Rabbit anti-Human, Mouse FKBP10 Polyclonal Antibody | anti-FKBP10 antibody
FKBP10 Polyclonal Antibody
IHC: 1:50-1:200
NCBI and Uniprot Product Information
NCBI Description
The protein encoded by this gene belongs to the FKBP-type peptidyl-prolyl cis/trans isomerase (PPIase) family. This protein localizes to the endoplasmic reticulum and acts as a molecular chaperone. Alternatively spliced variants encoding different isoforms have been reported, but their biological validity has not been determined.[provided by RefSeq, Nov 2009]
Uniprot Description
FKBP10: PPIases accelerate the folding of proteins during protein synthesis. Defects in FKBP10 are the cause of osteogenesis imperfecta type 6 (OI6). OI6 is a moderate to severe, autosomal recessive form of osteogenesis imperfecta characterized by increased serum alkaline phosphatase levels and bone histology exhibiting a fish scale-like lamellar pattern. Osteogenesis imperfecta defines a group of connective tissue disorders characterized by bone fragility and low bone mass.
Protein type: EC 5.2.1.8; Isomerase
Chromosomal Location of Human Ortholog: 17q21.2
Cellular Component: endoplasmic reticulum membrane; endoplasmic reticulum lumen
Molecular Function: peptidyl-prolyl cis-trans isomerase activity; FK506 binding; calcium ion binding
Biological Process: protein peptidyl-prolyl isomerization
Disease: Osteogenesis Imperfecta, Type Xi; Bruck Syndrome 1