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anti-Human PRICKLE1 Antibodies:
anti-Mouse (Murine) PRICKLE1 Antibodies:
anti-Rat (Rattus) PRICKLE1 Antibodies:
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Human Polyclonal PRICKLE1 Primary Antibody for EIA, IF - ABIN1450074
Katoh, Katoh: Identification and characterization of human PRICKLE1 and PRICKLE2 genes as well as mouse Prickle1 and Prickle2 genes homologous to Drosophila tissue polarity gene prickle. in International journal of molecular medicine 2003
Our experimental data demonstrate that high expression of Prickle1 and Vangl2 (show VANGL2 Antibodies) reduce the growth of neuroblastoma (show ARHGEF16 Antibodies) cells and indicate different roles of PCP (show PRCP Antibodies) proteins in tumorigenic cells compared to normal cells.
these findings suggest PRICKLE1 mutations contribute to ASD (show ARSD Antibodies) by disrupting the interaction with SYN1 (show SYN1 Antibodies) and regulation of synaptic vesicles.
study demonstrates that PRICKLE1 could act as a predisposing factor to human neural tube defects
MINK1 (show MINK1 Antibodies) interacts with and phosphorylates PRICKLE1 and PRICKLE2 (show PRICKLE2 Antibodies).
Mutations in prickle1 causes seizures.
PRICKLE1 mutations are not a frequent cause of progressive myoclous epilepsies in Southern Italy.
PRICKLE1 and PRICKLE2 (show PRICKLE2 Antibodies) mRNAs were expressed together in brain, eye and testis.
appears to serve as a nuclear receptor for REST/NRSF (show REST Antibodies), REST4, and possibly other transcription factors
NRSF (show REST Antibodies)/REST functions as a repressor of TH transcription in NSCs via a mechanism dependent on the TH NRSE/RE1 (show NPC2 Antibodies) sites.
Prickle-1 is a negative regulator of the Wnt/beta-catenin signaling pathway and is a putative tumor suppressor in human hepatocellular carcinoma
Prickle1 is part of a molecular mechanism that regulates facial branchiomotor neurons caudal (show CAD Antibodies) migration.
these findings suggest PRICKLE1 mutations contribute to ASD (show GUSB Antibodies) by disrupting the interaction with SYN1 (show SYN1 Antibodies) and regulation of synaptic vesicles.
Data suggest Prickle1 is part of the Wnt5a (show WNT5A Antibodies)/PCP (show BMP1 Antibodies) signaling, regulating cell polarity and affecting expression of multiple factors to stunt limb growth through altered patterns of gene expression, including the PCP (show BMP1 Antibodies) genes Wnt5a (show WNT5A Antibodies) and Vangl2 (show VANGL2 Antibodies).
Pk1 function in axonal-dendritic development associated with the maturation of CNS neurons.
Prickle1 and Prickle2 (show PRICKLE2 Antibodies) promote neurite-like process formation of C1300 cells via the Dvl1 (show DVL1 Antibodies)-dependent mechanism
These results suggest that RILP(also known as Prickle) expression and function control REST action more so than does REST expression and is an important regulatory role in cardiomyocyte differentiation.
both Prickle1 and Prickle2 (show PRICKLE2 Antibodies) promote neurite-like process formation of C1300 neuroblastoma (show ARHGEF16 Antibodies) cells via the Dishevelled (show DVL2 Antibodies) dependent pathway
mouse Prickle1 and Prickle2 (show PRICKLE2 Antibodies) possibly regulate positive neurite formation during brain development
Results demonstrate a role for prickle1 in AB polarity formation rather than expected role as a PCP (show BMP1 Antibodies) gene.
This gene encodes a nuclear receptor that may be a negative regulator of the Wnt/beta-catenin signaling pathway. The encoded protein localizes to the nuclear membrane and has been implicated in the nuclear trafficking of the transcription repressors REST/NRSF and REST4. Mutations in this gene have been linked to progressive myoclonus epilepsy. Alternate splicing results in multiple transcript variants. A pseudogene of this gene is found on chromosome 3.
, prickle-like protein 1
, REST/NRSF-interacting LIM domain protein 1
, REST (RE-1 silencing transcription factor)/NRSF (neuron-restrictive silencer factor)-interacting LIM domain protein
, prickle like 1