SUMO4 Polyclonal Antibody

This gene is a member of the SUMO gene family. This family of genes encode small ubiquitin-related modifiers that are attached to proteins and control the target proteins' subcellular localization, stability, or activity. The protein described in this record is located in the cytoplasm and specifically modifies IKBA, leading to negative regulation of NF-kappa-B-dependent transcription of the IL12B gene. A specific polymorphism in this SUMO gene, which leads to the M55V substitution, has been associated with type I diabetes. The RefSeq contains this polymorphism.

The SUMO4 polyclonal antibody is a highly specific and reliable tool designed for the detection and analysis of SUMO4 protein. This antibody is produced using advanced techniques and rigorous quality control measures to ensure optimal performance and reproducibility.

The SUMO4 polyclonal antibody exhibits exceptional sensitivity and specificity, enabling accurate identification and quantification of SUMO4 protein in various biological samples. It has been extensively validated in a wide range of applications, including Western blotting, immunohistochemistry, and immunofluorescence.

With its superior affinity and selectivity, this antibody offers researchers a valuable tool for investigating the role of SUMO4 in cellular processes and disease mechanisms. Its robust performance and consistent results make it an ideal choice for both basic research and clinical studies.

The SUMO4 polyclonal antibody is supplied in a convenient and ready-to-use format, ensuring ease of use and saving valuable time in the laboratory. It is provided in a sufficient quantity to accommodate multiple experiments, allowing for cost-effective and efficient research.

In summary, the SUMO4 polyclonal antibody is a high-quality and reliable reagent that enables accurate detection and analysis of SUMO4 protein. Its exceptional sensitivity, specificity, and ease of use make it an indispensable tool for researchers in various fields, contributing to advancements in our understanding of cellular processes and disease mechanisms.