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Fibromodulin is a member of a family of small interstitial proteoglycans, containing a central region composed of leucine-rich repeats with 4 keratan sulfate chains flanked by disulfide-bonded terminal domains. Additionally we are shipping Fibromodulin Kits (47) and Fibromodulin Proteins (10) and many more products for this protein.
Showing 10 out of 67 products:
Human Polyclonal Fibromodulin Primary Antibody for EIA, FACS - ABIN952324
Ehret, OConnor, Weder, Cooper, Chakravarti: Follow-up of a major linkage peak on chromosome 1 reveals suggestive QTLs associated with essential hypertension: GenNet study. in European journal of human genetics : EJHG 2009
Show all 2 references for ABIN952324
Cow (Bovine) Polyclonal Fibromodulin Primary Antibody for WB - ABIN2785800
Kalamajski, Oldberg: Fibromodulin binds collagen type I via Glu-353 and Lys-355 in leucine-rich repeat 11. in The Journal of biological chemistry 2007
Human Polyclonal Fibromodulin Primary Antibody for WB - ABIN515774
Yang, Culshaw, Liu, Lu, French, Clements, Corcoran: Canine tissue-specific expression of multiple small leucine rich proteoglycans. in Veterinary journal (London, England : 1997) 2012
fibromodulin is involved in the inflammatory processes that characterize atherosclerotic plaque vulnerability
The results suggest that regions within FMOD is associated with ACL (show ACLY Antibodies) injury susceptibility and that genetic sequence variability within genes encoding proteoglycans may potentially modulate the ligament fibril properties.
Melanocyte-secreted factor FMOD is a key regulator of angiogenesis.
Hepatic fibromodulin activates hepatic stellate cells and promotes collagen I deposition, which leads to liver fibrosis.
lumican (show LUM Antibodies) and fibromodulin display different behaviors and that lumican (show LUM Antibodies) may promote regeneration of the TMJ after degeneration and deformation induced by IL-1 beta (show IL1B Antibodies).
study shows (1) a detailed description of ectopic ossification (EO) formed by Bgn (show BGN Antibodies), Fmod or combined depletion, (2) the role of exercise in modulating EO and (3) that Bgn (show BGN Antibodies) and Fmod are critical in controlling motor function.
Fibromodulin is shown for the first time to be naturally processed and presented as a tumor-associated antigen in primary chronic lymphocytic leukemia cells, enabling the expansion of autologous tumor-specific T cells.
Fibromodulin has a role in progression of B-cell chronic lymphocytic leukemia and mantle cell lymphoma
fibromodulin activates the classical pathway of complement by directly binding C1q
complement control protein 6-8 is able to interact with DNA and necrotic cells, but in contrast the His-384 allotype binds these ligands more strongly than the Tyr (show TYR Antibodies)-384 variant
There are discrete populations of fibromodulin within articular cartilage, which may have differing impacts upon tissue processes.
MMP-13 (show MMP13 Antibodies) treatment of fresh articular cartilage results in cleaved fibromodulin fragments
fibromodulin and decorin (show DCN Antibodies) have similarities and differences that may represent the biochemical basis of redundancy in small leucine-rich proteoglycan (show Vcan Antibodies) function
tyrosine sulfate-rich domains of the LRR proteins fibromodulin and osteoadherin (show OMD Antibodies) bind motifs of basic clusters in a variety of heparin-binding proteins, including bioactive factors
Suggest a more complex role for collagen in plaque stability than previously anticipated in fibromodulin-deficient/ApoE (show APOE Antibodies)-null atherosclerotic mice.
The differential effects of Fmod deficiency on bones and teeth appear to diverge in adult mice.
Fibromodulin suppresses nuclear factor-kappaB activity by inducing the delayed degradation of IKBA (show NFKBIA Antibodies) via a JNK (show MAPK8 Antibodies)-dependent pathway coupled to fibroblast apoptosis.
FMOD presence is critical for proper temporospatial coordination of wound healing events and normal TGF-beta (show TGFB1 Antibodies) bioactivity.
fibromodulin plays important roles in the regulation of region-specific fibrillogenesis required for the integration of the corneal and scleral matrices and sulcus development required for establishment of the visual axis
Biglycan (show BGN Antibodies) and fibromodulin are novel key players in regulating chondrogenesis and extracellular matrix turnover during temoporomandibular joint osteoarthritis pathology.
deficiency combined with lumican (show LUM Antibodies) deficiency manifest several clinical features or Ehlers-Danlos syndrome
Dual functions may be related to the different forms of Fmod found in bone versus teeth.
Homologous sequence in lumican (show LUM Antibodies) and fibromodulin leucine-rich repeat 5-7 competes for collagen binding.
Fibromodulin is a member of a family of small interstitial proteoglycans, containing a central region composed of leucine-rich repeats with 4 keratan sulfate chains flanked by disulfide-bonded terminal domains. It may participate in the assembly of the extracellular matrix as it interacts with type I and type II collagen fibrils and inhibits fibrillogenesis in vitro. It may also regulate TGF-beta activities by sequestering TGF-beta into the extracellular matrix.
, KSPG fibromodulin
, collagen-binding 59 kDa protein
, keratan sulfate proteoglycan fibromodulin