Mer [p Tyr754, p Tyr749, p Tyr753] Antibody
Novus Biologicals | Catalog # NB300-690
Key Product Details
Species Reactivity
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Antibody Source
Product Specifications
Immunogen
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Theoretical MW
Disclaimer note: The observed molecular weight of the protein may vary from the listed predicted molecular weight due to post translational modifications, post translation cleavages, relative charges, and other experimental factors.
Scientific Data Images for Mer [p Tyr754, p Tyr749, p Tyr753] Antibody
Western Blot: Mer [p Tyr754, p Tyr749, p Tyr753] Antibody [NB300-690]
Western Blot: Mer [p Tyr749, p Tyr753] Antibody [NB300-690] - Phospho & non-Phospho-MerTK with Phospho-MERTK Antibody (NB300-690). Phosphorylated (1) & un-phosphorylated (2, 3) MERTK was immunoprecipitated with MERTK and blotted with Phospho-MerTK antibody (NB300-690). MW of MERTK is 174 kDa. Lower broad band is of IgGs in the immunoprecipitates.Immunocytochemistry/ Immunofluorescence: Mer [p Tyr754, p Tyr749, p Tyr753] Antibody [NB300-690]
Mer-[p-Tyr754--p-Tyr749--p-Tyr753]-Antibody-Immunocytochemistry-Immunofluorescence-NB300-690-img0005.jpgImmunocytochemistry/ Immunofluorescence: Mer [p Tyr754, p Tyr749, p Tyr753] Antibody [NB300-690]
Mer-[p-Tyr754--p-Tyr749--p-Tyr753]-Antibody-Immunocytochemistry-Immunofluorescence-NB300-690-img0004.jpgImmunocytochemistry/ Immunofluorescence: Mer [p Tyr754, p Tyr749, p Tyr753] Antibody [NB300-690] -
GAS6 overexpression activates the phosphorylation of Mer signaling in prostate epithelial cells or cancer cells(A) GAS6 mRNA expression as quantified by by real-time PCR in PCaControl cells or PCaGAS6OE cells. (B) GAS6 protein as quantified by ELISA in PCaControl cells or PCaGAS6OE cells. Data in Figure 4A, B are representative of mean with s.d. (Student's t-test). (C, D). PCaControl cells or PCaGAS6OE cells were starved for 24 hours and then exposed to 10% FBS of culture condition for 1 hour and phosphorylation of Mer was evaluated by (C) Western blot or (D) immunofluorescence staining. Bar = 50 μm. (E, F) GAS6 and Mer mRNA expression in the PrEPGAS6+/+ cells or PrEPGAS6−/− cells by real-time PCR. (G) Mer (red)/GAS6 (green) or p-Mer (red)/GAS6 (green) in the PrEPGAS6+/+ cells or PrEPGAS6−/− cells was evaluated by immunofluorescence staining. Bar = 50 μm. Image collected and cropped by CiteAb from the following open publication (https://pubmed.ncbi.nlm.nih.gov/27028863), licensed under a CC-BY license. Not internally tested by Novus Biologicals.Immunocytochemistry/ Immunofluorescence: Mer [p Tyr754, p Tyr749, p Tyr753] Antibody [NB300-690] -
GAS6 overexpression increases CSCs through activation of Mer signaling in PCa cells(A, B) Percent of cells expressing the CSC phenotype in coculture of PCaControl or PCaGAS6OE with osteoblasts as quantified by FACS analysis. Data in Figure 5A, 5B are representative of mean with s.d. (Student's t-test). (C) The sphere formation of PCaControl cells or PCaGAS6OE cells in suspended sphere culture conditions following the treatment with a Mer inhibitor, UNC1062. Bar = 50 μm. (D) Quantification of prostatospheres in suspended sphere culture condition. *Denotes p < 0.05 between vehicle vs. a Mer inhibitor, UNC1062 treatments by Student's t-test. (E, F) MTT assays of PCaControl cells or PCaGAS6OE following the treatment with a Mer inhibitor, UNC1062 at 3 day cultures in adherent culture conditions. N.S. denotes no significance (p > 0.05) between vehicle vs. a Mer inhibitor, UNC1062 treatments by Student's t-test. (G, H) % CSC from DTC population in bone marrow at 24 hours after intracardiac injection of PCaControl cells or PCaGAS6OE in SCID mice (n = 5) as quantified by FACS analysis. Data are representative of mean with s.d. (Student's t-test). (I) Left panel: Immunofluorescence staining of p-Mer (red)/GAS6 (green) in PCa cells in bone marrow of a PCa patient. Blue, DAPI nuclearstain. Bar = 50 μm. Right panel: p-Mer (red)/GAS6 (green) positive cells (white arrows) in the magnification of the white rectangle from left panel. Bar = 20 μm. Image collected and cropped by CiteAb from the following open publication (https://pubmed.ncbi.nlm.nih.gov/27028863), licensed under a CC-BY license. Not internally tested by Novus Biologicals.Applications for Mer [p Tyr754, p Tyr749, p Tyr753] Antibody
ELISA
Flow Cytometry
Immunocytochemistry/ Immunofluorescence
Immunohistochemistry
Western Blot
Flow Cytometry Panel Builder
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Advanced Features
- Spectra Viewer - Custom analysis of spectra from multiple fluorochromes
- Spillover Popups - Visualize the spectra of individual fluorochromes
- Antigen Density Selector - Match fluorochrome brightness with antigen density
Formulation, Preparation, and Storage
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Background: Mer
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Product Documents for Mer [p Tyr754, p Tyr749, p Tyr753] Antibody
Certificate of Analysis
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Product Specific Notices for Mer [p Tyr754, p Tyr749, p Tyr753] Antibody
This product is for research use only and is not approved for use in humans or in clinical diagnosis. Primary Antibodies are guaranteed for 1 year from date of receipt.
Citations for Mer [p Tyr754, p Tyr749, p Tyr753] Antibody
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Protocols
Find general support by application which include: protocols, troubleshooting, illustrated assays, videos and webinars.
- 7-Amino Actinomycin D (7-AAD) Cell Viability Flow Cytometry Protocol
- Antigen Retrieval Protocol (PIER)
- Antigen Retrieval for Frozen Sections Protocol
- Appropriate Fixation of IHC/ICC Samples
- Cellular Response to Hypoxia Protocols
- Chromogenic IHC Staining of Formalin-Fixed Paraffin-Embedded (FFPE) Tissue Protocol
- Chromogenic Immunohistochemistry Staining of Frozen Tissue
- ClariTSA™ Fluorophore Kits
- Detection & Visualization of Antibody Binding
- ELISA Sample Preparation & Collection Guide
- ELISA Troubleshooting Guide
- Extracellular Membrane Flow Cytometry Protocol
- Flow Cytometry Protocol for Cell Surface Markers
- Flow Cytometry Protocol for Staining Membrane Associated Proteins
- Flow Cytometry Staining Protocols
- Flow Cytometry Troubleshooting Guide
- Fluorescent IHC Staining of Frozen Tissue Protocol
- Graphic Protocol for Heat-induced Epitope Retrieval
- Graphic Protocol for the Preparation and Fluorescent IHC Staining of Frozen Tissue Sections
- Graphic Protocol for the Preparation and Fluorescent IHC Staining of Paraffin-embedded Tissue Sections
- Graphic Protocol for the Preparation of Gelatin-coated Slides for Histological Tissue Sections
- How to Run an R&D Systems DuoSet ELISA
- How to Run an R&D Systems Quantikine ELISA
- How to Run an R&D Systems Quantikine™ QuicKit™ ELISA
- ICC Cell Smear Protocol for Suspension Cells
- ICC Immunocytochemistry Protocol Videos
- ICC for Adherent Cells
- IHC Sample Preparation (Frozen sections vs Paraffin)
- Immunocytochemistry (ICC) Protocol
- Immunocytochemistry Troubleshooting
- Immunofluorescence of Organoids Embedded in Cultrex Basement Membrane Extract
- Immunofluorescent IHC Staining of Formalin-Fixed Paraffin-Embedded (FFPE) Tissue Protocol
- Immunohistochemistry (IHC) and Immunocytochemistry (ICC) Protocols
- Immunohistochemistry Frozen Troubleshooting
- Immunohistochemistry Paraffin Troubleshooting
- Intracellular Flow Cytometry Protocol Using Alcohol (Methanol)
- Intracellular Flow Cytometry Protocol Using Detergents
- Intracellular Nuclear Staining Flow Cytometry Protocol Using Detergents
- Intracellular Staining Flow Cytometry Protocol Using Alcohol Permeabilization
- Intracellular Staining Flow Cytometry Protocol Using Detergents to Permeabilize Cells
- Preparing Samples for IHC/ICC Experiments
- Preventing Non-Specific Staining (Non-Specific Binding)
- Primary Antibody Selection & Optimization
- Propidium Iodide Cell Viability Flow Cytometry Protocol
- Protocol for Heat-Induced Epitope Retrieval (HIER)
- Protocol for Liperfluo
- Protocol for Making a 4% Formaldehyde Solution in PBS
- Protocol for VisUCyte™ HRP Polymer Detection Reagent
- Protocol for the Characterization of Human Th22 Cells
- Protocol for the Characterization of Human Th9 Cells
- Protocol for the Fluorescent ICC Staining of Cell Smears - Graphic
- Protocol for the Fluorescent ICC Staining of Cultured Cells on Coverslips - Graphic
- Protocol for the Preparation & Fixation of Cells on Coverslips
- Protocol for the Preparation and Chromogenic IHC Staining of Frozen Tissue Sections
- Protocol for the Preparation and Chromogenic IHC Staining of Frozen Tissue Sections - Graphic
- Protocol for the Preparation and Chromogenic IHC Staining of Paraffin-embedded Tissue Sections
- Protocol for the Preparation and Chromogenic IHC Staining of Paraffin-embedded Tissue Sections - Graphic
- Protocol for the Preparation and Fluorescent ICC Staining of Cells on Coverslips
- Protocol for the Preparation and Fluorescent ICC Staining of Non-adherent Cells
- Protocol for the Preparation and Fluorescent ICC Staining of Stem Cells on Coverslips
- Protocol for the Preparation and Fluorescent IHC Staining of Frozen Tissue Sections
- Protocol for the Preparation and Fluorescent IHC Staining of Paraffin-embedded Tissue Sections
- Protocol for the Preparation of Gelatin-coated Slides for Histological Tissue Sections
- Protocol for the Preparation of a Cell Smear for Non-adherent Cell ICC - Graphic
- Protocol: Annexin V and PI Staining by Flow Cytometry
- Protocol: Annexin V and PI Staining for Apoptosis by Flow Cytometry
- Quantikine HS ELISA Kit Assay Principle, Alkaline Phosphatase
- Quantikine HS ELISA Kit Principle, Streptavidin-HRP Polymer
- R&D Systems Quality Control Western Blot Protocol
- Sandwich ELISA (Colorimetric) – Biotin/Streptavidin Detection Protocol
- Sandwich ELISA (Colorimetric) – Direct Detection Protocol
- TUNEL and Active Caspase-3 Detection by IHC/ICC Protocol
- The Importance of IHC/ICC Controls
- Troubleshooting Guide: ELISA
- Troubleshooting Guide: Fluorokine Flow Cytometry Kits
- Troubleshooting Guide: Immunohistochemistry
- Troubleshooting Guide: Western Blot Figures
- Western Blot Conditions
- Western Blot Protocol
- Western Blot Protocol for Cell Lysates
- Western Blot Troubleshooting
- Western Blot Troubleshooting Guide
- View all Protocols, Troubleshooting, Illustrated assays and Webinars
FAQs for Mer [p Tyr754, p Tyr749, p Tyr753] Antibody
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Q: What is the composition of buffer?
A: The antibody stabilization buffer contains Tris-Glycine buffer pH7.4, glycerol, stabilizing protein BSA, preservative Sodium azide at 0.02% final concentration; however, the exact composition of this buffer is proprietary.