ConstructionofBACLibraries：MegabaseDNAIsolation
Megabase DNA IsolationMegabase-size DNA isolation from plantsTo construct large insert DNA libraries in BAC and YAC vectors, methods must be developed to isolate very high molecular weight DNA - megabase-size DNA - from plants. To isolate such DNA, protoplasts or nuclei must first be embedded in agarose plugs or microbeads. The agarose acts as a solid porous matrix which allows for the diffusion of various reagents f......阅读全文
Construction－of－BAC－Libraries：Megabase－DNA－Isolation
Megabase DNA IsolationMegabase-size DNA isolation from plantsTo construct large insert DNA libraries in BAC and YAC vectors, methods must be developed
Construction－of－BAC－Libraries：Construction－of－a－BAC－library
Once high molecular weight (HMW) DNA has been prepared it must somehow be fragmented and DNA in the desired size range isolated. In general, as the de
Construction－of－BAC－Libraries：SOLUTIONS－FOR－BAC－LIBRARY－CONSTRUCTION
SOLUTIONS FOR BAC LIBRARY CONSTRUCTION10X Homogenization Buffer (HB) stock: (1 liter)IngredientAmountFinal ConcentrationTrisma base12.1 g0.1 MKCl59.7
DNA－Isolation－From－BAC－－PAC－Clones
DNA Isolation From BAC & PAC Clones This is a rapid alkaline lysis miniprep method for isolating DNA from large PAC clones. It is a modifi
Protocol－for－Construction－of－BAC－Libraries
Protocol for Construction of BAC Libraries The bacterial artificial chromosome cloning (BAC) system is emerging as the system of choice f
BAC－DNA分离方法－Isolation－of－BAC－DNA－from－Largescale－Cultures
Isolation of BAC DNA from Large-scale Cultures Joseph Sambrook Peter Maccallum Cancer Institute and The University of Melbourne, Austral
Large－Scale－Plasmid,－Cosmid,－BAC,－PAC,－and－Fosmid－DNA－Isolation
DNA Isolation by a Cleared Lysate Method Followed by Double Acetate Precipitation Version 3b - updated September 26, 1999The Most Recent Roe Lab Imple
细菌人工染色体
The Construction of Bacterial Artificial Chromosome (BAC) Libraries (complete manuscript) (Clemson University Genomics Institute) Construction of BAC
Organelle－DNA－Library－Construction
Organelle DNA Library Construction (version MAY-1998) I. NEBULIZATION of DNA 1. 0.5 - 5 ug DNA in TE (10mM/1mM), 25% glycerol, final vol
DNA－isolation－extraction
CTAB TECHNIQUE / Method / Schedule / Protocol FOR DNA ISOLATION / DNA EXTRACTION FROM PLANT LEAF / LEAVES SAMPLES (see also DNA RNA double isolati
Chromosomal－DNA－Isolation
Chromosomal DNA Isolation METHOD: Grow cells in 2-5 ml broth to late log phase. Pellet 1-2 ml cells in microfuge. Resuspend cells in 400
Cosmid－DNA－Isolation
实验概要 Isolation of high yields of highly pure cosmid DNA using PureLink™ HiPure Plasmid Purification Kits. 实验原理 The PureLink™ HiPure Plasmid Purif
Fungal－DNA－Isolation
Fungal DNA IsolationSaghai-Maroof MA, Soliman KM, Jorgensen RA, & Allard RW (1984) PNAS 81:8014-8018DNA successfully isolated from fungal species of C
Insect－DNA－Isolation－Protocol
实验概要The E.Z.N.A.® Insect DNA Kit is designed for efficient recovery of genomic DNA up to 60 kb in size from insects, arthropods, roundworms, flatw
小量培养物中分离－BAC－DNA
实验方法原理 小量 BAC DNA 是从 5 ml BAC 转化细胞培养物中制备的。DNA 的制备采用碱裂解法。BAC DNA 的产量可达 0.1~0.4 μg，足够用于限制酶切分析、PCR 或 Southern 印迹。
大量培养物中分离－BAC－DNA
BAC 重组子的精细分析，包括详细的限制酶切图谱、DNA 测序或亚克隆，所需 DNA 量都超过小量制备所能提供的量。本方案的制备流程适用于重组 BAC 的大规模培养物。500 ml BAC 转化菌的平均产量为 20~25 μg BAC DNA。还可用柱层析对 DNA 产物进一步纯化。本实验来源「分子
小量培养物中分离－BAC－DNA
实验方法原理 小量 BAC DNA 是从 5 ml BAC 转化细胞培养物中制备的。DNA 的制备采用碱裂解法。BAC DNA 的产量可达 0.1~0.4 μg，足够用于限制酶切分析、PCR 或 Southern 印迹。实验材料 限制性内切核酸酶大肠杆菌试剂、试剂盒 乙醇异丙醇DNA提取液碱性裂解
小量培养物中分离－BAC－DNA
小量 BAC DNA 是从 5 ml BAC 转化细胞培养物中制备的。DNA 的制备采用碱裂解法。BAC DNA 的产量可达 0.1~0.4 μg，足够用于限制酶切分析、PCR 或 Southern 印迹。本实验来源「分子克隆实验指南第三版」黄培堂等译。实验方法原理小量 BAC DNA 是从 5
大量培养物中分离－BAC－DNA
实验方法原理 BAC 重组子的精细分析，包括详细的限制酶切图谱、DNA 测序或亚克隆，所需 DNA 量都超过小量制备所能提供的量。本方案的制备流程适用于重组 BAC 的大规模培养物。500 ml BAC 转化菌的平均产量为 20~25 μ
大量培养物中分离－BAC－DNA
实验方法原理 BAC 重组子的精细分析，包括详细的限制酶切图谱、DNA 测序或亚克隆，所需 DNA 量都超过小量制备所能提供的量。本方案的制备流程适用于重组 BAC 的大规模培养物。500 ml BAC 转化菌的平均产量为 20~25 μg BAC DNA。还可用柱层析对 DNA 产物进一步
Isolation－of－genomic－DNA－from－bacteria
Note: This procedure does not work well with Gram + cocci. Transfer 1.5 mL overnight culture to a 1.5 mL microfuge tube, centrifuge for 30 sec, de
DNA抽提
DNA抽提（主要内容如下）· Working with DNA· DNA Extraction from Bacteria and Other Organisms· DNA Extraction from Cell and Tissue· Mitochondria DNA Isola
A－simple,－rapid－procedure－for－the－isolation－of－DNA－for－PCR
N.M. DuTeau and J.F. Leslie - Department of Plant Pathology, Throckmorton Hall, Kansas State University, Manhattan, KS 66506-5502 The polymerase cha
A－simple,－rapid－procedure－for－the－isolation－of－DNA－for－PCR
The polymerase chain reaction (PCR) is a method for amplifying specific segments of DNA defined by the small primers used to start the reaction. Using
Quick－Yeast－DNA－Prep:－Isolation－of－Total－DNA－(genomic－and－plasmid)
Grow a 5 ml YPD O/N culture inoculated with a single yeast colony at 30 deg. Transfer culture to a small 13 x 100 glass tube. Spin down cells 2
Quick－and－Easy－Isolation－of－Genomic－DNA－from－Yeast
Procedure Transfer 1.5 ml of liquid culture of yeast grown for 20 - 24 h at 30°C in YPD (1% yeast extract, 2% peptone, 2% dextrose) into a microce
One－step－miniprep－method－for－the－isolation－of－plasmid－DNA
plasmid miniprepAll ''miniprep'' methods reported so far for the isolation of plasmid DNA involve multiple pipetting, extraction, cent
Isolation－and－Quantification－of－Genomic－DNA－from－Mycobacterium－tuberculosis
Part A. Isolation of Nucleic AcidsNOTE: CAUTION! STEPS 1-10 SHOULD BE PERFORMED USING APPROPRIATE PROCEDURES FOR HANDLING MATERIAL POTENTIALLY CONTAMI
质粒的大量制备
· Plasmid Mini and Maxi Prep Methods (Gimila Lab) · Maxi-preps and all media, solutions (NWFSC)Isolation of cosmid, plasmid and P1 DNA
质粒的大量制备
· Plasmid Mini and Maxi Prep Methods (Gimila Lab) · Maxi-preps and all media, solutions (NWFSC)Isolation of cosmid, plasmid and P1 DNA