Oxytetracyline ELISA Test Kit

Catalog No. LSY-10044

1. Principle

This test kit is based on the competitive enzyme immunoassay for the detection ofOxytetracyline in the sample. The coupling antigens are pre-coated on the micro-well stripes. TheOxytetracyline in the sample and the coupling antigens pre-coated on the micro-well stripes compete for the anti- Oxytetracyline antibody. 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 theOxytetracyline in it. This value is compared to the standard curve and theOxytetracyline concentration is subsequently obtained.

 

2. Technical specifications

Sensitivity: 0.4 ppb

Incubation Temperature: 25℃

Incubation Time: 30min—15min

Detection limit:

Tissue,Honeyabout20ppb

Milk (method 1)about20ppb

Milk (method 1)about40ppb

Feedabout600ppb

Note:ppb=ng/mLorng/g

Cross-reaction rate:

Oxytetracyline100%

Tetracycline200%

Chlortetracycline240%

Doxycycline20%

Recovery rate:  90±15%

 

3. Components

1） Micro-well strips: 12 strips with 8 removable wells each

2） 10×concentratedstandard solution: 0 ppb,4ppb,12ppb,36ppb,108ppb (0.5ml/bottle)

3） Enzyme conjugate (7 mL)

4） Antibody working solution (7 mL)

5） Substrate A (7 mL)

6） Substrate B (7 mL)

7） Stop solution (7 mL)

8） 20× concentrated washing buffer (30 mL)

9） 20× concentrated redissolving solution (10 mL)  

 

4. Materials required but not provided

1) Equipments: microplate reader (450nm, 630nm),rotary evaporator/nitrogen-drying device, homogenizer, oscillator, centrifuge (4000g and above), balance (a sensibility reciprocal of 0.01 g), measuring pipets, incubator (adjustable25℃、37℃、60℃),timer

2) Micropipettors: single-channel 20~200 µL and 100~1000 µL, and multi-channel30~300 µL;

3) Reagents: deionized water, HCl, N,N-Dimethylformamide(DMF) 

 

5. Sample pre-treatment

Instructions

The following points must be dealt with before the pre-treatment of any kind of sample:

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 equipment 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) Dilute20× concentrated redissolving solution withdeionized water at 1:19(1 partconcentrated redissolving solution + 19 parts deionized water ).  

2) Washing buffer: 1 part 20× concentrated washing buffer + 19 parts deionized water

3) 1M HCl: take 1ml concentrated HCl, add 11ml deionized water to dissolve and mix it evenly.

5.1Tissue

1. Take1± 0.01 g of the homogenized sample into10 mL centrifugetube, add1 mLN,N-Dimethylformamide(DMF), shakewithoscillator for5min,to make sample completely dispersed, fully contact with the organic phase.

2. Centrifuge at above4000g for10 minutes.

3. Take100ul up-layer clear liquid, add900uldiluted redissolving solution, shake withoscillator for10min;

4. Take 50 µL for analysis.

Fold of dilution of the sample:20      

5.2 Honey

1) Take1± 0.01ghoney sample into10 mL centrifugetube; Add 2ml deionized water, shakewithoscillator fully for 1 min to dissolve; take 100ul dissolved solution, add 400uldiluted redissolving solution,oscillator for 10S to mix it evenly;

2) Take 50ul for analysis immediately.

   Fold of dilution of the sample:10

5.3 Milk (method 1)

1) Thaw the collected liquid milk sample, then put at room temperature for 30min;

2) Put tips in the down-layer of milk, take 1ml sample into 2ml centrifuge tube(note: do not take the up-layer cream);

3) Add 50ul 1M HCl, shake strongly for 1min(oroscillator for30s);

4) Centrifuge at above4000 r/min at room temperature (20 - 25 ℃) for 10 minutes;

5) Take up-layer clear liquid 50ul into another clean centrifuge tube(note: do not take the up-layer cream), add 450uldiluted redissolving solution, shake strongly for 1min(oroscillator for30s);

6) Take 50ul for analysis immediately.

   Fold of dilution of the sample:10

 Milk (method 2)

1) Take 50ul liquid sample into 1950uldiluted redissolving solution;oscillator fullyfor1min evenly;

2) Take 50ul for analysis immediately.

 Fold of dilution of the sample:40

5.4 Feed (Cattle feed, pig feed)

1.Take1± 0.01 gfeed sample into50 mL centrifugetube, add5 mLdeionized water, shakewithoscillator for 2min until feed separate completely, centrifuge at above4000 r/min for 10 minutes.

2.Take40ul up-layer clear liquid into a new centrifuge tube, add1560uldiluted redissolving solution, shake withoscillator for30s;

3.Take 50 µL for analysis.

Fold of dilution of the sample:200  

6.ELISA procedures

 Instructions

1. Bring all reagents and micro-well strips to the room temperature (20-25 ℃).

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 the procedures of ELISA.

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.

 Operation procedures

1. Take out all the necessary reagents from the kit and place at the room temperature (20 to 25 ℃) for at least 30 minutes. Note that each liquid reagent must be shaken to mix evenly before use.

2. Dilute the 5 concentrated standard solution separately: take 5 pieces of 2ml centrifuge tube, mark 0、0.4、1.2、3.6、10.8ppb accordingly, add 900µL thediluted redissolving solution into each tube, then add the five10X concentrated standard solution into above 5 tubes accordingly, 100ul/tube. The5 diluted standard solutions will be:0—0、0.4—4、1.2—12、3.6—36、10.8—108.

3. Take the required micro-well strips and plate frames. Re-sealed the unused microplate, stored at 2-8℃, not frozen.

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 50µL of the sample or standard solution to separate duplicate wells,then add enzyme conjugate, 50µL each well, thenadd 50 µL of the antibody solution into each well. Mix gently by shaking the plate manually, seal the microplate with the cover membrane, andincubate at25 ℃ at darkfor30 minutes.

6. Pour liquid out of microwell, add 250 µL/well of washing buffer for 15-30 seconds, repeatthreeto four times, then flap to dry (if there are the bubbles after flapping, cut them with the clean tips).

7. Coloration: add100 µLmixture ofthe substrate A andsubstrateB into each well (Note: mix Substrate A and Substrate B at 1:1, the mixture should be used in 10min, never use metal container or metal to stir the solution, otherwise the substrate may be invalid.). Mix gently by shaking the plate manually, andincubate at25 ℃ for15 minutes at dark for coloration.

8. Determination: add 50 µL of the stop solution into each well (The substrate color from blue to yellow, it means the stop succeeds). Mix gently by shaking the plate manually. Set the wavelength of the microplate reader at 450 nm to determine the OD value (Recommend to read the OD value at the dual-wavelength 450/630 nm within 5 minutes).

 

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 the content ofOxytetracyline in the sample.

7.1 Qualitative determination

The concentration range (ng/mL) can be obtained from the comparison the average OD value of the sample with that of the standard solution. Assuming that the OD value of the sampleⅠ is 0.3, and that of the sampleⅡ is1.0, while those of the standard solutions are as the followings:2.243 for 0ppb,1.816 for0.4ppb, 1.415 for1.2ppb,0.74 for3.6ppb, 0.313 for10.8ppb,accordingly the concentration range of the sampleⅠis3.6 to10.88ppb, and that of the sampleⅡ is 0.4 to 1.2 ppb.

7.2 Quantitative determination

The mean values of the absorbance values is equivalent to the percentage of 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 the standard solutions and the semilogarithm values of theOxytetracyline 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 corresponding dilution fold, thus finally obtainingOxytetracyline 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.

3. Mix every reagent and reaction mixture evenly and wash the microplate thoroughly,  otherwise there will be the undesirable reproducibility.

4. The stop solution is the 2 M sulfuric acid solution, avoid contacting with the skin.

5. 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.

6. 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.

7. Discard the colouration solution with any color that indicates the degeneration of this solution. The detecting value of the 0 standard solution of less than 0.5 indicates its degeneration.

8. The optimum reaction temperature is25 ℃, 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 the box.

Note: If the Vacuum package of microplate has leakage, it is still valid to use, do not affect the test result, be relax to use.