如標(biāo)本中待測物質(zhì)含量過高（樣本OD值大于標(biāo)準(zhǔn)品孔第一孔的OD值），請先用樣品稀釋液稀

14、釋一定倍數(shù)（n倍）后再測定，計算時請最后乘以總稀釋倍數(shù)（×n×5）。</p><p>　　封板膜只限一次性使用，以避免交叉污染。</p><p><b>　　底物請避光保存。</b></p><p>　　嚴(yán)格按照說明書的操作進(jìn)行，試驗結(jié)果判定必須以酶標(biāo)儀讀數(shù)為準(zhǔn).</p><p>　　所有樣品，洗滌液

15、和各種廢棄物都應(yīng)按傳染物處理。</p><p>　　本試劑不同批號組分不得混用。</p><p>　　10. 如與英文說明書有異，以英文說明書為準(zhǔn)。</p><p><b>　　計算：</b></p><p>　　以標(biāo)準(zhǔn)物的濃度為橫坐標(biāo)，OD值為縱坐標(biāo)， </p><p>　　在坐標(biāo)紙上繪出

16、標(biāo)準(zhǔn)曲線，根據(jù)樣品的OD </p><p>　　值由標(biāo)準(zhǔn)曲線查出相應(yīng)的濃度；再乘以稀釋 </p><p>　　倍數(shù)；或用標(biāo)準(zhǔn)物的濃度與OD值計算出標(biāo) </p><p>　　準(zhǔn)曲線的直線回歸方程式，將樣品的OD值 </p><p>　　代入方程式，計算出樣品濃度，再乘以稀釋 </p>

17、<p>　　倍數(shù)，即為樣品的實際濃度。 </p><p><b>　　（此圖僅供參考）</b></p><p><b>　　試劑盒性能：</b></p><p>　　1.樣品線性回歸與預(yù)期濃度相關(guān)系數(shù)R值為0.990以上。</p><p>　　2.批內(nèi)

18、與批見應(yīng)分別小于9%和11%</p><p>　　檢測范圍： </p><p>　　1000 pg/ml - 4500pg/ml </p><p><b>　　保存條件及有效期：</b&

19、gt;</p><p>　　1.試劑盒保存：；2-8℃。</p><p><b>　　2．有效期：6個月</b></p><p>　　Rat D-Dimer(D2D)</p><p>　　Drug Names</p><p>　　Generic Name：Rat D-Dimer(D2D) ELIS

20、A Kit.</p><p><b>　　Purpose</b></p><p>　　This kit allows for the determination of D2D concentrations in Rat serum, blood plasma, and other biological fluids.</p><p>　　Pri

21、nciple of the assay</p><p>　　The kit assay Rat D2D level in the sample，use Purified Rat D2D antibody to coat microtiter plate wells, make solid-phase antibody, then add D2D to wells, Combined D2D antibody wh

22、ich With HRP labeled goat anti-Human become antibody - antigen - enzyme-antibody complex, after washing Completely, Add TMB substrate solution, TMB substrate becomes blue color At HRP enzyme-catalyzed, reaction is termin

23、ated by the addition of a sulphuric acid solution and the color change is measured spectrophotometrica</p><p>　　Materials provided with the kit</p><p>　　Specimen requirements</p><p>

24、;　　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.</p><p>　　plasma-use suited EDTA o

25、r 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.</p><p>　　Urine-collect sue a ster

26、ile 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.</p><

27、;p>　　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 suspens

28、ion 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 superna

29、tant, If precipitation appeared, Centrifugal again.</p><p>　　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 me

30、lting,add PBS（PH7.4）, Homogenized by hand or Grinders, centrifugation 20-min at the speed of 2000-3000 r.p.m. remove supernatant.</p><p>　　extract as soon as possible after Specimen collection,and according

31、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.</p><p>　　Can’t detect

32、 the sample which contain NaN3, because NaN3 inhibits HRP active.</p><p>　　Assay procedure</p><p>　　1.Dilute and add sample to Standard: set 10 Standard wells on the ELISA plates coated, add Sta

33、ndard 100μl to the first and the second well, then add Standard dilution 50μl to the first and the second well, mix; take out 100μl form the first and the second well then add it to the third and the forth well separatel

34、y. then add Standard dilution 50μl to the third and the forth well ,mix ; then take out 50μl from the third and the forth well discard, add 50μl to the fifth and the sixth well ,then add</p><p>　　2.add sampl

35、e：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

36、sample 10μl (sample final dilution is 5-fold), add sample to wells , don’t touch the well wall as far as possible, and Gently mix.</p><p>　　3.Incubate: After closing plate with Closure plate membrane ,incuba

37、te for 30 min at 37℃.</p><p>　　4.Configurate liquid: 30-fold (or 20-fold)wash solution diluted 30-fold (or 20-fold) with distilled water and reserve.</p><p>　　5.washing：Uncover Closure plate mem

38、brane, discard Liquid, dry by swing, add washing buffer to every well, still for 30s then drain, repeat 5 times, dry by pat.</p><p>　　6.add enzyme：Add HRP-Conjugate reagent 50μl to each well, except blank w

39、ell. </p><p>　　7.incubate：Operation with 3.</p><p>　　8.washing：Operation with 5.</p><p>　　9.color：Add Chromogen Solution A 50ul and Chromogen Solution B to each well, evade the ligh

40、t preservation for 15 min at 37℃</p><p>　　10.Stop the reaction：Add Stop Solution50μl to each well, Stop the reaction(the blue color change to yellow color).</p><p>　　11.assay：take blank well as

41、zero , Read absorbance at 450nm after Adding Stop Solution and within 15min.</p><p>　　Important notes</p><p>　　The kit takes out from the refrigeration environment should be balanced 15-30 minut

42、es in the room temperature, ELISA plates coated if has not use up after opened, the plate should be stored in Sealed bag.</p><p>　　washing buffer will Crystallization separation, it can be heated the water h

43、elps dissolve when dilute . Washing does not affect the result.</p><p>　　add Sample with sampler Each step, And proofread its accuracy frequently, avoids the experimental error. add sample within 5 mins, if

44、the number of sample is much , recommend to use Volley .</p><p>　　if the testing material content is excessively higher (The sample OD is bigger than the first standard well ),please dilute Sample (n-fold),

45、Please diluente and multiplied by the dilution factor.（×n×5）.</p><p>　　Closure plate membrane only limits the disposable use, to avoid cross-contamination.</p><p>　　The substrate evade

46、 the light preservation.</p><p>　　Please according to use instruction strictly, The test result determination must take the microtiter plate reader as a standard.</p><p>　　All samples, washing b

47、uffer and each kind of reject should according to infective material process.</p><p>　　Do not mix reagents with those from other lots.</p><p><b>　　Calculate</b></p><p>