Food safety kits |

FOOD SAFETY KITS

Food safety is an increasingly concerned problem all around the world. In order to ensure the safety of food and feed, more than 100 countries have formulated food and feed related regulations. Elabscience® is a global supplier of food and feed safety solutions. We provide a wide range of innovative testing solutions and services for qualitative and quantitative detection of mycotoxins, residues and contaminants in food and feed.

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Products

CTC(Chlortetracycline) ELISA Kit

This kit uses Competitive-ELISA as the method. It can detect Chlortetracycline (CTC) in samples, such as meat, honey, eggs. This kit is composed of ELISA Microtiter plate, HRP conjugate, antibody working solution, standard and other supplementary reagents. The microtiter plate in this kit has been pre-coated with coupled antigen. During the reaction, CTC in the samples or standard competes with coupled antigen on the solid phase supporter for sites of anti-CTC antibody. Then Horseradish Peroxidase (HRP) conjugate is added to each microtiter plate well, and substrate reagent is added for color development. There is a negative correlation between the OD value of samples and the concentration of CTC. The concentration of CTC in the samples can be calculated by comparing the OD of the samples to the standard curve.

TMP(Trimethoprim) ELISA Kit

This kit uses Competitive-ELISA as the method. It can detect Trimethoprim (TMP) in samples, such as muscle, feed, etc. This kit is composed of ELISA Microtiter plate, HRP conjugate, standard liquid and other supplementary reagents. The microtiter plate in this kit has been pre-coated with coupled antigen. During the reaction, TMP in the samples or standard competes with coupled antigen on the solid phase supporter for sites of anti-TMP antibody. Then Horseradish Peroxidase (HRP) conjugate is added to each microtiter plate well, and substrate reagent is added for color development. There is a negative correlation between the OD value of samples and the concentration of TMP. The concentration of TMP in the samples can be calculated by comparing the OD of the samples to the standard curve.

SAL(Salbutamol) ELISA Kit

This kit uses Competitive-ELISA as the method. It can detect Salbutamol (SAL) in samples, such as muscle, feed, urine, etc. This kit is composed of ELISA Microtiter plate, HRP conjugate, antibody working solution, standard and other supplementary reagents. The microtiter plate in this kit has been pre-coated with coupled antigen. During the reaction, SAL in the samples or standard competes with coupled antigen on the solid phase supporter for sites of anti-SAL antibody. Then Horseradish Peroxidase (HRP) conjugate is added to each microtiter plate well, and substrate reagent is added for color development. There is a negative correlation between the OD value of samples and the concentration of SAL. The concentration of SAL in the samples can be calculated by comparing the OD of the samples to the standard curve.

SUD(Sudan I) ELISA Kit

This kit uses Competitive-ELISA as the method. It can detect Sudan Ⅰ (SUD) in samples, such as tomato juice, chilli sauce, eggs, etc. This kit is composed of ELISA Microtiter plate, HRP conjugate, antibody working solution, standard and other supplementary reagents. The microtiter plate in this kit has been pre-coated with coupled antigen. During the reaction, SUD in the samples or standard competes with coupled antigen on the solid phase supporter for sites of anti-SUD antibody. Then Horseradish Peroxidase (HRP) conjugate is added to each microtiter plate well, and substrate reagent is added for color development. There is a negative correlation between the OD value of samples and the concentration of SUD. The concentration of SUD in the samples can be calculated by comparing the OD of the samples to the standard curve.

PHEA( Phenylethanolamine A) ELISA Kit

This kit uses Competitive-ELISA as the method. It can detect Phenylethanolamine A (PHE A) in samples, such as muscle, feed. This kit is composed of ELISA Microtiter plate, HRP conjugate, antibody working solution, standard and other supplementary reagents. The microtiter plate in this kit has been pre-coated with coupled antigen. During the reaction, PHE A in the samples or standard competes with coupled antigen on the solid phase supporter for sites of anti-PHE A antibody. Then Horseradish Peroxidase (HRP) conjugate is added to each microtiter plate well, and substrate reagent is added for color development. There is a negative correlation between the OD value of samples and the concentration of PHE A. The concentration of PHE A in the samples can be calculated by comparing the OD of the samples to the standard curve.

FB1(Fumonisin B1) ELISA Kit

This kit is a competitive enzyme immunoassay for the quantitative determination of Fumonisin B1 in Corn, Feed, Edible oil etc.

MG(Malachite Green) ELISA Kit

This kit uses Competitive-ELISA as the method. It can detect Malachite Green (MG) in samples, such as muscle, etc. This kit is composed of ELISA Microtiter plate, HRP conjugate, antibody working solution, standard and other supplementary reagents. The microtiter plate in this kit has been pre-coated with coupled antigen. During the reaction, MG in the samples or standard competes with coupled antigen on the solid phase supporter for sites of anti-MG antibody. Then Horseradish Peroxidase (HRP) conjugate is added to each microtiter plate well, and substrate reagent is added for color development. There is a negative correlation between the OD value of samples and the concentration of MG. The concentration of MG in the samples can be calculated by comparing the OD of the samples to the standard curve.

RAC(Ractopamine) ELISA Kit

This kit uses Competitive-ELISA as the method. It can detect Ractopamine (RAC) in samples, such as muscle, feed, Liver, etc. This kit is composed of ELISA Microtiter plate, HRP conjugate, antibody working solution, standard and other supplementary reagents. The microtiter plate in this kit has been pre-coated with coupled antigen. During the reaction, RAC in the samples or standard competes with coupled antigen on the solid phase supporter for sites of anti-RAC antibody. Then Horseradish Peroxidase (HRP) conjugate is added to each microtiter plate well, and substrate reagent is added for color development. There is a negative correlation between the OD value of samples and the concentration of RAC. The concentration of RAC in the samples can be calculated by comparing the OD of the samples to the standard curve.

MNZ(Metronidazole) ELISA Kit

This kit uses Competitive-ELISA as the method. It can detect Metronidazole (MNZ) in samples, such as muscle, honey, etc. This kit is composed of ELISA Microtiter plate, HRP conjugate, antibody working solution, standard and other supplementary reagents. The microtiter plate provided in this kit has been pre-coated with coupled antigen. During the reaction, MNZ in the samples or standard competes with coupled antigen on the solid phase supporter for sites of anti- MNZ antibody. Then Horseradish Peroxidase (HRP) conjugate is added to each micro plate well, and substrate reagent is for color development. There is a negative correlation between the OD value of samples and the concentration of MNZ. The concentration of MNZ in the samples can be calculated by comparing the OD of the samples to the standard curve.

MEL(Melamine) ELISA Kit

This kit uses Competitive-ELISA as the method. It can detect Melamine (MEL) in samples, such as milk, muscle, feed, etc. This kit is composed of ELISA Microtiter plate, HRP conjugate, antibody working solution, standard and other supplementary reagents. The microtiter plate in this kit has been pre-coated with coupled antigen. During the reaction, MEL in the samples or standard competes with coupled antigen on the solid phase supporter for sites of anti-MEL antibody. Then Horseradish Peroxidase (HRP) conjugate is added to each microtiter plate well, and substrate reagent is added for color development. There is a negative correlation between the OD value of samples and the concentration of MEL. The concentration of MEL in the samples can be calculated by comparing the OD of the samples to the standard curve.