Porcine transforming growth factor β1 (TGF-β1)ELISA Kit
Catalog No. CSB-E06843p
(96 T)
This immunoassay kit allows for the in vitro quantitative determination of porcine TGF-β1 concentrations in serum, plasma a-n-d Cell Culture Supernates.
Expiration date six months from the date of manufacture
FOR RESEARCH USE ONLY. NOT FOR USE IN DIAGNOSTIC PROCEDURES.
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PRINCIPLE OF THE ASSAY
The microtiter plate provided in this kit has been pre-coated with an antibody specific to TGF-β1. Sta-n-dards or samples are then added to the appropriate microtiter plate wells with a biotin-conjugated antibody preparation specific for TGF-β1 a-n-d Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well a-n-d incubated. Then a TMB (3,3',5,5' tetramethyl-benzidine) substrate solution is added to each well. Only those wells that contain TGF-β1, biotin-conjugated antibody a-n-d enzyme-conjugated Avidin will exhibit a change in color. The enzyme-substrate reaction is terminated by the addition of a sulphuric acid solution a-n-d the color change is measured spectrophotometrically at a wavelength of 450 nm ±2 nm. The concentration of TGF-β1 in the samples is then determined by comparing the O.D. of the samples to the sta-n-dard curve.
DETECTION RANGE
0.78 ng/ml-50 ng/ml. The sta-n-dard curve concentrations used for the
1.56 ng/ml, 0.78 ng/ml.
ELISA’s were 50 ng/ml, 25 ng/ml, 12.5 ng/ml, 6.25 ng/ml, 3.12 ng/ml,
SPECIFICITY
This assay recognizes porcine TGF-β1. No significant cross-reactivity or interference was observed.
SENSITIVITY
The minimum detectable dose of porcine TGF-β1 is typically less than 0.2 ng/ml. The sensitivity of this assay, or Lower Limit of Detection (LLD) was defined as the lowest protein concentration that could be differentiated from zero.
MATERIALS PROVIDED
Reagent Quantity
Assay plate 1 Sta-n-dard 2 Sample Diluent 1 x 20 ml Biotin-antibody Diluent 1 x 10 ml HRP-avidin Diluent 1 x 10 ml Biotin-antibody 1 x 120μl HRP-avidin 1 x 120μl
1 x20 ml
Wash Buffer
(25×concentrate) TMB Substrate 1 x 10 ml Stop Solution 1 x 10 ml
1 x 10 ml1 N HCI (May be stored for up to 1 month at room temperature)
1 x 10 ml
1.2 N NaOH/0.5 M HEPES (May be stored for up to 1 month at room temperature)
STORAGE
1. Unopened test kits should be stored at 2-8?C upon receipt a-n-d the microtiter plate should be kept in a sealed bag. The test kit may be used throughout the expiration date of the kit, provided it is stored as prescribed above. Refer to the package label for the expiration date.
2. Opened test plate should be stored at 2-8?C in the aluminum foil bag with desiccants to minimize exposure to damp air. The kits will remain stable until the expiring date shown, provided it is stored as prescribed above.
3. A microtiter plate reader with a ba-n-dwidth of 10 nm or less a-n-d an optical density range of 0-3 OD or greater at 450nm wavelength is acceptable for use in absorbance measurement.
REAGENT PREPARATION
Bring all reagents to room temperature before use.
1 Wash Buffer If crystals have formed in the concentrate, warm up to room temperature a-n-d mix gently until the crystals have compley dissolved. Dilute 20 ml of Wash Buffer Concentrate into deionized or distilled water to prepare 500 ml of Wash Buffer.
2 Biotin-antibody Centrifuge the vial before opening. Dilute to the working concentration using Biotin-antibody Diluent(1:100), respectively.
3 HRP-avidin Centrifuge the vial before opening. Dilute to the working concentration using HRP-avidin Diluent(1:100), respectively.
4 Sta-n-dard Centrifuge the sta-n-dard vial at 6000-10000rpm for 30s. Reconstitute the Sta-n-dard with 1.0 ml of Sample Diluent. This reconstitution produces a stock solution of 50 ng/ml. Allow the sta-n-dard to sit for a minimum of 15 minutes with gentle agitation prior to making serial dilutions. The undiluted sta-n-dard serves as the high sta-n-dard (50 ng/ml). The Sample Diluent serves as the zero sta-n-dard (0 ng/ml). Prepare fresh for each assay. Use within 4 hours a-n-d discard after use.
Precaution: The Stop Solution provided with this kit is an acid solution. Wear eye, ha-n-d, face, a-n-d clothing protection when using this material.
OTHER SUPPLIES REQUIRED
1 Microplate reader capable of measuring absorbance at 450 nm, with the correction wavelength set at 540 nm or 570 nm.
2 Pipettes a-n-d pipette tips.
3 Deionized or distilled water.
4 Squirt bottle, manifold dispenser, or automated microplate washer.
5 An incubator which can provide stable incubation conditions up to 37°C±0.5°C.
6 Serum Use a serum separator tube (SST) a-n-d allow samples to clot for 30 minutes before centrifugation for 15 minutes at 1000 g. Remove serum a-n-d assay immediay or aliquot a-n-d store samples at -20°C. Centrifuge the sample again after thawing before the assay. Avoid repeated freeze-thaw cycles.
7 Plasma Collect plasma using citrate, EDTA, or heparin as an anticoagulant. Centrifuge for 15 minutes at 1000 g within 30 minutes of collection. Assay immediay or aliquot a-n-d store samples at -20°C. Centrifuge the sample again after thawing before the assay. Avoid repeated freeze-thaw cycles.
8 Cell Culture Supernates Remove particulates by centrifugation for 15 minutes at 1000 x g, 2 -8°C a-n-d assay immediay or aliquot a-n-d store samples at -20° C or -80℃. Avoid repeated freeze-thaw cycles.
SAMPLE COLLECTION A-N-D STORAGE
Note: Grossly hemolyzed samples are not suitable for use in this assay.
SAMPLE ACTIVATION PROCEDURE
To activate latent TGF-β1 to the immunoreactive form, prepare the following solutions for acid activation a-n-d neutralization (provided in our kit) .The solutions may be stored in polypropylene bottles at room temperature for up to one month. To activate latent TGF-β1 to immunoreactive TGF-β1 detectable by the TGF-β1 ELISA assay, follow the activation procedure outlined below. Assay samples after neutralization (pH 7.2 -7.6). Use polypropylene test tubes.
| Cell Culture Supernates | Serum/Plasma | | To 100μl of cell culture supernate, add 20μl of 1 N HCI. Mix well. | To 80μl serum/plasma, add 20μl of 1 N HCl Mix well. | | Incubate 10 minutes at room temperature. | Incubate 10 minutes at room temperature. | | Neutralize the acidified sample by adding 13 μl of 1.2 N NaOH/0.5 M HEPES. | Neutralize the acidified sample by adding 16μl of 1.2 N NaOH/0.5 M HEPES. | | Mix well. | Mix well. | | Assay immediay. | Assay immediay. | |
ASSAY PROCEDURE
Bring all reagents a-n-d samples to room temperature before use. It is recommended that all samples, sta-n-dards, a-n-d controls be assayed in duplicate. All the reagents should be added directly to the liquid level in the well. The pipette should avoid contacting the inner wall of the well.
1 Add 100μl of Sta-n-dard, Blank, or Sample per well. Cover with the adhesive strip. Incubate for 2 hours at 37°C.
2 Remove the liquid of each well, don’t wash.
3 Add 100μl of Biotin-antibody working solution to each well. Incubate for 1 hour at 37°C. Biotin-antibody working solution may appear cloudy. Warm up to room temperature a-n-d mix gently until solution appears uniform.
4 Aspirate each well a-n-d wash, repeating the process three times for a total of three washes. Wash: Fill each well with Wash Buffer (200μl) a-n-d let it sta-n-d for 2 minutes, then remove the liquid by flicking the plate over a sink. The remaining drops are removed by patting the plate on a paper towel. Complete removal of liquid at each step is essential to good performance.
5 Add 100μl of HRP-avidin working solution to each well. Cover the microtiter plate with a new adhesive strip. Incubate for 1 hour at 37°C.
6 Repeat the aspiration a-n-d wash five times as step 4.
7 Add 90μl of TMB Substrate to each well. Incubate for 10-30 minutes at 37°C. Keeping the plate away from drafts a-n-d other temperature fluctuations in the dark.
8 Add 50μl of Stop Solution to each well when the first four wells containing the highest concentration of sta-n-dards develop obvious blue color. If color change does not appear uniform, gently tap the plate to ensure thorough mixing.
9 Determine the optical density of each well within 30 minutes, using a microplate reader set to 450 nm.
CALCULATION OF RESULTS
Using the professional soft "Curve Exert 1.3" to make a sta-n-dard curve is recommended, which can be downloaded from our web.
Average the duplicate readings for each sta-n-dard, control, a-n-d sample a-n-d subtract the average zero sta-n-dard optical density. Create a sta-n-dard curve by reducing the data using computer software capable of generating a four parameter logistic (4-PL) curve-fit. As an alternative, construct a sta-n-dard curve by plotting the mean absorbance for each sta-n-dard on the x-axis against the concentration on the y-axis a-n-d draw a best fit curve through the points on the graph. The data may be linearized by plotting the log of the TGF-β1 concentrations versus the log of the O.D. a-n-d the best fit line can be determined by regression analysis. This procedure will produce an adequate but less precise fit of the data. If samples have been diluted, the concentration read from the sta-n-dard curve must be multiplied by the dilution factor.
LIMITATIONS OF THE PROCEDURE
1 The kit should not be used beyond the expiration date on the kit label.
2 Do not mix or substitute reagents with those from other lots or sources.
3 It is important that the Sta-n-dard Diluent selected for the sta-n-dard curve be consistent with the samples being assayed.
4 If samples generate values higher than the highest sta-n-dard, dilute the samples with the appropriate Sta-n-dard Diluent a-n-d repeat the assay.
5 Any variation in Sta-n-dard Diluent, operator, pipetting technique, washing technique, incubation time or temperature, a-n-d kit age can cause variation in binding.
6 ? This assay is designed to eliminate interference by soluble receptors, binding proteins, a-n-d other factors present in biological samples. Until all factors have been tested in the Immunoassay, the possibility of interference cannot be excluded. TECHNICAL HINTS
7 Centrifuge vials before opening to collect contents.
8 When mixing or reconstituting protein solutions, always avoid foaming.
9 To avoid cross-contamination, change pipette tips between additions of each sta-n-dard level, between sample additions, a-n-d between reagent additions. Also, use separate reservoirs for each reagent.
10 When using an automated plate washer, adding a 30 second soak period following the addition of wash buffer, a-n-d/or rotating the plate 180 degrees between wash steps may improve assay precision.
11 To ensure accurate results, proper adhesion of plate sealers during incubation steps is necessary.
12 Substrate Solution should remain colorless or light blue until added to the plate. Keep Substrate Solution protected from light. Substrate Solution should change from colorless or light blue to gradations of blue.
13 Stop Solution should be added to the plate in the same order as the Substrate Solution. The color developed in the wells will turn from blue to yellow upon addition of the Stop Solution. Wells that are green in color indicate that the Stop Solution has not mixed thoroughly with the Substrate Solution.
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