Sulfonylurea Herbicides antibody

Antigen: Sulfonylurea Herbicides

Clonality: Polyclonal

Host: Rabbit

Application: ELISA

Catalog no.: ABIN289632

Additional Information

Immunogen: Phenylsulfonyl derivative-KLH. (1-[2-(methyl ester)phenylsulfonyl]monoamidosuccinic acid-Keyhole Limpet Hemocyanine) prepared by the mixed anhydride method

Format: Neat antiserum, Liquid

Description: Sulfonylurea herbicides (SUs) were first introduced in 1982 by DuPont Crop Protection. Structurally common to all SU herbicides is the sulfonylurea group which is attached to two chemical structures. One structural element can constitute an aliphatic, aromatic, or heterocyclic group. The second structure mostly is a triazine or pyrimidine, but can also be a triazole. They are used for weed control in cereals such as wheat, rice, corn, and other crops such as potatoes, sugar beet, and turnip.

Specificity: Cross-reactivity: mesosulfuron-methyl 1246%; chlorimuron-ethyl 271%, imazosulfuron 223%; chlorsulfuron 166%, cyclosulfamuron 152%; sulfosulfuron 142%; pyrazosulfuron-ethyl 141%; triasulfuron 104%; metsulfuron-methyl 91%; iodosulfuron-methyl 79%; halosulfuron-methyl 77%; ethametsulfuron-methyl 66%; primisulfuron-methyl 66%; flazasulfuron 55%; prosulfuron 47%; thifensulfuron-methyl 30%; cinosulfuron 19%; azimsulfuron 16%; sulfometuron-methyl 14%; flupyrsulfuron-methyl-sodium 3%; tribenuron-methyl 2%, triflusulfuron-methyl 1%.

Application Details

Concentration: 50.000 tests/ml (HRP/TMB/H202 system)

Buffer: Preservative: None

Restrictions: For Research Use only

Images

Chemical Structure of Sulfonylurea (Source: PubChem)

Dose?response curves for three selected sulfonylurea herbicides obtained with spiked ultrapure water samples. Error bars represent

Publications

Publications: Degelmann, Wenger, Niessner et al.: "Development of a class-specific ELISA for sulfonylurea herbicides (sulfuron screen)." in: Environmental science & technology, Vol. 38, Issue 24, pp. 6795-802, 2005 (PubMed).