Glu-Glu Epitope Tag Antibody - BSA Free
Novus Biologicals | Catalog # NB600-354
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Scientific Data Images for Glu-Glu Epitope Tag Antibody - BSA Free
Western Blot: Glu-Glu Epitope Tag AntibodyBSA Free [NB600-354]
Western Blot: Glu-Glu Epitope Tag Antibody [NB600-354] - Analysis using the HRP conjugate of NB600-354. Detection of 200, 100, or 50 ng of E. coli whole cell lysate expressing a multi-tag fusion protein. Antibody used at 0.2 ug/ml (1:5,000).Western Blot: Glu-Glu Epitope Tag AntibodyBSA Free [NB600-354]
Western Blot: Glu-Glu Epitope Tag Antibody [NB600-354] - 200, 100, or 50 ng of E. coli whole cell lysate expressing a multi-tag fusion protein. Antibody used at 0.04 ug/ml (1:25,000).Western Blot: Glu-Glu Epitope Tag AntibodyBSA Free [NB600-354]
Western Blot: Glu-Glu Epitope Tag Antibody [NB600-354] - Triton X-100(1%0 Whole cell lysate(20mcg) from Cos7 cells transiently transfected with control vector (v) or an expression vector driving expression of Glu-Glu tagged RalBP1 (a to d).Applications for Glu-Glu Epitope Tag Antibody - BSA Free
ELISA
Immunocytochemistry/ Immunofluorescence
Immunoprecipitation
Western Blot
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Background: Glu-Glu Epitope Tag
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Product Specific Notices for Glu-Glu Epitope Tag Antibody - BSA Free
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.
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Application: Flow CytometrySample Tested: NMuMG mouse mammary gland epithelial cell line and Mouse bloodSpecies: MouseVerified Customer | Posted 08/24/2023Histogram results from flow cytometry on mouse polyomavirus infected and non-infected NMuMg cells and mouse blood. No difference is seen between the infected and non-infected groups.Based on the principle that the Glu-Glu epitope tag is derived from the sequence for mouse polyomavirus Middle T we hypothesized that the anti-Glu-Glu tag might be able to stain middle T antigen in mouse polyomavirus infected cells. We grew two groups of mice NMuMg cells, infecting one with A2 strain mouse polyomavirus for 24 hours and leaving one culture uninfected. The cells were lifted from the plates and prepped for flow cytometry including permeabilizing and staining with the anti-Glu-Glu Tag. The antibody stained a majority of the cells in both groups as positive, demonstrating that the antibody is not specific. Unstained cells were included for comparison. The same experiment was repeated with mouse blood from both infected and non-infected animals producing the same results. In conclusion the Glu-Glu tag antibody does not specifically recognize middle T in cells infected by mouse polyomavirus by flow cytometry. This was an unvalidated application.Bio-Techne ResponseThis review was submitted through the legacy Novus Innovators Program, reflecting a new species or application tested on a primary antibody.
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Protocols
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- Appropriate Fixation of IHC/ICC Samples
- Cellular Response to Hypoxia Protocols
- ClariTSA™ Fluorophore Kits
- Detection & Visualization of Antibody Binding
- ELISA Sample Preparation & Collection Guide
- ELISA Troubleshooting Guide
- 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
- Immunocytochemistry (ICC) Protocol
- Immunocytochemistry Troubleshooting
- Immunofluorescence of Organoids Embedded in Cultrex Basement Membrane Extract
- Immunohistochemistry (IHC) and Immunocytochemistry (ICC) Protocols
- Immunoprecipitation Protocol
- Preparing Samples for IHC/ICC Experiments
- Preventing Non-Specific Staining (Non-Specific Binding)
- Primary Antibody Selection & Optimization
- Protocol for VisUCyte™ HRP Polymer Detection Reagent
- 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 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 of a Cell Smear for Non-adherent Cell ICC - Graphic
- 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: 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