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細(xì)胞消化與解離試劑
在組織細(xì)胞的體外培養(yǎng)和原代細(xì)胞培養(yǎng)的過程中,需要使用組織細(xì)胞消化與解離試劑使組織細(xì)胞得以解離和分散,以便進(jìn)行單個(gè)細(xì)胞懸液的制備或貼壁生長傳代細(xì)胞培養(yǎng)。常用的消化液有胰蛋白酶(Trypsin)-EDTA、膠原酶和分散酶等。NEST?提供多種效能不同的細(xì)胞消化液,以滿足您在原代細(xì)胞分離和貼壁細(xì)胞傳代培養(yǎng)中的不同需求。
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產(chǎn)品詳情
胰蛋白酶(Trypsin)是一種絲氨酸水解酶,它能夠把多肽鏈中賴氨酸和精氨酸殘基中的羥基側(cè)切段,水解細(xì)胞間的蛋白質(zhì),破壞細(xì)胞間的連接,從而使組織或貼壁細(xì)胞離散成單個(gè)細(xì)胞。胰酶分散細(xì)胞的活性與組織或細(xì)胞的特性、胰酶濃度、溫度和作用時(shí)間有關(guān),在pH8.0和37°C時(shí),胰酶的作用能力最強(qiáng)。因此,在使用胰酶時(shí),應(yīng)當(dāng)把握好濃度、溫度和時(shí)間,以免消化過度造成細(xì)胞損傷。一般常用胰酶的工作濃度為0.25%,而半貼壁細(xì)胞或?qū)σ让该舾械募?xì)胞常采用低濃度(0.05%)的胰酶進(jìn)行細(xì)胞消化。由于EDTA能夠螯合Ca2+和Mg2+,從而破壞細(xì)胞連接促進(jìn)細(xì)胞的解離,因此在胰酶溶液中常常會(huì)加入一定量的EDTA混合使用,以增強(qiáng)解離效果。對(duì)于EDTA可能會(huì)干擾后續(xù)的測(cè)試分析時(shí),推薦選擇不含EDTA的消化液。具體請(qǐng)參考以下表格選擇合適的胰蛋白酶產(chǎn)品。

儲(chǔ)存:-20度,干冰運(yùn)輸

產(chǎn)品信息

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