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anti-Rat (Rattus) MCPH1 Antikörper:
anti-Human MCPH1 Antikörper:
anti-Mouse (Murine) MCPH1 Antikörper:
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Human Polyclonal MCPH1 Primary Antibody für IHC, IHC (p) - ABIN4333221
Venkatesh, Nagashri, Swamy, Mohiyuddin, Gopinath, Kumar: Primary microcephaly gene MCPH1 shows signatures of tumor suppressors and is regulated by miR-27a in oral squamous cell carcinoma. in PLoS ONE 2013
Human Monoclonal MCPH1 Primary Antibody für ICC, IF - ABIN1042622
Richardson, Shaaban, Kamal, Alisary, Walker, Ellis, Speirs, Green, Bell: Microcephalin is a new novel prognostic indicator in breast cancer associated with BRCA1 inactivation. in Breast cancer research and treatment 2011
MCPH1 interacts with and promotes the E3 ligase betaTrCP2 to degrade Cdc25A (zeige CDC25A Antikörper) independent of DNA damage. Overexpression of betaTrCP2 or the knockdown of Cdc25A (zeige CDC25A Antikörper) remedies the high mitotic index and rescues the premature differentiation of Mcph1-deficient neuroprogenitors in vivo MCPH1 itself is degraded by APC (zeige APC Antikörper)/CCdh1, but not APC (zeige APC Antikörper)/CCdc20, in late mitosis and G1 phase.
Candidate tumor suppressor gene MCPH1 is mutated in colorectal and gastric cancers.
Characterization of the effects of MCPH1 loss-of-function on chromosome morphology.
Results show that in addition to the scaffolding function in complex formation, BRUCE (zeige BIRC6 Antikörper) has an E3 ligase function to promote BRIT1 deubiquitination by USP8 (zeige USP8 Antikörper) leading to accumulation of BRIT1 at DNA double-strand break.
Data indicate splice-acceptor site homozygous mutation in intron 4 of microcephalin (MCPH1) gene in 2 children.
in addition to its role in brain development, MCPH1 also functions as a tumor suppressor gene and is directly regulated by miR (zeige MLXIP Antikörper)-27a.
BRUCE (zeige BIRC6 Antikörper) acts as a scaffold, bridging the ubiquitin-specific peptidase 8 (USP8 (zeige USP8 Antikörper)) and BRIT1 in a complex to coordinate USP8 (zeige USP8 Antikörper)-catalyzed deubiquitination of BRIT1.
SNTB1 (zeige SNTB1 Antikörper) and MCPH1 are located on chromosome 8, which may be involved in neuroticism, avoidant personality and depression.
Phosphorylation of BRIT1 protein coordinates TopBP1 protein recruitment and amplifies ATR signaling in cell DNA damage.
MCPH1 has an important role in regulating cell growth through regulating the cell cycle and apoptosis
sequence comparison of vertebrate species suggested that the identified E2F1 (zeige E2F1 Antikörper) binding motif is primate specific, consistent with the previous observation of rapid evolution of MCPH1 protein sequence in primates
MCPH1 is a bona fide tumor suppressor gene.
Mcph1-deficient mice reveal a role for MCPH1 in otitis media. Expression of Mcph1 in the epithelial cells of middle ear cavities supported its involvement in the development of otitis media.
MCPH1, through its function in the Chk1 (zeige CHEK1 Antikörper)-Cdc25 (zeige CDC25C Antikörper)-Cdk1 (zeige CDK1 Antikörper) pathway to couple the centrosome cycle with mitosis, is required for precise mitotic spindle orientation and thereby regulates the progenitor division mode to maintain brain size.
VIP (zeige Vip Antikörper) blockade induces microcephaly through Mcph1 signaling; VIP (zeige Vip Antikörper)/Mcph1/Chk1 (zeige CHEK1 Antikörper) signaling is key for normal cortical development
SET is an important regulator of chromosome condensation (zeige RCC1 Antikörper)/decondensation and disruption of the MCPH1-SET interaction might be important for the pathogenesis of primary microcephaly
Data did not show clear signs of premature malignant disease development due to the perturbed Mcph1 function.
Craniosynostosis-microcephaly with chromosomal breakage and other abnormalities is caused by a truncating MCPH1 mutation
MCPH1 is essential for mitotic and meiotic recombination DNA repair and maintaining genomic stability.
This gene encodes a DNA damage response protein. The encoded protein may play a role in G2/M checkpoint arrest via maintenance of inhibitory phosphorylation of cyclin-dependent kinase 1. Mutations in this gene have been associated with primary autosomal recessive microcephaly 1 and premature chromosome condensation syndrome. Alternatively spliced transcript variants have been described.
microcephaly, primary autosomal recessive 1
, microcephalin 1
, BRCT-repeat inhibitor of TERT expression 1