• 介紹：
  SDS說明：生化研究，用于從蛋白質(zhì)中分離核酸，從宿主細(xì)胞中脫落某些病毒；蛋白電泳試劑，也可用于質(zhì)粒提取
  SDS生物學(xué)應(yīng)用：
  (1)SDS是陰離子表面活性劑常用于蛋白質(zhì)和類脂類的電泳分離。當(dāng)其與蛋白質(zhì)混合,質(zhì)量比達(dá)到1.4:1時，SDS能破壞蛋白質(zhì)分子間以及其他物質(zhì)分子間的非共價鍵使蛋白質(zhì)的構(gòu)象發(fā)生變化繼而使蛋白質(zhì)變性解離成單一亞基，從而降低或消除了各種蛋白質(zhì)分子間的天然電荷差異。電泳常用10%的SDS作為儲備液。
  (2)SDS可以迅速破壞組織結(jié)構(gòu)，抑制RNase和脫氧核糖核苷酶（DNase）活性，所以SDS也是核酸純化試劑的關(guān)鍵組分。通常使用10%或者20%的SDS儲備液，SDS的工作濃度是0.1-0.5%。
  SDS貯存條件：密封陰涼干燥保存；
  SDS毒性：低毒，大鼠經(jīng)口半數(shù)致死量為1288mg/kg。有刺激性。

• 熔點(diǎn)： 204-207℃

• 外觀： 白色粉末

• 溶解性： Souble  in  H2O

• 敏感性： 易吸潮

• 儲存條件： RT

• 用途： 生化分析，電泳，離子對試劑

• 注意：部分產(chǎn)品我司僅能提供部分信息，我司不保證所提供信息的權(quán)威性，僅供客戶參考交流研究之用。

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輸入產(chǎn)品批號：

本計(jì)算器可幫助您計(jì)算出特定溶液中溶質(zhì)的質(zhì)量、溶液濃度和體積之間的關(guān)系，公式為：

質(zhì)量 (mg) = 濃度 (mM) x 體積 (mL) x 分子摩爾量 (g/mol)

• pg ng μg mg g kg =
  fM pM nM μM mM M *
  nL μL mL L *