Login
欢迎浏览恩派尔生物资料网
我要投稿 请登录 免费注册 安全退出

  • Northern Blotting

    Northern Blotting

    Northern BlottingAdapted from Molecular Cloning (Maniatis), Current Protocols in

    2024-11-05 105
  • Top Ten Ways to Ensure Valid RNAi Data

    Top Ten Ways to Ensure Valid RNAi Data

    1.Confirm results with a second or third siRNA to the same target.   One of the

    2024-11-05 83
  • Northern protocol(RULES FOR RNA WORK)

    Northern protocol(RULES FOR RNA WORK)

    1. Wear gloves at all time including filling pipet tip in racks, filling

    2024-11-05 69
  • How to prepare Molecular Biology grade glycogen

    How to prepare Molecular Biology grade glycogen

    How to prepare Molecular Biology grade glycogenAuthor: Roberto SalviSource: Cont

    2024-11-05 77
  • Purification of poly(A)+ RNA from total RNA

    Purification of poly(A)+ RNA from total RNA

    Purification of poly(A)+ RNA from total RNA0. (Optional)Before using Oligotex-dT

    2024-11-05 74
  • RNA interference:The short answer

    RNA interference:The short answer

    One way of seeing what a gene does is to block its messenger RNA and note the ef

    2024-11-05 86
  • RNAi——制备siRNAs的几种方法

    RNAi——制备siRNAs的几种方法

    越来越多的研究人员开始采用小分子干扰RNA(small interfering RNAs,siRNAs)来抑制特定的哺乳动物基因表达。siRNA是一种短片断双链

    2024-11-05 100
  • Preparation of single-stranded probes from cloned cDNA

    Preparation of single-stranded probes from cloned cDNA

    a) 2-5 µg of plasmid DNA containing the cDNA insert is linearized using an appro

    2024-11-05 88
  • IN SITU HYBRIDIZATION ON FROZEN SECTIONS

    IN SITU HYBRIDIZATION ON FROZEN SECTIONS

    Remove slides from freezer, thaw for 5 min. at 55C. Fix 10 min. in 4% paraformal

    2024-11-05 79
  • 如何确定RNA质量的经验谈!

    如何确定RNA质量的经验谈!

    1) 检测RNA溶液的吸光度 280、320、230、260nm下的吸光度分别代表了核酸、背景(溶液浑浊度)、盐浓度和蛋白等有机物的值。一般的,我们只看OD26

    2024-11-05 116
  • How to Maintain an RNase-free Lab

    How to Maintain an RNase-free Lab

    How to Maintain an RNase-free LabLet's admit it, everyone who has worked wit

    2024-11-05 92
  • 35S-RIBOPROBE SYNTHESIS FOR ISOTOPIC In Situ HYBRIDIZATION

    35S-RIBOPROBE SYNTHESIS FOR ISOTOPIC In Situ HYBRIDIZATION

    Pipet 12.5µl 35S-UTP (1200 Ci/mmol) into 1.5ml microfuge tube. Final concentrati

    2024-11-05 77
  • S1 analysis of yeast mRNA using oligonucleotide probes

    S1 analysis of yeast mRNA using oligonucleotide probes

    S1 analysis of yeast mRNA using oligonucleotide probesSteve Hahn. last modified

    2024-11-05 151
  • 推荐:RNAi及其在植物遗传改良中的应用

    推荐:RNAi及其在植物遗传改良中的应用

    RNAi即RNA干涉(或RNA干扰)是指双链RNA导入细胞后并被切割成21~23个核苷酸长度的短核苷酸双链,在其它作用因子的参与下能够特异地与其同源的mRNA结

    2024-11-05 92
  • 哺乳动物RNAi技术全面实验方法

    哺乳动物RNAi技术全面实验方法

    WHENVIRUSESINFECTEUKARYOTICCELLS domly integrate into host genomes, double-stran

    2024-11-05 85