Molecular Cloning: A Laboratory Manual, Book 3 |
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Page 68
Thus , using mammalian expression , genes and gene products can be identified
by ( 1 ) the appearance of a selectable or identifiable new phenotype in the cells ,
( 2 ) the production of a biologically active molecule that can be isolated and ...
Thus , using mammalian expression , genes and gene products can be identified
by ( 1 ) the appearance of a selectable or identifiable new phenotype in the cells ,
( 2 ) the production of a biologically active molecule that can be isolated and ...
Page 2
Corning Glass Works , Science Products Division , MP - 21 - 5 - 8 , Corning , NY
14831 , USA . Telephone 607 - 737 - 1667 . Fax 607 - 737 - 1636 . Curtin
Matheson Scientific Inc . , 9999 Veterans Memorial Drive , Houston , TX 77038 ,
USA .
Corning Glass Works , Science Products Division , MP - 21 - 5 - 8 , Corning , NY
14831 , USA . Telephone 607 - 737 - 1667 . Fax 607 - 737 - 1636 . Curtin
Matheson Scientific Inc . , 9999 Veterans Memorial Drive , Houston , TX 77038 ,
USA .
Page 4
A Laboratory Manual Joseph Sambrook, E. F. Fritsch, Tom Maniatis.
Biotechnology Systems Division , NEN Research Products , Postfach 40 12 40 ,
6072 Dreieich 4 , Federal Republic of Germany . Telephone ( 49 ) - ( 0 ) 6103 -
803 - 155 .
A Laboratory Manual Joseph Sambrook, E. F. Fritsch, Tom Maniatis.
Biotechnology Systems Division , NEN Research Products , Postfach 40 12 40 ,
6072 Dreieich 4 , Federal Republic of Germany . Telephone ( 49 ) - ( 0 ) 6103 -
803 - 155 .
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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