Skip to main content
. Author manuscript; available in PMC: 2008 Oct 15.
Published in final edited form as: Anal Chem. 2007 Sep 11;79(20):7799–7806. doi: 10.1021/ac071323h

Table 1.

Cross reactivity (%) of molinate and atrazine PHAIA

Compound Structure Chemical hapten 19 Clone 1M CSTWDTTGWC Clone 2EM CRSHWDTWC
molinate graphic file with name nihms62652t1.jpg 100 100 100
thiobencarb graphic file with name nihms62652t2.jpg 1 0 0
butylate graphic file with name nihms62652t3.jpg 1 0 0
EPTC graphic file with name nihms62652t4.jpg 1 5 15
cycloate graphic file with name nihms62652t5.jpg 1 9 0
pebulate graphic file with name nihms62652t6.jpg 4 7 13
Vernolate graphic file with name nihms62652t7.jpg 4 4 5
Compound Structure Chemical hapten 17 Clone 13A CTPVRWFDMC
graphic file with name nihms62652t8.jpg R1 R2 R3
atrazine Cl C2H5 CH(CH3)2 100 100
simazine Cl C2H5 C2H5 48 0
propazine Cl CH(CH3)2 CH(CH3)2 116 144
cyanazine Cl C2H5 C2N(CH3)2 91 0
ametryn SCH3 C2H5 CH(CH3)2 0 0
simetryn SCH3 C2H5 C2H5 0 0
prometryn SCH3 CH(CH3)2 CH(CH3)2 0 0
terbutryn SCH3 C2H5 C(CH3)3 0 0

All data are the mean of two independent experiments. A value of 0 means that there was no observable cross reactivity with the highest concentration tested 104 ng/ml