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The protein encoded by LOX is an extracellular copper enzyme that initiates the crosslinking of collagens and elastin. Zusätzlich bieten wir Ihnen LOX Antikörper (194) und LOX Proteine (14) und viele weitere Produktgruppen zu diesem Protein an.
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Human LOX ELISA Kit für Sandwich ELISA - ABIN418267
Tadmor, Bejar, Attias, Mischenko, Sabo, Neufeld, Vadasz: The expression of lysyl-oxidase gene family members in myeloproliferative neoplasms. in American journal of hematology 2013
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Mouse (Murine) LOX ELISA Kit für Sandwich ELISA - ABIN425766
Tsukasaki, Hamada, Okamoto, Nagashima, Terashima, Komatsu, Win, Okamura, Nitta, Yasuda, Penninger, Takayanagi: LOX Fails to Substitute for RANKL in Osteoclastogenesis. in Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research 2016
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Rat (Rattus) LOX ELISA Kit für Sandwich ELISA - ABIN432937
Wang, Wan, Li, Zhang, Wan, Ji, Li, Liu, Han: Lysyl oxidase is involved in synovial hyperplasia and angiogenesis in rats with collagen‑induced arthritis. in Molecular medicine reports 2017
Partial knockdown of lysyl oxidase genes sensitizes the developing embryo to dithiocarbamate exposure.
Data reveal a role for lysyl oxidase in early morphogenesis, especially in muscle development and neurogenesis, and resume some aspects of physiopathology of copper metabolism.
LOX expression was mildly but significantly upregulated in CD34 (zeige CD34 ELISA Kits)+-derived primary myelofibrosis megakaryocytes and platelets compared with controls. These megakaryocytes showed a greater tendency to adhere and spread to monomeric collagen, and this was inhibited by the LOX-specific inhibitor BAPN (zeige ANPEP ELISA Kits).
Data suggest that a missense mutation in lysyl oxidase (LOX) is associated with aortic disease.
Our findings suggest that LOX has a role in cancer cell mitosis
Our findings provide new evidence that LOX regulates SNAI2 expression and that SNAI2-mediated TIMP4 (zeige TIMP4 ELISA Kits) secretion plays a role in cancer progression.
UXT (zeige UXT ELISA Kits) Is a LOX-PP Interacting Protein That Modulates Estrogen Receptor Alpha (zeige ESR1 ELISA Kits) Activity in Breast Cancer Cells.
LOX is a prognostic factor for poor progression free survival in patients with ER- breast cancer. LOX overexpression was positively correlated with resistance to radiation and drug therapy.
This preliminary study indicated that LOX gene polymorphisms, such as rs2303656, rs3900446, and rs763497, may play crucial roles in intracranial aneurysm formation in the Korean population.
Results show that CTGF (zeige CTGF ELISA Kits) mediates the GDF8 (zeige MSTN ELISA Kits)-induced up-regulation of LOX expression and increases in LOX activity in human granulosa cells.
The LOXL1 (zeige LOXL1 ELISA Kits) SNPs, rs1048661 and rs3825942, are associated with PXF (zeige PEX19 ELISA Kits) in the South Indian population correlating with lowered LOX activity in the aqueous humor. The increased level of total TGF-beta (zeige TGFB1 ELISA Kits) in the aqueous humor of PXF (zeige PEX19 ELISA Kits) cases is possibly associated with LOX regulation which needs further investigation.
These findings suggest that LOX induces an age-dependent disturbance of diastolic function and aggravates Ang II (zeige AGT ELISA Kits)-induced hypertrophy, which provides novel insights into the role of LOX in cardiac performance.
Statins normalize vascular lysyl oxidase (LOX) down-regulation induced by proatherogenic risk factors.
These results indicate that proLOX could be processed by two different mechanisms producing two forms of active LOX.
Lysyl oxidase enhances elastin (zeige ELN ELISA Kits) synthesis and matrix formation by vascular smooth muscle cells
Lysyl oxidase has a role in oxidizing basic fibroblast growth factor (zeige FGF2 ELISA Kits) and inactivating its mitogenic potential
In cases of vascular calcification, the decreased expression of LOX may be partially responsible for decreased vascular elasticity and also for the decreased formation of new elastic fibers.
Statins normalize vascular lysyl oxidase down-regulation induced by proatherogenic risk factors.
These results suggest that LOX has the ability to induce RANKL (zeige TNFSF11 ELISA Kits) expression on stromal cells; however, it fails to substitute for RANKL (zeige TNFSF11 ELISA Kits) in osteoclastogenesis.
Data show that LOX-PP enhances adipogenesis at least partially through inhibition of FGF-2 (zeige FGF2 ELISA Kits) receptor signaling.
LOX targeting reduces peritoneal fibrosis.
Absence of lysyl oxidase (Lox) causes thoracic aortic aneurysms. The aortic mechanical behavior of Lox(-/-) mice is consistent with reduced elastin (zeige ELN ELISA Kits) and collagen cross-linking but demonstrates vascular location-specific differences. Lox(-/-) aortas show upregulation of matrix remodeling genes and location-specific differential expression of other matrix and smooth muscle cell gene sets.
Findings from this study indicate that preventing LOX overexpression may be protective against high glucose-induced apoptosis in retinal vascular cells associated with diabetic retinopathy.
LOX family members contribute significantly to the detrimental effects of cardiac remodelling, highlighting LOX inhibition as a potential therapeutic strategy for post-infarction recovery
Findings suggest that the lysyl oxidase (LOX)-mediated organization of collagen fibers in the extracellular matrix is an important regulator of osteoblastogenesis.
The data suggest a fibromodulin (zeige FMOD ELISA Kits)-modulated collagen cross-linking mechanism where fibromodulin (zeige FMOD ELISA Kits) binds to a specific part of the collagen domain and also forms a complex with lysyl oxidase, targeting the enzyme toward specific cross-linking sites.
Data suggest of pharmacologic targeting of lysyl oxidase (LOX) pathway to inhibit liver fibrosis and promote its resolution.
The protein encoded by this gene is an extracellular copper enzyme that initiates the crosslinking of collagens and elastin. The enzyme catalyzes oxidative deamination of the epsilon-amino group in certain lysine and hydroxylysine residues of collagens and lysine residues of elastin. In addition to crosslinking extracellular matrix proteins, the encoded protein may have a role in tumor suppression. Defects in this gene are a cause of autosomal recessive cutis laxa type I (CL type I). Two transcript variants encoding different isoforms have been found for this gene.
, protein-lysine 6-oxidase-like
, protein-lysine 6-oxidase
, ras excision protein
, ras recision gene (rrg)
, Lysyl oxidase (an H-rev gene with its expression down-regulated in HRAS-transformed rat 208F fibroblasts)