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F9 encodes vitamin K-dependent coagulation factor IX that circulates in the blood as an inactive zymogen. Zusätzlich bieten wir Ihnen Coagulation Factor IX Kits (73) und Coagulation Factor IX Proteine (38) und viele weitere Produktgruppen zu diesem Protein an.
Showing 10 out of 308 products:
Human Polyclonal Coagulation Factor IX Primary Antibody für IF (p), IHC (p) - ABIN1387087
Yang, Bae, Jung, Park, Chung, Seok, Roh, Han, Oh, Sohn, Jeong, Cho: Surface functionalization-specific binding of coagulation factors by zinc oxide nanoparticles delays coagulation time and reduces thrombin generation potential in vitro. in PLoS ONE 2017
Higher FIX antigen levels are associated with incident coronary heart disease in blacks but not in whites; the association of FXI (zeige F11 Antikörper) levels with ischemic stroke is slightly attenuated after adjusting for stroke risk factors.
Report a diagnostic algorithm that can reliably identify pathogenic variants of factor 8/9 and von Willebrand factor (zeige VWF Antikörper) and diagnose patients with hemophilia A, hemophilia B or von Willebrand disease.
a computational approach was conducted to select suitable location(s) for introducing new N-glycosylation sites into the human coagulation factor IX.
caspase-3 (zeige CASP3 Antikörper) inhibitors also suppressed the attenuation of cell adhesion and phosphorylation of p38 MAPK (zeige MAPK14 Antikörper) by EGF (zeige EGF Antikörper)-F9. Our data indicated that EGF (zeige EGF Antikörper)-F9 activated signals for apoptosis and induced de-adhesion in a caspase-3 (zeige CASP3 Antikörper) dependent manner.
Data suggest that coagulation factor IX (hFIX) minigene containing beta-globin (hBG) introns could represent a particular interest in stem cell-based gene therapy of hemophilias.
miR (zeige MLXIP Antikörper)-128 and miR (zeige MLXIP Antikörper)-125 could help to increase the nonsense-mutant F9 levels by repressing nonsense-mediated mRNA decay.
In 293T cells, the addition of 0.5 mM Ca(+2) and 1 mM Mg(+2) resulted in higher recombinant human Factor IX concentration. SK-Hep-1 cell line proved to be very effective in rhFIX production, and it can be used as a novel biotechnological platform for the production of recombinant proteins.
Authors investigated the interaction of coagulation factor IX in the development of atherosclerosis. Severe deficiency of FIX did not protect the animals from the development of atherosclerotic plaques in the aortic areas.
structural features within residues of the 39-loop contribute to the resistance of FIXa (zeige ETFB Antikörper) to inhibition by plasma inhibitors ZPI (zeige SERPINA10 Antikörper) and TFPI (zeige TFPI Antikörper).
hnRNP A3 (zeige HNRNPA3 Antikörper) is a major liver nuclear protein (zeige HEMGN Antikörper) binding to age related increase element of the factor IX gene.
functional role of binding of F9 to collagen IV (zeige COL4 Antikörper) in hemostasis.
FIX and FXI (zeige F11 Antikörper) deficiency cause similar effects in the carotid artery injury model
findings show coagulation factor IX & complement component C4-binding protein can bind Adenovirus fiber knob domain & provide a bridge for virus uptake through cell surface heparan sulfate proteoglycans & low-density lipoprotein receptor (zeige LDLR Antikörper)-related protein (zeige LRP1 Antikörper)
Mice lacking plasminogen (zeige PLG Antikörper) and fIX (Plg (zeige PLG Antikörper)(-/-)/fIX-/-) have lower mortality at age 6 months than Plg (zeige PLG Antikörper)(-/-)/fIX+/+ mice
important role for Lyn (zeige LYN Antikörper) in VWF (zeige VWF Antikörper)/GPIb-IX-induced integrin activation mediated via the cGMP signaling pathway independently of TXA2 (zeige TBXA2R Antikörper) synthesis and also indicate that Lyn (zeige LYN Antikörper) is critically important in GPIb-IX-mediated activation of the cGMP pathway
the heparin-binding exosite of factor IXa is a critical regulator of plasma thrombin (zeige F2 Antikörper) generation and venous thrombosis
Mg2 (zeige MCOLN1 Antikörper)+ ions are required to maintain native conformation and in vivo function of factor IX gamma-carboxyglutamic acid domain
This gene encodes vitamin K-dependent coagulation factor IX that circulates in the blood as an inactive zymogen. This factor is converted to an active form by factor XIa, which excises the activation peptide and thus generates a heavy chain and a light chain held together by one or more disulfide bonds. The role of this activated factor IX in the blood coagulation cascade is to activate factor X to its active form through interactions with Ca+2 ions, membrane phospholipids, and factor VIII. Alterations of this gene, including point mutations, insertions and deletions, cause factor IX deficiency, which is a recessive X-linked disorder, also called hemophilia B or Christmas disease.
coagulation factor IX
, coagulation factor 9 (plasma thromboplastic component, Christmas disease, hemophilia B)
, gla domain
, coagulation factor 9
, Coagulation factor IX
, coagulation factor IX-like
, Christmas factor
, F9 p22
, FIX F9
, factor 9
, factor IX F9
, plasma thromboplastic component
, plasma thromboplastin component
, christmas factor
, Coagulation factor IX (plasma thromboplastic component, Christmas disease, hemophilia B)
, coagulation factor IX (plasma thromboplastic component, Christmas disease, hemophilia B)
, factor IX activated protein
, factor IX