PEX16 Polyclonal Antibody

The protein encoded by this gene is an integral peroxisomal membrane protein. An inactivating nonsense mutation localized to this gene was observed in a patient with Zellweger syndrome of the complementation group CGD/CG9. Expression of this gene product morphologically and biochemically restores the formation of new peroxisomes, suggesting a role in peroxisome organization and biogenesis. Alternative splicing has been observed for this gene and two variants have been described.

The PEX16 Polyclonal Antibody is a highly specific and sensitive antibody that has been developed for the detection of PEX16 protein in various biological samples. This antibody has been extensively validated for its specificity and sensitivity, making it an ideal tool for researchers and scientists working in the field of peroxisome biology.

The PEX16 Polyclonal Antibody has been produced using high-quality immunogens and has undergone rigorous purification and characterization processes to ensure its purity and specificity. This antibody has been shown to recognize PEX16 protein in a variety of species, including human, mouse, and rat.

The PEX16 Polyclonal Antibody is suitable for use in a range of applications, including Western blotting, immunohistochemistry, and immunofluorescence. It has been shown to produce strong and specific signals in these assays, making it a reliable tool for the detection and quantification of PEX16 protein.

Overall, the PEX16 Polyclonal Antibody is a high-quality and reliable tool for researchers and scientists working in the field of peroxisome biology. Its specificity, sensitivity, and versatility make it an ideal choice for a wide range of applications.