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Human Polyclonal NDN Primary Antibody pour IC, IF - ABIN2452057
Kurita, Kuwajima, Nishimura, Yoshikawa: Necdin downregulates CDC2 expression to attenuate neuronal apoptosis. dans The Journal of neuroscience : the official journal of the Society for Neuroscience 2006
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Human Monoclonal NDN Primary Antibody pour IF, IHC (p) - ABIN518218
François, DOrlando, Fatone, Touvier, Pessina, Meneveri, Brunelli: Necdin enhances myoblasts survival by facilitating the degradation of the mediator of apoptosis CCAR1/CARP1. dans PLoS ONE 2012
Overall, these results demonstrate that an increase of SERT (Montrer SLC6A4 Anticorps) activity is sufficient to cause the apneas in Necdin-knockout pups.
The Necdin expression was further associated with suppression of both cell proliferation and death in osteoblasts.
Data reveal that necdin promotes mitochondrial biogenesis through stabilization of endogenous PGC-1alpha to exert neuroprotection against mitochondrial insults.
Our data suggest that necdin suppresses PIAS1 both by inhibiting SUMO E3 ligase activity and by promoting ubiquitin-dependent degradation.
Necdin is a candidate downstream effector for Galphao (Montrer GNAO1 Anticorps).
Myc (Montrer MYC Anticorps) overexpression in the cpk kidney results from the dysregulation of the cystin-necdin regulatory complex and c-Myc (Montrer MYC Anticorps), in turn, contributes to cystogenesis in the cpk mouse.
Antagonistic interplay between necdin and Bmi1 (Montrer BMI1 Anticorps) controls proliferation of neural precursor cells in the embryonic mouse neocortex.
using several mouse models, we reveal a competition between non-imprinted Ndn promoters which results in monoallelic (paternal or maternal) Ndn expression, suggesting that Ndn allelic exclusion occurs in the absence of imprinting regulation.
oxygen tension regulates the necdin protein level in NSCs through HIF-2alpha (Montrer EPAS1 Anticorps)-mediated proteasomal
necdin exerts its pro-survival activity by counteracting the action of the pro-apoptotic protein Cell Cycle Apoptosis Regulatory Protein (Montrer TGFB1 Anticorps) (CCAR1/CARP1 (Montrer CCAR1 Anticorps))
In the skeletal muscle of neonate pigs, both NECD and SNRPN (Montrer SNRPN Anticorps) were maternally imprinted, while UBE3A (Montrer ube3a Anticorps) was not imprinted.
Imprinting analysis showed that NDN and MAGEL2 (Montrer MAGEL2 Anticorps) are paternally expressed in all tissues of pig where the genes were expressed as in human and mouse.
this study shows that hypermethylation of NDN promotes cell proliferation by activating the Wnt (Montrer WNT2 Anticorps) signaling pathway in colorectal cancer
One candidate variant was located in an alpha helix of Necdin (NDN), phased to the paternally inherited allele. NDN is maternally imprinted within the 15q11.2 Prader-Willi Syndrome (PWS) region
NDN is an imprinted tumor suppressor gene which affects cancer cell motility, invasion and growth and that its loss of function in ovarian cancer can be caused by both genetic and epigenetic mechanisms.
Germline single nucleotide polymorphism in necdin gene is associated with breast cancer.
NDN and CD1A (Montrer CD1A Anticorps) are novel prognostic methylation markers in patients with head and neck squamous carcinomas
Necdin expression declined during replicative aging of IMR90 primary human fibroblasts or after induction of premature senescence.Showed that in normal human cells, Necdin expression mimicked the effect of p53 (Montrer TP53 Anticorps) inactivation by increasing radioresistance.
Hypermethylation and mutation of necdin is associated with neoplasms.
necdin exerts its pro-survival activity by counteracting the action of the pro-apoptotic protein Cell Cycle Apoptosis Regulatory Protein (CCAR1/CARP1 (Montrer CCAR1 Anticorps))
necdin has multiple roles within protein complexes in different subcellular compartments, and indicate that it can utilize multiple karyopherin-dependent pathways to modulate its localization.
In pre-adipocytes, necdin over-expression inhibits adipogenesis, while reducing necdin levels enhances adipogenic differentiation in tissue culture cell
This intronless gene is located in the Prader-Willi syndrome deletion region. It is an imprinted gene and is expressed exclusively from the paternal allele. Studies in mouse suggest that the protein encoded by this gene may suppress growth in postmitotic neurons.
, Prader-Willi syndrome chromosome region
, necdin homolog