OAT Polyclonal Antibody

OAT encodes the mitochondrial enzyme ornithine aminotransferase, which is a key enzyme in the pathway that converts arginine and ornithine into the major excitatory and inhibitory neurotransmitters glutamate and GABA. Mutations that result in a deficiency of this enzyme cause the autosomal recessive eye disease Gyrate Atrophy. Alternatively spliced transcript variants encoding different isoforms have been described. Related pseudogenes have been defined on the X chromosome.

The OAT Polyclonal Antibody is a highly specific and reliable tool designed for the detection and quantification of the Ornithine Aminotransferase (OAT) protein in various biological samples. This antibody is produced through a rigorous process, ensuring its high affinity and specificity towards the target protein. With its exceptional sensitivity, this antibody enables accurate and precise measurements of OAT levels, making it an invaluable asset for researchers and clinicians alike.

The OAT Polyclonal Antibody exhibits exceptional performance across a wide range of applications, including Western blotting, immunohistochemistry, and immunofluorescence. Its versatility allows for the exploration of OAT expression patterns and localization in different tissues and cell types. Furthermore, this antibody has been extensively validated, guaranteeing consistent and reproducible results.

This antibody is supplied in a convenient and ready-to-use format, eliminating the need for time-consuming preparations. Its long shelf life ensures its stability and reliability, making it an ideal choice for long-term experiments and storage. Additionally, the OAT Polyclonal Antibody is compatible with various detection systems, providing flexibility and convenience for researchers working with different experimental setups.

In summary, the OAT Polyclonal Antibody is a highly specific, sensitive, and versatile tool that enables accurate detection and quantification of the OAT protein. Its exceptional performance, convenience, and compatibility make it an indispensable resource for researchers and clinicians in the field of molecular biology and biomedical research.