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Topic Aflatoxin B1 ELISA Test Kit 
Name NICOLE 
Company REAGEN 
Address 102 Commerce Dr. Unit 8, Moorestown, NJ 08057  
Phone  
Mobile  
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Country USA 
Date Created 9/28/2013 12:30:22 PM 
Message Product Description

REAGEN™ Aflatoxin B1 ELISA Test Kit is a competitive enzyme immunoassay for the quantitative analysis of Aflatoxin B1 in cereals, meat/fish, feed, milk ,oils,peanuts and pistachios .The unique features of the kit are:
 High recovery (80-105%),rapid(10-40minutes), cost-effective extraction methods.
 High sensitivity (0.05 ng/g or ppb).
 High reproducibility.
 A quick ELISA assay (less than 2 hours regardless of number of samples).

Procedure Overview

REAGEN™ Aflatoxin B1 ELISA Test Kit 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. 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 second antibody, tagged with a peroxidase enzyme, targets 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.

Kit Contents, Storage and Shelf Life

REAGEN™ Aflatoxin B1 ELISA Test Kit has the Aflatoxin B1acity for 96 determinations or testing of 42 samples in duplicate (assuming 12 wells for standards). Return any unused microwells to the foil bag and reseal them with the desiccant provided in the original package. Store the kit at 2-8C *. The shelf life is 12 months when the kit is properly stored.
Kit Contents Amount Storage
Aflatoxin B1 Antibody-Coated Plate 1x 96-well Plate (8 wells x 12 strips) 2-8C
Aflatoxin B1 Standards:
Negative control (white cap tube)
0.05ng/mL (yellow cap tube)
0.1ng/mL (orange cap tube)
0.2 ng/mL (pink cap tube)
0.4ng/mL (purple cap tube)
0.8 ng/mL (blue cap tube)
100 ng/mL (spiking, red cap tube)
1.0 mL
1.0 mL
1.0 mL
1.0 mL
1.0 mL
1.0 mL
1.0 mL
2-8C


2-8C



Aflatoxin B1 Antibody #1 8ml 2-8C
HRP Conjugated Antibody #2 18mL
20X Wash Solution 30 mL
Stop Buffer 20 mL
TMB Substrate 10 mL
Concentrate of Feed Extraction Buffer (Optional)
Feed Clean Up Mix (Optional) 60g
6g

* If you are not planning to use the kit for over 3 months, store Aflatoxin B1 Antibody #1 and HRP-Conjugated Antibody #2 at -20C or in a freezer.

Sensitivity

Sample Type Detection Limit (ng/g or ppb)
Meat/fish/sereal/feed/seed/starch 0.5(Rapid Method); 2.5(Organic Solvent Method)
Meat/liver/kidney 0.5
Milk 0.5
Peanut butter 0.5
Vegetable/bean/peanut/olive oils 0.25

Specificity

Analytes Cross-Reactivity (%)
Aflatoxin B1 100.0
Aflatoxin B2 49
Aflatoxin M1 45
Aflatoxin M2 24
Aflatoxin G1 37
Aflatoxin G2 8

Required Materials Not Provided With the Kit

 Microtiter plate reader (450 nm)
 Incubator
 Tissue Mixer (e.g. Omni TissueMaster Homogenizer)
 Vortex mixer (e.g. Gneie Vortex mixer from VWR)
 10, 20, 100 and 1000 L pipettes
 Multi-channel pipette: 50-300 L (Optional)
 Methanol

Warnings and Precautions

 The standards contain Aflatoxin B1 . Handle with particular care.
 Do not use the kit past the expiration date.
 Do not intermix reagents from different kits or lots except for components with the same part No’s within their expiration dates.
 Try to maintain a laboratory temperature of 20°–25°C (68°–77°F). Avoid running assays under or near air vents, as this may cause excessive cooling, heating and/or evaporation. Also, do not run assays in direct sunlight, as this may cause excessive heat and evaporation. Cold bench tops should be avoided by placing several layers of paper towel or some other insulation material under the assay plates during incubation.
 Make sure you are using only distilled or deionized water since water quality is very important.
 When pipetting samples or reagents into an empty microtiter plate, place the pipette tips in the lower corner of the well, making contact with the plastic.
 Incubations of assay plates should be timed as precisely as possible. Be consistent when adding standards to the assay plate. Add your standards first and then your samples.
 Add standards to plate only in the order from low concentration to high concentration as this will minimize the risk of compromising the standard curve.
 Always refrigerate plates in sealed bags with a desiccant to maintain stability. Prevent condensation from forming on plates by allowing them equilibrate to room temperature (20 – 25C / 68 – 77F) while in the packaging.
 
 
      
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