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CTCF is a member of the BORIS + CTCF gene family and encodes a transcriptional regulator protein with 11 highly conserved zinc finger (ZF) domains. Additionally we are shipping CTCF Kits (8) and CTCF Proteins (7) and many more products for this protein.
Showing 10 out of 74 products:
Human Monoclonal CTCF Primary Antibody for IF, WB - ABIN968757
Bell, West, Felsenfeld: The protein CTCF is required for the enhancer blocking activity of vertebrate insulators. in Cell 1999
Show all 4 references for ABIN968757
Human Monoclonal CTCF Primary Antibody for EIA, WB - ABIN1106844
Grbesa, Marinkovic, Ivkic, Kruslin, Novak-Kujundzic, Pegan, Bogdanovic, Bedekovic, Gall-Troselj: Loss of imprinting of IGF2 and H19, loss of heterozygosity of IGF2R and CTCF, and Helicobacter pylori infection in laryngeal squamous cell carcinoma. in Journal of molecular medicine (Berlin, Germany) 2008
Show all 3 references for ABIN1106844
Human Monoclonal CTCF Primary Antibody for ELISA, WB - ABIN969071
Majumder, Gomez, Chadwick, Boss: The insulator factor CTCF controls MHC class II gene expression and is required for the formation of long-distance chromatin interactions. in The Journal of experimental medicine 2008
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Chicken Polyclonal CTCF Primary Antibody for ChIP, WB - ABIN2780790
Defossez, Kelly, Filion, Pérez-Torrado, Magdinier, Menoni, Nordgaard, Daniel, Gilson: The human enhancer blocker CTC-binding factor interacts with the transcription factor Kaiso. in The Journal of biological chemistry 2005
We propose that cohesin and CTCF have distinct functions in the regulation of runx1 (show RUNX1 Antibodies) during zebrafish embryogenesis.
Data conclude that CTCF modulates MRF (show C11orf9 Antibodies) functional interactions in the orchestration of myogenesis.
TGF-beta (show TGFB1 Antibodies)/beta2-spectrin/CTCF-regulated tumor suppression in human stem cell disorder Beckwith-Wiedemann syndrome.
Results indicate that CTCF binding polarity plays a functional role in the formation of higher-order chromatin structure.
Firre is X-linked and expressed from a macrosatellite repeat locus associated with a cluster of CTCF and cohesin binding sites, and is preferentially located adjacent to the nucleolus
CTCF controls the homeostatic maintenance and migration of Langerhans cells.
MyoD (show MYOD1 Antibodies) affects chromatin looping at CCCTC-binding factor-binding sites represents the first evidence that a differentiation factor regulates chromatin-loop dynamics
Findings establish CTCF as a prominent tumor-suppressor gene and point to CTCF-mediated epigenetic stability as a major barrier to neoplastic progression.
CTCF is recruited in a locus-specific manner and CTCF-RNA interactions may be involved in long-range chromosomal interactions.
TET1 (show TET1 Antibodies)/DNA methylation (show HELLS Antibodies)-dependent nucleosome repositioning is the main mechanism that drives differential CTCF binding site selection during stem cell development.
NURF regulation occurs partly through physical and functional interactions with the ubiquitous and multivalent factors Ctcf and cohesin
CTCF is involved in regulating endocrine function of pancreatic islet cells by suppression of Pax6 (show PAX6 Antibodies) expression.
The action of SNF2H (show SMARCA5 Antibodies) at CTCF sites is functionally important as depletion of CTCF or SNF2H (show SMARCA5 Antibodies) affects transcription of a common group of genes.
CSB (show ERCC6 Antibodies) and CTCF can regulate each other's chromatin association, thereby modulating chromatin structure and coordinating gene expression in response to oxidative stress.
CTCF binds to the provirus at a sharp border in epigenetic modifications in the pX region of the HTLV-1 provirus in T cells naturally infected with HTLV-1. This may cause widespread abnormalities in host cell chromatin structure and gene expression.
CTCF/cohesin coordinates HOXA cluster higher-order chromatin structure and expression during development
CTCF has a role in regulating SLC45A3-ELK4 (show ELK4 Antibodies) Chimeric RNA
CTCF helps recruit CENP-E (show CENPE Antibodies) to the centromere during mitosis and that it may do so through a structure stabilized by the CTCF/CENP-E (show CENPE Antibodies) complex.
Here, the authors reveal the methylcytosine dioxygenases TET1 (show TET1 Antibodies) and TET2 (show TET2 Antibodies) as active regulators of CTCF-mediated alternative splicing through conversion of 5-methylcytosine to its oxidation derivatives.
These results demonstrate the existence of definitive CTCF binding motifs corresponding to CTCF's diverse functions.
the CTCF-associated boundary element, CBS5, employs both Cohesin and noncoding RNA to establish and maintain topologically associated domains at the HOXA locus.
This gene is a member of the BORIS + CTCF gene family and encodes a transcriptional regulator protein with 11 highly conserved zinc finger (ZF) domains. This nuclear protein is able to use different combinations of the ZF domains to bind different DNA target sequences and proteins. Depending upon the context of the site, the protein can bind a histone acetyltransferase (HAT)-containing complex and function as a transcriptional activator or bind a histone deacetylase (HDAC)-containing complex and function as a transcriptional repressor. If the protein is bound to a transcriptional insulator element, it can block communication between enhancers and upstream promoters, thereby regulating imprinted expression. Mutations in this gene have been associated with invasive breast cancers, prostate cancers, and Wilms' tumors. Alternatively spliced transcript variants encoding different isoforms have been found for this gene.
transcriptional repressor CTCF
, CCCTC-binding factor (zinc finger protein)
, transcriptional repressor CTCF-like
, 11-zinc finger protein
, CTCFL paralog
, 11 zinc finger transcriptional repressor