SHOX Polyclonal Antibody

This gene belongs to the paired homeobox family and is located in the pseudoautosomal region 1 (PAR1) of X and Y chromosomes. Defects in this gene are associated with idiopathic growth retardation and in the short stature phenotype of Turner syndrome patients. This gene is highly conserved across species from mammals to fish to flies. Alternatively spliced transcript variants encoding different isoforms have been noted for this gene.

The SHOX polyclonal antibody is a highly specific and reliable tool for the detection and analysis of the Short Stature Homeobox (SHOX) protein. This antibody has been meticulously developed and rigorously tested to ensure its exceptional quality and performance.

The SHOX polyclonal antibody exhibits a high affinity towards the SHOX protein, enabling accurate and sensitive detection in various experimental applications. It has been extensively validated for use in Western blotting, immunohistochemistry, and immunofluorescence assays, providing researchers with a versatile tool for their investigations.

With its exceptional specificity, the SHOX polyclonal antibody ensures minimal cross-reactivity with other proteins, guaranteeing reliable and precise results. Its robust performance allows for the detection of even low abundance SHOX protein levels, facilitating the study of this crucial regulator of skeletal development.

Manufactured under stringent quality control measures, the SHOX polyclonal antibody offers consistent and reproducible results, ensuring the reliability of experimental data. Its long shelf life and stability make it an ideal choice for long-term storage and repeated use, providing researchers with a cost-effective solution.

In summary, the SHOX polyclonal antibody is a highly specific and reliable tool for the detection and analysis of the SHOX protein. Its exceptional quality, versatility, and robust performance make it an invaluable asset for researchers in the field of skeletal development and related studies.