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. 2016 Apr 27;11(4):e0153349. doi: 10.1371/journal.pone.0153349

Table 1. ELISA analyses.

protein control antibodies anti-Gag-H antibody clones
anti-His anti-GST protein specific 1B3H7 1D7D11 2H2D6 14H11G1
HERV-E (matrix) 4.010 0.155 3.141 0.136 0.143 0.130 0.129
HERV-K HML-2 (matrix) 3.948 0.142 3.183 0.140 0.145 0.144 0.176
HERV-K HML-2 (capsid) 4.187 0.135 3.143 0.140 0.133 0.131 0.148
HERV-W (matrix) GST 1.183 0.535 3.230 0.164 0.131 0.224 0.134
HERV-W (capsid) 4.193 0.154 3.020 0.131 0.186 0.126 0.157
HERV-K HML-5 (matrix) 3.242 0.136 3.500 0.131 0.980 0.127 0.130
GST 2.477 0.518 3.154 0.138 0.229 0.123 0.126
Gag-H GST 0.748 0.331 n.d. 3.951 1.531 4.237 1.373

The OD405 values in the control antibody columns give information on the integrity of the proteins used, which are named in the first column. Antibodies used (distinguished in control and anti-Gag-H clones) are given in the headlines. Underlined values in the GST column can be considered background since the tested proteins have no GST-tag. Integrity of all proteins used is demonstrated with values above background of the anti-His antibody, of the anti-GST antibody (against the proteins with GST tag only) and of the different antibodies directed against the HERV control proteins.

Cross reactivity of the anti-Gag-H antibody clones with other HERV family proteins was also tested. Generally, values were at background level with the exception of 1D7D11 against HERV-K HML-5 (matrix), thus, we can exclude cross reactivity with the exception of 1D7D11 for HERV-K HML-5 (matrix). n.d., not done.