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F10 encodes the vitamin K-dependent coagulation factor X of the blood coagulation cascade. 再加上，我们可以发Coagulation Factor X 试剂盒 (59) 和 Coagulation Factor X 蛋白 (28)和数多这个蛋白质的别的产品。
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Data suggest that, for all coagulation proteins tested (prothrombin, factor X, activated factor VII, activated protein C), tighter binding to lipid bilayers (lower Kd) is observed as the proportion of anionic phospholipid increases. These studies were conducted in high-throughput screening using phospholipid bilayers in nanodiscs with multiplexed silicon photonic sensor (micro-ring resonator) array technology.
A coagulation initiating pathway is revealed in which the TF-FVIIa-nascent FXa complex activates FVIII (显示 F8 抗体) apart from thrombin (显示 F2 抗体) feedback.
Data suggest oxidized lipid vesicles with phosphatidylserine/polyunsaturated fatty acids promote inactivation of ZPI (显示 SERPINA10 抗体)-PZ complex or free ZPI (显示 SERPINA10 抗体); binding of PZ-complexed or free ZPI (显示 SERPINA10 抗体) to oxidized vesicles mediates inactivation of ZPI (显示 SERPINA10 抗体) (an inhibitor of FXa); blocking heparin- (anticoagulant-)binding site on ZPI (显示 SERPINA10 抗体) interferes with binding to lipid or PZ. (ZPI (显示 SERPINA10 抗体) = protein Z-dependent protease inhibitor (显示 SERPINA10 抗体); PZ = protein Z (显示 PROZ 抗体); FXa = factor Xa)
Factor Va reduced by 100-fold the apparent Kd of myosin for factor Xa (Kd approximately 0.48 nM), primarily by reducing koff, indicating formation of a stable ternary complex of myosin:Xa:Va.
PTX2 (显示 APCS 抗体) was identified PTX2 (显示 APCS 抗体) as a novel partner for FX, and both proteins cooperated to prevent their SR-AI (显示 MSR1 抗体)-mediated uptake by macrophages.
annexin A2 (显示 ANXA2 抗体) contributes to lung injury and fibrotic disease by mediating the fibrogenic actions of FXa.
Individuals suffering from relapsing-remitting and secondary progressive multiple sclerosis had significantly higher prothrombin (显示 F2 抗体) and factor X levels than healthy donors, whereas levels were unchanged in primary progressive MS and neuromyelitis optica patients.
Low concentrations of TF and exogenous FXIa, each too low to elicit a burst in thrombin (显示 F2 抗体) production alone, act synergistically when in combination to cause substantial thrombin (显示 F2 抗体) production.
analysis of how physiological concentrations of Tissue factor pathway inhibitor (显示 TFPI 抗体) inhibit FXa
According to our study, compounds 1a, 1g and 1s displayed evident FXa inhibitory activity and excellent selectivity over thrombin (显示 F2 抗体) in in vitro inhibition activities studies.
PTX2 (显示 PITX2 抗体) was identified PTX2 (显示 PITX2 抗体) as a novel partner for FX, and both proteins cooperated to prevent their SR-AI (显示 MSR1 抗体)-mediated uptake by macrophages.
Enhanced FXa and PAR2 (显示 F2RL1 抗体) exacerbate DN and that both are promising targets for preventing diabetic nephropathy.
Macrophages regulate FX plasma levels in an SR-AI (显示 MSR1 抗体)-dependent manner.
Factor Xa has a role in inhibiting HMGB1 (显示 HMGB1 抗体)-induced septic responses in human umbilical vein endothelial cells and in mice
Selective inhibition of FXa improves the left ventricular function during CVB3-induced myocarditis and seems to be associated with an improved myocardial remodeling.
Activated factor X signaling via protease-activated receptor 2 (显示 F2RL1 抗体) suppresses pro-inflammatory cytokine production from lipopolysaccharide-stimulated myeloid cells.
There was no detectable increase in plasma levels of mouse FX after active-site inhibited human APC (显示 APC 抗体) administration to mice overexpressing human EPCR (显示 PROCR 抗体). FX does not effectively interact with EPCR (显示 PROCR 抗体) in vivo, at least in regards to the mouse system.
investigation of role of F10a in progression of diabetic nephropathy: data from studies using inhibitor of F10a suggest that F10a does play a role in development of proteinemia, glomerular hypertrophy, and protein deposition in kidney of db/db (显示 LEPR 抗体) mice
Data suggest that tissue factor (显示 F3 抗体) and factor V induction by LPS (显示 TLR4 抗体) may in part accelerate mesangioproliferative glomerulonephritis through activation of factor X and downstream proinflammatory and procoagulant mechanisms.
Data suggest factor Xa (FXa) and factor Va (FVa) compete to bind FXa on both PS model membranes and microparticles from activated platelets; this competition between dimerization/prothrombinase (显示 FGL2 抗体) complex formation appears to regulate blood coagulation.
thrombin (显示 F2 抗体) and factor Xa diffusion along the heparin molecule explains the effects of extended heparin chain lengths
Factor Xa (fXa), a key serine protease (显示 F2 抗体) of the coagulation system, was used as a model enzyme to test the canonical conformation hypothesis.
These findings as well as the prolonged survival of f10(-/-) mutants will enable us to expand our understanding of the molecular mechanisms of hemostasis, including a platform for screening variants of uncertain significance in patients with F10 deficiency and other coagulation disorders
This gene encodes the vitamin K-dependent coagulation factor X of the blood coagulation cascade. This factor undergoes multiple processing steps before its preproprotein is converted to a mature two-chain form by the excision of the tripeptide RKR. Two chains of the factor are held together by 1 or more disulfide bonds\; the light chain contains 2 EGF-like domains, while the heavy chain contains the catalytic domain which is structurally homologous to those of the other hemostatic serine proteases. The mature factor is activated by the cleavage of the activation peptide by factor IXa (in the intrisic pathway), or by factor VIIa (in the extrinsic pathway). The activated factor then converts prothrombin to thrombin in the presence of factor Va, Ca+2, and phospholipid during blood clotting. Mutations of this gene result in factor X deficiency, a hemorrhagic condition of variable severity.
, factor Xa
, stuart factor
, coagulation factor 10
, factor XA light chain
, virus activating protease
, virus-activating protease
, coagulation factor X
, vitamin K dependent serine protease
, coagulation factor X preproprotein
, blood coagulation factor X
, Coagulation factor X
, coagulation factor 10 L homeolog