VEGFR1 (vascular endothelial growth factor receptor 1; Flt-1) binds to VEGF-A, VEGF-B, and PlGF and functions in vasculogenesis, angiogenesis, lymphangiogenesis, and wound healing. It is expressed on endothelial cells, osteoblasts, placental trophoblasts, renal mesangial cells, and some hematopoietic stem cells. It can heterodimerize with VEGFR2 and modulate VEGFR2 mediated endothelial cell proliferation and vessel branching. VEGFR1 engagement on monocyte/macrophage lineage cells enhances their migration, and release of growth factors and cytokines.
Human Phospho-VEGFR1/Flt-1 DuoSet IC ELISA
R&D Systems | Catalog # DYC4170-2
Key Product Details
Assay Type
Sample Type
Reactivity
Human Phospho-VEGFR1/Flt-1 DuoSet IC ELISA Features
- Optimized capture and detection antibody pairings and recommended concentrations save lengthy development time
- Development protocols are provided to guide further assay optimization
- Assay can be customized to your specific needs
- Available in 2, 5, and 15-(96-well) plate pack sizes
- Economical alternative to Western blot
Product Summary for Human Phospho-VEGFR1/Flt-1 DuoSet IC ELISA
Product Specifications
Assay Format
Sample Volume Required
Detection Method
Conjugate
Specificity
Label
Kit Contents for Human Phospho-VEGFR1/Flt-1 DuoSet IC ELISA
- Capture Antibody
- Conjugated Detection Antibody
- Calibrated Immunoassay Standard or Control
Other Reagents Required
PBS: (Catalog # DY006), or 137 mM NaCl, 2.7 mM KCl, 8.1 mM Na2HPO4, 1.5 mM KH2O4, pH 7.2 - 7.4, 0.2 µm filtered
Wash Buffer: (Catalog # WA126), or equivalent
Lysis Buffer*
IC Diluent*
Blocking Buffer*
Substrate Solution: 1:1 mixture of Color Reagent A (H2O2) and Color Reagent B (Tetramethylbenzidine) (Catalog # DY999)
Stop Solution: 2 N H2SO4 (Catalog # DY994)
Microplates: R&D Systems (Catalog # DY990), or equivalent
Plate Sealers: ELISA Plate Sealers (Catalog # DY992), or equivalent
*For the Lysis Buffer, IC Diluent, and Blocking BUffer recommended for a specific DuoSet ELISA Development Kit, please see the product
Preparation and Storage
Shipping
Stability & Storage
Background: VEGFR1/Flt-1
Long Name
Alternate Names
Gene Symbol
Additional VEGFR1/Flt-1 Products
Product Documents for Human Phospho-VEGFR1/Flt-1 DuoSet IC ELISA
Certificate of Analysis
To download a Certificate of Analysis, please enter a lot or batch number in the search box below.
Note: Certificate of Analysis not available for kit components.
Product Specific Notices for Human Phospho-VEGFR1/Flt-1 DuoSet IC ELISA
For research use only
Citations for Human Phospho-VEGFR1/Flt-1 DuoSet IC ELISA
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Protocols
Find general support by application which include: protocols, troubleshooting, illustrated assays, videos and webinars.
- ELISA Sample Preparation & Collection Guide
- ELISA Troubleshooting Guide
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- Quantikine HS ELISA Kit Principle, Streptavidin-HRP Polymer
- Sandwich ELISA (Colorimetric) – Biotin/Streptavidin Detection Protocol
- Sandwich ELISA (Colorimetric) – Direct Detection Protocol
- Troubleshooting Guide: ELISA
- View all Protocols, Troubleshooting, Illustrated assays and Webinars
FAQs for Human Phospho-VEGFR1/Flt-1 DuoSet IC ELISA
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Q: What are the recommended methods for removal of adherent cells for preparation of cell lysates?
A: Enzymatic and chemical methods for the removal of cells is not recommended, as they may interfere with the assay. As stated in the datasheet, wash the adherent cells twice with PBS, then add Lysis Buffer #9. Finally, we recommend scraping to remove the adherent cells and resuspend them in the lysis buffer.
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Q: Which phosphorylated sites are recognized by this assay?
A: This assay utilizes an anti-phosphorylated tyrosine monoclonal detection antibody, and it recognizes all phosphorylated tyrosine residues.
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Q: What are the recommended methods for removal of adherent cells for preparation of cell lysates?
A: Enzymatic and chemical methods for the removal of cells is not recommended, as they may interfere with the assay. As stated in the datasheet, wash the adherent cells twice with PBS, then add Lysis Buffer #9. Finally, we recommend scraping to remove the adherent cells and resuspend them in the lysis buffer.
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Q: Which phosphorylated sites are recognized by this assay?
A: This assay utilizes an anti-phosphorylated tyrosine monoclonal detection antibody, and it recognizes all phosphorylated tyrosine residues.