RBM10 Polyclonal Antibody

This gene encodes a nuclear protein that belongs to a family proteins that contain an RNA-binding motif. The encoded protein associates with hnRNP proteins and may be involved in regulating alternative splicing. Defects in this gene are the cause of the X-linked recessive disorder, TARP syndrome. Alternate splicing results in multiple transcript variants.

The RBM10 Polyclonal Antibody is a highly specific and reliable tool designed for the detection and analysis of RBM10 protein expression in various biological samples. This antibody is produced using a polyclonal approach, ensuring a diverse range of antibodies that recognize different epitopes of the RBM10 protein.

The RBM10 Polyclonal Antibody exhibits exceptional sensitivity and specificity, enabling accurate and precise quantification of RBM10 protein levels. It has been extensively validated in multiple experimental settings, including Western blotting, immunohistochemistry, and immunofluorescence.

With its superior performance, the RBM10 Polyclonal Antibody is an indispensable tool for researchers studying RBM10 protein function and its involvement in various cellular processes. Its versatility allows for a wide range of applications, including protein expression profiling, protein-protein interaction studies, and functional analysis of RBM10 in disease models.

The RBM10 Polyclonal Antibody is manufactured using state-of-the-art techniques and undergoes rigorous quality control measures to ensure consistent and reliable results. It is supplied in a convenient format, ready for immediate use in laboratory experiments.

Choose the RBM10 Polyclonal Antibody for its exceptional performance, reliability, and versatility, and unlock new insights into the role of RBM10 in cellular biology and disease mechanisms.