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OriGene Antibodies in recent publications
A common polymorphism in the LDL receptor gene has multiple effects on LDL receptor function Hum. Mol. Genet., Apr 2013; 22: 1424 - 1431. [anti-DDK]

Excitotoxicity Upregulates SARM1 Protein Expression and Promotes Wallerian-Like Degeneration of Retinal Ganglion Cells and Their Axons Invest. Ophthalmol. Vis. Sci., Apr 2013; 54: 2771 - 2780. [SARM1]

Modulation of TET2 expression and 5-methylcytosine oxidation by the CXXC domain protein IDAX Nature 497, 122-126 doi:10.1038/nature12052 [anti-DDK]

Natriuretic Peptide Receptor-3 Gene (NPR3): Nonsynonymous Polymorphism Results in Significant Reduction in Protein Expression Because of Accelerated Degradation Circ Cardiovasc Genet, Apr 2013; 6: 201 - 210. [NPR3]

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Home All anti-F9 antibodies

Anti-F9 Antibody EPR6187

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Specifications Related Products Conjugation/Bulk FAQs
SKU Description Amount Price Availability*  
TA310474
  • Rabbit Monoclonal antibody against Factor IX (F9)
  • FREE positive control: HEK293T cell transient overexpression lysate (LC400045) , 20ug
100ul $325 3-7 Days Add to Shopping Cart
Gene NameHomo sapiens coagulation factor IX (F9)
Synonyms:FIX; HEMB; P19; PTC; THPH8
ImmunogenA synthetic peptide corresponding to residues in human Factor IX was used as an immunogen.
BufferStore at -20 °C. Buffer: Antibody buffer, sodium azide, glycerol, and BSA. Stable for 12 months from date of receipt.
Clone NameEPR6187 Isotype
Species ReactivityHuman Concentration
Guaranteed Application * Suggested DilutionsWB: 1:1,000 - 10,000; ICC: 1:50 - 100;
BackgroundFactor IX is 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 protein, including point mutations, insertions and deletions, cause factor IX deficiency, which is a recessive X-linked disorder, also called hemophilia B or Christmas disease (1).
Related Pathway
Hemostasis

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