人B-淋巴細(xì)胞趨化因子1試劑盒  檢測范圍：96T

2pg/ml-80pg/ml

使用目的：

人B-淋巴細(xì)胞趨化因子1試劑盒 用于測定人血清、血漿及相關(guān)液體樣本中B-淋巴細(xì)胞趨化因子1(BLC-1/CXCL13)含量。

實(shí)驗(yàn)原理

本試劑盒應(yīng)用雙抗體夾心法測定標(biāo)本中人BLC-1/CXCL13水平。用純化的人BLC-1/CXCL13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BLC-1/CXCL13，再與HRP標(biāo)記的BLC-1/CXCL13抗體結(jié)合，形成抗體-抗原-酶標(biāo)抗體復(fù)合物，經(jīng)過*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BLC-1/CXCL13呈正相關(guān)。用酶標(biāo)儀在450nm波長下測定吸光度（OD值），通過標(biāo)準(zhǔn)曲線計(jì)算樣品中人BLC-1/CXCL13濃度。

試劑盒組成

標(biāo)本要求 

1．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(shí)驗(yàn)。若不能馬上進(jìn)行試驗(yàn)，可將標(biāo)本放于-20℃保存，但應(yīng)避免反復(fù)凍融

2．不能檢測含NaN3的樣品，因NaN3抑制辣根過氧化物酶的（HRP）活性。

操作步驟

• 標(biāo)準(zhǔn)品的稀釋：本試劑盒提供原倍標(biāo)準(zhǔn)品一支，用戶可按照下列圖表在小試管中進(jìn)行稀釋。

• 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）、標(biāo)準(zhǔn)孔、待測樣品孔。在酶標(biāo)包被板上標(biāo)準(zhǔn)品準(zhǔn)確加樣50μl，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，輕輕晃動(dòng)混勻。
• 溫育：用封板膜封板后置37℃溫育30分鐘。   
• 配液：將30倍濃縮洗滌液用蒸餾水30倍稀釋后備用
• 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。
• 加酶：每孔加入酶標(biāo)試劑50μl，空白孔除外。
• 溫育：操作同3。
• 洗滌：操作同5。
• 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.
• 終止：每孔加終止液50μl，終止反應(yīng)（此時(shí)藍(lán)色立轉(zhuǎn)黃色）。
• 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。

• Calculate

  Take the standard density as the horizontal, the OD value for the vertical ,draw the standard curve on graph paper, Find out the corresponding density according to the sample OD value by the Sample curve, multiplied by the dilution multiple, or calculate the straight line regression equation of the standard curve with the standard density and the OD value ,with the sample OD value in the equation, calculate the sample density, multiplied by the dilution factor, the result is the sample actual density.

  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 min, 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 diluente and multiplied by the dilution factor.（×n×5）.
• Closure plate membrane only 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 the microtiter plate reader as 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.

• Storage and validity

  1．Storage：  2-8℃.

  2．validity： six months