考馬斯亮藍(lán)染色原理

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 bca法是常用蛋白濃度測(cè)定方法之一。其他蛋白濃度測(cè)定方法還有考馬斯亮藍(lán)法、bradford法測(cè)蛋白濃度等。本文是用bca法測(cè)定蛋白濃度。是使用索萊寶BCA蛋白濃度測(cè)定試劑盒完成本實(shí)驗(yàn)。

下面是bca法測(cè)蛋白濃度步驟:

1. 標(biāo)準(zhǔn)曲線的繪制:取一塊酶標(biāo)板,按照下表加入試劑 ;

2. 根據(jù)樣品數(shù)量,按50體積BCA試劑A加1體積BCA試劑B(50:1)配制適量BCA工作液,充分混勻;    

3. 各孔加入200μL BCA工作液;    

4. 把酶標(biāo)板放在振蕩器上振蕩30sec,37℃放置30分鐘,然后在562nm下比色測(cè)定。以蛋白含量(μg)為橫坐標(biāo),吸光值為縱坐標(biāo),繪出標(biāo)準(zhǔn)曲線;   

5. 稀釋待測(cè)樣品至合適濃度,使樣品稀釋液總體積為20μL,加入BCA工作液200μL,充分混勻,37℃放置30分鐘后,以標(biāo)準(zhǔn)曲線0號(hào)管做參比,在 562nm波長(zhǎng)下比色,記錄吸光值;     

6. 根據(jù)所測(cè)樣品的吸光值,在標(biāo)準(zhǔn)曲線上即可查得相應(yīng)的蛋白含量(μg),除以樣品稀釋液總體積(20μL),乘以樣品稀釋倍數(shù)即為樣品實(shí)際濃度(單 位:μg/μL)。

【bca法優(yōu)缺點(diǎn)】 

(一) 操作簡(jiǎn)單,快速,45分鐘內(nèi)完成測(cè)定,比經(jīng)典的Lowary法快4倍且更加方便; 

(二) 準(zhǔn)確靈敏,試劑穩(wěn)定性好,BCA試劑的蛋白質(zhì)測(cè)定范圍是20-200μg/ml,微量BCA測(cè)定范圍在0.5-10μg/ml。 

(三) 經(jīng)濟(jì)實(shí)用,除 試管 外,測(cè)定可在微板孔中就進(jìn)行,大大節(jié)約樣品和試劑用量; 

(四) 抗試劑干擾能力比較強(qiáng),如去垢劑,尿素等均無(wú)影響


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