Monoclonal antibody to a supertypic determinant associated with HLA-DRw52.

Standard

Monoclonal antibody to a supertypic determinant associated with HLA-DRw52. / Eiermann, Thomas; Krause, S; Wölpl, A; Ballas, M; Goldmann, S F.

in: HYBRIDOMA, Jahrgang 8, Nr. 4, 4, 1989, S. 467-474.

Publikationen: SCORING: Beitrag in Fachzeitschrift/ZeitungSCORING: ZeitschriftenaufsatzForschungBegutachtung

Harvard

Eiermann, T, Krause, S, Wölpl, A, Ballas, M & Goldmann, SF 1989, 'Monoclonal antibody to a supertypic determinant associated with HLA-DRw52.', HYBRIDOMA, Jg. 8, Nr. 4, 4, S. 467-474. <http://www.ncbi.nlm.nih.gov/pubmed/2476377?dopt=Citation>

APA

Eiermann, T., Krause, S., Wölpl, A., Ballas, M., & Goldmann, S. F. (1989). Monoclonal antibody to a supertypic determinant associated with HLA-DRw52. HYBRIDOMA, 8(4), 467-474. [4]. http://www.ncbi.nlm.nih.gov/pubmed/2476377?dopt=Citation

Vancouver

Eiermann T, Krause S, Wölpl A, Ballas M, Goldmann SF. Monoclonal antibody to a supertypic determinant associated with HLA-DRw52. HYBRIDOMA. 1989;8(4):467-474. 4.

Bibtex

@article{a7965046b2b749ed93c174808a90a59f,
title = "Monoclonal antibody to a supertypic determinant associated with HLA-DRw52.",
abstract = "A cytotoxic mouse monoclonal antibody UL-52 (IgG2b) was obtained after immunization of a BALB/c mouse with the lymphoblastoid cell line STA homozygous for HLA-A3, B8, Cw7, DR3, DRw52, DQw2, DPw2. Fluorescence analysis on a panel of B lymphoblastoid cell lines from the 10th International Histocompatibility Workshop 1987 showed almost exact concordance of UL-52 reactivity with the presence of the HLA-DRw52 antigen. Cytotoxicity testing of UL-52 on mononuclear cells of HLA-typed individuals revealed a pattern of reactivity closely associated with the HLA-DRw52 specificity as defined by conventional alloantisera (R = 0.77). UL-52 precipitated appropriate 29,000- and 33,000-dalton bands on SDS- polyacrylamide gels under reducing conditions from an HLA-DRw52 positive B lymphoblastoid cell line. Thus, by serological and biochemical criteria UL-52 defines a supertypic determinant associated with HLA-DRw52. In contrast to most DRw52- like monoclonal antibodies, UL-52 binds to DRw8 positive cells.",
author = "Thomas Eiermann and S Krause and A W{\"o}lpl and M Ballas and Goldmann, {S F}",
year = "1989",
language = "Deutsch",
volume = "8",
pages = "467--474",
number = "4",

}

RIS

TY - JOUR

T1 - Monoclonal antibody to a supertypic determinant associated with HLA-DRw52.

AU - Eiermann, Thomas

AU - Krause, S

AU - Wölpl, A

AU - Ballas, M

AU - Goldmann, S F

PY - 1989

Y1 - 1989

N2 - A cytotoxic mouse monoclonal antibody UL-52 (IgG2b) was obtained after immunization of a BALB/c mouse with the lymphoblastoid cell line STA homozygous for HLA-A3, B8, Cw7, DR3, DRw52, DQw2, DPw2. Fluorescence analysis on a panel of B lymphoblastoid cell lines from the 10th International Histocompatibility Workshop 1987 showed almost exact concordance of UL-52 reactivity with the presence of the HLA-DRw52 antigen. Cytotoxicity testing of UL-52 on mononuclear cells of HLA-typed individuals revealed a pattern of reactivity closely associated with the HLA-DRw52 specificity as defined by conventional alloantisera (R = 0.77). UL-52 precipitated appropriate 29,000- and 33,000-dalton bands on SDS- polyacrylamide gels under reducing conditions from an HLA-DRw52 positive B lymphoblastoid cell line. Thus, by serological and biochemical criteria UL-52 defines a supertypic determinant associated with HLA-DRw52. In contrast to most DRw52- like monoclonal antibodies, UL-52 binds to DRw8 positive cells.

AB - A cytotoxic mouse monoclonal antibody UL-52 (IgG2b) was obtained after immunization of a BALB/c mouse with the lymphoblastoid cell line STA homozygous for HLA-A3, B8, Cw7, DR3, DRw52, DQw2, DPw2. Fluorescence analysis on a panel of B lymphoblastoid cell lines from the 10th International Histocompatibility Workshop 1987 showed almost exact concordance of UL-52 reactivity with the presence of the HLA-DRw52 antigen. Cytotoxicity testing of UL-52 on mononuclear cells of HLA-typed individuals revealed a pattern of reactivity closely associated with the HLA-DRw52 specificity as defined by conventional alloantisera (R = 0.77). UL-52 precipitated appropriate 29,000- and 33,000-dalton bands on SDS- polyacrylamide gels under reducing conditions from an HLA-DRw52 positive B lymphoblastoid cell line. Thus, by serological and biochemical criteria UL-52 defines a supertypic determinant associated with HLA-DRw52. In contrast to most DRw52- like monoclonal antibodies, UL-52 binds to DRw8 positive cells.

M3 - SCORING: Zeitschriftenaufsatz

VL - 8

SP - 467

EP - 474

IS - 4

M1 - 4

ER -