Download Recombinant DNA Part F by Kaplan N.P. (ed.), Colowick N.P. (ed.), Wu R. (ed.) PDF

By Kaplan N.P. (ed.), Colowick N.P. (ed.), Wu R. (ed.)

The looks of one other quantity in that very good sequence, tools in Enzymology, is often a reason for appreciation when you desire to effectively perform a specific process or organize an enzyme or metabolic intermediate with no the tiresome prospect of looking through surprising literature and maybe opting for an unproven approach which isn't simply reproduced.

Show description

Read Online or Download Recombinant DNA Part F PDF

Best biology books

Bioscience Entrepreneurship In Asia: Creating Value with Biology

It is a well-researched booklet that may entice either teachers and entrepeneurs. Dr. Teng is a widely known professional during this box and provides a powerful point of view. I hugely suggest the booklet.

Biology of the Antarctic Seas VI

In regards to the ProductPublished through the yankee Geophysical Union as a part of the Antarctic examine sequence. Species within the genera Hyarachna, Echinozone, Pseudarachna, and Aspidarachna, all within the kin Hyarachnidae, are reviewed and severely mentioned. A key to genera is gifted besides a desk of the species in every one genus from antarctic waters.

Molecular Biology of RNA Tumor Viruses

Molecular Biology of RNA Tumor Viruses summary: Molecular Biology of RNA Tumor Viruses

Additional resources for Recombinant DNA Part F

Example text

L. Hamilton, Nucleic Acids Res. 13, 2827 (1985). 13 I. Nur, M. Szyf, A. Razin, G. Glaser, S. Rottem, and S. Razin, J. Bacteriol. 164, 19 (1985). 14 D. B. Willis, R. Goorha, and A, Granoff, J. Virol. 49, 86 (1984). METHODS IN ENZYMOLOGY, VOL. 155 Copyright © 1987 by Academic Press, Inc. All rights of reproduction in any form reserved. 19 Purification procedures for several Type II modification methylases have been published. 2°-35 In general, purifications have been based upon DNA protection assays: specific DNA methylases are detected in those chromatographic fractions which protect bacteriophage DNA from cleavage by a particular restriction endonuclease.

MbolI using this substrate. In this case, M. TaqI recognition sequence (TCGA) is formed upon 36 M. B, Mann, in "Gene Amplification and Analysis" (J. G. ), Vol. II, pp. 229-237. Elsevier/North-Holland, New York, 1981. 37 A. H. Bolden, C. N. Nalin, C. A. Ward, M. S. Poonian, W. W. McComans, and A. Weissbach, Nucleic Acids Res. 13, 3479 (1985). 3s A. Quint and H. Cedar, Nucleic Acids Res. 9, 633 (1981). 39 M. McClelland and M. Nelson, unpublished observations. 36 RESTRICTION ENZYMES [5] ligation of the oligonucleotide.

82, 2674 (1985). ii R. -H. -Y. Zhang, and M. Ehrlich, Nucleic Acids Res. 14, 1599 (1986). 12 R. H. Grafstrom, R. Yuan, and D. L. Hamilton, Nucleic Acids Res. 13, 2827 (1985). 13 I. Nur, M. Szyf, A. Razin, G. Glaser, S. Rottem, and S. Razin, J. Bacteriol. 164, 19 (1985). 14 D. B. Willis, R. Goorha, and A, Granoff, J. Virol. 49, 86 (1984). METHODS IN ENZYMOLOGY, VOL. 155 Copyright © 1987 by Academic Press, Inc. All rights of reproduction in any form reserved. 19 Purification procedures for several Type II modification methylases have been published.

Download PDF sample

Rated 4.87 of 5 – based on 28 votes