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RNA purification --- hot phenol protocol
Hot phenol may also be used to remove DNA.1. Add equal volume of TE-saturated ph
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Emobservations of microsomes
LEVEL I Figure 7.3 Isolated microsomes Figure 7.4 TEM of hepatocyteMATERIALS 1
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Total RNA extraction from Arabidopsis and tobacco
RNA extraction buffer: 0.1M NaCl 2% SDS 50mM Tris/HCl (pH9) 10mM EDTA 20mM %26sz
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染色体的制片程序
1、取对数生长期细胞一个T75或T25瓶。2、将培养基换成10ml DMEM(H)+10%FBS+0.1ug/ml秋水仙素的培养基，处理1~2小时。3、将细胞培
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变性RNA在膜上的转移和固定
多数情况下，为检测特定的靶mRNA，需先将RNA通过琼脂糖电泳分离后，再从胶上转移到二维支持物上（通常为尼龙膜），再与特异的标记探针杂交。本文主要介绍RNA在上
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用一步法从细胞和组织中同时制备DNA、RNA和蛋白质
本文所述的是RNA提取的一步法的改进，可从少量组织和细胞中同时回收DNA、RNA和蛋白质。这种方法包括用含异硫氰酸胍和酚的一种单相液来裂解细胞，加入氯仿产生第二
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植物RNA提取--Methods for Plant RNA Isolation
AMES/Chloroform extraction in our lab to extract total from potato leaves for v
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Total RNA extraction from Arabidopsis and tobacco--拟南芥和烟草总RNA提取
RNA extraction buffer:0.1M NaCl2% SDS50mM Tris/HCl (pH9)10mM EDTA20mM ß-mercapto
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Human FastTrack mRNA Isolation
Preparation of Cells1.Prepare or collect between 2x107 cells for each mRNA prep
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Protocol for FastTrack 2.0 mRNA Extraction Human Cells
Preparation of CellsPrepare or collect between 2x107 cells for each mRNA prep （w
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Extraction of RNA for Bacteria
一、实验原理 The E.Z.N.A. HP Total RNA Kit uses the reversible binding properties of H
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Invitro RNA synthesis from plasmid-borne sequences
N.B: Gloves should be worn at all times during preparation of in vitro RNA. All
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Acid Phenol Yeast RNA Preparation
This is the preferred method for yeast RNA preparationuse Gloves and RNAse free
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Human RNA Extraction protocol(哈佛RNA提取方法)
REAGENTSGuanadinium Thiocyanate1.0 M Sodium Citrate pH 7.010% Sarcosyl2-mercapto
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RNA Isolation from Yeast
RNA Isolation - Volumes and weights are for 10 ml cultures (1-2 x 107 cells/ml).
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