Molecular Cloning: A Laboratory Manual, Book 3 |
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Page 38
Return the cells to the incubator for 48 hours before assaying for transient
expression of transfected genes ( step 6a , page 16 . 36 ) or replating the cells in
selective medium for isolation of stable transformants ( step 6b , page 16 . 36 ) .
Note If ...
Return the cells to the incubator for 48 hours before assaying for transient
expression of transfected genes ( step 6a , page 16 . 36 ) or replating the cells in
selective medium for isolation of stable transformants ( step 6b , page 16 . 36 ) .
Note If ...
Page 25
8 ) with BamHI and remove protruding termini with mung - bean nuclease or
nuclease S1 ( see step 8 , page 17 . 23 , or step 4 , page 17 . 19 , respectively ) .
PASI provides a bacteriophage , promoter , pu , and the ribosome - binding site of
the ...
8 ) with BamHI and remove protruding termini with mung - bean nuclease or
nuclease S1 ( see step 8 , page 17 . 23 , or step 4 , page 17 . 19 , respectively ) .
PASI provides a bacteriophage , promoter , pu , and the ribosome - binding site of
the ...
Page 32
23 , step 5a and b , and page 17 . 22 , step 3g - h ) . Cleave the vector at an
appropriate downstream site ( EcoRI , Smal , BamHI ) . 3 . Clone the fragment into
the vector , transform E . coli strain YK537 , and plate on LB medium containing ...
23 , step 5a and b , and page 17 . 22 , step 3g - h ) . Cleave the vector at an
appropriate downstream site ( EcoRI , Smal , BamHI ) . 3 . Clone the fragment into
the vector , transform E . coli strain YK537 , and plate on LB medium containing ...
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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