Molecular Cloning: A Laboratory Manual, Book 3 |
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Page 31
TABLE 18 . 1 Properties of Commonly Used Protease Inhibitors Effective Inhibitor
Active against Inactive against concentration - Stock solution Aprotinin kallikrein
papain 1 - 2 ug / ml 10 mg / ml in 0 . 01 M ( Trasylol ) trypsin HEPES ( pH 8 .
TABLE 18 . 1 Properties of Commonly Used Protease Inhibitors Effective Inhibitor
Active against Inactive against concentration - Stock solution Aprotinin kallikrein
papain 1 - 2 ug / ml 10 mg / ml in 0 . 01 M ( Trasylol ) trypsin HEPES ( pH 8 .
Page 32
1 % SDS 100 ug / ml phenylmethylsulfonyl fluoride ( PMSF ) 1 ug / ml aprotinin 1
% Nonidet P - 40 ( NP - 40 ) 0 . 5 % sodium deoxycholate Single - detergent lysis
buffer 50 mm Tris . Cl ( pH 8 . 0 ) 150 mm NaCl 0 . 02 % sodium azide 100 ug ...
1 % SDS 100 ug / ml phenylmethylsulfonyl fluoride ( PMSF ) 1 ug / ml aprotinin 1
% Nonidet P - 40 ( NP - 40 ) 0 . 5 % sodium deoxycholate Single - detergent lysis
buffer 50 mm Tris . Cl ( pH 8 . 0 ) 150 mm NaCl 0 . 02 % sodium azide 100 ug ...
Page 6
TABLE A . 1 Antibiotic Solutions Working concentration Stock solution stringent
relaxed concentration storage plasmids plasmids Ampicillin 50 mg / ml in H , O -
20°C 20 ug / ml 60 ug / ml Carbenicillin 50 mg / ml in H , O - 20°C 20 ug / ml 60
ug ...
TABLE A . 1 Antibiotic Solutions Working concentration Stock solution stringent
relaxed concentration storage plasmids plasmids Ampicillin 50 mg / ml in H , O -
20°C 20 ug / ml 60 ug / ml Carbenicillin 50 mg / ml in H , O - 20°C 20 ug / ml 60
ug ...
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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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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