CUL7 Polyclonal Antibody

The protein encoded by this gene is a component of an E3 ubiquitin-protein ligase complex. The encoded protein interacts with TP53, CUL9, and FBXW8 proteins. Defects in this gene are a cause of 3M syndrome type 1 (3M1). Two transcript variants encoding different isoforms have been found for this gene.

The CUL7 Polyclonal Antibody is a highly reliable and efficient tool designed for the detection and analysis of CUL7 protein expression in various biological samples. This antibody is produced using advanced techniques and high-quality materials to ensure superior performance and accuracy.

The CUL7 Polyclonal Antibody exhibits exceptional specificity towards CUL7, a crucial component of the cullin-RING ubiquitin ligase complex. This complex plays a pivotal role in the regulation of protein degradation and cell cycle progression. By targeting CUL7, this antibody enables researchers to investigate the intricate mechanisms underlying cellular processes and disease pathogenesis.

With its polyclonal nature, this antibody offers enhanced sensitivity and versatility, making it suitable for a wide range of applications, including Western blotting, immunohistochemistry, and immunofluorescence. Its robust performance ensures reliable and reproducible results, facilitating precise and accurate data interpretation.

The CUL7 Polyclonal Antibody is meticulously validated to ensure its exceptional quality and performance. It has been extensively tested on various cell lines and tissues, demonstrating its reliability and consistency. Furthermore, this antibody exhibits minimal cross-reactivity with other proteins, ensuring specific and reliable detection of CUL7.

In summary, the CUL7 Polyclonal Antibody is a highly reliable and efficient tool for the detection and analysis of CUL7 protein expression. Its exceptional specificity, enhanced sensitivity, and versatility make it an invaluable asset for researchers in the fields of molecular biology, cell biology, and biomedical research.