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VSNL1 is a member of the visinin/recoverin subfamily of neuronal calcium sensor proteins. Additionally we are shipping Visinin-Like 1 Proteins (23) and Visinin-Like 1 Kits (12) and many more products for this protein.
Showing 10 out of 205 products:
Human Polyclonal VSNL1 Primary Antibody for ICC, IF - ABIN1580470
Hatakenaka, Kuo, Miki: Analysis of a distinctive protein in chick retina during development. in Brain research 1984
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Human Monoclonal VSNL1 Primary Antibody for ICC, IF - ABIN1580471
Kuno, Kajimoto, Hashimoto, Mukai, Shirai, Saheki, Tanaka: cDNA cloning of a neural visinin-like Ca(2+)-binding protein. in Biochemical and biophysical research communications 1992
Show all 8 references for ABIN1580471
Human Polyclonal VSNL1 Primary Antibody for EIA, IHC (p) - ABIN357108
Lin, Jeanclos, Treuil, Braunewell, Gundelfinger, Anand: The calcium sensor protein visinin-like protein-1 modulates the surface expression and agonist sensitivity of the alpha 4beta 2 nicotinic acetylcholine receptor. in The Journal of biological chemistry 2002
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Human Monoclonal VSNL1 Primary Antibody for WB - ABIN393301
Xu, Li, Zhang, Zhang, Zhang, Huang, Sun, Ren, Sui, Liu: MicroRNAs and target site screening reveals a pre-microRNA-30e variant associated with schizophrenia. in Schizophrenia research 2010
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Human Polyclonal VSNL1 Primary Antibody for IHC (p), WB - ABIN388387
Spilker, Dresbach, Braunewell: Reversible translocation and activity-dependent localization of the calcium-myristoyl switch protein VILIP-1 to different membrane compartments in living hippocampal neurons. in The Journal of neuroscience : the official journal of the Society for Neuroscience 2002
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Human Polyclonal VSNL1 Primary Antibody for EIA, IHC (p) - ABIN955518
: Special issue dedicated to the memory of Professor John M. Cleghorn. in Schizophrenia research 1994
Show all 2 references for ABIN955518
These findings suggest a unique role for cerebrospinal fluid Vilip-1 as a biomarker of entorhinal cortex neuron loss in Alzheimer disease
The results suggest that both serum and cerebrospinal fluid levels of VILIP-1 may be one of predictive markers of acute encephalopathy with biphasic seizures.
We show for the first time that the C-terminus of VILIP-1, containing Cys187, might represent a novel redox-sensitive motif and that VILIP-1 dimerization and aggregation are hallmarks of amyotrophic lateral sclerosis
Results show that in the presence of calcium, N-myristoylation significantly increases the kinetic rate of VILIP adsorption to the membrane.
The results showed that the CSF (show CSF2 Antibodies) VILIP-1 level had significantly increased in Alzheimer disease patients compared with both normal controls and Lewy body dementia patients.
SNPs upstream of SLC2A9 (show SLC2A9 Antibodies) and within VSNL1 showed strongest evidence for association with AD + P when compared with controls.
VSNL1 single-nucleotide polymorphisms and pathological changes in VILIP-1 protein expression, possibly occurring during brain development, may contribute to the morphological and functional deficits observed in schizophrenia.
Patients with high VSNL-1 expression had significantly poorer prognosis than those with low expression in stage III disease
The findings suggest that CSF (show CSF2 Antibodies) VILIP-1 and VILIP-1/Abeta42 predict rates of global cognitive decline similarly to tau and tau/Abeta42, and may be useful CSF (show CSF2 Antibodies) surrogates for neurodegeneration in early Alzheimer disease.
VSNL1 may play a role in the pathophysiology of aldosterone-producing adenomas harboring mutations in the potassium channel (show KCNAB2 Antibodies) KCNJ5 (show KCNJ5 Antibodies) via its antiapoptotic function in response to calcium cytotoxicity and its effect on aldosterone production.
Findings indicate that VILIP-1 is involved in epithelial-mesenchymal transition (EMT (show ITK Antibodies)) of squamous cell carcinoma (SCC (show CYP11A1 Antibodies)) cells by regulating the transcription factor Snail1 (show SNAI1 Antibodies) in a cAMP-dependent manner.
VSNL1 expresses exclusively in atrial cardiomyocytes during embryogenesis.
VILIP-1 overexpression decreases the susceptibility to skin carcinogenesis in experimental mouse cancer models, thus supporting its role as a tumor suppressor gene
Data show that VILIP-1 led to reduced migration of aggressive SCC (show CYP11A1 Antibodies) cells depending on cAMP levels.
Vsnl1 marks ureteric bud tips in embryonic kidneys, and its mosaic pattern demonstrates a heterogeneity of cell types that may be critical for normal ureteric branching.
Decreased or absent VILIP-1 expression in SCC (show CYP11A1 Antibodies) cell subpopulations may lead to a more advanced malignant phenotype characterized by changes in adhesive ability and increased cell motility, suggestive of a tumor suppressor function
VILIP1 constitutively binds to P2X2 (show P2RX2 Antibodies) receptors and displays enhanced interactions in an activation- and calcium-dependent manner owing to exposure of its binding segment in P2X2 (show P2RX2 Antibodies) receptors
This gene is a member of the visinin/recoverin subfamily of neuronal calcium sensor proteins. The encoded protein is strongly expressed in granule cells of the cerebellum where it associates with membranes in a calcium-dependent manner and modulates intracellular signaling pathways of the central nervous system by directly or indirectly regulating the activity of adenylyl cyclase. Alternatively spliced transcript variants have been observed, but their full-length nature has not been determined.
, visinin-like protein 1
, hippocalcin-like protein 3
, neural visinin-like protein 1
, 21 kDa CABP
, neurocalcin alpha