Molecular Cloning: A Laboratory Manual, Book 3 |
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Page 61
A number of different TLC plates and solvents can be used to separate acetylated
forms of chloramphenicol . ... Place the TLC plate in the chromatography
chamber , close the chamber , and allow the solvent front to move approximately
75 ...
A number of different TLC plates and solvents can be used to separate acetylated
forms of chloramphenicol . ... Place the TLC plate in the chromatography
chamber , close the chamber , and allow the solvent front to move approximately
75 ...
Page 22
Plan the experiment , and draw a key so that you will know what each well on the
plate contains . 2 . To each well of a PVC plate , add 50 ul of IgG solution ( 20 ug /
ml in 0 . 2 M NaHCO , ) . Cover the plate , and incubate it for 2 hours at room ...
Plan the experiment , and draw a key so that you will know what each well on the
plate contains . 2 . To each well of a PVC plate , add 50 ul of IgG solution ( 20 ug /
ml in 0 . 2 M NaHCO , ) . Cover the plate , and incubate it for 2 hours at room ...
Page 23
Cover the plate and incubate it for 20 minutes at room temperature in a
humidified atmosphere . The bovine serum albumin serves as a blocking agent
by binding to sites on the PVC plate that are not occupied by immunoglobulin
molecules .
Cover the plate and incubate it for 20 minutes at room temperature in a
humidified atmosphere . The bovine serum albumin serves as a blocking agent
by binding to sites on the PVC plate that are not occupied by immunoglobulin
molecules .
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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