PEX13 Polyclonal Antibody

This gene encodes a peroxisomal membrane protein that binds the type 1 peroxisomal targeting signal receptor via a SH3 domain located in the cytoplasm. Mutations and deficiencies in peroxisomal protein importing and peroxisome assembly lead to peroxisomal biogenesis disorders, an example of which is Zellweger syndrome.

The PEX13 Polyclonal Antibody is a highly specific and reliable tool designed for the detection and analysis of peroxisomal biogenesis factor 13 (PEX13) protein. This antibody has been extensively validated for its exceptional performance in various applications, including Western blotting, immunohistochemistry, and immunofluorescence.

The PEX13 Polyclonal Antibody exhibits a high affinity towards PEX13 protein, ensuring accurate and sensitive detection even at low expression levels. Its polyclonal nature allows for enhanced recognition of multiple epitopes, resulting in improved specificity and reduced background noise.

This antibody is produced using state-of-the-art techniques, ensuring batch-to-batch consistency and high purity. It has been rigorously tested to ensure optimal performance and reliability, providing researchers with confidence in their experimental results.

The PEX13 Polyclonal Antibody is suitable for a wide range of research applications, including studies on peroxisome biogenesis, cellular metabolism, and organelle dynamics. Its versatility and robustness make it an indispensable tool for scientists working in the fields of cell biology, molecular biology, and biochemistry.

With its exceptional specificity, sensitivity, and reliability, the PEX13 Polyclonal Antibody is an invaluable asset for researchers seeking to unravel the intricate mechanisms underlying peroxisomal biogenesis and function.