Beta Agonist ELISA Kit For Milk Egg Urine Serum Test Chicken Pork 96 Wells/Kit

Beta Agonist ELISA Kit For Milk Egg Urine Serum Chicken Pork 96 Wells/Kit

1. Principle

The β-agonists test kit is based on the competitive enzyme immunoassay for the detection of β-agonists in the sample. The coupling antigen is pre-coated on the micro-well stripes. The β-agonists in the sample and the coupling antigens pre-coated on the micro-well stripes compete for the anti-β-agonists antibodies. 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 β-agonists in the sample. This value is compared to the standard curve and the β-agonists residues is subsequently obtained.

2. Technical specifications

Sensitivity: 0.1 ppb
Incubation Temperature: 25℃
Incubation Time: 30min～15min

Detection limit:
Porcine urine 0.3ppb
Pork 0.6ppb

Cross-reaction rate:Clenbuterol 100%, Cimaterol <4%, Brombuterol 60%, Mabuterol 108%, Bambuterol <5%, Clorprenaline <1%, Salbutamol 75%, Terbutaline 25%, Penbutolol 19%, Tulobuterol 23%, Fenoterol <0.1%, Ractopamine <0.1%

Recovery rate:
Porcine urine, pork 90%±30%

3. Components

4. Materials required but not provided

1) Equipments:microplate reader, printer, homogenizer, vortex, oscillator, centrifuge, Incubator, measuring pipets, balance (a sensibility reciprocal of 0.01 g)
2) Micropipettors: single-channel 20-200µL, 100-1000µL, and multi-channel 30-300µL;
3) Reagents: NaOH, HCI.

5. Sample pre-treatment

Instructions(The following points must be dealt with before the pre-treatment )
1) Only the disposable tips can be used for the experiments and the tips must be changed when used for absorbing different reagents;
2) Before the experiment, each experimental utensil must be clean and should be re-cleaned if necessary, in order to avoid the contamination that interferes with the experimental results.

Solution preparation before sample pre-treatment:
1) 0.2M HCI: dissolve 17.2mL HCI in deionized water to 1L.
2) 1M NaOH: dissolve 4g NaOH in deionized water to 100 mL.
3) Sample extracting solution: 1 part 5X sample extracting solution + 4 parts deionized water, mix evenly.

5.1 Porcine urine
Take 20 µL clear urine, directly detect it (If urine are muddy, must filter or centrifuge at 4000 r/min for 10 min, then take clear urine). Store at frozen environment if don’t use.
Fold of dilution of sample: 1

5.2 Pork
1. Weigh 2±0.05g homogenized tissue sample into a 50ml centrifuge tube, add 3ml 0.2M HCl, shake for 3 min.
2. Then add 600ul 1M NaOH solution and 2.4ml Sample extracting solution, shake for 3min, centrifuge at 4000 r/min at room temperature (20-25 ℃) for 10 min.
3. Take 20µL up-layer liquid for analysis.(Note: if there is fat layer after centrifuge, remove fat layer or separate fat layer, take clear liquid for analysis)
Fold of dilution of sample:4

6. ELISA procedures

6.1Instructions
1. Bring all reagents and micro-well strips to the room temperature (20-25 ℃) before use;
2. Return all reagents to 2-8 ℃ immediately after use;
3. The reproducibility of the ELISA analysis, to a large degree, depends on the consistency of plate washing. The correct operation of plate washing is the key point in ELISA the procedures;
4. For the incubation at constant temperatures, all the samples and reagents must avoid light exposure, and each microplate should be sealed by the cover membrane.

6.2Operation procedures
1. Bring test kit to the room temperature (20-25 ℃) for at least 30 min, note that each reagent must be shaken evenly before use;
2. Put the required micro-well strips into plate frames. Re-sealed the unused microplate, stored at 2-8 ℃, not frozen.
3. Dilute the 40ml 20X concentrated washing buffer at 1:19 with deionized water (1 part 20X concentrated washing buffer + 19 part deionized water). Or prepare as quantity needed.
4. Numbering: number the micro-wells according to samples and standard solution; each sample and standard solution should be performed in duplicate; record their positions.
5. Add 20µL of the sample or the standard solution into separate duplicate wells, then add enzyme conjugate, 50ul/well; then add antibody working solution, 80µL/well. Mix gently by shaking the plate manually, seal the microplate with the cover membrane,incubate at 25 ℃ for 30 min.
6. Pour liquid out of microwell, add 250µL/well of washing buffer, wash for 4-5 times, 15-30s each time, then take out and flap to dry with absorbent paper(if there are the bubbles after flapping, cut them with the clean tips).
7. Coloration: add 50µL of substrate A, then add 50µL substrate B into each well. Mix gently by shaking the plate manually,and incubate at 25 ℃ for 15 minin the dark for coloration.
8. Determination: add 50µL of the stop solution into each well. Mix gently by shaking the plate manually. Set the wavelength of the microplate reader at 450nm to determine the OD value of every well. (Recommend to read the OD value at the dual-wavelength 450/630nm within 5 min).

7. Result judgment

There are two methods to judge the results; the first one is the rough judgment, while the second is the quantitative determination. Note that the OD value of the sample has a negative correlation with β-agonists concentration in the sample.

7.1 Qualitative determination
The concentration range (ng/mL) obtained from comparing the average OD value of the sample with that of the standard solution. Assuming that the OD value of the sample Ⅰ is 0.3, and that of the sample Ⅱ is 1.0, the OD value of standard solutions is: 2.243 for 0ppb, 1.816 for 0.1ppb, 1.415 for 0.3ppb, 0.74 for 0.9ppb, 0.313 for 2.7ppb, 0.155 for 8.1ppb, accordingly the concentration range of the sample Ⅰ is 2.7 to 8.1ppb, and that of the sample Ⅱ is 0.3 to 0.9ppb.

7.2 Quantitative determination
The mean values of the absorbance values obtained for the average OD value (B) of the sample and the standard solution divided by the OD value (B0) of the first standard solution (0 standard) and subsequently multiplied by 100%, that is

B—the average (double wells) OD value of the sample or the standard solution
B0—the average OD value of the 0 ng/mL standard solution
Draw the standard curve with the absorption percentages of standard solutions and the semilogarithm values of β-agonists standard solutions (ng/mL) as Y- and X-axis, respectively. Read the corresponding concentration of the sample from the standard curve by incorporating its absorption percentage into the standard curve. The resulting value is subsequently multiplied by the dilution fold, finally obtaining β-agonists concentration in the sample.

8. Precautions

1.The room temperature below 25 ℃ or the temperature of the reagents and the samples being not returned to the room temperature (20-25 ℃) will lead to a lower standard OD value.
2.Dryness of the microplate in the washing process will be accompanied by the situations including the non-linear standard curves and the undesirable reproducibility; So continue to next step immediately after washing.
3.Mix evenly, otherwise there will be the undesirable reproducibility.
4.The stop solution is the 2 M sulfuric acid solution, avoid contacting with the skin.
5. Do not use the kit exceeding its expiry date. The use of diluted or adulterated reagents from the kits will lead to the changes in the sensitivity and the detecting OD values. Do not exchange the reagents from the kits of different lot numbers to use.
6. Put the unused microplate into an auto-sealing bag to re-seal it. The standard substance and the colourless color former is light sensitive, and thus they cannot be directly exposed to the light.
7. Discard the colouration solution with any color that indicates the degeneration of this solution. The detecting value of the 0 standard solution (0 ppb) of less than 0.5 indicates its degeneration.
8. The optimum reaction temperature is 25 ℃, and too high or too low temperatures will result in the changes in the detecting sensitivity and OD values.

9. Storage and expiry date

Storage: store at 2-8 ℃, not frozen.
Expiry date: 12 months; date of production is on box.
Remarks: If the vacuum package of microtiter plates has leakage, the microtiter plate is normal and effective, do not affect the experimental result. Please feel free to use.

Q1: When will it be shipped?
A1: We will ship the goods for you as soon as possible within 7 working days after receiving the payment. (In case of external factors such as the epidemic, the delivery may be delayed)

Q2: Does it support OEM/ODM?
A2: It can be supported, but the specific quantity needs to be more than 100,000 pieces, which is convenient for customized products.

Q3: How is your factory doing in terms of quality control?
A3: We have nationally certified ISO9001 and ISO13485. Our production process conforms to standard procedures to ensure optimum product quality.

Q4: How to provide after-sales service?
A4: We provide professional online technical after-sales service. We can provide you with one-on-one guidance via video, telephone, etc.

Q5: What is the payment method?
A5: We receive payment by T/T.

Q6: How to ship?
A6: Choose the best shipping method for you by getting quotes from our many cooperative carriers, and also ship according to your requirements.

Shenzhen Wensidun Technology Co., Ltd. was established in 2018 and is located in Longgang District, Shenzhen, Guangdong Province, China. We have in-depth cooperation with Green Spring, which has 20 years of production and R&D experience.

We have more than 2000 square meters of GMP clean production workshop and more than 1000 square meters of R&D center in Shenzhen. Products cover over 100 varieties of food safety test kits, animal diseases diagnostic kits, in vitro diagnostic reagents, genetic antibody antigen preparation and form a complete set of testing instrument.Currently,our food safety test kit and animal disease diagnostic kit are widely used in many governments,enterprises and research institutes.Our products are sold to more than 40 countries and areas.

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