MYO7A Polyclonal Antibody

This gene is a member of the myosin gene family. Myosins are mechanochemical proteins characterized by the presence of a motor domain, an actin-binding domain, a neck domain that interacts with other proteins, and a tail domain that serves as an anchor. This gene encodes an unconventional myosin with a very short tail. Defects in this gene are associated with the mouse shaker-1 phenotype and the human Usher syndrome 1B which are characterized by deafness, reduced vestibular function, and (in human) retinal degeneration. Alternative splicing results in multiple transcript variants.

The MYO7A Polyclonal Antibody is a highly specific and reliable tool designed for the detection and analysis of MYO7A protein expression in various biological samples. This antibody is produced through a rigorous process, ensuring its high affinity and specificity towards MYO7A.

The MYO7A Polyclonal Antibody exhibits exceptional sensitivity, enabling the detection of even low levels of MYO7A protein. It has been extensively validated for use in various applications, including Western blotting, immunohistochemistry, and immunofluorescence.

This antibody is manufactured using state-of-the-art techniques and undergoes stringent quality control measures to ensure consistent and reliable performance. It is supplied as a liquid formulation, allowing for easy and convenient handling.

The MYO7A Polyclonal Antibody is suitable for use in both research and diagnostic settings. Its versatility and high specificity make it an ideal choice for studying MYO7A protein expression and its role in various biological processes.

Order the MYO7A Polyclonal Antibody today and unlock new insights into the function and regulation of MYO7A protein.