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NAT8L encodes a single-pass membrane protein, which contains a conserved sequence of the GCN5 or NAT superfamily of N-acetyltransferases and is a member of the N-acyltransferase (NAT) superfamily. Additionally we are shipping N-Acetyltransferase 8-Like (GCN5-Related, Putative) Antibodies (18) and N-Acetyltransferase 8-Like (GCN5-Related, Putative) Kits (10) and many more products for this protein.
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Results showed that both Shati+/- and Shati-/- mice demonstrated lower levels of NAA in the brain than Shati+/+ mice, suggesting that SHATI predominantly regulates NAA content in the brain
Study shows that Shati/Nat8l in the neuron may induce axon outgrowth by ATP synthesis and not through mGluR3 (show GRM3 Proteins) signaling.
Dysregulated expression of Nat8L is associated with deficits in oxidative phosphorylation in 5xFAD model of Alzheimer disease.
results indicate that Shati/Nat8l in the Nucleus Accumbens, but not in the dorsal striatum, plays a suppressive role in the behavioral responses to METHamphetamine by controlling the dopaminergic system via activation of group II mGlutamate receptors
The results of this study showed that Deletion of NAT8L increases dopamine D1 receptor on the cell surface in the nucleus accumbens, accelerating methamphetamine dependence in mice.
Nat8l impacts on the brown adipogenic phenotype
Deficiency of SHATI may affect behavior.
shati expression affects emoutional behaivors in mice
Nat8l is highly specific to aspartate. It is localized in mitochondria and microsomes, with a pattern comparable to the localization of NAA in brain. It is similar to NAG synthetase in catalytic mechanism without the involvement of cysteine.
Results indicated that NAT8L, but not NAT14 (show NAT14 Proteins), catalysed the synthesis of NAA from L-aspartate and acetyl-CoA (show LPCAT1 Proteins).
This study demonistrated that the human NAT8L gene related to reward dependence, a personality trait, and grey matter volume in the caudate nucleus in healthy subjects, suggesting that NAT8L might also affect human personality
Results indicated that NAT8L, but not NAT14 (show NAT14 Proteins), catalysed the synthesis of NAA from L-aspartate and acetyl-CoA (show LPCAT2 Proteins).
This gene encodes a single-pass membrane protein, which contains a conserved sequence of the GCN5 or NAT superfamily of N-acetyltransferases and is a member of the N-acyltransferase (NAT) superfamily. This protein is a neuron-specific protein and is the N-acetylaspartate (NAA) biosynthetic enzyme, catalyzing the NAA synthesis from L-aspartate and acetyl-CoA. NAA is a major storage and transport form of acetyl coenzyme A specific to the nervous system. The gene mutation results in primary NAA deficiency (hypoacetylaspartia).
, N-acetylaspartate synthetase
, N-acetyltransferase 8-like protein
, NAA synthetase
, camello 3
, protein Shati
, camello-like protein 3