Zeranol detection method and kit in grains
A technology of zearalenol and zearalenol, which is applied in the field of detection, can solve the problems of undetectable and harmful effects of edible animals, reduce the operation steps and labor intensity, shorten the detection time, and overcome the problems of long detection cycle Effect
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Embodiment 1
[0011] The method and kit for detecting zearalenol in grains of the present invention include a standard product of zearalenol, a standard product of β-zearalenol, a standard product of α-zearalenol, and a standard product of β-zearalenol , Zearalenone standard, zearalenone standard, biotinylated zearalenol, anti-mouse IgG coupled receptor magnetic beads, streptavidin donor magnetic beads, anti-zearalenol monogram Anti-antibody and detection buffer, wherein the anti-mouse IgG coupled receptor magnetic beads include 100μg / mL receptor magnetic beads, 0.05% Proclin-300 and pH7.4 PBS solution; streptavidin donor magnetic beads Including 100μg / mL donor magnetic beads, 25mM HEPES, 100mM NaCl solution and 0.1% Proclin-300; Weigh 1g agarose gel matrix powder, dissolve it in 1mmol / L HCl, and place it in a sintered glass filter Wash with 1mmol / L HCl for 15 minutes; for ligand coupling, use coupling buffer 0.2mol / L NaHCO3pH8.3 to dissolve the β-zearalenol antibody and chloramphenicol anti...
Embodiment 2
[0013] Methods and kits for the detection of zearalenol in grains, including standard zearalenol, β-zearalenol standard, α-zearalenol standard, β-zearalenol standard, and corn Gibberellone standard, zearalenone standard, biotinylated zearalenol, anti-mouse IgG coupled receptor magnetic beads, streptavidin donor magnetic beads, anti-zearalenol monoclonal antibody And detection buffer, wherein the anti-mouse IgG-coupled acceptor magnetic beads include 100μg / mL acceptor magnetic beads, 0.05% Proclin-300 and pH7.4 PBS solution; streptavidin donor magnetic beads include 100μg / mL donor magnetic beads, 25mM HEPES, 100mM NaCl solution and 0.2% Proclin-300; Weigh 1g agarose gel matrix powder, dissolve it in 1mmol / L HCl, and then place it in a sintered glass filter and use 1mmol / LHCl wash for 15min; ligand coupling use coupling buffer 0.2mol / LNaHCO3pH8.3 to dissolve the β-zearalenol antibody and chloramphenicol antibody to be coupled to obtain the antibody solution, and quickly transfe...
Embodiment 3
[0015] The method and kit for detecting zearalenol in grains of the present invention include a standard product of zearalenol, a standard product of β-zearalenol, a standard product of α-zearalenol, and a standard product of β-zearalenol , Zearalenone standard, zearalenone standard, biotinylated zearalenol, anti-mouse IgG coupled receptor magnetic beads, streptavidin donor magnetic beads, anti-zearalenol monogram Anti-antibody and detection buffer, wherein the anti-mouse IgG-coupled acceptor magnetic beads include 100μg / mL acceptor magnetic beads, 0.05% Proclin-300 and pH7.4 PBS solution; streptavidin donor magnetic beads Including 100μg / mL donor magnetic beads, 25mM HEPES, 100mM NaCl solution and 0.15% Proclin-300; Weigh 1g agarose gel matrix powder, dissolve it in 1mmol / L HCl, and place it in a sintered glass filter Wash with 1mmol / L HCl for 15min; use coupling buffer 0.2mol / LNaHCO3pH8.3 to dissolve the β-zearalenol antibody and chloramphenicol antibody to be coupled to obta...
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