SMN1 Monoclonal Antibody, 100ul[BT-MCA1144] Culture Media and a mitogen

and a mitogen

Defects in the cathepsin C have been shown to be a cause of Papillon-Lefevre syndrome

tissue specificity:Expressed in lymphocyte-rich tissues

and mutations in this gene have been associated with achromatopsia 3

Mutations in this gene have been associated with disruption of the retinal pigment epithelium (RPE) phagocytosis pathway and onset of autosomal recessive retinitis pigmentosa (RP)

SMN1 Monoclonal Antibody, 100ul[BT-MCA1144] Culture Media and a mitogenThis gene is part of a 500 kb inverted duplication on chromosome 5q13. This duplicated region contains at least four genes and repetitive elements which make it prone to rearrangements and deletions. The repetitiveness and complexity of the sequence have also caused difficulty in determining the organization of this genomic region. The telomeric and centromeric copies of this gene are nearly identical and encode the same protein. However, mutations in