Literature DB >> 54374

Conjugation methods in immunofluorescence.

R McKinney, L Thacker, G A Hebert.   

Abstract

We have described methods of labeling antibody preparations with FITC, TMRI, and RBI. The degree of labeling with FITC can be precisely controlled by using well-defined conjugation procedures and FITC of a known degree of purity. Our experience shows that relatively high F/P ratios of the order of 20 to 25 mug/mg are desirable for antibacterial conjugates. Many commercial preparations of rhodamine isothiocyanate are of very poor quality and are unsatisfactory for use in conjugate preparation. Therefore, one should analyze the rhodamine isothiocyanate product before preparing immune conjugates. Our experience indicates that very satisfactory conjugates of immune IgG or pure antibody can be prepared with TMRI of about 60% purity by using a dye-protein ratio of 20 mug/mg. The optimal dye-IgG ratio for labeling with RBI appears to be about two times that for labeling with TMRI because of the lower specific absorbance and fluorescence emission of RBI. Rhodamine conjugates may be preferred to FITC conjugates in certain situations where tissue autofluorescence interferes with the observation of the yellow-green emission of FITC. Furthermore, mixed rhodamine and FITC conjugates of different specificity can be used to great advantage in double-staining techniques that allow simultaneous screening for two antigenically different organisms on a single microscope slide.

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Year:  1976        PMID: 54374     DOI: 10.1177/002203457605500117011

Source DB:  PubMed          Journal:  J Dent Res        ISSN: 0022-0345            Impact factor:   6.116


  8 in total

1.  Effector CD8 T cells possess suppressor function after 4-1BB and Toll-like receptor triggering.

Authors:  Lara Myers; Chikara Takahashi; Robert S Mittler; Robert J Rossi; Anthony T Vella
Journal:  Proc Natl Acad Sci U S A       Date:  2003-04-14       Impact factor: 11.205

2.  Low-resolution structure and fluorescence anisotropy analysis of protein tyrosine phosphatase eta catalytic domain.

Authors:  Huita C Matozo; Maria A M Santos; Mario de Oliveira Neto; Lucas Bleicher; Luís Mauricio T R Lima; Rodolfo Iuliano; Alfredo Fusco; Igor Polikarpov
Journal:  Biophys J       Date:  2007-03-30       Impact factor: 4.033

3.  Detection of Legionnaires disease bacteria by direct immunofluorescent staining.

Authors:  W B Cherry; B Pittman; P P Harris; G A Hebert; B M Thomason; L Thacker; R E Weaver
Journal:  J Clin Microbiol       Date:  1978-09       Impact factor: 5.948

4.  Fluorescent treponemal antibody-absorption double-staining procedure.

Authors:  E F Hunter; B J Pender; E J Kennedy; D E Pettit; C M Schubert; J C Feeley; S A Larsen; B E McGrew
Journal:  J Clin Microbiol       Date:  1981-08       Impact factor: 5.948

5.  Demonstration of Actinomyces and Arachnia species in cervicovaginal smears by direct staining with species-specific fluorescent-antibody conjugate.

Authors:  L Pine; G B Malcolm; E M Curtis; J M Brown
Journal:  J Clin Microbiol       Date:  1981-01       Impact factor: 5.948

6.  Specific immunofluorescent staining of pathogenic treponemes with a monoclonal antibody.

Authors:  F Ito; E F Hunter; R W George; V Pope; S A Larsen
Journal:  J Clin Microbiol       Date:  1992-04       Impact factor: 5.948

7.  Double-staining procedure for the fluorescent treponemal antibody absorption (FTA-ABS) test.

Authors:  E F Hunter; R M McKinney; S E Maddison; D D Cruce
Journal:  Br J Vener Dis       Date:  1979-04

8.  Rapid method for identification and enumeration of oral Actinomyces.

Authors:  P T Marucha; P H Keyes; C L Wittenberger; J London
Journal:  Infect Immun       Date:  1978-09       Impact factor: 3.441

  8 in total

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