Pax3/Pax7 /Pax7 Antibody (274212)
R&D Systems | Catalog # MAB2457
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Key Product Details
Species Reactivity
Validated:
Cited:
Applications
Validated:
Cited:
Label
Antibody Source
Product Specifications
Immunogen
Met1-Ser215
Accession # NP_000429
Specificity
Clonality
Host
Isotype
Scientific Data Images for Pax3/Pax7 /Pax7 Antibody (274212)
Detection of Pax3/Pax7 in B16-F1 cells by Flow Cytometry
B16-F1 cells were stained with Mouse Anti-Human/Mouse Pax3/Pax7 /Pax7 Monoclonal Antibody (Catalog # MAB2457, filled histogram) or isotype control antibody (Catalog # MAB003, open histogram) followed by Allophycocyanin-conjugated Anti-Mouse IgG Secondary Antibody (Catalog # F0101B). To facilitate intracellular staining, cells were fixed with Flow Cytometry Fixation Buffer (Catalog # FC004) and permeabilized with Flow Cytometry Permeabilization/Wash Buffer I (Catalog # FC005). View our protocol for Staining Intracellular Molecules.Pax3/Pax7 in B16‑F1 Mouse Cell Line.
Pax3/Pax7 was detected in immersion fixed B16-F1 mouse melanoma cell line using Mouse Anti-Human/Mouse Pax3/Pax7 Monoclonal Antibody (Catalog # MAB2457) at 2 µg/mL for 3 hours at room temperature. Cells were stained using the NorthernLights™ 557-conjugated Anti-Mouse IgG Secondary Antibody (red; Catalog # NL007) and counterstained with DAPI (blue). Specific staining was localized to nuclei. View our protocol for Fluorescent ICC Staining of Cells on Coverslips.Detection of Human Pax3/Pax7 by Immunocytochemistry/Immunofluorescence
Characterization of iMPCs during monolayer differentiation. a–e Representative immunostaining of Pax3 (a), Myf5 (b), MyoD (c), and MyoG (d), and corresponding quantification (e) during iMPC expansion. Scale bar=100 µm. f Representative FACS analysis for CD56 in H9 and TRiPSC derived iMPCs. g Representative immunostaining (top) and quantification (bottom) of Pax7+ and MyoG+ cell populations for H9 and TRiPS derived myotubes at 2 weeks of monolayer differentiation. (n = 6 samples from 2 differentiations for each cell line). h Representative immunostaining and quantification of GFP+/Pax7+ and GFP-/Pax7+ cell pools at 2 weeks of monolayer differentiation. Scale bar=50 µm. (n = 4 samples from 2 differentiations for each cell line). i Representative immunostaining and quantification of myotube diameter at 1, 2, and 4 weeks of monolayer differentiation. (*P < 0.05 vs. 1 week, #P < 0.05 vs. 4 week, Tukey–Kramer HSD test; n = 6 samples from 2 differentiations for each cell line). Scale bars=50 µm. Data are presented as mean ± SEM Image collected and cropped by CiteAb from the following publication (https://pubmed.ncbi.nlm.nih.gov/29317646), licensed under a CC-BY license. Not internally tested by R&D Systems.Detection of Pax3/Pax7/Pax7 by Immunohistochemistry
Immunofluorescent analysis of Pax3 expression in the developing mouse cerebellum.(A) Bar plot showing the percentage of Pax3 + cells co-stained (y-axis) with cerebellar cell markers Pax2, Foxp2 and Calbindin at E12, E15, and P3 (x-axis). (B) Top: Immunofluorescent co-staining of Pax3 (red) and Foxp2 (green) in embryonic cerebellum at E15. Merged image is a composite image of the Pax3, Foxp2, and DAPI. Bottom: Immunofluorescent co-staining of Pax3 (red) and Calb (green) in the postnatal cerebellum at P0. Merged image is a composite image of the Pax3, Foxp2, and DAPI. Labels: VZ: Ventricular zone, EGL: External granular layer, PCL: Purkinje cell layer, ML: Molecular layer, Scalebars = 100 µm. (C) Immunofluorescent staining of Pax3 (red) in the developing cerebellum at P9. Image collected and cropped by CiteAb from the following open publication (https://pubmed.ncbi.nlm.nih.gov/35942939), licensed under a CC-BY license. Not internally tested by R&D Systems.Detection of Pax3/Pax7/Pax7 by Immunohistochemistry
Immunofluorescent analysis of Pax3 expression in the developing mouse cerebellum.(A) Bar plot showing the percentage of Pax3 + cells co-stained (y-axis) with cerebellar cell markers Pax2, Foxp2 and Calbindin at E12, E15, and P3 (x-axis). (B) Top: Immunofluorescent co-staining of Pax3 (red) and Foxp2 (green) in embryonic cerebellum at E15. Merged image is a composite image of the Pax3, Foxp2, and DAPI. Bottom: Immunofluorescent co-staining of Pax3 (red) and Calb (green) in the postnatal cerebellum at P0. Merged image is a composite image of the Pax3, Foxp2, and DAPI. Labels: VZ: Ventricular zone, EGL: External granular layer, PCL: Purkinje cell layer, ML: Molecular layer, Scalebars = 100 µm. (C) Immunofluorescent staining of Pax3 (red) in the developing cerebellum at P9. Image collected and cropped by CiteAb from the following open publication (https://pubmed.ncbi.nlm.nih.gov/35942939), licensed under a CC-BY license. Not internally tested by R&D Systems.Applications for Pax3/Pax7 /Pax7 Antibody (274212)
CyTOF-ready
Immunocytochemistry
Sample: Immersion fixed B16-F1 mouse melanoma cell line
Intracellular Staining by Flow Cytometry
Sample: B16‑F1 mouse melanoma cell line fixed with paraformaldehyde and permeabilized with saponin
Western Blot
Sample: Recombinant Human Pax3
Reviewed Applications
Read 2 reviews rated 4.5 using MAB2457 in the following applications:
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
Purification
Reconstitution
Reconstitute at 0.5 mg/mL in sterile PBS. For liquid material, refer to CoA for concentration.
Formulation
Shipping
Stability & Storage
- 12 months from date of receipt, -20 to -70 °C as supplied.
- 1 month, 2 to 8 °C under sterile conditions after reconstitution.
- 6 months, -20 to -70 °C under sterile conditions after reconstitution.
Calculators
Background: Pax3/Pax7
Long Name
UniProt
Additional Pax3/Pax7 Products
Product Documents for Pax3/Pax7 /Pax7 Antibody (274212)
Certificate of Analysis
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Product Specific Notices for Pax3/Pax7 /Pax7 Antibody (274212)
For research use only
Related Research Areas
Citations for Pax3/Pax7 /Pax7 Antibody (274212)
Customer Reviews for Pax3/Pax7 /Pax7 Antibody (274212) (2)
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Customer Images
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Application: Western BlotSample Tested: B16-F1 mouse melanoma cell lineSpecies: MouseVerified Customer | Posted 09/13/2021
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Application: Western BlotSample Tested: See PMID 21078671Species: OtherVerified Customer | Posted 02/19/2015
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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
- Appropriate Fixation of IHC/ICC Samples
- Cellular Response to Hypoxia Protocols
- ClariTSA™ Fluorophore Kits
- Detection & Visualization of Antibody Binding
- 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
- 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
- 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 Liperfluo
- 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 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
- Protocol: Annexin V and PI Staining by Flow Cytometry
- Protocol: Annexin V and PI Staining for Apoptosis by Flow Cytometry
- R&D Systems Quality Control Western Blot Protocol
- TUNEL and Active Caspase-3 Detection by IHC/ICC Protocol
- The Importance of IHC/ICC Controls
- Troubleshooting Guide: Fluorokine Flow Cytometry Kits
- 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