首页> 美国卫生研究院文献>Biochemical Journal >Tissue-culture cell fractionation. Fractionation of membranes from tissue-culture cells homogenized by glycerol-induced lysis.
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Tissue-culture cell fractionation. Fractionation of membranes from tissue-culture cells homogenized by glycerol-induced lysis.

机译:组织培养细胞分级分离。组织培养细胞膜的馏分通过甘油诱导的裂解而被均质化。

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摘要

1. The disruption of various types of tissue-culture cells by (a) incubation in solutions of 1.2 M-glycerol and (b) transfer of the glycerol-loaded cells to relatively hypo-osmotic solutions of 0.25 M-sucrose was studied. 2. Bivalent cations (2mM-Mg2+) were generally included to preserve the nuclei, but some cells (polyoma-virus-transformed baby-hamster kidney cells) failed to be disrupted adequately under these conditions. 3. Other cells (mouse-embryo fibroblasts) required additional gentle Dounce homogenization to effect complete cell breakage. 4. Purification of the whole homogenate was carried out by a combination of differential centrifugation and sedimentation or flotation through sucrose gradients. 5. Enzyme analysis showed that plasma-membrane, endoplasmic-reticulum and mitochondrial fractions were obtained in good yield and purity.
机译:1.研究了通过(a)在1.2 M-甘油溶液中孵育和(b)将甘油负载细胞转移至0.25 M-蔗糖的低渗溶液中来破坏各种类型的组织培养细胞。 2.通常包含二价阳离子(2mM-Mg2 +)来保存细胞核,但是在这些条件下某些细胞(多瘤病毒转化的仓鼠肾细胞)未能被充分破坏。 3.其他细胞(小鼠胚胎成纤维细胞)需要额外的温和的Dounce匀浆作用才能完全破坏细胞。 4.通过差速离心和通过蔗糖梯度的沉降或浮选的组合来进行整个匀浆的纯化。 5.酶分析表明,获得的血浆膜,内质网和线粒体级分均具有良好的收率和纯度。

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