FA58A Polyclonal Antibody

Mutations in this gene have been shown to cause an X-linked dominant STAR syndrome that typically manifests syndactyly, telecanthus and anogenital and renal malformations. The protein encoded by this gene contains a cyclin-box-fold domain which suggests it may have a role in controlling nuclear cell division cycles. Alternative splicing results in multiple transcript variants encoding distinct isoforms.

The FA58A Polyclonal Antibody is a highly specific and sensitive immunological reagent designed for use in various research applications. This antibody is produced by immunizing rabbits with a synthetic peptide corresponding to a specific region of the human FA58A protein. The resulting polyclonal antibody exhibits high affinity and specificity for the target protein, making it an ideal tool for detecting and quantifying FA58A in various biological samples.

The FA58A Polyclonal Antibody is suitable for use in a variety of applications, including Western blotting, immunohistochemistry, and ELISA. It has been extensively validated for use in human samples and has been shown to exhibit minimal cross-reactivity with other proteins. The antibody is supplied as a purified IgG fraction, which has been affinity-purified from rabbit serum using a specific antigen.

The FA58A Polyclonal Antibody is a reliable and effective tool for researchers studying the role of FA58A in various biological processes. Its high specificity and sensitivity make it an ideal reagent for detecting and quantifying FA58A in complex biological samples. With its proven performance and ease of use, the FA58A Polyclonal Antibody is an essential tool for any researcher studying this important protein.