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  • 肝中DNA的分离与鉴定原理

    肝中DNA的分离与鉴定原理

    细胞内的核酸多以核蛋白的形式存在,其中脱氧核糖核蛋白主要存在于细胞核中,核糖核蛋白主要存在于细胞质中。这两类核蛋白在0.14mol/L氯化钠溶液中的溶解度相差很

    2024-10-16
  • Freeze Squeeze PCR Product Purification from Agorose Gel

    Freeze Squeeze PCR Product Purification from Agorose Gel

    Abstract: The “Freeze squeeze” method is a cost effective and technically simple

    2024-10-16
  • 寡核苷酸纯化

    寡核苷酸纯化

    Purpose: Purification of oligonucleotides (which have already been purified by r

    2024-10-16
  • Injection DNA Preparation

    Injection DNA Preparation

    ) Culture 400 mls of bacteria harboring transposon overnight at 37oC.2) Harvest

    2024-10-16
  • DNA isolation extraction

    DNA isolation extraction

    CTAB TECHNIQUE / Method / Schedule / Protocol FOR DNA ISOLATION / DNA EXTRACTION

    2024-10-16
  • 真菌基因组DNA的提取方法

    真菌基因组DNA的提取方法

    Fungal Genomic DNA Extraction OverviewHigh throughput of many fungal isolates ca

    2024-10-16
  • 细菌基因组DNA提取方法综述

    细菌基因组DNA提取方法综述

    细菌基因组DNA的提取方法综述,提供了5种方法。 1 快速微量提取法 A.取1.5ml菌体培养物于一灭菌Ep管中,12000rpm离心1min, 丢去上清夜,收

    2024-10-16
  • Recovering DNA from agarose gels

    Recovering DNA from agarose gels

    Recovering DNA from agarose gelsPaul N. Hengen, Ph.D. (July 14, 1999)Introductio

    2024-10-16
  • 间接荧光免疫标记的基础方法

    间接荧光免疫标记的基础方法

    BackgroundThis is the method for indirect immunofluorescence labeling; that is,

    2024-10-16
  • 核酸生物合成

    核酸生物合成

    一、直接检出病毒核酸   1.核酸杂交(Nucleic acid hybridization) -临床病毒学中报速诊断方法通常是检测标本中的病毒抗原,然而

    2024-10-16
  • 丙烯酰胺胶分离DNA

    丙烯酰胺胶分离DNA

    1.Pour a vertical acrylamide gel using TEA buffer.A 4 % non denaturing gel is co

    2024-10-16
  • DEAE membrane吸附法分离与纯化DNA片段

    DEAE membrane吸附法分离与纯化DNA片段

    利用离子交换的原理,在低盐情况下使DNA 吸附在带正电荷的滤膜上,再利用含有高浓度盐类的缓冲液将DNA 自膜上溶离下来。仪器用具:Mupid II 迷你电泳槽;

    2024-10-16
  • Sephadex G-50 spun column purificati

    Sephadex G-50 spun column purificati

    Sephadex G-50 spun column purificationSpin column purification can be used to ch

    2024-10-16
  • Isolation of DNA fragments using glass milk (GENE-CLEAN)

    Isolation of DNA fragments using glass milk (GENE-CLEAN)

    1.Excise DNA section from gel into eppendorf tube.2.Add 2-3 volumes of NaI (NaI

    2024-10-16
  • PLASMID MIDI-PREP FROM BACTERIA

    PLASMID MIDI-PREP FROM BACTERIA

    PREPARE SOLUTIONS1. Glycerol mix (1 L):Weigh 25 grams (liquid weight) of glycero

    2024-10-16