Identification of repertoires of surface antigens on leukemias using an antibody microarray
We have previously described a microarray of cluster of differentiation (CD) antibodies that enables concurrent determination of more than 60 CD antigens on leukocytes. This procedure does not require protein purification or labeling, or a secondary detection system. Whole cells are captured by a mi...
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Published in | Proteomics (Weinheim) Vol. 3; no. 11; pp. 2147 - 2154 |
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Main Authors | , , , , |
Format | Journal Article |
Language | English |
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Weinheim
WILEY-VCH Verlag
01.11.2003
WILEY‐VCH Verlag |
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Abstract | We have previously described a microarray of cluster of differentiation (CD) antibodies that enables concurrent determination of more than 60 CD antigens on leukocytes. This procedure does not require protein purification or labeling, or a secondary detection system. Whole cells are captured by a microarray of 10 nL antibody dots immobilized on a nitrocellulose film on a microscope slide. Distinct patterns of cell binding are observed for different leukemias or lymphomas. These haematological malignancies arise from precursor cells of T‐ or B‐lymphocytic, or myeloid lineages of hematopoiesis. The dot patterns obtained from patients are distinct from those of peripheral blood leukocytes from normal subjects. This microarray technology has recently undergone a number of refinements. The microarray now contains more CD antibodies, and a scanner for imaging dot patterns and software for data analysis provide an extensive immunophenotype sufficient for diagnosis of common leukemias. The technology is being evaluated for diagnosis of leukemias with parallel use of conventional diagnostic criteria. |
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AbstractList | We have previously described a microarray of cluster of differentiation (CD) antibodies that enables concurrent determination of more than 60 CD antigens on leukocytes. This procedure does not require protein purification or labeling, or a secondary detection system. Whole cells are captured by a microarray of 10 nL antibody dots immobilized on a nitrocellulose film on a microscope slide. Distinct patterns of cell binding are observed for different leukemias or lymphomas. These haematological malignancies arise from precursor cells of T- or B-lymphocytic, or myeloid lineages of hematopoiesis. The dot patterns obtained from patients are distinct from those of peripheral blood leukocytes from normal subjects. This microarray technology has recently undergone a number of refinements. The microarray now contains more CD antibodies, and a scanner for imaging dot patterns and software for data analysis provide an extensive immunophenotype sufficient for diagnosis of common leukemias. The technology is being evaluated for diagnosis of leukemias with parallel use of conventional diagnostic criteria. We have previously described a microarray of cluster of differentiation (CD) antibodies that enables concurrent determination of more than 60 CD antigens on leukocytes. This procedure does not require protein purification or labeling, or a secondary detection system. Whole cells are captured by a microarray of 10 nL antibody dots immobilized on a nitrocellulose film on a microscope slide. Distinct patterns of cell binding are observed for different leukemias or lymphomas. These haematological malignancies arise from precursor cells of T‐ or B‐lymphocytic, or myeloid lineages of hematopoiesis. The dot patterns obtained from patients are distinct from those of peripheral blood leukocytes from normal subjects. This microarray technology has recently undergone a number of refinements. The microarray now contains more CD antibodies, and a scanner for imaging dot patterns and software for data analysis provide an extensive immunophenotype sufficient for diagnosis of common leukemias. The technology is being evaluated for diagnosis of leukemias with parallel use of conventional diagnostic criteria. |
Author | Christopherson, Richard I. Barber, Nicole Belov, Larissa Mulligan, Stephen P. Huang, Pauline |
Author_xml | – sequence: 1 givenname: Larissa surname: Belov fullname: Belov, Larissa organization: School Molecular and Microbial Biosciences, University of Sydney, Sydney, NSW, Australia – sequence: 2 givenname: Pauline surname: Huang fullname: Huang, Pauline organization: School Molecular and Microbial Biosciences, University of Sydney, Sydney, NSW, Australia – sequence: 3 givenname: Nicole surname: Barber fullname: Barber, Nicole organization: School Molecular and Microbial Biosciences, University of Sydney, Sydney, NSW, Australia – sequence: 4 givenname: Stephen P. surname: Mulligan fullname: Mulligan, Stephen P. organization: School Molecular and Microbial Biosciences, University of Sydney, Sydney, NSW, Australia – sequence: 5 givenname: Richard I. surname: Christopherson fullname: Christopherson, Richard I. email: ric@mmb.usyd.edu.au organization: School Molecular and Microbial Biosciences, University of Sydney, Sydney, NSW, Australia |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/14595814$$D View this record in MEDLINE/PubMed |
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SubjectTerms | Antibodies - immunology Antibody antibody microarrays Antigens, Surface - immunology Antigens, Surface - metabolism Cluster of differentiation antigens Collodion - chemistry HL-60 Cells Humans Leukemia Leukemia - diagnosis Leukemia - drug therapy Leukemia - immunology Leukocytes - immunology Lymphoma Lymphoma - diagnosis Lymphoma - drug therapy Lymphoma - immunology Microarray Tretinoin - pharmacology |
Title | Identification of repertoires of surface antigens on leukemias using an antibody microarray |
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