SOX13 Rabbit Polyclonal Antibody, 20ul Buffers & Solutions a complex involved in various

a complex involved in various cellular and developmental processes

Defects in EDA are a cause of ectodermal dysplasia

Proton-linked monocarboxylate transporter

Mutations in this gene cause Charcot-Marie-Tooth disease types 1F (CMT1F) and 2E (CMT2E)

SOX13 Rabbit Polyclonal Antibody, 20ul Buffers & Solutions a complex involved in variousThis gene encodes a member of the SOX (SRY related HMG box) family of transcription factors involved in the regulation of embryonic development and in the determination of cell fate. The encoded protein may act as a transcriptional regulator after forming a protein complex with other proteins. It has also been determined to be a type 1 diabetes autoantigen also known as islet cell antibody 12.