MALD2 Polyclonal Antibody

The protein encoded by this gene is a membrane protein found at the tight junctions between epithelial cells. The encoded protein helps establish epithelial barriers such as those in the organ of Corti, where these barriers are required for normal hearing. Defects in this gene are a cause of deafness autosomal recessive type 49 (DFNB49). Two transcript variants encoding different isoforms have been found for this gene.

The MALD2 Polyclonal Antibody is a highly specific and sensitive antibody designed for use in various research applications. This antibody is produced by immunizing rabbits with a synthetic peptide corresponding to the C-terminal region of the human MALD2 protein. The resulting polyclonal antibody has been purified using a combination of protein A and peptide affinity chromatography to ensure high specificity and purity.

The MALD2 Polyclonal Antibody has been extensively validated for use in Western blotting, immunohistochemistry, and immunofluorescence assays. It has been shown to specifically recognize the MALD2 protein in a variety of human tissues and cell lines. This antibody is suitable for use in both basic research and clinical applications.

The MALD2 Polyclonal Antibody is supplied as a liquid in phosphate-buffered saline (PBS) with 0.02% sodium azide as a preservative. It is available in various sizes to meet the needs of different research applications. This antibody is recommended for use at a dilution of 1:1000 for Western blotting and 1:200 for immunohistochemistry and immunofluorescence assays.

In summary, the MALD2 Polyclonal Antibody is a highly specific and sensitive antibody that is ideal for use in various research applications. Its high purity and specificity make it a valuable tool for researchers studying the function and expression of the MALD2 protein in human tissues and cell lines.