Human ELF3 Antibody

Catalog # Availability Size / Price Qty
MAB57871
MAB57871-SP
ELF3 in Human Prostate.
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Human ELF3 Antibody Summary

Species Reactivity
Human
Specificity
Detects human ELF3 in direct ELISAs. In direct ELISAs, no cross-reactivity with recombinant human ELF5 is observed.
Source
Monoclonal Mouse IgG1 Clone # 662516
Purification
Protein A or G purified from hybridoma culture supernatant
Immunogen
E. coli-derived recombinant human ELF3
Met1-Gly173
Accession # P78245
Formulation
Lyophilized from a 0.2 μm filtered solution in PBS with Trehalose. *Small pack size (SP) is supplied either lyophilized or as a 0.2 µm filtered solution in PBS.

Applications

Recommended Concentration
Sample
Immunohistochemistry
8-25 µg/mL
See below

Please Note: Optimal dilutions should be determined by each laboratory for each application. General Protocols are available in the Technical Information section on our website.

Scientific Data

Immunohistochemistry ELF3 antibody in Human Prostate by Immunohistochemistry (IHC-P). View Larger

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.

Immunohistochemistry Detection of Human ELF3/ESE-1 by Immunohistochemistry View Larger

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.

Immunohistochemistry Detection of Human ELF3/ESE-1 by Immunohistochemistry View Larger

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.

Immunohistochemistry Detection of Human ELF3/ESE-1 by Immunohistochemistry View Larger

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.

Reconstitution Calculator

Reconstitution Calculator

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Preparation and Storage

Reconstitution
Sterile PBS to a final concentration of 0.5 mg/mL.
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Shipping
Lyophilized product is shipped at ambient temperature. Liquid small pack size (-SP) is shipped with polar packs. Upon receipt, store immediately at the temperature recommended below.
Stability & Storage
Use a manual defrost freezer and avoid repeated freeze-thaw cycles.
  • 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.

Background: ELF3

ELF3 (E74-Like Factor 3; also ESE-1, ESX, ERT and JEN) is a 41-43 kDa member of the ETS family of proteins. During uncomplicated (non-inflammatory) periods of cell differentiation, ELF3 is expressed exclusively by epithelial cells, repressing genes needed during early differentiation, and promoting genes needed for full differentiation. Under conditions of inflammation, cells such as monocytes, endothelial cells and chrondrocytes will express ELF3 and produce molecules such as Ang1 and COX2. Human ELF3 is 371 amino acids (aa) in length. It contains one PNT/pointed dimerization domain (aa 46-132), a protein stabilizing PEST sequence (aa 210‑225), an A/T Hook region that binds to AT-rich DNA sequences (aa 236-252), and an ETS DNA binding domain (aa 273-355). ELF3 interacts with CREBBP, EP300, KU70 and KU86. There is one splice variant that shows a deletion of aa 174-200. Over aa 1-173, human ELF3 shares 87% aa identity with mouse ELF3.

Long Name
E74-like factor 3
Entrez Gene IDs
1999 (Human); 13710 (Mouse); 304815 (Rat)
Alternate Names
E74-like factor 3 (ets domain transcription factor, epithelial-specific ); E74-like factor 3; ELF3; Epithelial-restricted with serine box; epithelial-specific); Epithelium-restricted Ets protein ESX; Epithelium-specific Ets transcription factor 1; EPR1; EPR-1; ERT; ESX; ets domain transcription factor, serine box (epithelial-specific); ETS-related transcription factor Elf-3; JEN; serine box

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