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  • AMethodforMicroScaleIsolationandPurificationofGangliosides

    A Method for Micro-Scale Isolation and Purification of GangliosidesStephan Ladisch~Director, Center for Cancer and Transplant Biology, Children's National Medical Center, Washington, D.C. 22010 This solvent partition method permits the isolation of gangliosides from small samples and from samples in which the ganglioside concentration is low, especially relative to the concentration of potentially contaminat......閱讀全文

    Protein-A-Purification-of-Antibody

    1. Reagents(1) Affi-gel Protein-A Agarose (BioRad #153-6153)(2) MAPS II Binding Buffer (BioRad # 153-6161)(3) 0.314 g/ml diH2O(4) MAPS II Elution Buff

    Protein-purification;-actin

    Protein purification; actin ? ? ?Overview?? ACTINThe most abundant muscle and non-muscle cytoskeletal protein. MW 42 kDa, 374/375 amino acids; various

    DNA電泳

    DNA電泳(主要內容如下)??Preparation of Agarose Gel and Electrophoresis??Extraction of DNA From Agarose Gel??Extraction of DNA from Acrylamide Gels??DNA Marker?

    Method:-Lymphocyte-Transformation

    Method: Lymphocyte TransformationMay 30, 1990Rosalie VeilePrinciple:Lymphocytes are transformed to establish cell lines. Mononuclear cells (lymphocyte

    其它PCR方法

    ·?????????Standard PCR Protocol?(Molecular Biology Techniques Manual)The followings are described in detailRecommended Reagent ConcentrationsRecommend

    Column-Purification-of-Demethylated-Sphingomyelin

    Packing column:1) To 20 g of 100-200 mesh Bio-Sil A silica gel add 80 mls of chloroform.2) Place a small portion of glass wool at the base of the colu

    Purification-of-GST-Fused-Proteins

    Day 1Set up an overnight culture in 100 ml LMM broth or 100 ml terrific broth containing 100ul 100 mg/mlAmpDay 2Add 40-50 ml o/n culture to 1 lt terri

    Protein-Expression-and-Purification-Protocol

    Step 1:?Transform?appropriate DNA plasmid into BL21(DE3)?E. coli?cells. These cells must be competent. (Protocol for how to make competent cells.)a) T

    Protein-G-Purification-of-Antibodies

    1. Reagent and Materials(1) Hi-Trap Protein G Column (Pharmacia Biotech #17-0404-01)(2) 20 mM Sodium Phosphate Buffer, pH 7.01.084 g NaH2PO4, anhydrou

    Isolation-of-bone-marrow

    (contributed by Chris Jackson (chris.jackson@bris.ac.uk))A protocol I have used to isolate rat bone marrow is:?1. Kill the rat and dissect out the fem

    Methods-for-the-Measurement-of-a-Bacterial-Enzyme-Activity-in-Cell-Lysates4

    The use of a micro-titre based colorimetric assay provided a third method for the study of ACTase activity, and the most useful for large scale measur

    A-quick-method-to-isolate-plant

    Use from 0.01 - 0.1 gram plant material. Grind the plant material with liq.N2 in a mortar.We normally use some alumina to crush hard tissue.

    A-Method-for-Structure1

    A Method for Structure–Activity Analysis of Quorum-Sensing Signaling Peptides from Naturally Transformable StreptococciMany species of streptococci se

    A-Method-for-Structure2

    CD SpectroscopyCD spectra for peptides and reference solutions were recorded at 298?K on a Jasco J-920 CD spectrometer with a 1-mm quartz cuvette. Spe

    A-Method-for-Structure3

    CSP-Dependent Transformation AssayTo determine if synthetic peptides activated quorum sensing for induction of genetic competence, we used the?comC?de

    A-Method-for-Structure4

    We also used this mutant (SMdC) as a host to generate two types of?lacZ?transcriptional reporter fusion strains to assay the promoter activity of QS-c

    A-Method-for-Structure5

    ConclusionsQuorum-sensing signaling systems involving the interaction between a signaling peptide and its cognate histidine kinase receptor are widely

    Easy-YAC-Preparation-Method

    YAC TRANSFORMATION OF C. ELEGANS USING TOTAL YEAST GENOMIC DNA[This method is described in The Worm Breeder's Gazette (1997) A. Davies and J. Shaw

    Isolation-of-Functional-Photosystem-II-Core-Particles-From-the-Cyanoba...

    This chapter contains the description of several methods used for the isolation of functional photosystem (PS)II core particles from wild-type (wt

    ELISA

    Gangliosides ELISA protocol?(Contributed by?pingsunjim)This protocol can be used for detection of gangliosides.Specific antibodies to gangliosides are

    E.Z.N.A.?-Total-RNA-Midi-Kit-Protocol-DNase-I-digestion-Protocol

    實驗概要E.Z.N.A.? ?Total RNA Midiprep Kit provides a rapid and easy method for the ?isolation of up to 600 ug of total RNA from cultured eukaryotic cells,

    Purification-of-human-mononuclear-cells-and-neutrophils

    PurposeMaterials10ml 6% dextran + 7ml citrate/citric acidDextran: T500 --> 6g+100ml PBSCitrate solution: 25g Na Citrate + 8g citric acid + 500 ml PBS4

    DNA-Purification-from-Agarose-Gels

    1. Separate DNA fragments in an agarose gel cast with 0.5 mg/mL Ethidium bromide. Locate bands with a hand-held long-wave UV lamp.2. Slice the gel wit

    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

    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

    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

    Isolation-of-Zebrafish-embryos

    Zebrafish will mate and deposit fertilized eggs on the bottom of the tank at 'dawn'. They can be accustomed to lay at any convenient time by k

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