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HCFC1 is a member of the host cell factor family and encodes a protein with five Kelch repeats, a fibronectin-like motif, and six HCF repeats, each of which contains a highly specific cleavage signal. Additionally we are shipping HCFC1 Proteins (26) and HCFC1 Kits (2) and many more products for this protein.
Showing 10 out of 36 products:
Human Polyclonal HCFC1 Primary Antibody for IP, PLA - ABIN261124
Parker, Palchaudhuri, Yin, Wei, Chakravarti: A transcriptional regulatory role of the THAP11-HCF-1 complex in colon cancer cell function. in Molecular and cellular biology 2012
Show all 2 references for ABIN261124
Human Polyclonal HCFC1 Primary Antibody for IHC, ELISA - ABIN1533760
Wilson, LaMarco, Peterson, Herr: The VP16 accessory protein HCF is a family of polypeptides processed from a large precursor protein. in Cell 1993
Show all 2 references for ABIN1533760
Cow (Bovine) Polyclonal HCFC1 Primary Antibody for WB - ABIN2780671
Vrabec, Liu, Li, Leal: Sequence variants in host cell factor C1 are associated with Ménière's disease. in Otology & neurotology : official publication of the American Otological Society, American Neurotology Society [and] European Academy of Otology and Neurotology 2008
Human Polyclonal HCFC1 Primary Antibody for IP, WB - ABIN261125
Yu, Mashtalir, Daou, Hammond-Martel, Ross, Sui, Hart, Rauscher, Drobetsky, Milot, Shi, Affar: The ubiquitin carboxyl hydrolase BAP1 forms a ternary complex with YY1 and HCF-1 and is a critical regulator of gene expression. in Molecular and cellular biology 2010
survival of the heterozygous Hcfc1(epiKO/+) female embryos llustrates the developmental plasticity of the post-implantation mouse embryo - in this instance, permitting survival of females heterozygous for an X-linked embryonic lethal allele
our work identifies plausible cellular consequences of missense HCFC1 variants and identifies likely and relevant disease mechanisms that converge on embryonic stages of brain development.
These results indicate that HCF-1 represents a novel transcriptional regulator required for maintaining pancreatic b-cell function.
Ronin (show THAP11 Antibodies)/Hcf-1 controls a genetic program that contributes to the unimpeded growth of embryonic stem cells.
HCF-1 is an important component of the viral latency-reactivation cycle and it is regulated by association with a component that is distinct from the identified HCF-1 interaction factors
Bap1 (show BAP1 Antibodies) helps to control cell proliferation by regulating HCF-1 protein levels and by associating with genes involved in the G(1)-S transition
O-GlcNAcylation of the transcription regulators Host Cell Factor-1 (HCF-1) and Ten-Eleven Translocation protein 2 (TET2 (show TET2 Antibodies)) could be readily observed. Our study raises questions on the occurrence and abundance of O-GlcNAcylation as a histone modification
These results demonstrate that distinct OGT (show OGT Antibodies)-binding sites in HCF-1 promote proteolysis, and provide novel insights into the mechanism of this unusual protease activity.
We report here two brothers with dysmorphic features and complex malformations resulting from an X-linked inherited cobalamin deficiency due to HCFC1 gene mutation.
THAP11 (show THAP11 Antibodies), ZNF143 (show ZNF143 Antibodies), and HCF-1 form a mutually dependent complex on chromatin, which is independent of E2F (show E2F1 Antibodies) occupancy.
study reports the tetratricopeptide-repeat domain of O-GlcNAc (show OGT Antibodies) transferase binds the carboxyl-terminal portion of an HCF-1 proteolytic repeat such that the cleavage region lies in the glycosyltransferase (show GTDC2 Antibodies) active site above uridine diphosphate-GlcNAc; protein glycosylation and HCF-1 cleavage occur in the same active site
A missense mutation in a global transcriptional coregulator, HCFC1, was identified as the genetic basis of an X-linked form of combined methylmalonic acidemia and hyperhomocysteinemia.
HCFC1 is a common component of active human CpG-island promoters and coincides with ZNF143 (show ZNF143 Antibodies), THAP11 (show THAP11 Antibodies), YY1 (show YY1 Antibodies), and GABP transcription factor occupancy.
MLL5 (show MLL5 Antibodies) can associate with HCF-1 and then be recruited to E2F1 (show E2F1 Antibodies)-responsive promoters to stimulate H3K4 trimethylation and transcriptional activation.
A noncoding, regulatory mutation was identified in the binding site of transcription factor YY1 (show YY1 Antibodies) in the HCFC1 gene in patients with nonsyndromic intellectual disability.
HCFC1 plays a role in craniofacial development, which is in part mediated through the regulation of MMACHC (show MMACHC Antibodies) expression
This gene is a member of the host cell factor family and encodes a protein with five Kelch repeats, a fibronectin-like motif, and six HCF repeats, each of which contains a highly specific cleavage signal. This nuclear coactivator is proteolytically cleaved at one of the six possible sites, resulting in the creation of an N-terminal chain and the corresponding C-terminal chain. The final form of this protein consists of noncovalently bound N- and C-terminal chains. The protein is involved in control of the cell cycle and transcriptional regulation during herpes simplex virus infection. Alternatively spliced variants which encode different protein isoforms have been described\; however, not all variants have been fully characterized.
, VP16 accessory protein
, VP16-accessory protein
, host cell factor 1
, host cell factor C1