author_facet Bakker, P. J. M.
Stap, J.
Tukker, C. J.
van Oven, C. H.
Veenhof, C. H. N.
Aten, J.
Bakker, P. J. M.
Stap, J.
Tukker, C. J.
van Oven, C. H.
Veenhof, C. H. N.
Aten, J.
author Bakker, P. J. M.
Stap, J.
Tukker, C. J.
van Oven, C. H.
Veenhof, C. H. N.
Aten, J.
spellingShingle Bakker, P. J. M.
Stap, J.
Tukker, C. J.
van Oven, C. H.
Veenhof, C. H. N.
Aten, J.
Cytometry
An indirect immunofluorescence double staining procedure for the simultaneous flow cytometric measurement of iodo‐ and chlorodeoxyuridine incorporated into DNA
Cell Biology
Endocrinology
Hematology
Biophysics
Pathology and Forensic Medicine
author_sort bakker, p. j. m.
spelling Bakker, P. J. M. Stap, J. Tukker, C. J. van Oven, C. H. Veenhof, C. H. N. Aten, J. 0196-4763 1097-0320 Wiley Cell Biology Endocrinology Hematology Biophysics Pathology and Forensic Medicine http://dx.doi.org/10.1002/cyto.990120412 <jats:title>Abstract</jats:title><jats:p>In this paper we describe an indirect fluorescence double staining procedure for the simultaneous detection of IdUrd and CldUrd in the same cell nucleus. Two commercially available antibodies were selected for this purpose. A rat antiBrdUrd monoclonal antibody from Seralab was found to bind specifically to CldUrd and BrdUrd. A mouse monoclonal anti‐BrdUrd antibody from Becton Dickinson used in a 1:2 dilution binds to all halogenated deoxyuridines but, when the cells were extensively washed with Tris buffer with a high salt concentration, almost no binding to CldUrd was observed. An immunofluorescence procedure was developed, based on these primary antibodies, raised in different species (rat and mouse), in combination with highly purified second antibodies: FITC conjugated goat antirat and Texas‐Red conjugated goat antimouse.</jats:p> An indirect immunofluorescence double staining procedure for the simultaneous flow cytometric measurement of iodo‐ and chlorodeoxyuridine incorporated into DNA Cytometry
doi_str_mv 10.1002/cyto.990120412
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imprint Wiley, 1991
imprint_str_mv Wiley, 1991
issn 0196-4763
1097-0320
issn_str_mv 0196-4763
1097-0320
language English
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match_str bakker1991anindirectimmunofluorescencedoublestainingprocedureforthesimultaneousflowcytometricmeasurementofiodoandchlorodeoxyuridineincorporatedintodna
publishDateSort 1991
publisher Wiley
recordtype ai
record_format ai
series Cytometry
source_id 49
title An indirect immunofluorescence double staining procedure for the simultaneous flow cytometric measurement of iodo‐ and chlorodeoxyuridine incorporated into DNA
title_unstemmed An indirect immunofluorescence double staining procedure for the simultaneous flow cytometric measurement of iodo‐ and chlorodeoxyuridine incorporated into DNA
title_full An indirect immunofluorescence double staining procedure for the simultaneous flow cytometric measurement of iodo‐ and chlorodeoxyuridine incorporated into DNA
title_fullStr An indirect immunofluorescence double staining procedure for the simultaneous flow cytometric measurement of iodo‐ and chlorodeoxyuridine incorporated into DNA
title_full_unstemmed An indirect immunofluorescence double staining procedure for the simultaneous flow cytometric measurement of iodo‐ and chlorodeoxyuridine incorporated into DNA
title_short An indirect immunofluorescence double staining procedure for the simultaneous flow cytometric measurement of iodo‐ and chlorodeoxyuridine incorporated into DNA
title_sort an indirect immunofluorescence double staining procedure for the simultaneous flow cytometric measurement of iodo‐ and chlorodeoxyuridine incorporated into dna
topic Cell Biology
Endocrinology
Hematology
Biophysics
Pathology and Forensic Medicine
url http://dx.doi.org/10.1002/cyto.990120412
publishDate 1991
physical 366-372
description <jats:title>Abstract</jats:title><jats:p>In this paper we describe an indirect fluorescence double staining procedure for the simultaneous detection of IdUrd and CldUrd in the same cell nucleus. Two commercially available antibodies were selected for this purpose. A rat antiBrdUrd monoclonal antibody from Seralab was found to bind specifically to CldUrd and BrdUrd. A mouse monoclonal anti‐BrdUrd antibody from Becton Dickinson used in a 1:2 dilution binds to all halogenated deoxyuridines but, when the cells were extensively washed with Tris buffer with a high salt concentration, almost no binding to CldUrd was observed. An immunofluorescence procedure was developed, based on these primary antibodies, raised in different species (rat and mouse), in combination with highly purified second antibodies: FITC conjugated goat antirat and Texas‐Red conjugated goat antimouse.</jats:p>
container_issue 4
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container_title Cytometry
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author Bakker, P. J. M., Stap, J., Tukker, C. J., van Oven, C. H., Veenhof, C. H. N., Aten, J.
author_facet Bakker, P. J. M., Stap, J., Tukker, C. J., van Oven, C. H., Veenhof, C. H. N., Aten, J., Bakker, P. J. M., Stap, J., Tukker, C. J., van Oven, C. H., Veenhof, C. H. N., Aten, J.
author_sort bakker, p. j. m.
container_issue 4
container_start_page 366
container_title Cytometry
container_volume 12
description <jats:title>Abstract</jats:title><jats:p>In this paper we describe an indirect fluorescence double staining procedure for the simultaneous detection of IdUrd and CldUrd in the same cell nucleus. Two commercially available antibodies were selected for this purpose. A rat antiBrdUrd monoclonal antibody from Seralab was found to bind specifically to CldUrd and BrdUrd. A mouse monoclonal anti‐BrdUrd antibody from Becton Dickinson used in a 1:2 dilution binds to all halogenated deoxyuridines but, when the cells were extensively washed with Tris buffer with a high salt concentration, almost no binding to CldUrd was observed. An immunofluorescence procedure was developed, based on these primary antibodies, raised in different species (rat and mouse), in combination with highly purified second antibodies: FITC conjugated goat antirat and Texas‐Red conjugated goat antimouse.</jats:p>
doi_str_mv 10.1002/cyto.990120412
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id ai-49-aHR0cDovL2R4LmRvaS5vcmcvMTAuMTAwMi9jeXRvLjk5MDEyMDQxMg
imprint Wiley, 1991
imprint_str_mv Wiley, 1991
institution DE-Brt1, DE-Zwi2, DE-D161, DE-Gla1, DE-Zi4, DE-15, DE-Pl11, DE-Rs1, DE-105, DE-14, DE-Ch1, DE-L229, DE-D275, DE-Bn3
issn 0196-4763, 1097-0320
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language English
last_indexed 2024-03-01T15:06:58.937Z
match_str bakker1991anindirectimmunofluorescencedoublestainingprocedureforthesimultaneousflowcytometricmeasurementofiodoandchlorodeoxyuridineincorporatedintodna
mega_collection Wiley (CrossRef)
physical 366-372
publishDate 1991
publishDateSort 1991
publisher Wiley
record_format ai
recordtype ai
series Cytometry
source_id 49
spelling Bakker, P. J. M. Stap, J. Tukker, C. J. van Oven, C. H. Veenhof, C. H. N. Aten, J. 0196-4763 1097-0320 Wiley Cell Biology Endocrinology Hematology Biophysics Pathology and Forensic Medicine http://dx.doi.org/10.1002/cyto.990120412 <jats:title>Abstract</jats:title><jats:p>In this paper we describe an indirect fluorescence double staining procedure for the simultaneous detection of IdUrd and CldUrd in the same cell nucleus. Two commercially available antibodies were selected for this purpose. A rat antiBrdUrd monoclonal antibody from Seralab was found to bind specifically to CldUrd and BrdUrd. A mouse monoclonal anti‐BrdUrd antibody from Becton Dickinson used in a 1:2 dilution binds to all halogenated deoxyuridines but, when the cells were extensively washed with Tris buffer with a high salt concentration, almost no binding to CldUrd was observed. An immunofluorescence procedure was developed, based on these primary antibodies, raised in different species (rat and mouse), in combination with highly purified second antibodies: FITC conjugated goat antirat and Texas‐Red conjugated goat antimouse.</jats:p> An indirect immunofluorescence double staining procedure for the simultaneous flow cytometric measurement of iodo‐ and chlorodeoxyuridine incorporated into DNA Cytometry
spellingShingle Bakker, P. J. M., Stap, J., Tukker, C. J., van Oven, C. H., Veenhof, C. H. N., Aten, J., Cytometry, An indirect immunofluorescence double staining procedure for the simultaneous flow cytometric measurement of iodo‐ and chlorodeoxyuridine incorporated into DNA, Cell Biology, Endocrinology, Hematology, Biophysics, Pathology and Forensic Medicine
title An indirect immunofluorescence double staining procedure for the simultaneous flow cytometric measurement of iodo‐ and chlorodeoxyuridine incorporated into DNA
title_full An indirect immunofluorescence double staining procedure for the simultaneous flow cytometric measurement of iodo‐ and chlorodeoxyuridine incorporated into DNA
title_fullStr An indirect immunofluorescence double staining procedure for the simultaneous flow cytometric measurement of iodo‐ and chlorodeoxyuridine incorporated into DNA
title_full_unstemmed An indirect immunofluorescence double staining procedure for the simultaneous flow cytometric measurement of iodo‐ and chlorodeoxyuridine incorporated into DNA
title_short An indirect immunofluorescence double staining procedure for the simultaneous flow cytometric measurement of iodo‐ and chlorodeoxyuridine incorporated into DNA
title_sort an indirect immunofluorescence double staining procedure for the simultaneous flow cytometric measurement of iodo‐ and chlorodeoxyuridine incorporated into dna
title_unstemmed An indirect immunofluorescence double staining procedure for the simultaneous flow cytometric measurement of iodo‐ and chlorodeoxyuridine incorporated into DNA
topic Cell Biology, Endocrinology, Hematology, Biophysics, Pathology and Forensic Medicine
url http://dx.doi.org/10.1002/cyto.990120412