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

DEX(Dexamethasone) ELISA Kit

This kit uses Competitive-ELISA as the method. It can detect Dexamethasone (DEX) in samples, such as muscle, milk, 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, DEX in the samples or standard competes with coupled antigen on the solid phase supporter for sites of anti-DEX 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 DEX. The concentration of DEX in the samples can be calculated by comparing the OD of the samples to the standard curve.

MQCA(3-methyl quinoxaline-2-carboxylic acid)ELISA Kit

This kit uses Competitive-ELISA as the method. It can detect 3-methyl quinoxaline-2-carboxylic acid (MQCA) in samples, such as muscle, 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, MQCA in the samples or standard competes with coupled antigen on the solid phase supporter for sites of anti-MQCA 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 MQCA. The concentration of MQCA in the samples can be calculated by comparing the OD of the samples to the standard curve.

OQX(Olaquindox) ELISA Kit

This kit uses Competitive-ELISA as the method. It can detect Olaquindox (OQX) in samples, such as 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, OQX in the samples or standard competes with coupled antigen on the solid phase supporter for sites of anti-OQX 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 OQX. The concentration of OQX in the samples can be calculated by comparing the OD of the samples to the standard curve.

SEM(Nitrofurazone) ELISA Kit

This kit uses Competitive-ELISA as the method. It can detect SEM in samples, such as honey, muscle, milk, feed, 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, SEM in the samples or standard competes with coupled antigen on the solid phase supporter for sites of anti- SEM 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 SEM. The concentration of SEM in the samples can be calculated by comparing the OD of the samples to the standard curve.

AHD(Nitrofurantoin) ELISA Kit

This kit uses Competitive-ELISA as the method. It can detect Nitrofurantoin (AHD) in samples, such as muscle, honey, milk, 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, AHD in the samples or standard competes with coupled antigen on the solid phase supporter for sites of anti-AHD 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 AHD. The concentration of AHD in the samples can be calculated by comparing the OD of the samples to the standard curve.

AOZ(Nitrofuran Furazolidone) ELISA Kit

This kit uses Competitive-ELISA as the method. It can detect Nitrofuran Furazolidone (AOZ) 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 in this kit has been pre-coated with coupled antigen. During the reaction, AOZ in the samples or standard competes with coupled antigen on the solid phase supporter for sites of anti-AOZ 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 AOZ. The concentration of AOZ in the samples can be calculated by comparing the OD of the samples to the standard curve.

AMOZ(Nitrofuran Furaltadone) ELISA Kit

This kit uses Competitive-ELISA as the method. It can detect Nitrofuran Furaltadone (AMOZ) in samples, such as honey, 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, AMOZ in the samples or standard competes with coupled antigen on the solid phase supporter for sites of anti- AMOZ 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 AMOZ. The concentration of AMOZ in the samples can be calculated by comparing the OD of the samples to the standard curve.

LSY-10007 Chloramphenicol(CAP) ELISA Test Kit (Tissue, egg) LSY

This test kit is based on theindirect competitive enzyme immunoassay for the detection of Chloramphenicol in the sample.The coupling antigenis pre-coated on the micro-well stripes. The Chloramphenicol in the sample and the coupling antigen pre-coated on the micro-well stripes compete for the anti-Chloramphenicolantibody. After the addition of the enzyme conjugate, the TMB substrate is added for coloration. The optical density (OD) value of the sample has a negative correlation with the Chloramphenicol in it. This value is compared to the standard curve and the Chloramphenicol concentration is subsequently obtained.