hygiena MYC-INS-5018-REVB Zearalenone Low Matrix Elisa Instruction Manual

hygiena MYC-INS-5018-REVB Zearalenone Low Matrix Elisa

Product Information

Specifications

• Product Name: Helica Zearalenone Low Matrix ELISA assay
• Intended Use: Quantitative detection of zearalenone in cereal crops and animal feeds
• Kit Contents: Antibody-coated microwell plate, dilution plate, standards, conjugate, assay diluent, substrate, stop solution, and PBS-T powder

Product Usage Instructions

• The assay is a competitive enzyme-linked immunoassay using a mouse anti-zearalenone monoclonal antibody to detect zearalenone.
• The kit includes a microwell plate coated with the antibody, standards for calibration, conjugate for detection, and other necessary solutions for the assay.
• You will need a blender, Whatman #1 filter paper, distilled or deionized water, and methanol for sample preparation and extraction.
• Grind a representative sample to fine particle size.
• Prepare extraction solution (70% methanol) by mixing water and methanol.
• Weigh out the sample and add the extraction solvent in the specified ratio.
• Mix well and filter the extract before testing.

FAQ

• Can this assay be used for human diagnostics?
• No, this assay is not approved for human diagnostic or treatment purposes.
• What crops can be tested using this kit?
• Cereal crops such as maize, barley, oats, wheat, rice, and sorghum can be tested using this kit.

Helica® Zearalenone Low Matrix ELISA
For the quantitative detection of zearalenone in cereal crops, such as maize, barley, oats, wheat, rice, and sorghum, as well as in animal feeds.

Introduction

Introduction – Zearalenone
Zearalenone (RAL/F-2 mycotoxin) is a potent, non-steroidal, estrogenic metabolite produced by several fungal genera, specifically Gibberella and Fusarium. Some Fusarium species are known to produce a diversity of harmful mycotoxins, including zearalenone, fumonisin, and deoxynivalenol, which result in severe health implications in domestic animals. Some more common adverse effects include breeding problems and infertility in farm animals, with female swine being the most susceptible to these estrogenic effects. Zearalenone is frequently found in cereal crops, including maize, barley, oats, wheat, rice, and sorghum. Due to the wide range of commodities in which zearalenone can be detected, an analytical method such as ELISA is a useful means to provide rapid screening and identification of samples containing high levels of zearalenone.

Intended Use

• Hygiena’s Helica® Mycotoxin ELISA kits are user-friendly, cost-effective kits for the detection of mycotoxins in a wide range of commodities including animal feeds, grains, corn, and animal urine, designed to protect humans and animals from dangerous side effects of mycotoxins.
• The Helica Zearalenone Low Matrix ELISA assay is a competitive enzyme-linked immunoassay intended for the quantitative detection of zearalenone in cereal crops, such as maize, barley, oats, wheat, rice, and sorghum, as well as in animal feeds.
• Data obtained from assays should not be used for human diagnostic or human treatment purposes. Assays are not approved by the United States Food and Drug Administration or any other US or non-US regulatory agency for use in human diagnostics or treatment. Helica assays should not be used as the sole basis for assessing the safety of products for release to consumers. The information generated is only to be used in conjunction with the user’s regular quality assurance program.
• Not approved for clinical diagnosis. Use for research and development, quality assurance, and quality control under the supervision of technically qualified persons.

Principle of the Method
The Helica Zearalenone Low Matrix ELISA assay is a solid-phase competitive inhibition enzyme immunoassay. A zearalenone-specific antibody optimized to react with zearalenone is coated to a polystyrene microwell. Toxins are extracted from a ground sample with 70% methanol. If zearalenone is present it will bind to the coated antibody. After wells are decanted and washed, zearalenone bound to horse-radish peroxidase (HRP) is added and binds to the antibody not already occupied by zearalenone present in the sample or standard. After this incubation period, the contents of the wells are decanted and washed and a chromogenic HRP substrate is added, which develops a blue color in the presence of the enzyme. The intensity of the color is directly proportional to the amount of bound conjugate and inversely proportional to the amount of zearalenone in the standard or sample. Therefore, as the concentration of zearalenone in the sample or standard increases, the intensity of the blue color will decrease. An acidic stop solution is added, which changes the chromogen color from blue to yellow. The microwells are measured optically by a microplate reader with an absorbance filter of 450 nm (OD450). The optical densities of the samples are compared to the ODs of the kit standards and a result is determined by interpolation from the standard curve.

Kit Contents

a microwell holder coated with a mouse anti-zearalenone monoclonal antibody, Ready-to-Use.
1X Plate| Dilution plate| 96 non-coated wells (12 eight-well strips) in a microwell holder,

Ready-to-Use. (Mixing wells)

6X Vials| Standards| 1.5 mL/vial of zearalenone at the following concentrations: 0.0, 0.1, 0.3, 0.6, 1.2 and 4.0 ng/mL in 70% methanol, Ready- to-Use.
1X Bottle| Conjugate| 12 mL of zearalenone conjugated to peroxidase in buffer with preservative, Ready-to-Use.
2X Bottles| Assay diluent| 2 x 12 mL proprietary sample diluent, Ready-to- Use.
1X Bottle| Substrate| 12 mL stabilized tetramethylbenzidine (TMB), Ready-to- Use.
1X Bottle| Stop solution| 12 mL acidic solution, ready to use.
1X Pouch| PBS-T powder| PBS with 0.05% Tween20®, bring to 1 Liter with distilled water and

store refrigerated. (Wash buffer)

Materials Required but Not Provided

• Grinder sufficient to render sample to a particle size of fine instant coffee
• Collection container: Minimum 125 mL capacity
• Balance: up to 20 g measuring capability
• Graduated cylinder: 100 mL
• Methanol: 70 mL reagent grade per sample
• Distilled or deionized water: 30 mL per sample
• Filter paper – Whatman #1 or equivalent
• Filter funnel
• Centrifuge
• Pipettor with tips: 100 μL and 200 μL
• Dilution tubes
• Timer
• Wash bottle
• Absorbent paper towels
• Microplate reader with 450 nm filter

Storage and Shelf Life

• Store reagents at 2 to 8 °C. Do not freeze.
• Reagents should be used by the expiration date stamped on the individual labels.
• HRP-labeled conjugate and TMB-substrates are photosensitive and are packaged in a light-protective opaque bottle. Store in the dark and return to storage after use.

Precautions and Waste Disposal

General Precautions

• Bring all reagents to room temperature (19 to 25 °C) before use.
• Do not interchange reagents between kits of different lot numbers.
• Do not return unused reagents to their original bottles. The assay procedure details the volumes required.
• Adhere to all time and temperature conditions stated in the procedure.
• During the sample extraction, avoid cross-contamination.
• Devices such as a blender must be cleaned after each sample preparation.
• Samples tested should have a pH of 7.0 (± 1.0). Excessive alkaline or acidic conditions may affect the test results.

Safety Precautions
Mycotoxins (aflatoxins, trichothecenes, and others) are well-known human carcinogens and are considered highly toxic. Because mycotoxins can cause human illness, appropriate safety precautions must be taken and personal protective equipment worn when handling samples, reagents, glassware, and other supplies and equipment that potentially could be contaminated with mycotoxins.

• Before using this assay, please review the Safety Data Sheet(s) available at www.hygiena.com.
• Refer to your site practices for safe handling of materials.
• It is strongly advised that protective gloves, a lab coat, and safety glasses be worn at all times while handling mycotoxin kits and their respective components. Consider all materials, containers and devices that are exposed to samples or standards to be contaminated with mycotoxins.
• Never pipette reagents or samples by mouth.
• Standards are flammable. Caution should be taken in the use and storage of these reagents.
• The stop solution contains sulfuric acid, which is corrosive. Please refer to the SDS. Do not allow to contact skin or eyes. If exposed, flush with water.

Disposal
Decontaminate materials and dispose of waste per your site practices and as required by local regulations. Do not dispose of these materials down the drain. Please note that there is a potential for mycotoxin contamination in or on any of the kit components provided.

• Dispose of all materials, containers, and devices in the appropriate receptacle after use.
• Before conducting the assay, prepare a waste container to act as a receptacle for your kit waste.
• Eject contaminated pipette tips and all other related materials into this container.
• Once the assay is completed, the container should be treated with a sufficient amount of 5 – 6% sodium hypochlorite (NaOCl) to saturate the contents of the container (approximately 1/10th the volume of the container). The NaOCl will denature the mycotoxins and neutralize the waste, making it safe for disposal. Invert the container several times to thoroughly coat all waste.
• In the case of an accidental toxin spill, treat the spill surface with 5 – 6% NaOCl for a minimum of 10 minutes followed by 5% aqueous acetone. Wipe dry with absorbent paper towels.

Preparation of Samples
Note: The sample must be collected according to the appropriate established sampling techniques.

Extraction Procedure Cereals

1. Grind a representative sample to the particle size of fine instant coffee (95% passes through a 20-mesh screen).

2. Prepare the extraction solution (70% methanol) by adding 30 mL of distilled or deionized water to 70 mL of methanol (reagent grade) for each sample to be tested.

3. Weigh out a 20 g ground portion of the sample and add 100 mL of the Extraction Solvent (70%).
   Note: The ratio of sample to extraction solvent is 1:5 (w/v).

4. Mix by shaking in a sealed container or a blender for a minimum of 3 minutes.

5. Allow the particulate matter to settle, then filter 5 – 10 mL of the extract through a Whatman #1 filter paper (or equivalent) and collect the filtrate to be tested.

6. Dilute an aliquot of the extract 1:10 with 70% methanol.

7. The sample is now ready for testing.

8. The final dilution for use in calculations is 1:50.

Animal feed

1. Grind a representative sample to the particle size of fine instant coffee (95% passes through a 20-mesh screen).

2. Prepare extraction solvent (70% methanol) by adding 30 mL of distilled or deionized water to 70 mL of methanol for each sample to be tested.

3. Transfer 100 mL of 70% methanol to a container and add 20 g of the ground sample.
   Note: The ratio of sample to extraction solvent is 1:5 (w/v).

4. Mix by shaking in a sealed container for a minimum of 3 minutes.

5. Allow the particulate matter to settle, then filter 5-10 mL of the extract through a Whatman #1 filter and collect the filtrate to be tested.

6. Dilute an aliquot of the extract at 1:50 with 70% methanol.

7. The sample is now ready for testing.

8. The final dilution for use in calculations is 1:250.

Assay Procedure

1. Bring all the reagents to room temperature before use. Prepare wash buffer by reconstituting the PBS-T powder packet by washing out the contents with a gentle stream of distilled or deionized water into a
   1-Liter container. Fill to 1 Liter with distilled or deionized water and store refrigerated when not in use.

2. Place one mixing well in a microwell holder for each standard and sample to be tested. Place an equal number of antibody-coated microwells in another microwell holder. Return unused wells to the foil pack with desiccant.

3. Mix each reagent by swirling the reagent bottle before use.

4. Dispense 200 μL of the Assay Diluent into each mixing well.

5. Using a new pipette tip for each, add 100 μL of each standard and prepare a sample to the appropriate mixing well-containing diluent. Mix by priming pipettor at least 3 times.
   Note: The operator must record the location of each standard and sample throughout the test.

6. Using a new pipette tip for each, transfer 100 μL of contents from each mixing well to a corresponding antibody-coated microtiter well. Incubate at room temperature for 10 minutes.
   Note: The mixing wells contain enough solution to run each standard and/or sample in duplicate (recommended). If running each standard or sample in singlets or if more replicates are needed, the volumes of assay diluent and sample/ standard should be scaled accordingly.

7. Decant the contents from microwells into a discard basin. Wash the microwells by filling each with PBS-T wash buffer, then decanting the wash into a discard basin. Repeat wash for a total of 3 washes.

8. Tap the microwells (face down) on a layer of absorbent towels to remove residual wash buffer.

9. Add 100 μL of zearalenone HRP-conjugate to each antibody-coated well and incubate at room temperature for 10 minutes. Cover to avoid direct light.

10. Repeat steps 6 and 7.

11. Measure the required volume of substrate solution (1 mL/strip or 120 μL/well) and place it into a separate container. Add 100 μL to each microwell. Incubate at room temperature for 10 minutes. Cover to avoid direct light.

12. Measure the required volume of stop solution (1 mL/strip or 120 μL/well) and place it into a separate container. Add 100 μL in the same sequence and at the same pace as the substrate solution was added.

13. Read the optical density (OD) of each microwell with a microtiter plate reader using a 450 nm filter. Record the optical density (OD) of each microwell.

14. Setting the zero standard as 100% binding (Bo), calculate % binding (%B) for each standard and sample as a percentage of the zero binding (%B/Bo).

Interpretation of Results
Construct a dose-response curve using the OD values expressed as a percentage (%B/Bo) of the OD of the zero (0.0 ng/mL) standard against the zearalenone content of the standard. Unknowns are measured by interpolation from the standard curve.
The information contained on the label of each standard vial refers to the contents of that vial. However, the sample has been diluted at a 1:5 ratio with 70% methanol in the extraction procedure, followed by an additional dilution of 1:10 or 1:50 in 70% methanol. Therefore, the level of zearalenone shown by the standard must be multiplied by 50 or 250, respectively, to indicate the ng per gram (ppb) of the commodity as follows.

Standard (ng/mL)| Cereal diluted 1:50 (ppb in sample)| Animal feed diluted 1:250 (ppb in sample)
---|---|---
0.0| 0.0| 0.0
0.1| 5.0| 25.0
0.3| 15.0| 75.0
0.6| 30.0| 150.0
1.2| 60.0| 300.0
4.0| 200.0| 1000.0

If a sample contains zearalenone at a greater concentration than the highest standard, it should be diluted appropriately in extraction solvent and retested. The extra dilution step should be taken into consideration when expressing the final result.

Assay Characteristics
Data from twelve consecutive standard curves gave the following results:

• The below figure is a representative standard curve for zearalenone based on the above data table.

• Recoveries of 500 ppb, 150 ppb, and 60 ppb zearalenone spiked into feed samples were as follows based on an average of six independent experiments (n=6).

• Recoveries from certified reference material (corn) were as follows based on an average of six independent experiments (n=6).

Cross-reactivity
The essay will cross-react with zearalenone analogues as follows:

Technical Assistance
For questions or comments, please contact your local distributor. You can also email techsupport@hygiena.com, visit our Contact Us page for regional phone numbers or request technical support at https://www.hygiena.com/hygiena/technical-support-request.html.

References

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