Molecular Cloning: A Laboratory Manual, Book 2 |
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Results 1-3 of 83
Page 8-57
Dilute an aliquot of the neutralized dNTP appropriately , and read the optical
density at the wavelengths given in the table ... Store in small aliquots at - 20°C .
Use strains C600 ( BNN93 ) for growth and BNN102 ( C600hflA ) for screening of
...
Dilute an aliquot of the neutralized dNTP appropriately , and read the optical
density at the wavelengths given in the table ... Store in small aliquots at - 20°C .
Use strains C600 ( BNN93 ) for growth and BNN102 ( C600hflA ) for screening of
...
Page 8-66
Remove two aliquots ( 2 ul each ) and place in small ( 0.5 - ml ) microfuge tubes .
Number these aliquots 1 and 2. Store at 0 ° C . It is important to use small
microfuge tubes to minimize evaporation of the sample during subsequent
incubation .
Remove two aliquots ( 2 ul each ) and place in small ( 0.5 - ml ) microfuge tubes .
Number these aliquots 1 and 2. Store at 0 ° C . It is important to use small
microfuge tubes to minimize evaporation of the sample during subsequent
incubation .
Page 15-65
In Falcon 2059 tubes , precooled to 0°C , combine 1 - and 5 - ul aliquots of the
undiluted reaction mixture and of each dilution of the reaction mixture with 200 -
ul aliquots of competent TG1 cells ( prepared as described in Chapter 1 , pages 1
.
In Falcon 2059 tubes , precooled to 0°C , combine 1 - and 5 - ul aliquots of the
undiluted reaction mixture and of each dilution of the reaction mixture with 200 -
ul aliquots of competent TG1 cells ( prepared as described in Chapter 1 , pages 1
.
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Contents
CONCENTRATING NUCLEIC ACIDS E | 8-10 |
SYNTHESIS OF THE FIRST STRAND OF DNA 8 | 8-11 |
MEASUREMENT OF RADIOACTIVITY IN NUCLEIC ACIDS E | 8-18 |
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Common terms and phrases
aliquots allow amount amplification antibody appropriate approximately bacteriophage bacteriophage T4 base binding buffer carried cDNA cells centrifugation Chapter chromatography cleaved clones colonies complete concentration constructed containing deletions denatured described detection determine digestion dNTPs double-stranded efficiency electrophoresis et al ethanol expression extraction Figure filters four fragment gene genomic DNA hybridization increase Incubate inserted interest isolated Klenow labeled length libraries ligation linear linkers membrane method minutes mixture molecules mRNA mutants nucleic acids nucleotides obtained oligonucleotide plaques plasmid DNA plate position possible precipitation prepared presence primer probe problem protein purified radioactivity radiolabeled reaction recombinant region remove restriction enzyme room temperature samples screening separate sequence single single-stranded solution step stored strand synthesis target DNA target sequence template termini transfer Tris tube units usually vector volume