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  • ChromosomalDNAIsolation

    Chromosomal DNA IsolationMETHOD:Grow cells in 2-5 ml broth to late log phase.Pellet 1-2 ml cells in microfuge.Resuspend cells in 400 μl TES (50 mM Tris-HCl, 10 mM NaCl, 10 mM EDTA, pH7.5).Add: 17 μl 30% (w/v) sarkosyl (final concentration of 1%) and 5 μl 10 mg/ml proteinase K (final concentration 100 μg/ml).Incubate at 37oC for 30-60 minutes, or until the solution clears.Add 400 μl 4 M NH4OAc and mix well.Extract 2X ......閱讀全文

    Chromosomal-DNA-Isolation

    Chromosomal DNA IsolationMETHOD:Grow cells in 2-5 ml broth to late log phase.Pellet 1-2 ml cells in microfuge.Resuspend cells in 400 μl TES (50 mM Tri

    Chromosomal-DNA-Extraction-from-Grampositive-Bacteria

    Chromosomal DNA Extraction from Gram-positive BacteriaThis procedure was originally developed for?Listeria monocytogenes?but has worked well with othe

    Cosmid-DNA-Isolation

    實驗概要Isolation of high yields of highly pure cosmid DNA using PureLink? HiPure Plasmid Purification Kits.實驗原理The ?PureLink? HiPure Plasmid Purification

    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

    DNA-isolation-extraction

    CTAB TECHNIQUE / Method / Schedule / Protocol FOR DNA ISOLATION / DNA EXTRACTION FROM PLANT LEAF / LEAVES SAMPLES (see also DNA RNA double isolation

    Insect-DNA-Isolation-Protocol

    實驗概要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

    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, decant

    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 modification of a

    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

    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 66506-5502The polymerase chain

    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

    細菌的核酸抽提

    DNA Extraction·?????????DNA Extraction from Bacteria?(Julie B. Wolf,UMBC)Phenol/chloroform method·?????????DNA Extraction From Bacteria (Triton Method

    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 min. in

    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

    Quick-and-Easy-Isolation-of-Genomic-DNA-from-Yeast

    ProcedureTransfer 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 microcentrif

    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

    Isolation-of-Genomic-DNA-from-Tissue-Using-ChargeSwitch?-Technology

    實驗概要?The ChargeSwitch? ?gDNA Mini and Micro Tissue Kits allow rapid and efficient purification ?of genomic DNA from mini (10-25 mg) or micro (3-5 mg)

    BAC-DNA分離方法-Isolation-of-BAC-DNA-from-Largescale-Cultures

    Isolation of BAC DNA from Large-scale CulturesJoseph SambrookPeter Maccallum Cancer Institute and The University of Melbourne, AustraliaDavid W. Russe

    Rapid-DNA-Isolation-from-Phyllanthus-Amarus-and-Other-Plant-Tissues

    Procedure Preheat Extraction Buffer at 60°C. Weigh 100 mg of fresh leaf tissue and grind it to powder in Liquid Nitrogen in a chilled mortar an

    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

    Mitochondrial-DNA-Isolation-from-Somatic-Embryogenic-Cell-Cultures-of-Larix

    Mitochondrial DNA is isolated by a modification of the methods described by Wilson and Chourey (1984) and Radetzky (1990).?Cell cultures at four days

    質粒的小量制備

    ·?????????Standard (alkaline lysis) Mini-Prep?(Goldberg Lab)Standard protocol for mini-prep and recipe for solution I, II and III.Alkaline Lysis Minip

    質粒的小量制備

    ·?????????Standard (alkaline lysis) Mini-Prep?(Goldberg Lab)Standard protocol for mini-prep and recipe for solution I, II and III.Alkaline Lysis Minip

    重組DNA的分離、克隆與測序實驗手冊8

    B. Midiprep double-stranded DNA isolationA midi-prep double-stranded DNA isolation has been developed to generate a sufficient amount of template DNA

    Isolation-of-colonic-epithelium

    實驗概要The ?method we use is based on work of Dr. Hazel Cheng, at the University of ?Toronto and works for both colon and the small intestine.First ?we e

    Poly(A)+RNA-Isolation

    Eukaryotic messenger RNA (mRNA) can be separated from the other RNA species in a total RNA preparation by affinity chromatography by virtue of the

    Isolation-of-papillary-cells

    Isolation of renal papillary cells1.?For isolation of papillary cells, kidneys were harvested and kept in HBSS containing 15 mM HEPES, penicillin/

    Isolation-of-liver-lymphocyte

    Isolation of liver lymphocyte???Several lymphocyte subpopulations reside in the normal adult human liver. Liver lymphocytes mainly include a large n

    mice-islet-isolation

    1.?Islets of Langerhans were isolated from 5- to 7-week-old nonobese diabetic (NOD) mice. 2.?Which involves cannulation of the common bile duct and

    Isolation-Of-PCR-Products

    實驗概要Rapid and efficient purification of PCR products from salts, primers, dNTPs, and other non-nucleic acid reagents.實驗原理The ChargeSwitch? TechnologyT

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