G6PD Monoclonal Antibody

This gene encodes glucose-6-phosphate dehydrogenase. This protein is a cytosolic enzyme encoded by a housekeeping X-linked gene whose main function is to produce NADPH, a key electron donor in the defense against oxidizing agents and in reductive biosynthetic reactions. G6PD is remarkable for its genetic diversity. Many variants of G6PD, mostly produced from missense mutations, have been described with wide ranging levels of enzyme activity and associated clinical symptoms. G6PD deficiency may cause neonatal jaundice, acute hemolysis, or severe chronic non-spherocytic hemolytic anemia. Two transcript variants encoding different isoforms have been found for this gene.

Introducing the G6PD Monoclonal Antibody, a highly specialized product designed to detect and quantify glucose-6-phosphate dehydrogenase (G6PD) in various biological samples. This monoclonal antibody is produced using advanced techniques and is of the highest quality, ensuring accurate and reliable results.

The G6PD Monoclonal Antibody is an essential tool for researchers and clinicians alike, as it enables the detection of G6PD deficiency, a genetic disorder that affects millions of people worldwide. This product is suitable for use in a range of applications, including enzyme-linked immunosorbent assays (ELISAs), Western blotting, and immunohistochemistry.

The G6PD Monoclonal Antibody is supplied in a convenient format, with ample quantities available for multiple experiments. It is also compatible with a range of detection systems, making it a versatile product that can be used in various laboratory settings.

In summary, the G6PD Monoclonal Antibody is a high-quality product that offers accurate and reliable detection of G6PD in biological samples. Its versatility and compatibility with various detection systems make it an essential tool for researchers and clinicians working in the field of G6PD deficiency.