Molecular Cloning: A Laboratory Manual, Book 3 |
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Page 49
After the Tris base has been dissolved in deionized water , the pH of the solution
should be adjusted with HCl as described in Appendix B . If Tris · Cl or Trizma is
used to prepare buffers , the concentration of salt will be too high and ...
After the Tris base has been dissolved in deionized water , the pH of the solution
should be adjusted with HCl as described in Appendix B . If Tris · Cl or Trizma is
used to prepare buffers , the concentration of salt will be too high and ...
Page 2
32 Å rise per base pair minor groove Inclination of base normals to helical axis =
- 1 . 2° Propeller twist of base pair ( mean ) = + 16° Number of base pairs per
helical turn = - 10 — helix packing diameter 23 . 7 Å — FIGURE C . 1 The B form
of ...
32 Å rise per base pair minor groove Inclination of base normals to helical axis =
- 1 . 2° Propeller twist of base pair ( mean ) = + 16° Number of base pairs per
helical turn = - 10 — helix packing diameter 23 . 7 Å — FIGURE C . 1 The B form
of ...
Page 13
H TABLE C . 9 Nucleoside Analogs Used as Chain Terminators in DNA
Sequencing Structure 요 요 요 Base HOP _ O _ P _ OP _ O _ CH , OH OH OH KW
2 , 3 ' - Dideoxyribonucleoside Molecular 5 ' - triphosphates H H weight 2 ' , 3 ...
H TABLE C . 9 Nucleoside Analogs Used as Chain Terminators in DNA
Sequencing Structure 요 요 요 Base HOP _ O _ P _ OP _ O _ CH , OH OH OH KW
2 , 3 ' - Dideoxyribonucleoside Molecular 5 ' - triphosphates H H weight 2 ' , 3 ...
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LibraryThing Review
User Review - iayork - LibraryThingthe BIBLE of every biologist: So few and so much to say about this bible of Biology at the bench... You'll really find everything you want in it, including the composition of all the buffers and ... Read full review
Contents
BOOK | 3 |
Identification and Analysis of Recombinants 2 108 | 30 |
TRANSFECTION MEDIATED BY DEAEDEXTRAN 16 | 41 |
Copyright | |
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acetate activity added Adjust aliquots allow amount antibody antigen Appendix appropriate approximately aqueous assay bacterial bacteriophage base binding buffer carried cells centrifugation Chapter chromatography Cl pH cloned coli column complete concentration containing culture deionized water described desired detected dilution Dissolve EDTA efficiency electrophoresis enzyme et al ethanol expression extract Figure filter final fragment gene growth hybridization Incubate levels ligation mammalian cells medium method mg/ml microfuge tube minutes mixture mRNAs nucleic acid pellet phase phosphate Place plasmid plate polymerase precipitation prepared procedure Products promoter protein radioactive radiolabeled reaction remove restriction room temperature sample screen selection sequence sodium solution specific step sterile stored strain TABLE Telephone termini tion transcription transfection transfer transformation Tris ug/ml usually vectors volume wash western blotting ОН