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MeSH Review

Fluorescent Antibody Technique

 
 
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Disease relevance of Fluorescent Antibody Technique

 

Psychiatry related information on Fluorescent Antibody Technique

 

High impact information on Fluorescent Antibody Technique

 

Chemical compound and disease context of Fluorescent Antibody Technique

 

Biological context of Fluorescent Antibody Technique

 

Anatomical context of Fluorescent Antibody Technique

 

Associations of Fluorescent Antibody Technique with chemical compounds

  • Both acetone and formaldehyde fixation were used for the immunofluorescence tests [2].
  • To test this hypothesis, we determined the level of fetal hemoglobin in dead and living infants in three different laboratories by three methods: high-performance liquid chromatography, polyacrylamide-gel electrophoresis, and cell-based immunofluorescence assays for fetal hemoglobin-containing red cells (F cells) [27].
  • The sensitivity of the three stains in detecting P. carinii was 45 of 49 (92 percent) for immunofluorescence; 37 of 49 (76 percent) for Diff-Quik (a Giemsa-type stain); and 39 of 49 (80 percent) for toluidine blue O [28].
  • Tunicamycin had only a slight effect on the initial times and rates of CSP appearance on the cell surface; some apparent intracellular redistribution of CSP was detected by immunofluorescence [29].
  • Genes for the lamina lucida protein, kalinin/laminin 5, have been proposed as candidates for some forms of JEB, based on immunofluorescence analysis recognizing kalinin epitopes [30].
 

Gene context of Fluorescent Antibody Technique

  • Immunofluorescence localization studies using affinity-purified antibody directed against the YPT1 protein showed punctate staining of the cytoplasm of growing yeast cells and very intense staining of small buds, where membrane growth and secretion are most active [31].
  • We have cloned a gene encoding one of these proteins (NUP1) and have confirmed the localization of the NUP1 protein to the pore complex by immunofluorescence, using an epitope-tagged construct to differentiate it from other members of this family [32].
  • Immunofluorescence studies demonstrate that both LANP and ataxin-1 colocalize in nuclear matrix-associated subnuclear structures [33].
  • Coimmunoprecipitations and immunofluorescence studies revealed that GIT1 and huntingtin associate in mammalian cells under physiological conditions [34].
  • Immunofluorescence analysis revealed a myelomonocytoid immunophenotype (expression of CD13 and CD68, and lack of lymphoid markers) [35].
 

Analytical, diagnostic and therapeutic context of Fluorescent Antibody Technique

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