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Profiling CD antigens on leukaemias with an antibody microarray
Authors:Nicole Barber  Swetlana Gez  Stephen P Mulligan  Adrian Woolfson
Institution:a School of Molecular and Microbial Biosciences, University of Sydney, Sydney, NSW 2006, Australia
b Department of Haematology, Royal North Shore Hospital, St. Leonards, NSW 2065, Australia
c University of Cambridge School of Clinical Medicine, Addenbrooke’s Hospital, Hills Road, Box 11, Cambridge CB2 2SP, United Kingdom
Abstract:Cluster of differentiation (CD) antigens are defined when a surface molecule found on some members of a standard panel of human cells reacts with at least one novel antibody, and there is good accompanying molecular data. Monoclonal antibodies to surface CD antigens on leukocytes have been used for flow cytometry, and more recently to construct microarrays that capture live cells. These DotScanTM microarrays enable the rapid and highly parallel characterization of repertoires of CD antigens whose expression patterns may be correlated with discrete leukaemia subtypes, or used to define biomarker ‘signatures’ for non-hematological diseases. DotScanTM with fluorescence multiplexing enables profiling of CD antigens for minor subsets of cells, such as colorectal cancer cells and tumour-infiltrating lymphocytes from a surgical sample.
Keywords:ALL  acute lymphocytic leukaemia  AML  acute myeloid leukaemia  APL  acute promyelocytic leukaemia  ATRA  all-trans retinoic acid  BMA  bone marrow aspirate  CD antigen  cluster of differentiation antigen  CEA  chorio-embryonic antigen  CLL  chronic lymphocytic leukaemia  1  25D3  1-α  25-dihydroxyvitamin D3  CRC  colorectal cancer  EpCAM  epithelial cell adhesion molecule  HLDA  human leukocyte differentiation antigens  TILs  tumour-infiltrating lymphocytes  PB  peripheral blood  TPA  12-O-tetradecanoyl phorbol-13-acetate
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