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The protein encoded by FKBP10 belongs to the FKBP-type peptidyl-prolyl cis/trans isomerase (PPIase) family. Zusätzlich bieten wir Ihnen FK506 Binding Protein 10, 65 KDa Proteine (8) und FK506 Binding Protein 10, 65 KDa Kits (1) und viele weitere Produktgruppen zu diesem Protein an.
Showing 10 out of 62 products:
Human Monoclonal FKBP10 Primary Antibody für 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 Polyclonal FKBP10 Primary Antibody für ELISA, WB - ABIN566216
Ahn, Kang, Kim, Lee: Mining of serum glycoproteins by an indirect approach using cell line secretome. in Molecules and cells 2010
Human Monoclonal FKBP10 Primary Antibody für 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
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 (zeige ELN Antikörper) 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 (zeige MOK Antikörper)
FKBP65 is linked to pyridinoline cross-linking by specifically mediating the dimerization of LH2 (zeige PLOD2 Antikörper).
observed changes in activity of six rER-resident PPIases, cyclophilin B (zeige PPIB Antikörper) (encoded by the PPIB (zeige PPIB Antikörper) gene), FKBP13 (FKBP2 (zeige FKBP2 Antikörper)), FKBP19 (FKBP11 (zeige FKBP11 Antikörper)), FKBP22 (FKBP14 (zeige FKBP14 Antikörper)), FKBP23 (FKBP7 (zeige FKBP7 Antikörper)), 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 (zeige COL1A2 Antikörper) without contractures, which expands the genotypic spectrum of Osteogenesis imperfecta (zeige COL1A2 Antikörper).
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 (zeige COL1A2 Antikörper).
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 (zeige CTSD Antikörper), FKBP10, and SLC2A1 (zeige SLC2A1 Antikörper) 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 (zeige PLOD2 Antikörper), 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