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Catalog Number | orb1958259 |
---|---|
Category | Small Molecules |
Description | Cyclophilin B Protein, Human, Recombinant (His) |
Purity | 98.00% |
MW | 22 kDa (predicted) |
Biological Activity | 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. |
Note | For research use only |
Expiration Date | 12 months from date of receipt. |
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