Features:
-UV wavelength available, including 340nm.
-3 test methods: End Point, Fixed time and Kinetic.
-Temperature control, incubation time and temperature adjustable.
-Compact design, PC controlled system, Windows XP.
-User-friendly software offers simple operation.
REAGEN Sulfaquinoxaline ELISA kit is a Competitive Enzyme immunoassay for the Quantitative Analysis of Sulfaquinoxaline (SQX) in fish, shrimp, Honey, kidney, liver, Meat (Beef, Chicken and pork), Milk, serum, urine and Water.
The unique features of the kit are:
Rapid extraction method for various samples with high recovery (> 80%)
High sensitivity (0.5 ng / g or ppb) and low detection limit (0.5 ng / g or ppb for shrimp)
A quick ELISA assay (less than 2 hours regardless of number of samples)
High reproducibility
Sample TypeDetection Limit (ng/g or ppb)
Fish/Shrimp/Meat/Liver/Kidney0.5
Honey2
Milk5
Serum5
Urine5
Water0.5
AnalytesCross-Reactivity (%)
Sulfaquinoxaline100
Sulfamethoxypyridazine70
Sulfadiazine4
Sulfamoxole1
Sulfisoxazole0.5
Sulfathiazole
REAGEN Dexamethasone ELISA Test Kit is a competitive enzyme immunoassay for the quantitative analysis of Dexamethasone, Betamethasone, Flumethasone in meat, fish, shrimp,urine and serum.
The unique features of the kit are:
High recovery(>75%), rapid (less than 30 minutes), and cost-effective extraction methods.
High sensitivity (0.1 ng/g or ppb) and low detection limit (e.g. 0.1 ng/g or ppb for meat).
High reproducibility.
A quick ELISA assay (less than 2 hours regardless of number of samples).
Procedure Overview
REAGEN Dexamethasone ELISA Test Kit is based on a competitive colorimetric ELISA assay. The drug of interest has been coated in the plate wells. During the analysis, sample is added along with the primary antibody specific for the target drug. If the target is present in the sample, it will compete for the antibody, thereby preventing the antibody from binding to the drug attached to the well. The secondary antibody, tagged with a peroxidase enzyme, targets the primary antibody that is complexed to the drug coated on the plate wells. The resulting color intensity, after addition of substrate, has an inverse relationship with the target concentration in the sample.
Sensitivity
Sample TypeDetection Limit (ng/g or ppb)
Milk0.1
Meat/Fish/Shrimp0.1
Serum0.25
Urine0.25
REAGEChloramphenicol (CAP) ELISA Test Kit is a competitive enzyme immunoassay for the quantitative analysis of chloramphenicol in feed, fish, eggs, honey, meat (beef, chicken and pork), milk, milk powder, serum, shrimp and urine.
The unique features of the kit are:
High recovery (80-105%), rapid (10 - 40 minutes), and cost-effective extraction methods.
High sensitivity (0.05 ng/g or ppb) and low detection limit (0.025 ng/g or ppb) for shrimp, fish and meat samples.
High reproducibility.
A quick ELISA assay (less than 2 hours regardless of number of samples).
Procedure Overview
The method is based on a competitive colorimetric ELISA assay. The CAP antibody has been coated in the plate wells. During the analysis, sample is added along with the CAP-horseradish peroxidase conjugate. If the CAP residue is present in the sample, it will compete for the CAP antibody, thereby preventing the CAP-HRP from binding to the antibody attached to the well. The resulting color intensity, after addition of the HRP substrate (TMB), has an inverse relationship with the CAP residue concentration in the sample.
Sensitivity
REAGEN Aflatoxin B1 ELISA Test Kit is a competitive enzyme immunoassay for the quantitative analysis of Aflatoxin B1 in cereals, meat/fish, feed, milk,milk powder ,oils,peanuts and pistachios .
l(91%)andα-zearalanol(69%).
High sensitivity (1 ng/g or ppb).
A quick ELISA assay (less than 1 hours regardless of number of samples).
High reproducibility.
Procedure Overview
The method is based on a competitive colorimetric ELISA assay. The toxin of interest has been coated in the plate wells. During the analysis, sample is added along with the primary antibody specific for the target toxin and enzyme-conjugate. If the target is present in the sample, it will compete for the antibody, thereby preventing the antibody from binding to the toxin attached to the well. The enzyme-conjugate, will bined with the primary antibody that is complexed to the toxin coated on the plate wells. The resulting color intensity, after addition of substrate, has an inverse relationship with the target concentration in the sample.
