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)

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with both 4-hydroxylation and 18-hydroxylation activities

Defects in MEF2A could be a cause of autosomal dominant coronary artery disease 1 with myocardial infarction (ADCAD1)

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