Molecular Cloning: A Laboratory Manual, Book 3 |
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Page 4
In some cases , it is possible to improve the response to such antigens by
physically coupling them to a carrier protein ... PHYSICAL STATE OF THE
ANTIGEN Aggregated protein is a much better immunogen than soluble ,
dispersed protein .
In some cases , it is possible to improve the response to such antigens by
physically coupling them to a carrier protein ... PHYSICAL STATE OF THE
ANTIGEN Aggregated protein is a much better immunogen than soluble ,
dispersed protein .
Page 5
The first of these booster injections should be given when the primary response
is past its peak ( about 4 - 6 weeks after the primary injection of antigen in the
case of rabbits ) . About 7 - 10 days after the first booster injection , test bleeds ...
The first of these booster injections should be given when the primary response
is past its peak ( about 4 - 6 weeks after the primary injection of antigen in the
case of rabbits ) . About 7 - 10 days after the first booster injection , test bleeds ...
Page 16
Purification of Immunospecific Antibodies Antibodies may be purified by
adsorption to , and elution from , their cognate antigen . In some cases ( e . g . ,
when the antigen is a protein ) , the antigen may be coupled to a matrix such as
cyanogen ...
Purification of Immunospecific Antibodies Antibodies may be purified by
adsorption to , and elution from , their cognate antigen . In some cases ( e . g . ,
when the antigen is a protein ) , the antigen may be coupled to a matrix such as
cyanogen ...
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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