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The protein encoded by FKBP14 is a member of the FK506-binding protein family of peptidyl-prolyl cis-trans isomerases. Additionally we are shipping FK506 Binding Protein 14, 22 KDa Antibodies (51) and FK506 Binding Protein 14, 22 KDa Proteins (14) and many more products for this protein.
the occurrence of umbilical skin redundancy in association with two other syndromes: Morquio syndrome and FKBP14-related Ehlers-Danlos syndrome (EDS), is reported.
FKBP22 catalyzes the folding of type III collagen (show COL3A1 ELISA Kits) and only interacts with type III type VI and type X collagen.
A 1.9 A resolution crystal structure for human FKBP22 has been determined. The EF-hand motifs of two FKBP22 molecules form a dimeric complex with an elongated and predominantly hydrophobic cavity that can potentially be occupied by an aliphatic ligand.
study demonstrated FKBP14 is localized in the endoplasmic reticulum (ER) and that deficiency of FKBP14 leads to enlarged ER cisterns in dermal fibroblasts in vivo.
The protein encoded by this gene is a member of the FK506-binding protein family of peptidyl-prolyl cis-trans isomerases. The encoded protein is found in the lumen of the endoplasmic reticulum, where it is thought to accelerate protein folding. Defects in this gene are a cause of a type of Ehlers-Danlos syndrome (EDS). Both a protein-coding variant and noncoding variants are transcribed from this gene.
FK506 binding protein 14, 22 kDa
, FK506-binding protein 14
, PPIase FKBP14
, peptidyl-prolyl cis-trans isomerase FKBP14
, 22 kDa FK506-binding protein
, 22 kDa FKBP