Cry1Ie toxin was an insect-resistant protein used in genetically modified crops (GMC). In this study， a large human VH gene nanobodies phage displayed library was employed to select anti-Cry1Ie toxin antibody by affinity panning. After 5 rounds of panning， total 12 positive monoclonal phage particles were obtained. One of the identified positive phage nanobody was expressed in E.coli BL21 and the purified protein was indicated as a molecular mass of approximately 20?kDa by sodium dodecyl sulfate polyacrylamide gel electrophoresis (SDS-PAGE). Then a sensitive indirect competitive time-resolved fluoroimmunoassay (IC-TRFIA) was established for detection of Cry1Ie toxin by the purified protein. The working range of detection for Cry1Ie toxin standards in the IC-TRFIA were 0.08-6.44?ng?mL and the medium inhibition of control (IC) was 0.73?ng?mL. It showed a weak cross-reactivity with Cry1Ab toxin (at 5.6%)， but did not recognize Cry1B， Cry1C， Cry1F， and Cry2A toxins (were <0.1%). The average recoveries of Cry1Ie toxin from respectively spiked in rice， corn and soil samples were in the range of 83.5%-96.6% and with a coefficient of variation (CV) among 2.0%-8.6%. These results showed the IC-TRFIA was promising for detection of Cry1Ie toxin in agricultural and environmental samples.