Molecular cloning: a laboratory manual, Volume 2 |
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Results 1-5 of 20
Page 8-6
... reaction mixture drops by more than a full unit , producing a buffer whose pH is ~ 7.2 . • Monovalent cations . Standard PCR buffer contains 50 mM KCl and works well for amplifica- tion of segments of DNA > 500 bp in length . Raising ...
... reaction mixture drops by more than a full unit , producing a buffer whose pH is ~ 7.2 . • Monovalent cations . Standard PCR buffer contains 50 mM KCl and works well for amplifica- tion of segments of DNA > 500 bp in length . Raising ...
Page 8-7
... reaction mixture . For example , cock- tails of Tbr and Taq , sold under the trade name DyNAzyme ( MJ Research Inc. ) exhibit high fideli- ty because of the proofreading function of Tbr and the high efficiency that is characteristic of ...
... reaction mixture . For example , cock- tails of Tbr and Taq , sold under the trade name DyNAzyme ( MJ Research Inc. ) exhibit high fideli- ty because of the proofreading function of Tbr and the high efficiency that is characteristic of ...
Page 8-21
... reaction mixture during PCR . Paraffin wax not only prevents evapora- tion , but also maintains separation between components ( e.g. , primer and template ) until the reaction mixture is heated . This separation prevents nonspecific ...
... reaction mixture during PCR . Paraffin wax not only prevents evapora- tion , but also maintains separation between components ( e.g. , primer and template ) until the reaction mixture is heated . This separation prevents nonspecific ...
Page 8-22
... reaction mixtures with 1 drop ( ~ 50 μl ) of light mineral oil to prevent ... mixture and the four control reactions and analyze them by electrophoresis ... reaction should yield a readily visible DNA fragment of the expected size . The ...
... reaction mixtures with 1 drop ( ~ 50 μl ) of light mineral oil to prevent ... mixture and the four control reactions and analyze them by electrophoresis ... reaction should yield a readily visible DNA fragment of the expected size . The ...
Page 8-23
... reaction mixture Use the minimum possible temperature during the annealing step . Consider adding adjuvants such as BSA ( 0.2-0.6 mg / ml ) , DMSO ( 5 % ) , or glycerol ( 5 % ) to the reaction mixture . Repurify the template DNA by ...
... reaction mixture Use the minimum possible temperature during the annealing step . Consider adding adjuvants such as BSA ( 0.2-0.6 mg / ml ) , DMSO ( 5 % ) , or glycerol ( 5 % ) to the reaction mixture . Repurify the template DNA by ...
Contents
8-6 | |
8-17 | |
8-23 | |
Analysis of Interacting Proteins with Surface Plasmon Resonance Spectroscopy 18 | 8-96 |
INFORMATION PANELS | 8-107 |
INFORMATION PANELS | 8-109 |
Chapter 9 | 8-120 |
Preparation of Radiolabeled DNA and RNA Probes 9 1 | 8-128 |
Exon Trapping and Amplification 11 80 | 11-80 |
INFORMATION PANELS | 11-98 |
Chain Reaction | 11-125 |
Chapter 1 | 12-1 |
Chapter 4 | 12-4 |
Chapter 12 | 12-12 |
Chapter 16 | 12-16 |
INTRODUCTION | 12-32 |
Chapter 15 | 9-15 |
Chapter 18 | 9-18 |
INTRODUCTION | 9-25 |
PROTOCOLS | 9-33 |
INFORMATION PANELS | 9-76 |
1 | 10-1 |
Chapter 10 | 10-10 |
Volume 1 | 10-11 |
Volume 2 | 10-16 |
INFORMATION PANELS | 10-43 |
Chapter 3 | 11-3 |
Chapter 5 | 11-5 |
Chapter 11 | 11-7 |
Chapter 8 | 11-8 |
PROTOCOLS | 11-13 |
INFORMATION PANELS | 12-94 |
1 | 12-115 |
Chapter 13 | 13-13 |
INFORMATION PANELS | 13-63 |
Purification of Closed Circular DNA by Equilibrium Centrifugation in CsClEthidium 1 69 | 13-69 |
INFORMATION PANELS | 14-1 |
Chapter 2 | 14-2 |
Chapter 14 | 14-3 |
INFORMATION PANELS | 14-9 |
INFORMATION PANELS | 7 |
1 | 1-1 |
Chapter 7 | 1-7 |
Eukaryotic Cells | 1-17 |
Other editions - View all
Molecular Cloning: Selected Applications in Medicine and Biology Gregory G. Brown Limited preview - 2011 |
Common terms and phrases
Acad agarose gel aliquots amplified DNA annealing Appendix bacteriophage M13 bands base Biol BioTechniques catalyzed cDNA clones cDNA libraries cells centrifuge Chapter cleavage concentration containing cycle ddNTP denatured detection digestion DNA fragments DNA sequencing DNA templates dNTPs double-stranded DNA efficiency Escherichia coli ethanol exonuclease gel electrophoresis gene H₂O hybridization information panel Klenow fragment labeled ligation method microfuge tube microtiter plate minutes molecules mRNA mutations Natl Nucleic Acids Nucleic Acids Res nucleotides oligonucleotide oligonucleotide primers PCR products phagemid plaques plasmid plasmid DNA pmoles polyacrylamide gel polymerase chain reaction polymerization polynucleotide kinase preparation probes protein Protocol purified radioactivity radiolabeled reaction mixture reagents listed recombinant requires the reagents residues restriction enzyme reverse transcriptase RNase room temperature samples screening Sequenase sequencing gel sequencing reactions single-stranded DNA Step strand synthesis target DNA template DNA termini thermal cycler thermostable DNA polymerase tion transcription vector vitro wild-type µg/ml
Popular passages
Page 9-91 - Melton, DA, Krieg, PA, Rebagliati, MR, Maniatis, T., Zinn, K., and Green, MR (1984) Efficient in vitro synthesis of biologically active RNA and RNA hybridization probes from plasmids containing a bacteriophage SP6 promoter. Nucleic Acids Res. 12, 7035-7056.
Page 14-37 - Towbin, H., Staehelin, T., and Gordon, J. (1979) Electrophoretic transfer of proteins from polyacrylamide gels to nitrocellulose sheets: procedure and some applications.
Page 9-88 - Eldeiry, WS, Tokino, T., Velculescu. VE, Levy, DB, Parsons. R., Trent, JM, Lin, D., Mercer, WE, Kinzler, KW, and Vogelstein, B.
Page 9-92 - Labeling deoxyribonucleic acid to high specific activity in vitro by nick translation with DNA polymerase.
Page 9-87 - Campbell, AP, Chenchik, A., Moqadam, F., Huang, B., Lukyanov, S., Lukyanov, K., Gurskaya, N., Sverdlov, ED, and Siebert, PD (1996).
Page 8-120 - Gilliland. G., Perrin. S., Blanchard. K., and Bunn, HF (1990) Analysis of cytokine mRNA and DNA detection and quantitation by competitive polymerase chain reaction.
Page 8-120 - Frohman, MA, Dush, MK, and Martin, GR (1988) Rapid production of full-length cDNAs from rare transcripts: amplification using a single gene-specific oligonucleotide primer. Proc. Natl. Acad. Sci. USA 85, 8998-9002. 2. Edwards, JBDM, Delort, J., and Mallet, J. (1991) Oligodeoxyribonucleotide ligation to single-stranded cDNAs: A new tool for cloning 5' ends of mRNAs and for constructing cDNA libraries by in vitro amplification.
Page 9-87 - DV, Angerer, LM, and Angerer, RC (1984) Detection of mRNAs in sea urchin embryos by in situ hybridization using asymmetric RNA probes. Dev. Biol. 101, 485-502.
Page 12-103 - Birnboim, HC and Doly, J. (1979) A rapid alkaline extraction procedure for screening recombinant plasmid DNA.
Page 9-88 - A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity.