KRT37 Polyclonal Antibody, 100ul High Speed Micro-Centrifuges Mutations in this gene are

Mutations in this gene are the most common cause of Fanconi anemia

Two transcript variants encoding different isoforms have been found for MAF

indicating that the scaffold protein can turn signaling "on" or "off" depending on the scaffold concentration

and appears to be the principal fatty acid transporter in enterocytes

KRT37 Polyclonal Antibody, 100ul High Speed Micro-Centrifuges Mutations in this gene areThe protein encoded by this gene is a member of the keratin gene family. As a type I hair keratin, it is an acidic protein which heterodimerizes with type II keratins to form hair and nails. The type I hair keratins are clustered in a region of chromosome 17q12 q21 and have the same direction of transcription.