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RERE encodes a member of the atrophin family of arginine-glutamic acid (RE) dipeptide repeat-containing proteins. Additionally we are shipping RERE Kits (7) and RERE Proteins (3) and many more products for this protein.
Showing 10 out of 46 products:
Human Polyclonal RERE Primary Antibody for FACS, IHC (p) - ABIN954511
Zhang, Sol-Church, Rydbeck, Stabley, Spotila, Devoto: High resolution linkage and linkage disequilibrium analyses of chromosome 1p36 SNPs identify new positional candidate genes for low bone mineral density. in Osteoporosis international : a journal established as result of cooperation between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA 2009
Show all 2 references for ABIN954511
Fruit Fly (Drosophila melanogaster) Polyclonal RERE Primary Antibody for WB - ABIN2780857
Olsen, Blagoev, Gnad, Macek, Kumar, Mortensen, Mann: Global, in vivo, and site-specific phosphorylation dynamics in signaling networks. in Cell 2006
Human Polyclonal RERE Primary Antibody for FACS, IHC (p) - ABIN653912
Kumar, Duester: Retinoic acid controls body axis extension by directly repressing Fgf8 transcription. in Development (Cambridge, England) 2014
Results suggest that atrophin2 plays a role in the feedback regulation of Fgf8 (show FGF8 Antibodies) signaling.
the Atro-Rpd3 (show HDAC1 Antibodies) complex plays a conserved role to function as a Ci(R) corepressor.
Tissue-specific transcriptional repression, by means of an REREa-Histone Deacetylase (show HDAC1 Antibodies) complex, modulates growth factor signaling during embryogenesis.
RERE-deficiency leads to delayed development of the principal fissures and delayed maturation and migration of Purkinje cells, abnormal cerebellar foliation and Purkinje cell maturation during postnatal cerebellar development.
RERE plays a critical role in the development.
a mutation in Rere (also known as atrophin2) leads to the formation of asymmetrical somites in mouse embryos, similar to embryos deprived of retinoic acid
act as transcriptional co-repressor during embryonic development.
Atrophin-1 (show ATN1 Antibodies) and the short form of Atrophin-2 can act as potent and evolutionarily conserved transcriptional activators.
The mouse ortholog of RERE is required for embryonic development
This gene encodes a member of the atrophin family of arginine-glutamic acid (RE) dipeptide repeat-containing proteins. The encoded protein co-localizes with a transcription factor in the nucleus, and its overexpression triggers apoptosis. A similar protein in mouse associates with histone deacetylase and is thought to function as a transcriptional co-repressor during embryonic development. Multiple transcript variants encoding different isoforms have been found for this gene.
, gaping mouth
, arginine-glutamic acid dipeptide (RE) repeats
, atrophin-1 like protein
, arginine-glutamic acid dipeptide repeats protein
, atrophin-1 related protein
, atrophin-1-like protein
, atrophin-1-related protein