After the preliminary clustering of the whole workshop panel using flowcytometry data, we selected those clusters that were composed of mAbs that bound a broad range of cells. To obtain evidence that mAbs in each of these preliminary clusters detected the same antigen, they were tested for their capacity to compete with each other for binding to a target cell and the molecular weights of their antigens were estimated after immunoprecipitation. Most preliminary clusters in the non-lineage panel contained control mAbs that had been characterised in one of the previous workshops, and this study therefore increased the number of mAbs available to each of these non-lineage antigens. One new interesting cluster, BoWC14, was described which define...
<p><b>(a)</b> Dot plots illustrating flow cytometry analysis of cells obtained after maturation in I...
A precise identification and phenotypic characterization of human B-cell subsets is of crucial impor...
Flow cytometry is used extensively to examine immune cells in non-lymphoid tissues. However, a metho...
Monoclonal antibodies potentially specific for antigens expressed or upregulated on activated leukoc...
Based on cluster groups from the first-round analyses of the Third International Swine CD Workshop, ...
The blind panel collected for the 8th Human Leucocyte Differentiation Antigens Workshop (HLDA8; http...
The reactivity of 155 monoclonal antibodies submitted to the Third International Workshop on Swine L...
We have attempted to clarify the characteristics of monoclonal antibodies (MAbs) detecting lymphocyt...
<p>Antigenicity analyses of antigens and mAbs targeted to CD4bs, V1V2, V2 and V3 regions.</p
This chapter presents the results of blind serological studies carried out by workshop participants ...
The balance of inflammation and immunosuppression driven by changed ratios in diverse myeloid and T ...
Five-dimensional flow cytometry was used to identify the 5 lineages of peripheral blood leukocytes s...
Classifying monoclonal antibodies, based on the similarity of their binding to the proteins (antigen...
Flow cytometry was used to identify mAbs that recognize conserved epitopes on hamster leukocyte diff...
<p>The right-hand margin provides the name of peptide sets. Rows and columns represent clusters of i...
<p><b>(a)</b> Dot plots illustrating flow cytometry analysis of cells obtained after maturation in I...
A precise identification and phenotypic characterization of human B-cell subsets is of crucial impor...
Flow cytometry is used extensively to examine immune cells in non-lymphoid tissues. However, a metho...
Monoclonal antibodies potentially specific for antigens expressed or upregulated on activated leukoc...
Based on cluster groups from the first-round analyses of the Third International Swine CD Workshop, ...
The blind panel collected for the 8th Human Leucocyte Differentiation Antigens Workshop (HLDA8; http...
The reactivity of 155 monoclonal antibodies submitted to the Third International Workshop on Swine L...
We have attempted to clarify the characteristics of monoclonal antibodies (MAbs) detecting lymphocyt...
<p>Antigenicity analyses of antigens and mAbs targeted to CD4bs, V1V2, V2 and V3 regions.</p
This chapter presents the results of blind serological studies carried out by workshop participants ...
The balance of inflammation and immunosuppression driven by changed ratios in diverse myeloid and T ...
Five-dimensional flow cytometry was used to identify the 5 lineages of peripheral blood leukocytes s...
Classifying monoclonal antibodies, based on the similarity of their binding to the proteins (antigen...
Flow cytometry was used to identify mAbs that recognize conserved epitopes on hamster leukocyte diff...
<p>The right-hand margin provides the name of peptide sets. Rows and columns represent clusters of i...
<p><b>(a)</b> Dot plots illustrating flow cytometry analysis of cells obtained after maturation in I...
A precise identification and phenotypic characterization of human B-cell subsets is of crucial impor...
Flow cytometry is used extensively to examine immune cells in non-lymphoid tissues. However, a metho...