E2F-1 Polyclonal Antibody, 50ul[BT-AP02788] NGS Oligos Mutations in SLC22A5 (solute carrier

Mutations in SLC22A5 (solute carrier family 22 member 5)are the cause of systemic primary carnitine deficiency (CDSP)

These genes play critical roles during fetal development

AHSG*1 has Thr-248/Thr-256

F-box proteins interact with SKP1 through the F box

This gene| a beta basic group member| is part of a gene cluster with beta-A4| beta-B1| and beta-B2

E2F-1 Polyclonal Antibody, 50ul[BT-AP02788] NGS Oligos Mutations in SLC22A5 (solute carrierThe protein encoded by E2F1 (E2F transcription factor 1) is a member of the E2F family of transcription factors. The E2F family plays a crucial role in the control of cell cycle and action of tumor suppressor proteins and is also a target of the transforming proteins of small DNA tumor viruses. The E2F proteins contain several evolutionally conserved domains found in most members of the family. These domains include a DNA binding domain, a