Molecular Cloning: A Laboratory Manual, Book 3 |
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Page 51
In an Erlenmeyer flask , prepare the appropriate volume of solution containing
the desired concentration of acrylamide for the resolving gel , using the values
given in Table 18 . 3 on page 18 . 52 . Mix the components in the order shown .
In an Erlenmeyer flask , prepare the appropriate volume of solution containing
the desired concentration of acrylamide for the resolving gel , using the values
given in Table 18 . 3 on page 18 . 52 . Mix the components in the order shown .
Page 12
TABLE C . 8 Unusual Bases Molecular A weight Name Structure 1 0 - ) OD280
OD 200 OH Hypoxanthine 136 . 1 249 . 5 10 . 7 0 . 09 H . ОН ОН Xanthine 152 . 1
267 10 . 3 0 . 61 IZ H TABLE C . 9 Nucleoside Analogs Used as Chain.
TABLE C . 8 Unusual Bases Molecular A weight Name Structure 1 0 - ) OD280
OD 200 OH Hypoxanthine 136 . 1 249 . 5 10 . 7 0 . 09 H . ОН ОН Xanthine 152 . 1
267 10 . 3 0 . 61 IZ H TABLE C . 9 Nucleoside Analogs Used as Chain.
Page 25
Sensitivity of Different Autoradiographic Methods Table E . 3 shows the sensitivity
of different autoradiographic methods for the detection of radioisotopes . The
amounts of radioactivity shown in the table are those required to obtain a ...
Sensitivity of Different Autoradiographic Methods Table E . 3 shows the sensitivity
of different autoradiographic methods for the detection of radioisotopes . The
amounts of radioactivity shown in the table are those required to obtain a ...
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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