GPT2 Antibody

Code CSB-PA070045
Size US$119
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Product Details

Uniprot No.
Target Names
GPT2
Alternative Names
AAT2 antibody; Alanine aminotransferase 2 antibody; ALAT2_HUMAN antibody; ALT2 antibody; Glutamate pyruvate transaminase 2 antibody; Glutamic alanine transaminase 2 antibody; Glutamic pyruvate transaminase (alanine aminotransferase) 2 antibody; Glutamic pyruvic transaminase 2 antibody; Glutamic--alanine transaminase 2 antibody; Glutamic--pyruvic transaminase 2 antibody; GPT 2 antibody; gpt2 antibody
Raised in
Rabbit
Species Reactivity
Human
Immunogen
Synthesized peptide derived from the Internal region of Human GPT2.
Immunogen Species
Homo sapiens (Human)
Conjugate
Non-conjugated
Isotype
IgG
Purification Method
The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
Concentration
It differs from different batches. Please contact us to confirm it.
Buffer
Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
Form
Liquid
Tested Applications
WB, ELISA
Recommended Dilution
Application Recommended Dilution
WB 1:500-1:2000
ELISA 1:40000
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.
Usage
For Research Use Only. Not for use in diagnostic or therapeutic procedures.

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Target Background

Function
Catalyzes the reversible transamination between alanine and 2-oxoglutarate to form pyruvate and glutamate.
Gene References into Functions
  1. The GPT2 gene demonstrates increasing expression in brain in the early postnatal period, and GPT2 protein localizes to mitochondria. Akin to the human phenotype, Gpt2-null mice exhibit reduced brain growth. Through metabolomics and direct isotope tracing experiments, we find a number of metabolic abnormalities associated with loss of Gpt2 PMID: 27601654
  2. Recessively inherited loss of function GPT2 mutations are a novel cause of intellectual disability. PMID: 25758935
  3. ATF4 silencing prevented the activating effect of histidinol and tunicamycin on ATF4 and ALT2 expression. Our findings point to ALT2 as an enzyme involved in the metabolic adaptation of the cell to stress PMID: 24418603
  4. expression of GPT2 especially in muscle and fat, suggests a unique and previously unrecognized role of this gene product in glucose, amino acid, and fatty acid metabolism and homeostasis. PMID: 11863375
  5. The biliary IL-6 and TNF-alpha levels were positively correlated with serum DBIL, TBA and gamma-GT levels in infantile hepatitis syndrome subjects. PMID: 17109502
  6. Elevation of liver enzymes and hepatic insulin resistance as reflected by fasting insulin occur in the early stages of insulin resistance and highlight the central role of the liver in insulin resistance in the general population. PMID: 17596883
  7. A clinical method for selective measurement of ALT1 and 2 in human plasma is described. PMID: 19360321

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Involvement in disease
Mental retardation, autosomal recessive 49 (MRT49)
Protein Families
Class-I pyridoxal-phosphate-dependent aminotransferase family, Alanine aminotransferase subfamily
Tissue Specificity
Expressed at high levels in muscle, adipose tissue, kidney and brain and at lower levels in the liver and breast.
Database Links

HGNC: 18062

OMIM: 138210

KEGG: hsa:84706

STRING: 9606.ENSP00000345282

UniGene: Hs.460693

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