Use your antibodies-online credentials, if available.
No Products on your Comparison List.
Your basket is empty.
Find out more
SYNJ1 encodes a phosphoinositide phosphatase that regulates levels of membrane phosphatidylinositol-4,5-bisphosphate. Additionally we are shipping Synaptojanin 1 Proteins (5) and many more products for this protein.
Showing 10 out of 43 products:
Rat (Rattus) Polyclonal SYNJ1 Primary Antibody for ICC, WB - ABIN1742316
Park, Kim, Lee, Park, Park, Sun, Kim, Chang: SNX18 shares a redundant role with SNX9 and modulates endocytic trafficking at the plasma membrane. in Journal of cell science 2010
Show all 7 references for ABIN1742316
Mouse (Murine) Monoclonal SYNJ1 Primary Antibody for WB - ABIN968786
Cestra, Castagnoli, Dente, Minenkova, Petrelli, Migone, Hoffmüller, Schneider-Mergener, Cesareni: The SH3 domains of endophilin and amphiphysin bind to the proline-rich region of synaptojanin 1 at distinct sites that display an unconventional binding specificity. in The Journal of biological chemistry 1999
Show all 3 references for ABIN968786
Rat (Rattus) Monoclonal SYNJ1 Primary Antibody for IHC (fro), WB - ABIN782444
Ramjaun, McPherson: Tissue-specific alternative splicing generates two synaptojanin isoforms with differential membrane binding properties. in The Journal of biological chemistry 1996
Show all 2 references for ABIN782444
Chicken Polyclonal SYNJ1 Primary Antibody for WB - ABIN2778875
Thole, Vermeer, Zhang, Gadella, Nielsen: Root hair defective4 encodes a phosphatidylinositol-4-phosphate phosphatase required for proper root hair development in Arabidopsis thaliana. in The Plant cell 2008
Mnb (show DYRK1A Antibodies) is a synaptic kinase that promotes efficient synaptic vesicle recycling by Synj function at the neuromuscular junction.
Findings imply that restoring the level of any one of these genes dap160/itsn1 (show ITSN1 Antibodies), synj/synj1, and nla/dscr1 (show RCAN1 Antibodies) may reduce endocytic defects seen in DS.
In the absence of synaptojanin or endophilin, vesicles undergo full fusion and re-formation.
Synaptojanin 1 is required for endolysosomal trafficking of synaptic proteins in cone photoreceptor inner segments.
This protein localized predominantly to cone photoreceptors. Using blastula stage transplantation experiments, study demonstrates that rods from mutants lacking SynJ1 develop normally and do not have the pronounced morphological defects detected in cones
Synj1 is required for anchoring of ribbons, for vesicle maintenance, and for synaptic transmission at cone photoreceptor ribbon synapses.
Synj1 is critical for retrieval of membrane in order to maintain the quantity, timing of fusion, and spontaneous release properties of synaptic vesicles at hair-cell ribbon synapses.
Mutations in SYNJ1 gene do not play a major role in early-onset or familial PD in our population.
This study demonstrated that SYNJ1 was significantly higher in Down syndrome and correlated with several measures of Abeta (show APP Antibodies). SYNJ1 was higher in down syndrome with Alzheimer disease and significantly higher than SYNJ1 in sporadic Alzheimer disease.
This is the third reported family with autosomal recessive, early-onset parkinsonism associated with the SYNJ1 p.Arg258Gln mutation. This work contributes to the definition of the genetic and clinical aspects of PARK20.
the clinical progression of the Italian siblings with SYNJ1-related early-onset atypical parkinsonism seems to present a more severe progression in the early stages
Our data suggest that the previously reported Arg258Gln mutation in SYNJ1 is not a frequent cause of Parkinson disease
This review presented that SYNJ1 in recessive forms of juvenile parkinsonism.
Findings suggest that SYNJ1 mutation is responsible for the early-onset Parkinsonism phenotype probably due to deficiencies in its phosphatase activity and consequent impairment of its synaptic functions.
Results indicate that SYNJ1 gene is a compelling candidate for Parkinsonism; mutations in the functionally linked protein auxilin (show DNAJC6 Antibodies) cause a similar early-onset phenotype, and other findings implicate endosomal dysfunctions in the pathogenesis.
a novel mechanism by which reduction of a PI(4,5)P2-degrading enzyme, synj1, improves amyloid-induced neuropathology and behavior deficits through accelerating cellular Abeta (show APP Antibodies) clearance.
Trisomy for SYNJ1 in Down syndrome is functionally linked to the enlargement of early endosomes.
These results implicate Pak5 (show PAK7 Antibodies) in Pacsin1 (show PACSIN1 Antibodies)- and Synaptojanin1-mediated synaptic vesicle trafficking.
PI(4,5)P-to-PI4P conversion achieved by Synj1 at sites of high curvature may cooperate with dynamin (show DNM1 Antibodies) to achieve membrane fission.
synaptojanin 1 function is needed for the progression of recycling vesicles to the functional synaptic vesicle pool.
PtdIns(4,5)P(2) dyshomeostasis caused by gene dosage imbalance for Synj1 may contribute to brain dysfunction and cognitive disabilities in down syndrome.
Synaptojanin 1 functions in constitutive and triggered internalization of AMPA (show GRIA3 Antibodies) receptors.
Synaptojanin-1 is involved phosphatidylinositol metabolism in astrogliogenesis, but not in neurogenesis.
This gene encodes a phosphoinositide phosphatase that regulates levels of membrane phosphatidylinositol-4,5-bisphosphate. As such, expression of this enzyme may affect synaptic transmission and membrane trafficking. Multiple transcript variants encoding different isoforms have been found for this gene.
, no optokinetic response c
, synaptojanin 1
, synaptojanin 1, isoform 1
, synaptic inositol 1,4,5-trisphosphate 5-phosphatase 1
, synaptic inositol-1,4,5-trisphosphate 5-phosphatase 1
, inositol 5'-phosphatase (synaptojanin 1)
, synaptojanin-1, polyphosphoinositide phosphatase