Molecular Cloning: A Laboratory Manual, Book 3 |
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Page xix
51 LABELING THE 3 ' TERMINI OF DOUBLE - STRANDED DNA USING THE
KLENOW FRAGMENT OF E . coli DNA POLYMERASE I 10 . 51 LABELING THE 3
' TERMINI OF DOUBLE - STRANDED DNA WITH BACTERIOPHAGE T4 DNA ...
51 LABELING THE 3 ' TERMINI OF DOUBLE - STRANDED DNA USING THE
KLENOW FRAGMENT OF E . coli DNA POLYMERASE I 10 . 51 LABELING THE 3
' TERMINI OF DOUBLE - STRANDED DNA WITH BACTERIOPHAGE T4 DNA ...
Page 1
Subcloning is a simple matter when the restriction sites at the termini of the target
fragment are identical to , or compatible with , those of the new vector . The target
fragment can then be ligated to the vector without enzymatic manipulation of ...
Subcloning is a simple matter when the restriction sites at the termini of the target
fragment are identical to , or compatible with , those of the new vector . The target
fragment can then be ligated to the vector without enzymatic manipulation of ...
Page 2
FILLING RECESSED 3 ' TERMINI Recessed 3 ' termini can be filled by the
polymerase activity of the Klenow fragment of E . coli DNA polymerase I in the
presence of the appropriate dNTPs . Which of the four dNTPs are added to the
reaction ...
FILLING RECESSED 3 ' TERMINI Recessed 3 ' termini can be filled by the
polymerase activity of the Klenow fragment of E . coli DNA polymerase I in the
presence of the appropriate dNTPs . Which of the four dNTPs are added to the
reaction ...
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Contents
BOOK | 3 |
Identification and Analysis of Recombinants 2 108 | 30 |
TRANSFECTION MEDIATED BY DEAEDEXTRAN 16 | 41 |
Copyright | |
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Common terms and phrases
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