CCL1 Polyclonal Antibody, 20ul Biochemical Reagents Defects in this gene are

Defects in this gene are a cause of xeroderma pigmentosum complementation group F (XP-F)

with both 4-hydroxylation and 18-hydroxylation activities

Huntington's disease and temporal lobe epilepsy

They form a three-tiered signaling module composed of MAPKKKs| MAPKKs| and MAPKs

Required for the amino acid-induced relocalization of mTORC1 to the lysosomes and its subsequent activation by the GTPase RHEB

CCL1 Polyclonal Antibody, 20ul Biochemical Reagents Defects in this gene areThis antimicrobial gene is one of several chemokine genes clustered on the q arm of chromosome 17. Chemokines form a superfamily of secreted proteins involved in immunoregulatory and inflammatory processes. The superfamily is divided into four subfamilies based on the arrangement of the N terminal cysteine residues of the mature peptide. This chemokine, a member of the CC subfamily, is secreted by activated T cells and displays chemotactic activity