CD6 Polyclonal Antibody, 50ul[BT-AP02008] CellSafe™ Mutations of PTCH1 have been

Mutations of PTCH1 have been associated with basal cell nevus syndrome

Mutations in this gene are associated with congenital cataracts| facial dysmorphism and neuropathy syndrome (CCFDN)

The product of PEX5 (peroxisomal biogenesis factor 5) binds to the C-terminal PTS1-type tripeptide peroxisomal targeting signal (SKL-type) and plays an essential role in peroxisomal protein import

The interleukin 4 receptor also binds to IL13

Recognizes and binds to the DNA sequence 5'-CGCCCCCGC-3'

CD6 Polyclonal Antibody, 50ul[BT-AP02008] CellSafe™ Mutations of PTCH1 have beenCMTM6 belongs to the chemokine like factor gene superfamily, a novel family that is similar to the chemokine and transmembrane 4 superfamilies. This gene is one of several chemokine like factor genes located in a cluster on chromosome 3. This gene is widely expressed in many tissues, but the exact function of the encoded protein is unknown.