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The protein encoded by FKBP10 belongs to the FKBP-type peptidyl-prolyl cis/trans isomerase (PPIase) family. Additionally we are shipping FK506 Binding Protein 10, 65 KDa Proteins (8) and FK506 Binding Protein 10, 65 KDa Kits (1) and many more products for this protein.
Showing 10 out of 62 products:
Human Monoclonal FKBP10 Primary Antibody for IF, IP - ABIN968087
Coss, Winterstein, Sowder, Simek: Molecular cloning, DNA sequence analysis, and biochemical characterization of a novel 65-kDa FK506-binding protein (FKBP65). in The Journal of biological chemistry 1996
Show all 2 Pubmed References
Human Monoclonal FKBP10 Primary Antibody for ELISA, WB - ABIN528460
Venturi, Monti, Dalle Carbonare, Corradi, Gandini, Valenti, Boner, Antoniazzi: A novel splicing mutation in FKBP10 causing osteogenesis imperfecta with a possible mineralization defect. in Bone 2011
Human Polyclonal FKBP10 Primary Antibody for ELISA, WB - ABIN566216
Ahn, Kang, Kim, Lee: Mining of serum glycoproteins by an indirect approach using cell line secretome. in Molecules and cells 2010
FKBP10 plays a crucial role in hypertrophic scar formation and maybe a therapeutic target for hypertrophic scars.
Data suggest a requirement for FKBP65 function during embryonic connective tissue development in mice; its expression is restricted postnatally in bone, ligaments and tendons.
FKBP65 may act as an elastin (show ELN Antibodies) chaperone in vivo by controlling both the coacervation and the maturation stages of its selfassembly into fibrils.
FKBP10 protein is overexpressed in renal cell carcinoma (show MOK Antibodies)
FKBP65 is linked to pyridinoline cross-linking by specifically mediating the dimerization of LH2 (show PLOD2 Antibodies).
observed changes in activity of six rER-resident PPIases, cyclophilin B (show PPIB Antibodies) (encoded by the PPIB (show PPIB Antibodies) gene), FKBP13 (FKBP2 (show FKBP2 Antibodies)), FKBP19 (FKBP11 (show FKBP11 Antibodies)), FKBP22 (FKBP14 (show FKBP14 Antibodies)), FKBP23 (FKBP7 (show FKBP7 Antibodies)), and FKBP65 (FKBP10), due to posttranslational modifications of proline residues in the substrate.
novel pathogenic mutations of FKBP10 can lead to the extremely rare type XI Osteogenesis imperfecta (show COL1A2 Antibodies) without contractures, which expands the genotypic spectrum of Osteogenesis imperfecta (show COL1A2 Antibodies).
Mutations in FKBP10, localised to chromosome 17q21, have been identified in a patient of Bruck syndrome. Additional cases are also discussed.
A pathogenic change was found in the FKBP10 gene in patients with osteogenesis imperfecta (show COL1A2 Antibodies).
findings further extend the body of evidence that supports the importance of FKBP10 gene in the development of skeletal system
Mutations in the HSP47 and FKBP65 produce a moderately severe form of Osteogenesis imperfect.
CTSD (show CTSD Antibodies), FKBP10, and SLC2A1 (show SLC2A1 Antibodies) are novel genes that participate in the acquisition and maintenance of the adriamycin-resistant phenotype in leukemia cells.
Results imply that FKBP10 mutations affect collagen indirectly, by ablating FKBP65 support for collagen telopeptide hydroxylation by lysyl hydroxylase 2 (show PLOD2 Antibodies), thus decreasing collagen cross-links in tendon and bone matrix.
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.
FK506 binding protein 10
, FK506 binding protein 10, 65 kDa
, peptidyl-prolyl cis-trans isomerase FKBP10
, FK506-binding protein
, peptidyl-prolyl cis-trans isomerase FKBP10-like
, 65 kDa FK506-binding protein
, 65 kDa FKBP
, FK506 binding protein 6 (65 kDa)
, FK506-binding protein 10
, PPIase FKBP10
, immunophilin FKBP65