MyoD(Phospho Ser200) Polyclonal Antibody

This gene encodes a nuclear protein that belongs to the basic helix-loop-helix family of transcription factors and the myogenic factors subfamily. It regulates muscle cell differentiation by inducing cell cycle arrest, a prerequisite for myogenic initiation. The protein is also involved in muscle regeneration. It activates its own transcription which may stabilize commitment to myogenesis.

The MyoD(Phospho Ser200) Polyclonal Antibody is a highly specific and sensitive tool designed for the detection and quantification of MyoD protein phosphorylated at Serine 200. This antibody is produced using a polyclonal approach, ensuring a high affinity and specificity towards the target protein.

MyoD is a crucial transcription factor involved in the regulation of myogenesis, the process of muscle cell differentiation and development. Phosphorylation of MyoD at Serine 200 has been shown to play a significant role in its activity and function. Therefore, the ability to detect and measure this phosphorylation event is of utmost importance in understanding the molecular mechanisms underlying myogenesis.

The MyoD(Phospho Ser200) Polyclonal Antibody has been rigorously validated for its specificity and sensitivity through various experimental approaches, including Western blotting, immunoprecipitation, and immunofluorescence. It exhibits minimal cross-reactivity with other phosphorylated or non-phosphorylated forms of MyoD, ensuring accurate and reliable results.

This antibody is supplied as a liquid formulation, ready for immediate use in various applications, including but not limited to Western blotting, immunohistochemistry, and flow cytometry. It is compatible with a wide range of sample types, including cell lysates, tissue extracts, and cultured cells.

With its exceptional performance and reliability, the MyoD(Phospho Ser200) Polyclonal Antibody is an indispensable tool for researchers studying myogenesis and its associated signaling pathways. Its high specificity and sensitivity make it an ideal choice for both qualitative and quantitative analysis of MyoD phosphorylation at Serine 200, facilitating a deeper understanding of the molecular mechanisms governing muscle cell differentiation and development.