VEGFR1 (Vascular Endothelial Growth Factor Receptor 1) is a receptor involved in blood vessel formation. The Porcine VEGFR1 ELISA kit allows researchers to gain insights into the role of VEGFR1 in angiogenesis and other processes related to blood vessel formation in pigs, providing valuable information for their studies.
Description
Porcine VEGFR1 / Flt1 / Vascular Endothelial Growth Factor Receptor 1 ELISA Kit
Key Features
| Save Time | Pre-coated 96 well plate | |
| Quick Start | Kit includes all necessary reagents | |
| Publication Ready | Reproducible and reliable results |
Overview
| Product Name: | Porcine VEGFR1/Flt1 (Vascular Endothelial Growth Factor Receptor 1) ELISA Kit |
| Product Code: | PRFI00163 |
| Size: | 96 Assays |
| Alias: | VEGFR1, FLT1, Vascular Endothelial Growth Factor Receptor 1, FLT1, Flt-1, FLT-1, Fms-like tyrosine kinase 1, fms-related tyrosine kinase 1, vascular endothelial growth factor, vascularpermeability factor receptor, FRT, Tyrosine-protein kinase FRT, Tyrosine-protein kinase receptor FLT, vascular endothelial growth factor receptor 1, Vascular permeability factor receptor, VEGFR1, VEGFR-1 |
| Detection Method: | Sandwich ELISA, Double Antibody |
| Reactivity: | Porcine |
| Sensitivity: | 18.75pg/ml |
| Range: | 31.25-2000pg/ml |
| Storage: | 4°C for 6 months |
| Note: | For Research Use Only |
Additional Information
| Recovery | Matrices listed below were spiked with certain level of Porcine VEGFR1/Flt1R1/Flt1R1/Flt1 and the recovery rates were calculated by comparing the measured value to the expected amount of Porcine VEGFR1/Flt1R1/Flt1R1/Flt1 in samples. Please contact us for more information. |
| Linearity: | The linearity of the kit was assayed by testing samples spiked with appropriate concentration of Porcine VEGFR1/Flt1R1/Flt1R1/Flt1 and their serial dilutions. The results were demonstrated by the percentage of calculated concentration to the expected. Please contact us for more information. |
| CV(%) | Intra Assay <8 Inter Assay <10 |
Kit Components
| Component | Quantity | Storage |
| ELISA Microplate (Dismountable) | 8x12 strips | 2-8°C/-20°C |
| Lyophilized Standard | 2 | 2-8°C/-20°C |
| Sample/Standard Dlution Buffer | 20ml | 2-8°C |
| Biotin-labeled Antibody (Concentrated) | 120ul | 2-8°C (Protection from light) |
| Antibody Dilution Buffer | 10ml | 2-8°C |
| HRP-Streptavidin Conjugate (SABC) | 120ul | 2-8°C(Protect from light) |
| SABC Dilution Buffer | 10ml | 2-8°C |
| TMB Substrate | 10ml | 2-8°C (Protection from light) |
| Stop Solution | 10ml | 2-8°C |
| Wash Buffer (25X) | 30ml | 2-8°C |
| Plate Sealer | 5 | - |
Other materials required:
- Microplate reader with 450 nm wavelength filter
- Multichannel Pipette, Pipette, microcentrifuge tubes and disposable pipette tips
- Incubator
- Deionized or distilled water
- Absorbent paper
- Buffer resevoir
Protocol
*Note: Protocols are specific to each batch/lot. For the exact instructions please follow the protocol included in your kit.
Before adding to wells, equilibrate the SABC working solution and TMB substrate for at least 30 min at 37°C. When diluting samples and reagents, they must be mixed completely and evenly. It is recommended to plot a standard curve for each test.
| Step | Procedure |
| 1. | Set standard, test sample and control (zero) wells on the pre-coated plate respectively, and then, record their positions. It is recommended to measure each standard and sample in duplicate. Wash plate 2 times before adding standard, sample and control (zero) wells! |
| 2. | Aliquot 0.1ml standard solutions into the standard wells. |
| 3. | Add 0.1 ml of Sample / Standard dilution buffer into the control (zero) well. |
| 4. | Add 0.1 ml of properly diluted sample ( Human serum, plasma, tissue homogenates and other biological fluids.) into test sample wells. |
| 5. | Seal the plate with a cover and incubate at 37 °C for 90 min. |
| 6. | Remove the cover and discard the plate content, clap the plate on the absorbent filter papers or other absorbent material. Do NOT let the wells completely dry at any time. Wash plate X2. |
| 7. | Add 0.1 ml of Biotin- detection antibody working solution into the above wells (standard, test sample & zero wells). Add the solution at the bottom of each well without touching the side wall. |
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