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Choline is a direct precursor of acetylcholine (ACh), a neurotransmitter of the central and peripheral nervous system that regulates a variety of autonomic, cognitive, and motor functions. Additionally we are shipping High Affinity Choline Transporter Antibodies (34) and and many more products for this protein.
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These data provide evidence for an epithelium-independent non-vesicular, non-quantal ACh (show FGFR3 ELISA Kits) release in the mouse trachea involving low-affinity choline transporters.
bacterial artificial chromosome CHT mice thus represent a novel tool to examine both the positive and negative impact of constitutively elevated cholinergic signaling capacity
These findings reveal compensatory mechanisms that, in the context of moderate cognitive challenges, can overcome the performance deficits expected from the significantly reduced ACh (show FGFR3 ELISA Kits) capacity of CHT+/- cholinergic terminals.
CHT association with cholesterol-rich rafts is critical for its function
This study showed that a constitutive loss of CHT expression in hemizygous mice leads to a significant reduction in basal extracellular dopamine levels in the nucleus accumbens.
This study demonistrated that CHT support for neuromuscular signaling involves contributions to ACh (show FGFR3 ELISA Kits) synthesis as well as cholinergic synaptic vesicle availability.
CHT1 knockout mice have tachycardia and hypertension at rest.
CHT1 binds to Par-4 (show F2RL3 ELISA Kits) and inhibits choline uptake when its incorporation is reduced on the cell surface
CHT is an essential and regulated presynaptic component of cholinergic signaling
CHT1 was expressed early in CNS development, predominantly in the regions containing cholinergic neurons. NGF (show NGFB ELISA Kits) AND BMP4 (show BMP4 ELISA Kits) increased CHT mRNA accumulation in primary septal cultures.
Here we describe an autosomal recessive presynaptic congenital myasthenic syndrome presenting with a broad clinical phenotype due to homozygous SLC5a7 missense mutations. Phenotype ranges from classical presentation of a congenital myasthenic syndrome in one patient (p.Pro210Leu), to severe neurodevelopmental delay with brain atrophy (p.Ser94Arg) and extend the clinical outcomes to infantile lethality (p.Val112Glu).
Impaired Presynaptic High-Affinity Choline Transporter Causes a Congenital Myasthenic Syndrome with Episodic Apnea: this study broadens the clinical spectrum of human diseases resulting from reduced CHT activity and highlights the complexity of cholinergic metabolism at the synapse
These data show that acute exposure of depolarized cells to insulin (show INS ELISA Kits) is coupled to transiently increased levels of CHT proteins at the cell surface, and that this is attenuated by chronic insulin (show INS ELISA Kits) exposure.
This study demonstrated a specific impairment in cognitive control associated with the Ile89Val polymorphism of SLC5A7.
This mini-review discusses structural requirements for both organic cationic transporters OCT1 (show POU2F1 ELISA Kits) and OCT2 versus the blood-brain barrier choline transporter (BBBCHT) are discussed and compared.
[review] The critical role of CHT in maintaining cholinergic transmission indicates that it could be a target for therapeutic intervention to promote acetylcholine synthesis, the accomplishment of which has not been adequately addressed.
CHT1 forms a homo-oligomer on the cell surface in cultured cells.
Our findings compel consideration of mutations in SLC5A7 or its functional partners in relation to unexplained motor neuronopathies.
Polymorphic variation in the CHT1 gene can predict early, subclinical measures of carotid atherosclerosis.
Nedd4-2 mediated ubiquitination regulates the cell surface expression of CHT1 in HEK293 cells.
Choline is a direct precursor of acetylcholine (ACh), a neurotransmitter of the central and peripheral nervous system that regulates a variety of autonomic, cognitive, and motor functions. SLC5A7 is a Na(+)- and Cl(-)- dependent high-affinity transporter that mediates the uptake of choline for acetylcholine synthesis in cholinergic neurons (Apparsundaram et al., 2000
high affinity choline transporter 1
, hemicholinium-3-sensitive choline transporter
, solute carrier family 5 member 7
, high affinity choline transporter; hemicholinium-3-sensitive choline transporter
, solute carrier family 5 (choline transporter), member 7
, solute carrier family 5, member 7
, choline transporter
, creatine transporter 1
, sodium- and chloride-dependent creatine transporter 1
, solute carrier family 6 (neurotransmitter transporter, creatine), member 8
, solute carrier family 6 member 8
, ChT1 thymocyte antigen
, V-set and immunoglobulin domain-containing protein 1