recombinant
expressed in E. coli
Quality Level
assay
≥80% (SDS-PAGE)
form
buffered aqueous glycerol solution
UniProt accession no.
shipped in
dry ice
storage temp.
−20°C
Gene Information
human ... E2F6(1876)
General description
E2F6 (E2F transcription factor 6) belongs to a family of eight transcription factors (E2F1-E2F8), called E2F. This family is divided into three groups, and E2F6, E2F7 and E2F8 belong to the third group. Its C-terminal lacks the pRb-binding domain, its N-terminal lacks the homology domain found in E2F1 to E2F3, and it also does not contain the transactivation domain found in E2F1 to E2F5. It acts as a polycomb group (PcG) transcriptional repressive complex-association protein. In humans, it is expressed in CD34+ hematopoietic progenitor cells.
Biochem/physiol Actions
E2F6 (E2F transcription factor 6) acts as a transcriptional repressor in a pocket-protein independent manner, and it is not transactivated and does not contain pocket-protein binding domains. Human parvovirus B19 (B19V) elevates E2F6 expression, thus, prevents cell division of human erythroid progenitors. HPV (human papilloma virus)16 E7 oncoprotein interacts with E2F6 and leads to the deregulation of its expression. It acts as an antagonist of E2F-1, which is pro-apoptotic in nature, and prevents the apoptosis of hematopoietic progenitor cells during proliferation. It interacts with BRCA1, through its C-terminal and suppresses the ultraviolet-induced apoptosis.
E2F6 is a member of the E2F family of transcription factors that play an important role in the regulation of cell cycle progression. In normal cells, E2F activity is regulated by binding to pRB, the product of the retinoblastoma gene, and by binding to "pocket proteins", p107 and p130.
Physical form
Solution in 50 mM Tris, pH 7 (25 °C), 150 mM NaCl, 1 mM EDTA, 1 mM DTT, and 30% (w/v) glycerol.
Analysis Note
The product may appear as a triplet in SDS-PAGE.
存储类别
10 - Combustible liquids
wgk
WGK 1
flash_point_f
Not applicable
flash_point_c
Not applicable
法规信息
新产品
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Zhihong Wan et al.
The Journal of clinical investigation, 120(10), 3530-3544 (2010-10-05)
Human parvovirus B19 (B19V) is the only human pathogenic parvovirus. It causes a wide spectrum of human diseases, including fifth disease (erythema infectiosum) in children and pure red cell aplasia in immunocompromised patients. B19V is highly erythrotropic and preferentially replicates
Margaret E McLaughlin-Drubin et al.
Journal of virology, 82(17), 8695-8705 (2008-06-27)
The papillomavirus life cycle is intimately coupled to the differentiation state of the infected epithelium. Since papillomaviruses lack most of the rate-limiting enzymes required for genome synthesis, they need to uncouple keratinocyte differentiation from cell cycle arrest and maintain or
Jiro Kikuchi et al.
Stem cells (Dayton, Ohio), 25(10), 2439-2447 (2007-06-30)
E2F-6 is a dominant-negative transcriptional repressor against other members of the E2F family. In this study, we investigated the expression and function of E2F-6 in human hematopoietic progenitor cells to clarify its role in hematopoiesis. We found that among E2F
W-W Yang et al.
Cell death and differentiation, 14(4), 807-817 (2006-11-11)
E2F6 is believed to repress E2F-responsive genes and therefore plays an important role in cell-cycle regulation. However, the role of E2F6 in the control of apoptosis remains unknown. We show here that the expression of E2F6 was downregulated with a
BAP1 immunohistochemistry and p16 FISH to separate benign from malignant mesothelial proliferations.
Brandon S Sheffield et al.
The American journal of surgical pathology, 39(7), 977-982 (2015-01-31)
A variety of immunohistochemical (IHC) stains have been proposed to mark either benign or malignant mesothelial proliferations. Loss of the p16 tumor suppressor (CDKN2A), through homozygous deletions of 9p21, is a good marker of mesotheliomas but lacks sensitivity. Recent reports
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