Cyclophilin B Protein, Human, Recombinant (His)

TargetMol Chemicals

Cyclophilin B Protein, Human, Recombinant (His)

16

Research Use Only

22 kDa (predicted); 22 kDa (reducing conditions)

PPIB is identified as a candidate gene for OI-IX. Osteogenesis imperfecta (OI) is an inherited disorder of connective tissue typically caused by defects in either COL1A1 or COL1A2. A number of other genes causative of this disorder have been found, including PPIB, which forms one subunit of the prolyl 3-hydroxylase enzyme complex. Patients with OI caused by PPIB mutation should have appropriate early and regular management of their hearing.

-20°C

12352200