C.D. O'Connor, J.N.B. Walker, and J.R. Saunders, RsrII: A Restriction Endonuclease with a Heptanucleotide Recognition Sequence. B.-Q. Qiang and I. Schildkraut, NotI and SfiI: Restricton Endonucleases with Octanucleotide Recognition Sequences. M. McClelland, Site-Specific Cleavage of DNA at 8-, 9-, and 10-bp Sequences. M. Nelson and M. McClelland, Purification and Assay of Type II DNA Methylases. M. Nelson and I. Schildkraut, The Use of DNA Methylases to Alter the Apparent Recognition Specificities of Restriction Endonucleases. Rapid Methods for DNA Sequence Analysis. A.T. Bankier, K.M. Weston, and B.G. Barrell, Random Cloning and Sequencing by the M13/Dideoxynucleotide Chain Termination Method. G.-F. Hong, The Use of DNase I, Buffer Gradient Gel, and 35S Label for DNA Sequencing. L. Dente and R. Cortese, pEMBL: A New Family of Single-Stranded Plasmids for Sequencing DNA. T.K. Misra, DNA Sequencing: A New Strategy to Create Ordered Deletions, Modified M13 Vector, and Improved Reaction Conditions for Sequencing by Dideoxy Chain Termination Method. R. Zagursky and K. Baumeister, Construction and Use of pBR322 Plasmids That Yield Single-Stranded DNA for Sequencing. S. Henikoff, Unidirectional Digestion with Exonuclease III in DNA Sequence Analysis. S. Labeit, H. Lehrach, and R.S. Goody, DNA Sequencing Using ga-Thiodeoxynucleotides. A. Ahmed, Use of Transposon-Promoted Deletions in DNA Sequence Analysis. R.M.K. Dale and A. Arrow, A Rapid Single-Stranded Cloning, Sequencing, Insertion, and Deletion Strategy. Z.-g. Peng and R. Wu, A New and Simple Rapid Method for Sequencing DNA. G. Volckaert, A Systematic Approach to Chemical DNA Sequencing by Subcloning in pGV451 and Derived Vectors. F.M. Pohl and S. Beck, Direct Transfer Electrophoresis Used for DNA Sequencing. L.M. Smith, R.J. Kaiser, J.Z. Sanders, and L.E. Hood, The Synthesis and Use of Fluorescent Oligonucleotides in DNA Sequence Analysis. A. Rosenthal, R. Jung, and H.-D. Hunger, Solid-Phase Methods for Sequencing of Oligodeoxynucleotides and DNA. Miscellaneous Methods. K.B. Mullis and F.A. Faloona, Specific Synthesis of DNA in Vitro via a Polymerase-Catalyzed Chain Reaction. D. Koshland and P. Hieter, Visual Assay for Chromosome Ploidy. S. Nishimura, N. Shindo-Okada, and P.F. Crain, Isolation of Amino Acid-Specific tRNA by High-Performance Liquid Chromatography. Y. Kuchino, N. Hanyu, and S. Nishimura, Analysis of Modified Nucleosides and Nucleotide Sequence of tRNA. P.A. Krieg and D.A. Melton, In Vitro RNA Synthesis with SP6 RNA Polymerase. H. Bujard, R. Gentz, M. Lanzer, D. Stueber, M. Mueller, I. Ibrahimi, M.-T. Haeuptle, and B. Dobberstein, A T5 Promoter-Based Transcriptionb1Translation System for the Analysis of Proteins in Vitro and in Vivo. G.L. Igloi and H. K"ssel, Use of Boronate-Containing Gels for Electrophoretic Analysis of Both Ends of RNA Molecules. C.L. Smith and C.R. Cantor, Purification, Specific Fragmentation, and Separation of Large DNA Molecules. G.F. Carle and M.V. Olson, Orthogonal-Field-Alternation Gel Electrophoresis. L.S. Lerman and K. Silverstein, Computational Simulation of DNA Melting and Its Application to Denaturing Gradient Gel Electrophoresis. R.M. Myers, T. Maniatis, and L.S. Lerman, Detection and Localization of Single Base Changes by Denaturing Gradient Gel Electrophoresis. J. Berman, S. Eisenberg, and B.-K. Tye, An Agarose Gel Electrophoresis Assay for the Detection of DNA-Binding Activities in Yeast Cell Extracts. T.D. Tullius, B.A. Dombroski, M.E.A. Churchill, and L. Kam, Hydroxyl Radical Footprinting: A High-Resolution Method for Mapping Protein*b1DNA Contacts. D.E. Hill, A.R. Oliphant, and K. Struhl, Mutagenesis with Degenerate Oligonucleotides: An Efficient Method for Saturating a Defined DNA Region with Base Pair Substitutions. A.R. Oliphant and K. Struhl, The Use of Random-Sequence Oligonucleotides for Determining Consensus Sequences. F.I. Lewitter and W.P. Rindone, Computer Programs for Analyzing DNA and Protein Sequences. Author Index. Subject Index.
The critically acclaimed laboratory standard, Methods in Enzymology, is one of the most highly respected publications in the field of biochemistry. Since 1955, each volume has been eagerly awaited, frequently consulted, and praised by researchers and reviewers alike. The series contains much material still relevant today - truly an essential publication for researchers in all fields of life sciences.
Biochemists, geneticists, microbiologists, genetic engineers, analytical chemists, clinical chemists, molecular biologists, industrial researchers working on protein products, plant scientists involved in plant breeding and plant pathology.
- No. of pages:
- © Academic Press 1987
- 9th December 1987
- Academic Press
- eBook ISBN:
@from:Praise for the Series @qu:"The Methods in Enzymology series represents the gold-standard." @source:--NEUROSCIENCE @qu:"Incomparably useful." @source:--ANALYTICAL BIOCHEMISTRY @qu:"It is a true 'methods' series, including almost every detail from basic theory to sources of equipment and reagents, with timely documentation provided on each page." @source:--BIO/TECHNOLOGY @qu:"The series has been following the growing, changing and creation of new areas of science. It should be on the shelves of all libraries in the world as a whole collection." @source:--CHEMISTRY IN INDUSTRY @qu:"The appearance of another volume in that excellent series, Methods in Enzymology, is always a cause for appreciation for those who wish to successfully carry out a particular technique or prepare an enzyme or metabolic intermediate without the tiresome prospect of searching through unfamiliar literature and perhaps selecting an unproven method which is not easily reproduced." @source:--AMERICAN SOCIETY OF MICROBIOLOGY NEWS @qu:"If we had some way to find the work most often consulted in the laboratory, it could well be the multi-volume series Methods in Enzymology...a great work." @source:--ENZYMOLOGIA @qu:"A series that has established itself as a definitive reference for biochemists." @source:--JOURNAL OF CHROMATOGRAPHY
California Institute of Technology, Division of Biology, Pasadena, U.S.A.
The Salk Institute, La Jolla, CA, USA
Division of Biological Sciences, Cornell University, Ithaca, New York, U.S.A.
Elsevier.com visitor survey
We are always looking for ways to improve customer experience on Elsevier.com.
We would like to ask you for a moment of your time to fill in a short questionnaire, at the end of your visit.
If you decide to participate, a new browser tab will open so you can complete the survey after you have completed your visit to this website.
Thanks in advance for your time.