Aflatoxin B1 ELISA Test Kit
CH8300A
Pre-Processing Three In One, Simple And Convenient Aflatoxin B1 ELISA Test Kit
Aflatoxin b1 ELISA Kit provides a competitive enzyme immunoassay for the quantitative analysis of aflatoxin b1 in cereals,bran cereals,peanut meal,DDGS,corn gluten meal,corn germ, corn syrup and animal feed.Up to 96tests or assaying about 42 samples in duplicate( assuming 12 wells for standards).
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The unique features of the kit are:
- LOD:2μg/kg
- LOQ:2.5μg/kg .
- Quantitative Range:2.5-100μg/kg
- 20min
- recovery for certificated reference material:85%~110%
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| 1.Sample Preparation |
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Reagent Preparation
The formulation of Extraction-solvent is as follow:
ethanol:distilled water=1:1(v/v); for exemple, ethanol 500mL+distilled water 500mL, then vortex homogeneous.
Cecreals, bran cereals, DDGS, corn gluten meal, corn germ, corn syrup and animal feed
A representative sample( according to accepted sampling techniques) should be ground and thoroughly mixed prior to proceeding with the extraction procedure.
- Weigh out 5g of the homogenize sample into a suitable vial and vortex thoroughly with 25mL of Extraction-solvent for 3min.
- Filter the extract with Whatman NO.1 filter(or equivalent), or centrifuge the extract at 4000×g for 3~5 minutes.
- An aliquot of 100μL the filtrate obtained after filtration(or 100μL the supernatant obtained after centifugation), is diluted with 300μL of the Universal Sample Diluent.
- Use 50μL of the diluted solution per well for the assay.
Note:
- For bran cereals extraction, it is recommended to extract the sample with 1:7(w/v) or more;
- the pH of the supernatant or the filtrate should be 6~8, can adjust it with 1N NaOH or 1N HCl
- The diluted solution can be used as the determination of deoxynivalenol, aflatoxin b1 and aflatoxin b1
Peanut meal
A representative sample( according to accepted sampling techniques) should be ground and thoroughly mixed prior to proceeding with the extraction procedure.
- Weigh out 5g of the homogenize sample into a suitable vial and vortex thoroughly with 10mL of acetonitrile for 3min.
- Filter the extract with Whatman NO.1 filter(or equivalent), or centrifuge the extract at 4000×g for 3~5 minutes.
- Evaporate clean the liquid of 0.2mL of the filtrate obtained after filtration(or 0.2mL the supernatant obtained after centifugation). Then resolve the remaining residue with 1mL of Extraction-solvent.
- An aliquot of 100μL the resolved solution, is diluted with 300μL of the Universal Sample Diluent.
- Use 50μL of the diluted solution per well for the assay.
Dilution factor:2
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| Kit Contents |
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| Components |
Amount |
Components |
Amount |
| Precoated Microtiter Plate |
1x 96well (8wells x12strips) |
aflatoxin b1 Antibody |
6mL |
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aflatoxin b1
Standards
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Zero standard |
1mL |
HRP-Conjugated Antibody |
6mL |
| 2.5ppb |
1mL |
Universal Sample-Diluent |
40mL |
| 7.5ppb |
1mL |
20 x Wash Solution |
30mL |
| 25ppb |
1mL |
Stop Buffer |
12mL |
| 100ppb |
1mL |
TMB Substrate |
12mL |
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