Semicarbazide (SEM) ELISA Quantitation Kit. Manual

Transcription

1 Semicarbazide (SEM) ELISA Quantitation Kit Manual Catalog number: Immunoperoxidase Assay for Determination of Semicarbazide (SEM) in the Tissue (Chicken, Fish and Shrimp), Milk and Honey. This kit is for research use only, and is not for use in diagnostic procedures. GenWay Biotech, Inc Nancy Ridge Drive San Diego, CA Phone: Fax:

2 1. PRINCIPLE OF THE TEST This test kit is based on the competitive enzyme immunoassay for the detection of semicarbazide (SEM) in the tissue (chicken, fish, shrimp), milk, honey. The conjugate antigen is pre-coated on the micro-well stripes. The SEM in the testing sample competes with the conjugate antigen pre-coated on the micro-well stripes, to interact with the antibody against SEM. After the addition of the enzyme conjugate, the TMB substrate is added for coloration. The optical density (OD) value of the testing sample has a negative correlation with the content of SEM in the sample. This value is compared to the standard curve and the content of the corresponding SEM is subsequently obtained. 2. TECHNICAL SPECIFICATIONS Sensitivity 0.1 ppb Detection Limit Tissue and Honey ppb Recovery Rate Tissue (Shrimp and Fish) ±10% Honey, Chicken, Meat/Liver ±15% Cross-Reaction Rate: SEM % AHD < 0.1% AMOZ < 0.1% AOZ < 0.1% 3. COMPONENTS 1. Micro-well strips: 12 strips with 8 removable wells each 2. 6 standard solution (1ml each): 0ppb, 0.1ppb, 0.3ppb, 0.9ppb, 2.7ppb and 8.1ppb 3. Enzyme conjugate (12ml). red cap 4. Antibody working solution (7ml)....blue cap 5. Substrate A solution (7ml).....white cap 6. Substrate B solution (7ml).... black cap 7. Stop solution (7ml).yellow cap concentrated washing buffer (40ml)....white cap 9. 2 concentrated re-dissolving solution (50ml)... transparent cap ml 2-Nitrobenzaldehyde (C 7 H 5 NO 3 )... white cap ml extract of Sample solution black cap For research use only; not for diagnostic or therapeutic use. Page 2

3 4. MATERIALS REQUIRED BUT NOT PROVIDED 1. Equipments Micro-plate reader Printer Mixer or stomacher Nitrogen-drying device Oscillator Centrifuge Measuring pipets Balance with a reciprocal sensibility of 0.01g 2. Micropipettors Single-channel 20 to 200µl and 100 to 1000µl Multi-channel 250µl 3. Reagents Methanol Sodium hydroxide Ethyl acetate, N-hexane Thick HCI Potassium Hydrogen phosphate anhydrous (K 2 HPO 4 ) K 2 Fe(CN) 5 NO.3H 2 O ZnSO 4.7H 2 O 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 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. The 2 concentrated re-dissolving solution is mixed with deionized water at equal volume. The resulting solution will be used for sample re-dissolving. 2. C solution (for milk sample): dissolve 12.5g of K 2 Fe(CN) 5 NO.3H 2 O in deionized water to 100ml D solution (for milk sample): dissolve 29.8g of ZnSO 4.7H 2 O in deionized water to 100ml M K 2 HPO 4 : dissolve 22.8g of K 2 HPO 4 3H 2 O in deionized water to 1L. 4. 1M HCl: dissolve 8.6ml of thick HCI in water to 100ml. For research use only; not for diagnostic or therapeutic use. Page 3

4 5. 1M NaOH: dissolve 4g of NaOH in water to 100ml. 5.1 Samples Preparation a) Shrimp, Fish and Meat Sample Homogenize the sample use mixer or stomacher, continued on method (d) b) Milk Put 5ml milk into centrifugal tube; add C and D solution, 250ul each. Mix thoroughly, use oscillator; centrifuge at above 4000r/min at 4-12 C for 10min with centrifuge of constant temperatures; if no centrifuge of constant temperature, reduce sample temperature to approx 8 C, then centrifuge. Continued on method (d). b) Honey Put 1±0.05 g into centrifugal tube, Add 4 ml deionized water, then 0.5ml1M HCI and 100µl 2-Nitrobenzaldehyde are added, mix with oscillator thoroughly, Continued on second step of (d) d) Continue Above Steps 1. Take 1± 0.05g of the homogenized sample (shrimp, fish and meat), 1.1 ml the supernatant of centrifugal milk(equivalent to 1ml of milk sample), add 4 ml deionized water, 5 ml 1 M HCI and 100 ul 2-Nitrobenzaldehyde to each well, by shaking properly. 2. Incubate at 37 C overnight (approx 16h). 3. Add 5ml 1 M K2HPO4, 0.4ml1M NaOH, 5ml extract of sample solution to each well, shake vigorously for 30 seconds. 4. Centrifuge at above 4000r/min at room temperature (20-25 C) for 10min. 5. Transfer 2.5ml of sample solution into a clean vessel and reduce to dryness by 50 nitrogen or air. 6. Dissolve the dry residue in 1ml N-hexane and mix properly with 1ml of dilute re-dissolving solution, centrifuge at above 4000r/min at room temperature (20-25 C) for 10min. 7. Take 50µl of the lower, aqueous phase per well in the assay. Fold of dilution of the sample: 2 For research use only; not for diagnostic or therapeutic use. Page 4

5 6. ASSAY PROCEDURE 1. Bring test kit to the room temperature (20 to 25 C) for at least 30min, note that each liquid reagent must be shaken evenly before use; put the required micro-well strips into plate frames. Re-sealed the unused microplate, stored at 2 to 8, not frozen. 2. Solution preparation: dilute 40 ml of the concentrated washing buffer (20 concentrated) with the distilled or deionized water to 800ml (or just to the required volume) for use. 3. Ordering: give different serial numbers to the different micro-wells each corresponding to a testing sample or a standard preparation; each testing sample or standard preparation has two duplicate micro-wells; record their locations. 4. Dissolve concentrated antibody in dilute re-dissolving solution by 1:11 (1 ml antibody is added in 10 ml of the dilute re-dissolving solution). 5. Add 50ul of standard preparation and 50ul of the sample to each well, then add 50 ml antibody to every well, Vortex gently to mix evenly, seal the micro-plate with the cover membrane, and incubate at 37 C for 30min. 6. Transfer out liquid of micro-well, soak the well with the washing buffer for 10S and then flap to dry (if there are the bubbles after flapping, cut them with the clean tips); wash the micro-plate with the washing buffer at 250µl/well for four to five times. 7. Add 100µl of the enzyme conjugate into each well; and incubate at 37 C for 30min.Take out micro-plate, wash the micro-plate 4-5 times according to above Coloration: add 50µl of the substrate A solution and then 50µl of the B solution into each well. Vortex gently to mix evenly, and incubate at 37 C for 30min at dark for coloration. 9. Determination: add 50µl of the stop solution into each well. Vortex gently to mix evenly. Set the wavelength of the micro-plate reader at 450nm to determine the OD value of every well. (Recommend to read the OD value at the dual-wavelength 450/630nm). 7. RESULTS There are two methods to judge the results; the first one is used for the rough judgment, while the second for the quantitative determination. Note that the OD value of the testing sample has a negative correlation with the content of Sulfonamides. 7.1 Qualitative Determination The concentration range (ng/ml) can be obtained form the comparison the average OD value of the testing sample with that of the standard preparation. Assuming that the OD value of the sample I is 0.268, and that of the sample II is 1.230, the OD value of standard preparations is: for 0ppb, for 0.1ppb, for 0.3ppb, for 0.9ppb, for 2.7ppb, for 8.1 ppb, accordingly the concentration range of the sample I is 0.9 to 2.7 ppb, and that of the sample II is 0.10 to 0.30 ppb. (multiplied by the corresponding dilution fold) For research use only; not for diagnostic or therapeutic use. Page 5

6 7.2 Quantitative Determination The mean values of the absorbance values is equivalent to the percentage of the average OD value (B) of the testing sample and the standard preparation divided by the OD value (B0) of the first standard preparation (0 standard) and subsequently multiplied by 100%, that is, Percentage of Absorbance Value = (B / B 0 ) x 100% B = the average (double wells) OD value of the testing sample or the standard preparation B 0 = the average OD value of the 0ng/ml standard preparation Draw the standard curve with the absorption percentages of the standard preparations and the semi logarithm values of the Semicarbazide standard preparations (ng/ml) as Y- and X-axis, respectively. Read the corresponding concentration of the testing 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 obtaining the actual concentration of Semicarbazide in the testing sample. Using the professional analyzing software of this kit will be more convenient for the accurate and rapid analysis of a large amount of samples. (Please contact us for this software) 8. PRECAUTIONS 1. The room temperature below 20 or the temperature of the reagents and the testing samples being not returned to the room temperature (20 to 25 C) will lead to a lower standard OD value. 2. Dryness of the micro-plate in the washing process will be accompanied by the situations including the nonlinear 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 2M sulfuric acid solution, being avoided 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 micro-plate into an auto-sealing bag to re-seal it. The standard substance and the colorless color former is light sensitive, and thus they cannot be directly exposed to the light. 7. Discard the coloration solution with any color that indicates the degeneration of this solution. The detecting value of the 0 standard preparation of less than 0.5 (A450nm< 0.5) indicates its degeneration. 9. STORAGE AND EXPIRATION DATE Storage: Store at 2-8 C, not frozen. Expiry Date: 1 Year; Date of production is on the box. For research use only; not for diagnostic or therapeutic use. Page 6

7 Troubleshooting The following are some common problems encountered with the use of ELISA kits, and some of the causes of these problems. 1. Problem: Low absorbance Improper incubation times Improper mixing of the TMB substrate. Each component is mixed in equal parts. Wrong filter on microtiter reader. Wavelength should be 450 nm for TMB, 490 nm for OPD, or 405 nm for ABTS. Incorrect reagents used. 2. Problem: High Absorbance Cross contamination from other samples or positive control. Improper washing. Wrong filter on microtiter reader. Contaminated buffers or enzyme substrate. Improper incubation times. 3. Problem: Poor Duplicates Poor mixing of specimens. Technical error. Inconsistency in following ELISA protocol. Inefficient washing. 4. Problem: All wells are positive Contaminated buffers or enzyme substrate. Inefficient washing. 5. Problem: All wells are negative Procedure not followed correctly. Contaminated buffers or enzyme substrate. Contaminated conjugate. For research use only; not for diagnostic or therapeutic use. Page 7