OCLN Polyclonal Antibody

This gene encodes an integral membrane protein that is required for cytokine-induced regulation of the tight junction paracellular permeability barrier. Mutations in this gene are thought to be a cause of band-like calcification with simplified gyration and polymicrogyria (BLC-PMG), an autosomal recessive neurologic disorder that is also known as pseudo-TORCH syndrome. Alternative splicing results in multiple transcript variants. A related pseudogene is present 1.5 Mb downstream on the q arm of chromosome 5.

The OCLN Polyclonal Antibody is a highly specific and sensitive tool designed for the detection and analysis of occludin, a key protein involved in the formation and maintenance of tight junctions. This antibody is produced using a polyclonal approach, ensuring a diverse range of antibodies that recognize different epitopes of the occludin protein.

The OCLN Polyclonal Antibody has been rigorously tested and validated for various applications, including Western blotting, immunohistochemistry, and immunofluorescence. It exhibits exceptional performance in detecting occludin in a wide range of sample types, including cell lysates, tissue sections, and cultured cells.

With its high affinity and specificity, the OCLN Polyclonal Antibody enables accurate and reliable quantification of occludin expression levels in both normal and disease states. Its superior sensitivity allows for the detection of low-abundance occludin protein, making it an ideal choice for researchers working with limited sample quantities.

The OCLN Polyclonal Antibody is supplied as a ready-to-use solution, eliminating the need for time-consuming and error-prone antibody preparation. It is provided in a convenient format, allowing for easy storage and handling.

Choose the OCLN Polyclonal Antibody for your research needs and unlock new insights into the role of occludin in tight junction biology.