Using Antibodies: A Laboratory Manual, Volume 286 |
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Page 4
... anti- gen . These types of methods have made antibodies one of the most useful reagents for studying molecules of interest . To produce specific antibodies , a selected antigen is injected into a laboratory ani- mal and serum samples ...
... anti- gen . These types of methods have made antibodies one of the most useful reagents for studying molecules of interest . To produce specific antibodies , a selected antigen is injected into a laboratory ani- mal and serum samples ...
Page 11
... anti- gen - binding domain . They do not contribute to the diversity of binding sites , but instead allow the replacement of one heavy - chain constant region with another . The rearrangement occurs downstream from the variable region ...
... anti- gen - binding domain . They do not contribute to the diversity of binding sites , but instead allow the replacement of one heavy - chain constant region with another . The rearrangement occurs downstream from the variable region ...
Page 14
... anti - idiotope . Nature 374 : 739-742 . Gally J.A. 1973. Structure of immunoglobu- lins . In The antigens ( ed . M. Sela ) , vol . 1 , pp . 162-298 . Academic Press , New York . Givol D. 1991. The minimal antigen - binding fragment of ...
... anti - idiotope . Nature 374 : 739-742 . Gally J.A. 1973. Structure of immunoglobu- lins . In The antigens ( ed . M. Sela ) , vol . 1 , pp . 162-298 . Academic Press , New York . Givol D. 1991. The minimal antigen - binding fragment of ...
Page 25
... anti- gens in close apposition to the antibody can be quite large , occupying as much as 500-750 Å2 and often involving contacts with multiple CDRs , and many times estab- lishing contact with all six . Although these studies have shown ...
... anti- gens in close apposition to the antibody can be quite large , occupying as much as 500-750 Å2 and often involving contacts with multiple CDRs , and many times estab- lishing contact with all six . Although these studies have shown ...
Page 26
... anti - phosphotyrosine antibodies , which specifically recognize the phosphorylated side chain of this amino acid in different local regions of many proteins . The ability of antibodies to recognize small epitopes in various structural ...
... anti - phosphotyrosine antibodies , which specifically recognize the phosphorylated side chain of this amino acid in different local regions of many proteins . The ability of antibodies to recognize small epitopes in various structural ...
Contents
43 | |
Immunostaining | 152 |
allows the partial | 222 |
Immunoblotting | 242 |
provides a reliable | 254 |
method to check | 268 |
purification takes | 312 |
Tagging Proteins | 345 |
Determining | 380 |
contains | 423 |
Protein Techniques | 430 |
covered in Appendix | 454 |
Other editions - View all
Using Antibodies: A Laboratory Manual, Volume 286 Edward Harlow,David Lane No preview available - 1999 |
Common terms and phrases
affinity allow amino acids anti antibody binding antibody solution antibody-antigen antigen Appendix ascites assay background problems beads biotin blot Caution cell staining chain chemical chloride column commercial commonly complex coverslips cross-reactions denatured detection methods detergents determine dilutions electrophoresis elution embryos enzyme epitopes fixation fixed fluorochromes gene hybridoma immune immunoaffinity purification immunoblotting immunoglobulin immunoprecipitation immunostaining Incubate interactions labeled antibody labeled secondary reagent lysate lysis buffer membrane methanol mg/ml microscope minutes at room molecular weight molecules monoclonal antibodies Needed solutions nitrocellulose nonspecific normally paraformaldehyde peptide polyclonal antibodies polypeptide preclearing primary antibody procedure protease protein antigens protein G protocols purified antibodies reaction recommend remove room temperature samples secondary antibodies sensitivity serum signal slides sodium azide specific antibody specimen step stored streptavidin structure substrate supernatant tein tibody tion tissue tissue-culture transfer Tris pH tube volume Wash Wear appropriate gloves µg/ml
Popular passages
Page 29 - Benjamin DC, Berzofsky JA, East IJ, Gurd, FRN, Hannum C., Leach SJ, Margoliash E., Michael JG, Miller A., Prager EM, Reichlin M., Sercarz EE, Smith-Gill SJ, Todd PE, and Wilson AC 1984. The antigenic structure of proteins: A reappraisal. Annu. Rev. Immunol. 2: 67-101.
Page 422 - Davis, BJ (1964) Disc electrophoresis — II. Method and application to human serum proteins.
Page 333 - K, Lys; L, Leu; M, Met; N, Asn; P, Pro; Q, Gin; R, Arg; S, Ser; T, Thr; V, Val; W, Trp; Y, Тут.
Page 10 - Segal, DM, Padlan, EA, Cohen, GH, Rudikoff, S., Potter, M., and Davies, D. R. (1974) The three-dimensional structure of a phosphorylcholine-binding mouse immunoglobulin Fab and the nature of the antigen binding site. Proc. Natl. Acad. Sci. USA 71, 4298^302.
Page 422 - Laskey, RA and Mills, AD (1975) Quantitative film detection of 3H and 14C in polyacrylamide gels by fluorography.
Page 422 - Bonner, WM, and Laskey, RA (1974) A film detection method for tritiumlabelled proteins and nucleic acids in polyacrylamide gels.
Page 30 - Amit AG, Mariuzza RA, Phillips SEV, and Poljak RJ 1986. Three-dimensional structure of an antigen-antibody complex at 2.8 A resolution.
Page 13 - Alt, FW/ Yancopoulos, GD/ Blackwell/ TK, Wood/ C./ Thomas/ E., Boss/ M./ Coffman/. R./ Rosenberg/ N., Tonegawa/ S. and Baltimore/ D.
Page 13 - Activity of multiple light 18 chain genes in murine myeloma cells producing a single, functional light chain. Cell 21: 1-12.