catalog number :
MBS9216916
products full name :
NAT8L Antibody (N-Term)
products short name :
[NAT8L]
products name syn :
[Purified Rabbit Polyclonal Antibody (Pab); N-acetylaspartate synthetase; NAA synthetase; 2.3.1.17; Camello-like protein 3; N-acetyltransferase 8-like protein; NAT8L; CML3]
other names :
[N-acetylaspartate synthetase; N-acetylaspartate synthetase; N-acetylaspartate synthetase; N-acetyltransferase 8-like (GCN5-related, putative); Camello-like protein 3; N-acetyltransferase 8-like protein]
products gene name :
[NAT8L]
other gene names :
[NAT8L; NAT8L; CML3; NACED; NAT8-LIKE; CML3; NAA synthetase]
uniprot entry name :
NAT8L_HUMAN
reactivity :
Human, Mouse . Predicted: Rat
form :
Purified polyclonal antibody supplied in PBS with 0.09% (W/V) sodium azide. This antibody is purified through a protein A column, followed by peptide affinity purification.
storage stability :
Maintain refrigerated at 2-8°C for up to 2 weeks. For long term storage store at -20°C in small aliquots to prevent freeze-thaw cycles.
tested application :
Western Blot (WB), ELISA
image1 heading :
Western Blot (WB)
other info1 :
Target/Specificity: This NAT8L antibody is generated from a rabbit immunized with a KLH conjugated synthetic peptide between 59-93 amino acids from human NAT8L. Calculated MW: 32837
other info2 :
Antigen Type: Synthesized Peptide. Cellular Location : Cytoplasm. Membrane; Single- pass membrane protein. Microsome membrane; Single-pass membrane protein Mitochondrion membrane; Single-pass membrane protein. Rough endoplasmic reticulum membrane; Single-pass membrane protein. Note=Its enzymatic activity contribution is quantitatively larger in mitochondrial compartment than in extramitochondrial compartment. Tissue Location: Expressed in brain.
products categories :
Metabolism; Signal Transduction
products description :
Plays a role in the regulation of lipogenesis by producing N-acetylaspartate acid (NAA), a brain-specific metabolite. NAA occurs in high concentration in brain and its hydrolysis plays a significant part in the maintenance of intact white matter. Promotes dopamine uptake by regulating TNF-alpha expression. Attenuates methamphetamine-induced inhibition of dopamine uptake.
products references :
Hillier L.W.,et al.Nature 434:724-731(2005). Brandenberger R.,et al.Nat. Biotechnol. 22:707-716(2004). Ota T.,et al.Nat. Genet. 36:40-45(2004). Popsueva A.E.,et al.Dev. Biol. 234:483-496(2001). Arun P.,et al.Neurochem. Int. 55:219-225(2009).
ncbi acc num :
NP_848652.2
ncbi gb acc num :
NM_178557.3
ncbi pathways :
Alanine, Aspartate And Glutamate Metabolism Pathway (101142); Alanine, Aspartate And Glutamate Metabolism Pathway (100063); Metabolic Pathways (132956); Metapathway Biotransformation (198837)
ncbi summary :
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). [provided by RefSeq, Dec 2010]
uniprot summary :
NAT8L: Plays a role in the regulation of lipogenesis by producing N-acetylaspartate acid (NAA), a brain-specific metabolite. NAA occurs in high concentration in brain and its hydrolysis plays a significant part in the maintenance of intact white matter. Promotes dopamine uptake by regulating TNF-alpha expression. Attenuates methamphetamine-induced inhibition of dopamine uptake. Defects in NAT8L are the cause of N-acetylaspartate deficiency (NACED). A metabolic disorder resulting in truncal ataxia, marked developmental delay, seizures, and secondary microcephaly. Belongs to the camello family. Protein type: EC 2.3.1.17; Membrane protein, integral; Acetyltransferase. Chromosomal Location of Human Ortholog: 4p16.3. Cellular Component: cytoplasm; integral to membrane; mitochondrial membrane; mitochondrion; rough endoplasmic reticulum membrane. Molecular Function: aspartate N-acetyltransferase activity. Biological Process: metabolic process. Disease: N-acetylaspartate Deficiency