Human ELF3 Antibody (662516)
R&D Systems | Catalog # MAB57871
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Key Product Details
Validated by
Species Reactivity
Applications
Label
Antibody Source
Product Specifications
Immunogen
Met1-Gly173
Accession # P78245
Specificity
Clonality
Host
Isotype
Scientific Data Images for Human ELF3 Antibody (662516)
ELF3 in Human Prostate.
ELF3 was detected in immersion fixed paraffin-embedded sections of human prostate using Mouse Anti-Human ELF3 Monoclonal Antibody (Catalog # MAB57871) at 15 µg/mL overnight at 4 °C. Before incubation with the primary antibody, tissue was subjected to heat-induced epitope retrieval using Antigen Retrieval Reagent-Basic (Catalog # CTS013). Tissue was stained using the Anti-Mouse HRP-DAB Cell & Tissue Staining Kit (brown; Catalog # CTS002) and counterstained with hematoxylin (blue). Specific staining was localized to nuclei of glandular epithelial cells. View our protocol for Chromogenic IHC Staining of Paraffin-embedded Tissue Sections.Detection of Human ELF3/ESE-1 by Immunohistochemistry
ELF3, EHF, and TGIF1 enhances the malignant phenotypes of LUAD cells.A, B Inhibition of invasive and migrate activity by knockdown master TFs, ELF3, EHF, and TGIF1. PC-9 cells were transfected with indicated siRNA-pool and subjected to invasion and migration assays (see “Materials and methods”). Invaded and migrated cells were stained with crystal violet and counted (see Fig. S3). Histograms represent the number of invasion or migration. Representative photographs were shown. C Colony assay performed on PC-9 cells transfected with either scramble or siRNA-pool targeting ELF3, EHF, and TGIF1. D Silencing of ELF3, EHF, and TGIF1 increased clonal cell growth in a 3D spheroid culture system. PC-9 cells transfected with scramble or siRNA-pool were cultured as spheroid in DMEM medium and the spheroids was observed after 48 h. E Inhibition of cell migration by knockdown master TFs, ELF3, EHF, and TGIF1. PC-9 cells were transfected with indicated siRNA-pool and subjected to scratch assay (see “Materials and methods”). Representative photographs were taken and migration areas were measured. Statistical analysis was performed by using t tests; data are shown as bar graphs of the mean ± SD. of three independent experiments. Scale bars (white) indicate 250 μm. F The effects of pcDNA3.1-ELF3 and/or pcDNA3.1-EHF co-transfected with TGIF1 siRNA on cell migration and invasiveness in LUAD cells were examined by Transwell assays using a Boyden chamber in the presence or absence of Matrigel, respectively. Histograms represent the number of invasion or migration. Data were representative of two to three separate experiments performed in triplicate. *p < 0.05; **p < 0.01; ***p < 0.001. Image collected and cropped by CiteAb from the following publication (https://pubmed.ncbi.nlm.nih.gov/33070167), licensed under a CC-BY license. Not internally tested by R&D Systems.Detection of Human ELF3/ESE-1 by Immunohistochemistry
ELF3, EHF, and TGIF1 enhances the malignant phenotypes of LUAD cells.A, B Inhibition of invasive and migrate activity by knockdown master TFs, ELF3, EHF, and TGIF1. PC-9 cells were transfected with indicated siRNA-pool and subjected to invasion and migration assays (see “Materials and methods”). Invaded and migrated cells were stained with crystal violet and counted (see Fig. S3). Histograms represent the number of invasion or migration. Representative photographs were shown. C Colony assay performed on PC-9 cells transfected with either scramble or siRNA-pool targeting ELF3, EHF, and TGIF1. D Silencing of ELF3, EHF, and TGIF1 increased clonal cell growth in a 3D spheroid culture system. PC-9 cells transfected with scramble or siRNA-pool were cultured as spheroid in DMEM medium and the spheroids was observed after 48 h. E Inhibition of cell migration by knockdown master TFs, ELF3, EHF, and TGIF1. PC-9 cells were transfected with indicated siRNA-pool and subjected to scratch assay (see “Materials and methods”). Representative photographs were taken and migration areas were measured. Statistical analysis was performed by using t tests; data are shown as bar graphs of the mean ± SD. of three independent experiments. Scale bars (white) indicate 250 μm. F The effects of pcDNA3.1-ELF3 and/or pcDNA3.1-EHF co-transfected with TGIF1 siRNA on cell migration and invasiveness in LUAD cells were examined by Transwell assays using a Boyden chamber in the presence or absence of Matrigel, respectively. Histograms represent the number of invasion or migration. Data were representative of two to three separate experiments performed in triplicate. *p < 0.05; **p < 0.01; ***p < 0.001. Image collected and cropped by CiteAb from the following publication (https://pubmed.ncbi.nlm.nih.gov/33070167), licensed under a CC-BY license. Not internally tested by R&D Systems.Detection of Human ELF3/ESE-1 by Immunohistochemistry
ELF3, EHF, and TGIF1 enhances the malignant phenotypes of LUAD cells.A, B Inhibition of invasive and migrate activity by knockdown master TFs, ELF3, EHF, and TGIF1. PC-9 cells were transfected with indicated siRNA-pool and subjected to invasion and migration assays (see “Materials and methods”). Invaded and migrated cells were stained with crystal violet and counted (see Fig. S3). Histograms represent the number of invasion or migration. Representative photographs were shown. C Colony assay performed on PC-9 cells transfected with either scramble or siRNA-pool targeting ELF3, EHF, and TGIF1. D Silencing of ELF3, EHF, and TGIF1 increased clonal cell growth in a 3D spheroid culture system. PC-9 cells transfected with scramble or siRNA-pool were cultured as spheroid in DMEM medium and the spheroids was observed after 48 h. E Inhibition of cell migration by knockdown master TFs, ELF3, EHF, and TGIF1. PC-9 cells were transfected with indicated siRNA-pool and subjected to scratch assay (see “Materials and methods”). Representative photographs were taken and migration areas were measured. Statistical analysis was performed by using t tests; data are shown as bar graphs of the mean ± SD. of three independent experiments. Scale bars (white) indicate 250 μm. F The effects of pcDNA3.1-ELF3 and/or pcDNA3.1-EHF co-transfected with TGIF1 siRNA on cell migration and invasiveness in LUAD cells were examined by Transwell assays using a Boyden chamber in the presence or absence of Matrigel, respectively. Histograms represent the number of invasion or migration. Data were representative of two to three separate experiments performed in triplicate. *p < 0.05; **p < 0.01; ***p < 0.001. Image collected and cropped by CiteAb from the following publication (https://pubmed.ncbi.nlm.nih.gov/33070167), licensed under a CC-BY license. Not internally tested by R&D Systems.Applications for Human ELF3 Antibody (662516)
Immunohistochemistry
Sample: Immersion fixed paraffin-embedded sections of human prostate
Formulation, Preparation, and Storage
Purification
Reconstitution
Sterile PBS to a final concentration of 0.5 mg/mL. 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: ELF3
Long Name
Alternate Names
Gene Symbol
UniProt
Additional ELF3 Products
Product Documents for Human ELF3 Antibody (662516)
Certificate of Analysis
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Product Specific Notices for Human ELF3 Antibody (662516)
For research use only
Related Research Areas
Citations for Human ELF3 Antibody (662516)
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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
- 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
- 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
- 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
- TUNEL and Active Caspase-3 Detection by IHC/ICC Protocol
- The Importance of IHC/ICC Controls
- Troubleshooting Guide: Immunohistochemistry
- View all Protocols, Troubleshooting, Illustrated assays and Webinars