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RELN encodes a large secreted extracellular matrix protein thought to control cell-cell interactions critical for cell positioning and neuronal migration during brain development. Additionally we are shipping Reelin Antibodies (52) and Reelin Proteins (12) and many more products for this protein.
Showing 6 out of 22 products:
Human Reelin ELISA Kit for Sandwich ELISA - ABIN821736
Hornig, Sturm, Fiebich, Tebartz van Elst: Increased Blood-Reelin-Levels in First Episode Schizophrenia. in PLoS ONE 2015
Developmental gene expression pattern of reelin, dab1 (show DAB1 ELISA Kits), vldlr (show VLDLR ELISA Kits), and apoer2 (show LRP8 ELISA Kits) in the central nervous system of zebrafish was compared, and their remarkable expression was detected in the developing laminar structures and also non-laminated structures.
reelin and cofilin (show CFL1 ELISA Kits) cooperate in controlling cytoskeletal dynamics during neuronal migration.
Results suggest that Reelin induces branching of the leading processes of migrating neurons and that of basal processes of radial glial cells when they arrive at the Reelin-containing marginal zone.
Results revealed that lack of functional reelin does not simply invert, but highly disorganize visual cortical layers, resulting in a massive intermingling of cells with different laminar fates.
Report demonstrated that the reelin subregion R5-6 consisting of 747 amino acids in the 5th and 6th repeats was sufficient for apoER2 (show LRP8 ELISA Kits) and VLDLR (show VLDLR ELISA Kits) binding, and inhibiting lipoprotein-induced cholesterol accumulation in macrophages.
Findings indicate the physiological importance of Reelin in protecting the brain against amyloid beta (Abeta (show APP ELISA Kits))-induced synaptic dysfunction and memory impairment.
suggest that Reelin-dependent signaling mechanisms may be split into Src (show SRC ELISA Kits)-AKT (show AKT1 ELISA Kits)-dependent and Src (show SRC ELISA Kits)-Go-dependent pathways
Results of this study point to the Reelin signaling pathway as a candidate target for the pharmacologic treatment of neuropsychiatric diseases.
Application of Reelin enhances long-term potentiation, increases dendritic spine density and improves associative and spatial learning and memory.
Reelin depletion and stress impaired spatial memory, whereas either one of those factors alone was not sufficient to elicit this effect. Findings extend understanding of the role of reelin-stress interactions in schizophrenia.
Study showed increased expression in striatum membranes and decreased expression in frontal cortex membranes for both DRD2 (show DRD2 ELISA Kits) and Htr2a receptors from heterozygous Reelin mutant mice compared to wild-type
Among men, but not in women certain genotypes of the RELN gene were significantly associated with the susceptibility to Alzheimer's disease.
The features of reelin expression in the brain of fetuses and newborns at 22-40 weeks' gestation with internal HC should be considered as morphological differential and diagnostic criteria for the disease in relation to its etiology.
Study shows that early neural cells transiently express Reelin at the time they leave the presumptive olfactory/vomeronasal epithelium and that Dab 1 (show DAB1 ELISA Kits) is present in the migratory cell mass and in the presumptive ensheathing cells in the absence of reelin.
the reelin protein blood concentration might be a relevant signal with respect to the pathophysiology of schizophrenia.
These findings suggest a central AKT (show AKT1 ELISA Kits)-FOXG1 (show FOXG1 ELISA Kits)-reelin signaling pathway in focal malformations of cortical development and support pathway inhibitors as potential treatments or therapies for some forms of focal epilepsy.
rs7341475 (A/G) and rs262355 (A/T) polymorphisms in RELN gene are inversely associated with SZ risk.
RELN SNPs were associated with Alzheimer disease and mild cognitive impairment. GG genotype at rs2299356 was associated with risk of AD. RELN-rs528528 CT genotype was protective for MCI.
pThis study roposed that RELN mutations contribute to the genetic heterogeneity of myoclonus-dystonia.
Heterozygous reelin mutations cause autosomal-dominant lateral temporal epilepsy.
A peak in Reelin mRNA and protein expression is present in the pig embryonic brain during the period of major neurogenesis and neuronal migration.
This gene encodes a large secreted extracellular matrix protein thought to control cell-cell interactions critical for cell positioning and neuronal migration during brain development. This protein may be involved in schizophrenia, autism, bipolar disorder, major depression and in migration defects associated with temporal lobe epilepsy. Mutations of this gene are associated with autosomal recessive lissencephaly with cerebellar hypoplasia. Two transcript variants encoding distinct isoforms have been identified for this gene. Other transcript variants have been described but their full length nature has not been determined.
, extracellular matrix serine protease
, reelin, extracellular