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ABAT cdna clone

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Catalog # MBS1276244
Unit / Price
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  0.01 mg Plasmid + 0.2 mL Glycerol-Stock  /  $285 +1 FREE 8GB USB
ABAT cdna clone
Product Name

ABAT, cDNA Clone

Full Product Name


Product Gene Name
Research Use Only
For Research Use Only. Not for use in diagnostic procedures.
atggcctcca tgttgctcgc ccagcgcctg gcctgcagct tccagcacag ctaccgcctg ctggtgcctg gatccagaca cattagtcaa gctgcagcca aagtcgacgt tgaatttgat tatgatgggc ctctgatgaa gacggaagtc ccagggccta gatctcagga gttaatgaaa cagctgaata taattcagaa tgcagaggct gtgcattttt tctgcaatta cgaagagagc cgaggcaatt acctggttga tgtggacggc aaccgaatgc tggatcttta ttcccagatc tcctctgtcc ccataggtta cagccacccc gccctgctga aactcatcca acagcctcaa aatgcgagca tgtttgtcaa cagacccgcc ctcggaatcc tgcctccgga gaactttgtg gagaagctcc ggcagtcctt gctctcggtg gctcccaaag ggatgtccca gctcatcacc atggcctgcg gctcctgctc caatgaaaac gccttaaaga ccatcttcat gtggtaccgg agcaaggaaa gagggcagag gggcttctcc caggaggagc tggagacgtg catgattaac caggcccctg gctgccccga ctacagcatc ctctccttca tgggcgcgtt ccatgggagg accatgggtt gcttagcgac cacgcactct aaagccattc acaagatcga catcccttcc tttgactggc ccatcgcacc gttcccacgg ctgaaatacc ctctggaaga gtttgtgaaa gagaaccaac aggaggaggc ccgctgtctg gaagaggtgg aggatctgat tgtgaaatat cggaaaaaga agaagacggt ggccgggatc atcgtggagc ccatccagtc cgagggtgga gacaaccacg catccgatga cttctttcgg aagctgagag acatcgccag gaagcatggc tgcgccttct tggtggacga ggtccagacc ggaggaggct gcacgggcaa gttctgggcc catgagcact ggggcctgga tgacccagca gacgtgatga ccttcagcaa gaagatgatg actgggggct tcttccacaa ggaggagttc aggcctaatg ctccctaccg gatcttcaac acctggctgg gggacccgtc caagaacctg ttgctggctg aggtcatcaa catcatcaag cgggaggacc tgctaaataa tgcagcccat gccgggaagg ccctgctcac aggactgctg gacctccagg cccggtaccc ccagttcatc agcagggtga gaggacgagg caccttttgc tccttcgata ctcccgatga ttccatacgg aataagctca ttttaattgc cagaaacaaa ggtgtggtgt tgggtggctg tggtgacaaa tccattcgtt tccgtcccac gctggtcttc agggatcacc acgctcacct gttcctcaat attttcagtg acatcttagc agacttcaag taa
Clone Sequence Report
Provided with product shipment
ISO Certification
Manufactured in an ISO 13485:2003 and EN ISO 13485:2012 Certified Laboratory.
Other Notes
Small volumes of ABAT cdna clone vial(s) may occasionally become entrapped in the seal of the product vial during shipment and storage. If necessary, briefly centrifuge the vial on a tabletop centrifuge to dislodge any liquid in the container`s cap. Certain products may require to ship with dry ice and additional dry ice fee may apply.
NCBI/Uniprot data below describe general gene information for ABAT. It may not necessarily be applicable to this product.
NCBI Accession #
UniProt Secondary Accession #
UniProt Related Accession #
Molecular Weight
56,439 Da
NCBI Official Full Name
Homo sapiens 4-aminobutyrate aminotransferase, mRNA
NCBI Official Synonym Full Names
4-aminobutyrate aminotransferase
NCBI Official Symbol
NCBI Official Synonym Symbols
  [Similar Products]
NCBI Protein Information
4-aminobutyrate aminotransferase, mitochondrial
UniProt Protein Name
4-aminobutyrate aminotransferase, mitochondrial
UniProt Synonym Protein Names
(S)-3-amino-2-methylpropionate transaminase (EC:; GABA aminotransferase; GABA-AT; Gamma-amino-N-butyrate transaminase; GABA transaminase; GABA-T; L-AIBAT
UniProt Gene Name
UniProt Synonym Gene Names
GABAT; GABA-AT; GABA transaminase; GABA-T  [Similar Products]
UniProt Entry Name
NCBI Summary for ABAT
4-aminobutyrate aminotransferase (ABAT) is responsible for catabolism of gamma-aminobutyric acid (GABA), an important, mostly inhibitory neurotransmitter in the central nervous system, into succinic semialdehyde. The active enzyme is a homodimer of 50-kD subunits complexed to pyridoxal-5-phosphate. The protein sequence is over 95% similar to the pig protein. GABA is estimated to be present in nearly one-third of human synapses. ABAT in liver and brain is controlled by 2 codominant alleles with a frequency in a Caucasian population of 0.56 and 0.44. The ABAT deficiency phenotype includes psychomotor retardation, hypotonia, hyperreflexia, lethargy, refractory seizures, and EEG abnormalities. Multiple alternatively spliced transcript variants encoding the same protein isoform have been found for this gene. [provided by RefSeq, Jul 2008]
UniProt Comments for ABAT
ABAT: 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. Defects in ABAT are a cause of GABA transaminase deficiency (GABATD). The phenotype of this deficiency includes psychomotor retardation, hypotonia, hyperreflexia, lethargy, refractory seizures, and EEG abnormalities. Belongs to the class-III pyridoxal-phosphate-dependent aminotransferase family.

Protein type: Carbohydrate Metabolism - propanoate; Amino Acid Metabolism - alanine, aspartate and glutamate; Transferase; Mitochondrial; EC; EC; Amino Acid Metabolism - valine, leucine and isoleucine degradation; Other Amino Acids Metabolism - beta-alanine; Carbohydrate Metabolism - butanoate

Chromosomal Location of Human Ortholog: 16p13.2

Cellular Component: 4-aminobutyrate transaminase complex; mitochondrial matrix; mitochondrion

Molecular Function: 4-aminobutyrate transaminase activity; protein homodimerization activity; pyridoxal phosphate binding; succinate-semialdehyde dehydrogenase binding

Biological Process: behavioral response to cocaine; gamma-aminobutyric acid catabolic process

Disease: Gaba-transaminase Deficiency
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While every efforts were made to ensure the accuracy of the information provided in this datasheet, MyBioSource will not be liable for any omissions or errors contained herein. MyBioSource reserves the right to make changes to this datasheet at any time without prior notice.

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