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12-Hydroxyeicosatetraenoic Acid (12-HETE) ELISA Kit
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12-Hydroxyeicosatetraenoic Acid (12-HETE) ELISA Kit
产品资料
12-Hydroxyeicosatetraenoic Acid (12-HETE) ELISA Kit
如果您对该产品感兴趣的话,可以
产品名称:
12-Hydroxyeicosatetraenoic Acid (12-HETE) ELISA Kit
产品型号:
abx251300
产品展商:
abbexa
产品文档:
无相关文档
简单介绍
12-Hydroxyeicosatetraenoic Acid (12-HETE) ELISA Kit
产品描述
12-Hydroxyeicosatetraenoic Acid (12-HETE) ELISA Kit is an ELISA Kit for the in vitro quantitative measurement of 12-Hydroxyeicosatetraenoic Acid (12-HETE) concentrations in serum, plasma and other biological fluids.
Target
12-Hydroxyeicosatetraenoic Acid (12-HETE)
Reactivity
General (All species)
Tested Applications
ELISA
Recommended dilutions
Optimal dilutions/concentrations should be determined by the end user.
Storage
Shipped at 4 °C. Upon receipt, store the kit according to the storage instruction in the kit's manual.
Validity
The validity for this kit is at least 6 months. Up to 12 months validity can be provided on request.
Stability
The stability of the kit is determined by the rate of activity loss. The loss rate is less than 5% within the expiration date under appropriate storage conditions. To minimize performance fluctuations, operation procedures and lab conditions should be strictly controlled. It is also strongly suggested that the whole assay is performed by the same user throughout.
Test Range
0.78 ng/ml - 50 ng/ml
Sensitivity
0.47 ng/ml
Standard Form
Lyophilized
Detection Method
Colorimetric
Assay Type
Competitive
Assay Data
Quantitative
Sample Type
Serum, plasma and other biological fluids.
Kit Components
The kit components listed are for reference only. The product manual may differ slightly. The product should be used as stated on the product manual included and delivered together with the product.
Pre-coated 96-Well Microplate
Standard
Standard Diluent Buffer
Wash Buffer
Detection Reagent A
Detection Reagent B
Diluent A
Diluent B
TMB Substrate
Stop Solution
Plate Sealer
Material Required But Not Provided
37°C incubator
Multi and single channel pipettes and sterile pipette tips
Squirt bottle or automated microplate washer
1.5 ml tubes
Distilled water
Absorbent filter papers
100 ml and 1 liter graduated cylinders
Microplate reader (wavelength: 450 nm)
ELISA Shaker
Sample Collection/Preparation
Serum: Samples should be collected into a serum separator tube. Coagulate the serum by leaving the tube undisturbed in a vertical position overnight at 4°C or at room temperature for up to 60 minutes. Centrifuge at approximately 1000 × g for 20 min. Analyze the serum immediately or aliquot and store at -20°C or -80°C.
Plasma: Collect plasma using heparin or EDTA as an anticoagulant. Centrifuge for 15 minutes at 1000 × g within 30 minutes of collection. Assay immediately or aliquot and store at -20°C or -80°C. Avoid hemolysis and high cholesterol samples.
Tissue homogenates: The preparation of tissue homogenates will vary depending upon tissue type – this is just an example. Rinse tissues with ice-cold PBS to remove the excess of blood. Weigh before homogenization. Finely mince tissues and homogenize with a tissue homogenizer on ice in PBS and sonicate the cell suspension. Centrifuge the homogenates at 5000 × g for 5 min and collect the supernatant. Assay immediately or aliquot and store at -20°C.
Reagent Preparation
This procedure is provided for reference only. The product manual may differ slightly. The product should be used as stated on the product manual included and delivered together with the product.
1) Standard: Prepare the standard with the recommended volume of Standard Diluent Buffer, to make the standard solution. Then use the Standard Diluent buffer to carry out serial dilutions of the standard solution, as instructed in the Protocol.
2) Wash Buffer: Dilute the concentrated Wash Buffer with distilled water, as instructed in the Protocol.
3) Detection Reagent Preparation: Calculate the total volume of working solution required. Dilute Detection Reagent A and Detection Reagent B with Diluent A and Diluent B, respectively, at 1:100.
Assay Procedure
This procedure is provided for reference only. The product manual may differ slightly. The product should be used as stated on the product manual included and delivered together with the product.
1) Set standard, test samples and control wells.
2) Aliquot 50 µl of diluted standard into the standard wells.
3) Aliquot 50 µl of Standard Diluent buffer into the control (zero) well.
4) Aliquot 50 µl of diluted samples into the sample wells.
5) Immediately aliquot 50 µl of Detection Reagent A to each well. Incubate for 45 mins at 37 °C.
6) Wash 3 times.
7) Aliquot 100 µl of Detection Reagent B to each well. Incubate for 30 mins at 37 °C.
8) Wash 5 times.
9) Aliquot 90 µl of TMB Substrate to each well. Incubate for 10-20 mins at 37 °C.
10) Aliquot 50 µl of Stop Solution.
11) Measure the OD at 450 nm.
Assay Precision
Intra-assay Precision (Precision within an assay): 3 samples with low, medium and high levels of 12-Hydroxyeicosatetraenoic Acid (12-HETE) were tested 20 times on one plate, respectively.
Inter-assay Precision (Precision between assays): 3 samples with low, medium and high levels of 12-Hydroxyeicosatetraenoic Acid (12-HETE) were tested on 3 different plates, 8 replicates in each plate.
CV (%) = (Standard Deviation / mean) × 100
Intra-Assay: CV<10%
Inter-Assay: CV<10%
Availability
Shipped within 5-7 working days.
Note
This product is for research use only.
The range and sensitivity is subject to change. Please contact us for the latest product information. For accurate results, sample concentrations must be diluted to mid-range of the kit. If you require a specific range, please contact us in advance or write your request in your order comments.
Please note that our ELISA and CLIA kits are optimised for detection of native samples, rather than recombinant proteins. We are unable to guarantee detection of recombinant proteins, as they may have different sequences or tertiary structures to the native protein.
Research Articles on 12-Hydroxyeicosatetraenoic Acid (12-HETE)
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