ABAT Recombinant Monoclonal Antibody

Code CSB-RA242969A0HU
Size US$210
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Image
  • IHC image of CSB-RA242969A0HU diluted at 1:100 and staining in paraffin-embedded human liver tissue performed on a Leica BondTM system. After dewaxing and hydration, antigen retrieval was mediated by high pressure in a citrate buffer (pH 6.0). Section was blocked with 10% normal goat serum 30min at RT. Then primary antibody (1% BSA) was incubated at 4℃ overnight. The primary is detected by a Goat anti-rabbit IgG polymer labeled by HRP and visualized using 0.05% DAB.
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Product Details

Uniprot No.
Target Names
Alternative Names
4-aminobutyrate aminotransferase, mitochondrial (EC 2.6.1.19) ((S)-3-amino-2-methylpropionate transaminase) (EC 2.6.1.22) (GABA aminotransferase) (GABA-AT) (Gamma-amino-N-butyrate transaminase) (GABA transaminase) (GABA-T) (L-AIBAT), ABAT, GABAT
Species Reactivity
Human
Immunogen
A synthesized peptide derived from human ABAT
Immunogen Species
Homo sapiens (Human)
Conjugate
Non-conjugated
Clonality
Monoclonal
Isotype
Rabbit IgG
Clone No.
5B6
Purification Method
Affinity-chromatography
Concentration
It differs from different batches. Please contact us to confirm it.
Buffer
Rabbit IgG in 10mM phosphate buffered saline , pH 7.4, 150mM sodium chloride, 0.05% BSA, 0.02% sodium azide and 50% glycerol.
Form
Liquid
Tested Applications
ELISA, IHC
Recommended Dilution
Application Recommended Dilution
IHC 1:50-1:200
Troubleshooting and FAQs
Storage
Upon receipt, store at -20°C or -80°C. Avoid repeated freeze.
Lead Time
Basically, we can dispatch the products out in 1-3 working days after receiving your orders. Delivery time maybe differs from different purchasing way or location, please kindly consult your local distributors for specific delivery time.
Description

ABAT, or 4-aminobutyrate aminotransferase, serves as a critical mitochondrial enzyme responsible for catabolizing gamma-aminobutyric acid (GABA), the primary inhibitory neurotransmitter in the central nervous system. By regulating GABA availability, ABAT influences neuronal excitability and has emerged as a significant target in neuroscience research, particularly in studies examining seizure disorders, neurological development, and GABAergic signaling pathways. Beyond its neurological roles, ABAT has garnered attention in cancer metabolism research, where altered GABA metabolism may contribute to tumor microenvironment modulation and cellular proliferation.

This recombinant monoclonal antibody, clone 5B6, offers researchers the reproducibility essential for longitudinal studies and multi-site collaborations. Developed using recombinant technology with a defined sequence, this antibody eliminates the lot-to-lot variability inherent in traditional hybridoma-derived reagents, ensuring consistent performance across experiments. The rabbit host origin provides high-affinity binding characteristics, while affinity chromatography purification delivers a clean preparation suitable for demanding applications.

Validation in immunohistochemistry demonstrates reliable detection in paraffin-embedded human liver tissue, where ABAT expression reflects the organ's role in amino acid metabolism. Using a citrate buffer antigen retrieval protocol at pH 6.0 with recommended dilutions of 1:50 to 1:200, researchers can expect clear, specific staining patterns visualized through standard HRP-DAB detection systems. The antibody is also validated for ELISA applications, providing flexibility for both tissue-based localization studies and quantitative protein measurement workflows.

This antibody supports investigations spanning neuroscience, cancer biology, metabolic disorders, and signal transduction research, making it a versatile tool for researchers exploring GABA metabolism and its broader physiological implications.

Usage
For Research Use Only. Not for use in diagnostic or therapeutic procedures.

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Target Background

Function
Catalyzes the conversion of gamma-aminobutyrate and L-beta-aminoisobutyrate to succinate semialdehyde and methylmalonate semialdehyde, respectively. Can also convert delta-aminovalerate and beta-alanine.
Gene References into Functions
  1. This study utilized ER+ IBC to identify a metagene including ABAT and STC2 as predictive biomarkers for endocrine therapy resistance. PMID: 25771305
  2. A-to-G transition at nucleotide 754 of the human ABAT gene identified in lymphoblast cDNA (c.754A>G) results in substitution of an invariant arginine at amino acid 220 by lysine (p.Arg220Lys). This point mutation results in destabilization of the binding of pyridoxal-5'-phosphate to GABA-transaminase (required for transamination of GABA to succinic semialdehyde) and thus results in GABA-transaminase deficiency. PMID: 25485164
  3. Findings point to a possible role of ABAT gene-regulated GABA catabolism for an altered processing of somatosensory stimuli as a potential vulnerability marker for affective disorders. PMID: 22225676
  4. direct involvement of ABAT in pathways affecting lower esophageal sphincter (LES) control in gastro esophageal reflux disease PMID: 21552517
  5. Observational study and genome-wide association study of gene-disease association. (HuGE Navigator) PMID: 20659789
  6. excessive prenatal GABA exposure in the central nervous system (CNS) is responsible for the clinical manifestations of GABA transaminase deficiency [case report] PMID: 20052547
  7. Marked differences in platelet uptake of GABA and activity of catabolic enzyme GABA-T between patients with generalized and localization-related epileptic syndromes. May indicate an impairment in function of brain GABAergic systems. PMID: 12694932
  8. results suggest that the Cys321 residue is essential for the catalytic function of GABAT, and that it is involved in the formation of a disulfide link between two monomers of human brain GABAT PMID: 15528998
  9. lysine 357 is essential for catalytic function of brain GABA transaminase, and is involved in binding PLP at the active site PMID: 15650327
  10. Analysis of the autistic disorder susceptibility locus suggests an association on chromosome 16p between GRIN2A and ABAT. PMID: 15830322

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Involvement in disease
GABA transaminase deficiency (GABATD)
Subcellular Location
Mitochondrion matrix.
Protein Families
Class-III pyridoxal-phosphate-dependent aminotransferase family
Tissue Specificity
Liver > pancreas > brain > kidney > heart > placenta.
Database Links

HGNC: 23

OMIM: 137150

KEGG: hsa:18

STRING: 9606.ENSP00000268251

UniGene: Hs.336768

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