TY - JOUR
T1 - Quantitative determination and visualization of herpes simplex virus type 1 antigen, free and cell-bound by ELISA
AU - Tirado, Rocío
AU - Sarmiento, Rosa Elena
AU - Gómez, Beatríz
N1 - Funding Information:
This work was partially supported by grant srv/lha/rjsp.90 from programa Universitario de InvestigaciBn en Salud. We thank M. en C. Jaime Bustos Martinez, Dr. Karl Mueller for helpful discussions and Michael Shea who revised the English.
PY - 1996
Y1 - 1996
N2 - A method of quantifying and visualizing herpes simplex virus type 1 antigen by indirect enzyme-linked immunosorbent assay (ELISA) is described. This assay is simplified by the use of polyclonal serum and can be applied to the quantification of free antigen as well cell-bound. Moreover, cell viral antigen can be visualized. Antigen sources were vital suspensions, infected cells and proteins extracted from infected cells. The assay was specific and its sensitivity was dependent on the antigen source. The technique was regarded as specific within a range showing a direct correlation (r>0.8) between the concentration of the antigen and the net absorbance value (the difference of the absorbance obtained with the vital antigen minus the control antigen). The technique has advantages over other ELISA procedures: does not require monoclonal antibodies, or labelled antiviral immunoglobulins or antiviral serum from two different species. In addition total free antigen can be measured.
AB - A method of quantifying and visualizing herpes simplex virus type 1 antigen by indirect enzyme-linked immunosorbent assay (ELISA) is described. This assay is simplified by the use of polyclonal serum and can be applied to the quantification of free antigen as well cell-bound. Moreover, cell viral antigen can be visualized. Antigen sources were vital suspensions, infected cells and proteins extracted from infected cells. The assay was specific and its sensitivity was dependent on the antigen source. The technique was regarded as specific within a range showing a direct correlation (r>0.8) between the concentration of the antigen and the net absorbance value (the difference of the absorbance obtained with the vital antigen minus the control antigen). The technique has advantages over other ELISA procedures: does not require monoclonal antibodies, or labelled antiviral immunoglobulins or antiviral serum from two different species. In addition total free antigen can be measured.
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U2 - 10.1080/01971529608005793
DO - 10.1080/01971529608005793
M3 - Research Article
C2 - 8842985
AN - SCOPUS:0029821374
SN - 0197-1522
VL - 17
SP - 277
EP - 291
JO - Journal of Immunoassay
JF - Journal of Immunoassay
IS - 3
ER -