BMPER Polyclonal Antibody

This gene encodes a secreted protein that interacts with, and inhibits bone morphogenetic protein (BMP) function. It has been shown to inhibit BMP2- and BMP4-dependent osteoblast differentiation and BMP-dependent differentiation of the chondrogenic cells. Mutations in this gene are associated with a lethal skeletal disorder, diaphanospondylodysostosis.

The BMPER Polyclonal Antibody is a highly specific and sensitive antibody designed for the detection of BMPER protein in various biological samples. This antibody is produced by immunizing rabbits with a synthetic peptide corresponding to the C-terminal region of human BMPER protein. The resulting polyclonal antibody has been purified using protein A affinity chromatography and is suitable for use in a variety of applications, including Western blotting, immunohistochemistry, and ELISA.

The BMPER protein is a member of the BMP (bone morphogenetic protein) family and plays a critical role in the regulation of angiogenesis and vascular development. Dysregulation of BMPER expression has been implicated in various diseases, including cancer and cardiovascular disorders. Therefore, the BMPER Polyclonal Antibody is an essential tool for researchers studying the role of BMPER in these diseases.

This antibody has been extensively validated for its specificity and sensitivity, ensuring accurate and reliable results. It exhibits minimal cross-reactivity with other proteins, making it an ideal choice for detecting BMPER protein in complex biological samples. Additionally, the antibody has been optimized for use in a variety of experimental conditions, including different sample types and detection methods.

In summary, the BMPER Polyclonal Antibody is a high-quality research tool that provides reliable and accurate detection of BMPER protein in various biological samples. Its specificity, sensitivity, and versatility make it an essential tool for researchers studying the role of BMPER in various diseases and biological processes.