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Mouse (Murine) LOC360919 ELISA Kit for Sandwich ELISA - ABIN424631
Sippel, Shimizu, Strnad, Traystman, Herson, Waziri: Arginase I release from activated neutrophils induces peripheral immunosuppression in a murine model of stroke. in Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism 2015
Show all 2 references for ABIN424631
Human LOC360919 ELISA Kit for Sandwich ELISA - ABIN414563
Yin, Wang, Huang, Mao, Zhou, Zhang et al.: Circulating CD14(+) HLA-DR(-/low) myeloid-derived suppressor cells in leukemia patients with allogeneic hematopoietic stem cell transplantation: novel clinical potential strategies for the prevention ... in Cancer medicine 2016
Rat (Rattus) LOC360919 ELISA Kit for Sandwich ELISA - ABIN431942
Klepeisz, Sagmeister, Haudek-Prinz, Pichlbauer, Grasl-Kraupp, Gerner: Phenobarbital induces alterations in the proteome of hepatocytes and mesenchymal cells of rat livers. in PLoS ONE 2013
RERE (show RERE ELISA Kits)-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 (show RERE ELISA Kits) plays a critical role in the development.
a mutation in Rere (show RERE ELISA Kits) (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- (show RERE ELISA Kits)repressor during embryonic development.
Atrophin-1 (show ATN1 ELISA Kits) and the short form of Atrophin-2 (show RERE ELISA Kits) can act as potent and evolutionarily conserved transcriptional activators.
suggest that mutations in RERE (show RERE ELISA Kits) cause a genetic syndrome and that haploinsufficiency of RERE (show RERE ELISA Kits) might be sufficient to cause many of the phenotypes associated with proximal 1p36 deletions
The mouse ortholog of RERE (show RERE ELISA Kits) 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.
arginine-glutamic acid dipeptide repeats protein
, atrophin 2
, atrophin-1 like protein
, atrophin-1 related protein
, atrophin-1-like protein
, atrophin-1-related protein
, alpha-fetoprotein related protein