Human Phospho-Mer DuoSet IC ELISA
R&D Systems, part of Bio-Techne | Catalog # DYC2579-2
Key Product Details
Assay Type
Sample Type
Reactivity
Human Phospho-Mer 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-Mer DuoSet IC ELISA
Product Specifications
Assay Format
Sample Volume Required
Detection Method
Conjugate
Specificity
Label
Scientific Data Images for Human Phospho-Mer DuoSet IC ELISA
The Human Phospho-Mer DuoSet IC ELISA is more sensitive than immunoprecipitation (IP)-Western analysis
NS0 cells transfected with human Mer (NS0-hMer) were treated with conditioned media from the human lung cell line, WI-38, for 15 minutes to induce tyrosine phosphorylation of Mer. Lysates were serially diluted and analyzed by (A) IP-Western blot and (B) this DuoSet IC ELISA. IPs were done using an anti-Mer monoclonal antibody and goat anti-mouse agarose. Immunoblots were incubated with an HRP-conjugated anti-phosphotyrosine monoclonal antibody (R&D Systems, Catalog # HAM1676) to detect phospho-Mer. Bands were visualized by chemiluminescent detection using WesternGloTM Chemiluminescent Detection Substrate (R&D Systems, Catalog # AR004). Human Phospho-Mer can be detected in this DuoSet IC ELISA by using approximately 5 to 10 times less lysate than is needed for a conventional IP-Western blot.The Human Phospho-MerDuoSet IC ELISA detects ligand-induced Mer tyrosine phosphorylation
NS0-hMer cells were untreated or treated with conditioned media from the human lung cancer cell line, WI-38, for 15 minutes. ELISA and IP-Western blot (inset) analyses were done using 100 μg and 400 μg of lysate, respectively. IP-Western blots for phospho-Mer (p-Mer) were done as described in Figure 1. Blots were stripped and total Mer was detected using a biotinylated anti-Mer polyclonal antibody (R&D Systems, Catalog #BAF891).The specificity of the Human Phospho-MerDuoSet IC ELISA is confirmed by receptor competition
NS0-hMer cells were treated with conditioned media from the human lung cell line, WI-38, for 15 minutes minutes. The indicated amounts of recombinant extracellular domains of human Mer/Fc (R&D Systems, Catalog #891-MR), human Axl/Fc (R&D Systems, Catalog #154-AL), human Dtk/Fc (R&D Systems, Catalog #859-DK) or human TrkA/Fc (R&D Systems, Catalog #175-TK) were added to 100 μg lysate and analyzed using this DuoSet IC ELISA. Competition was observed only with recombinant human Mer.Kit Contents for Human Phospho-Mer 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: Mer
Long Name
Alternate Names
Gene Symbol
Additional Mer Products
Product Documents for Human Phospho-Mer DuoSet IC ELISA
Product Specific Notices for Human Phospho-Mer DuoSet IC ELISA
For research use only