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Key Product Details
Species Reactivity
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Cited:
Applications
Validated:
Cited:
Label
Antibody Source
Product Specifications
Immunogen
aa 134-234
Specificity
Clonality
Host
Isotype
Scientific Data Images for GLP/EHMT1 Antibody (B0422)
Detection of GLP/EHMT1 by Western Blot
p65 is present in a complex with G9a and GLP under TNF alpha -stimulated conditions in 3T3-L1 adipocytes. Fully differentiated 3T3-L1 adipocytes were treated with 0.75 nM TNF alpha or an equivalent volume of vehicle (0.1% BSA/PBS) for 30 min. (A) Monolayers were collected and subjected to subcellular fractionation. As shown in the left-hand portion of the figure, cytosolic and nuclear protein extracts (300 μg total protein/sample) were immunoprecipitated (IP) with an anti-G9a antibody. The mock sample contained anti-G9a antibody without cell extract and was used as a negative control. (B) The left-hand portion of the figure shows IP of nuclear extract (300 μg total protein/sample) using anti-GLP antibody. The mock sample contained anti-G9a antibody (A) or anti-GLP antibody (B) without protein extract and was used as a negative control in each experiment. The samples on the right-hand portion of (A) or (B) are direct western blot controls containing 25 μg total protein that were analyzed via immunoblotting without IP. This is a representative figure of an experiment independently performed three times. (See Figures S6 and S7 for the original Western blot images). Image collected and cropped by CiteAb from the following open publication (https://pubmed.ncbi.nlm.nih.gov/37237488), licensed under a CC-BY license. Not internally tested by R&D Systems.Detection of GLP/EHMT1 by Western Blot
p65 is present in a complex with G9a and GLP under TNF alpha -stimulated conditions in 3T3-L1 adipocytes. Fully differentiated 3T3-L1 adipocytes were treated with 0.75 nM TNF alpha or an equivalent volume of vehicle (0.1% BSA/PBS) for 30 min. (A) Monolayers were collected and subjected to subcellular fractionation. As shown in the left-hand portion of the figure, cytosolic and nuclear protein extracts (300 μg total protein/sample) were immunoprecipitated (IP) with an anti-G9a antibody. The mock sample contained anti-G9a antibody without cell extract and was used as a negative control. (B) The left-hand portion of the figure shows IP of nuclear extract (300 μg total protein/sample) using anti-GLP antibody. The mock sample contained anti-G9a antibody (A) or anti-GLP antibody (B) without protein extract and was used as a negative control in each experiment. The samples on the right-hand portion of (A) or (B) are direct western blot controls containing 25 μg total protein that were analyzed via immunoblotting without IP. This is a representative figure of an experiment independently performed three times. (See Figures S6 and S7 for the original Western blot images). Image collected and cropped by CiteAb from the following open publication (https://pubmed.ncbi.nlm.nih.gov/37237488), licensed under a CC-BY license. Not internally tested by R&D Systems.Applications for GLP/EHMT1 Antibody (B0422)
Direct ELISA
Immunohistochemistry
Immunoprecipitation
Western Blot
Reviewed Applications
Read 8 reviews rated 4.3 using PP-B0422-00 in the following applications:
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Background: GLP/EHMT1
Long Name
Alternate Names
Gene Symbol
Additional GLP/EHMT1 Products
Product Documents for GLP/EHMT1 Antibody (B0422)
Certificate of Analysis
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Note: Certificate of Analysis not available for kit components.
Product Specific Notices for GLP/EHMT1 Antibody (B0422)
For research use only
Related Research Areas
Citations for GLP/EHMT1 Antibody (B0422)
Customer Reviews for GLP/EHMT1 Antibody (B0422) (8)
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Customer Images
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Application: ImmunohistochemistrySample Tested: Brain tissueSpecies: HumanVerified Customer | Posted 09/07/2021
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Application: Chromatin ImmunoprecipitationSample Tested: B cellsSpecies: HumanVerified Customer | Posted 06/26/2018ChIP was performed using PP-B0422-00 or isotype IgG (1 ug antibody/ 100 ug Chromatin). Realtime-PCR was performed using primers specific for promoter of gene of interest and the results are expressed as % input.
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Application: Western BlotSample Tested: 293TSpecies: HumanVerified Customer | Posted 06/22/2018293T whole cell lysate was immunoblotted with anti GLP anitibody.
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Application: Immunocytochemistry/ImmunofluorescenceSample Tested: CCD-1070Sk human foreskin fibroblast cell lineSpecies: HumanVerified Customer | Posted 06/19/2018
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Application: Western BlotSample Tested: RL human non-Hodgkin's lymphoma B cell lineSpecies: HumanVerified Customer | Posted 01/04/2018
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Application: ImmunocytochemistrySample Tested: Human Dermal Microvascular Endothelial cells - Paraformaldehyde fixed cellsSpecies: HumanVerified Customer | Posted 07/11/2017Immunofluorescence staining of paraformaldehyde fixed Human Dermal Microvascular Endothelial cells. PP-B0422-00 used at 1:100 dilution.
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Application: ImmunoprecipitationSample Tested: Human Dermal Microvascular Endothelial whole cell lysateSpecies: HumanVerified Customer | Posted 04/21/2017
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Application: Western BlotSample Tested: Human Dermal Microvascular Endothelial whole cell lysateSpecies: HumanVerified Customer | Posted 04/21/2017
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Protocols
Find general support by application which include: protocols, troubleshooting, illustrated assays, videos and webinars.
- 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
- 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
- IHC Sample Preparation (Frozen sections vs Paraffin)
- Immunofluorescent IHC Staining of Formalin-Fixed Paraffin-Embedded (FFPE) Tissue Protocol
- Immunohistochemistry (IHC) and Immunocytochemistry (ICC) Protocols
- Immunohistochemistry Frozen Troubleshooting
- Immunohistochemistry Paraffin Troubleshooting
- Immunoprecipitation Protocol
- Preparing Samples for IHC/ICC Experiments
- Preventing Non-Specific Staining (Non-Specific Binding)
- Primary Antibody Selection & Optimization
- Protocol for Heat-Induced Epitope Retrieval (HIER)
- Protocol for Making a 4% Formaldehyde Solution in PBS
- Protocol for VisUCyte™ HRP Polymer Detection Reagent
- 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 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
- 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: 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