EGR3 Protein

EGR3

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EGR3

Official Full Name early growth response 3
Background This gene encodes a transcriptional regulator that belongs to the EGR family of C2H2-type zinc-finger proteins. It is an immediate-early growth response gene which is induced by mitogenic stimulation. The protein encoded by this gene participates in the transcriptional regulation of genes in controling biological rhythm. It may also play a role in a wide variety of processes including muscle development, lymphocyte development, endothelial cell growth and migration, and neuronal development. Alternative splicing results in multiple transcript variants encoding distinct isoforms.[provided by RefSeq, Dec 2010]
Synonyms EGR3; early growth response 3; EGR-3; PILOT; early growth response protein 3; zinc finger protein pilot;
    • Species :
    • Human
    • Mouse
    • Rat
    • Zebrafish
    • Source :
    • E.coli
    • HEK293
    • HEK293T
    • Mammalian Cell
    • Sf9 Insect Cell
    • Wheat Germ
    • Tag :
    • GST
    • His
    • T7
    • Myc/DDK
    • Myc
    • DDK
    • N/A
    Species Cat.# Product name Source (Host) Tag Protein Length Price
    Human EGR3-2083H Recombinant Human Early Growth Response 3 Sf9 Insect Cell N/A
    Human EGR3-3125H Recombinant Human EGR3 Protein, GST-tagged Wheat Germ GST
    Human EGR3-398H Recombinant Human EGR3 Protein, MYC/DDK-tagged HEK293 Myc/DDK
    Human EGR3-6970H Recombinant Human EGR3 protein, His & T7-tagged E.coli His/T7
    Mouse EGR3-5054M Recombinant Mouse EGR3 Protein Mammalian Cell His
    Rat EGR3-2034R Recombinant Rat EGR3 Protein Mammalian Cell His
    Zebrafish EGR3-757Z Recombinant Zebrafish EGR3 Mammalian Cell His
    Human EGR3-243HCL Recombinant Human EGR3 lysate HEK293 N/A
    Human EGR3-2855H Recombinant Human EGR3 protein, His-tagged E.coli His
    Human EGR3-1826H Recombinant Human EGR3 Protein, Myc/DDK-tagged, C13 and N15-labeled HEK293T Myc/DDK
    Mouse Egr3-2762M Recombinant Mouse Egr3 Protein, Myc/DDK-tagged HEK293T Myc/DDK

    EGR3 involved in several pathways and played different roles in them. We selected most pathways EGR3 participated on our site, such as Calcineurin-regulated NFAT-dependent transcription in lymphocytes, Hepatitis B, Viral carcinogenesis, which may be useful for your reference. Also, other proteins which involved in the same pathway with EGR3 were listed below. Creative BioMart supplied nearly all the proteins listed, you can search them on our site.

    Pathway Name Pathway Related Protein
    Calcineurin-regulated NFAT-dependent transcription in lymphocytes EGR3; CSF2; POU2F1; JUNB; BATF3; EGR4; CDK4; IRF4; CTLA4; DGKA
    Hepatitis B STAT4; AKT2; MAPK3; IFNB1; TGFBR1; NFATC3; CASP8; TRP53; NRAS; SMAD4
    Viral carcinogenesis HIST1H2BE; HIST2H2BE; CDC42; KAT2B; PIK3R5; GTF2H2C_2; CCNE2; MAPK3; SCIN; YWHAZ

    EGR3 has several biochemical functions, for example, DNA binding, metal ion binding, transcription factor activity, sequence-specific DNA binding. Some of the functions are cooperated with other proteins, some of the functions could acted by EGR3 itself. We selected most functions EGR3 had, and list some proteins which have the same functions with EGR3. You can find most of the proteins on our site.

    Function Related Protein
    DNA binding SOX19A; RPS15; UNCX4.1; IFIH1; MAFA; BSX; HESX1; SMARCC1B; DLX6A; ZNF19
    metal ion binding RACGAP1; OSR1; ZNF680; MOCS3; PDE4A; CYGB2; ZNF711; IDO1; POLD1; ARAP3
    transcription factor activity, sequence-specific DNA binding GTF2H2; CREB5; CLOCKB; CEBPD; MAFGA; FOXG1A; TBX22; IRF6; SLC2A4RG; SCAND1

    EGR3 has direct interactions with proteins and molecules. Those interactions were detected by several methods such as yeast two hybrid, co-IP, pull-down and so on. We selected proteins and molecules interacted with EGR3 here. Most of them are supplied by our site. Hope this information will be useful for your research of EGR3.

    Shin, H; Kwon, S; et al. The Transcription Factor Egr3 Is a Putative Component of the Microtubule Organizing Center in Mouse Oocytes. PLOS ONE 9:-(2014).
    Darmanis, S; Cui, T; et al. Identification of Candidate Serum Proteins for Classifying Well-Differentiated Small Intestinal Neuroendocrine Tumors. PLOS ONE 8:-(2013).

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