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Coagulation Factor IX Proteins (F9)

F9 encodes vitamin K-dependent coagulation factor IX that circulates in the blood as an inactive zymogen. Additionally we are shipping Coagulation Factor IX Antibodies (142) and Coagulation Factor IX Kits (66) and many more products for this protein.

list all proteins Gene Name GeneID UniProt
F9 2158 P00740
F9 14071 P16294
F9 24946 P16296
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Top Coagulation Factor IX Proteins at antibodies-online.com

Showing 10 out of 31 products:

Catalog No. Origin Source Conjugate Images Quantity Supplier Delivery Price Details
HOST_Human Cells Mouse His tag 10 μg Log in to see 16 Days
$206.80
Details
HOST_Human Cells Human His tag 50 μg Log in to see 16 Days
$382.80
Details
HOST_Escherichia coli (E. coli) Mouse His tag „Crystallography Grade“ protein due to multi-step, protein-specific purification process 1 mg Log in to see 29 to 34 Days
$4,331.68
Details
HOST_Escherichia coli (E. coli) Human His tag „Crystallography Grade“ protein due to multi-step, protein-specific purification process 1 mg Log in to see 29 to 34 Days
$4,331.68
Details
HOST_Escherichia coli (E. coli) Human His tag 100 μg Log in to see 11 to 13 Days
$633.60
Details
HOST_Escherichia coli (E. coli) Mouse His tag 100 μg Log in to see 11 to 13 Days
$809.60
Details
HOST_Escherichia coli (E. coli) Rat His tag 100 μg Log in to see 11 to 13 Days
$823.90
Details
HOST_Escherichia coli (E. coli) Rabbit His tag,GST tag 100 μg Log in to see 11 to 13 Days
$859.10
Details
HOST_Wheat germ Human GST tag 10 μg Log in to see 9 Days
$405.71
Details
Yeast Sheep His tag   1 mg Log in to see 56 to 66 Days
$2,715.17
Details

F9 Proteins by Origin and Source

Origin Expressed in Conjugate
Human , , ,
,
Mouse (Murine) ,

Rat (Rattus) ,

Top referenced Coagulation Factor IX Proteins

  1. Human Coagulation Factor IX Protein expressed in Human Cells - ABIN2004307 : Espinós, Casaña, Haya, Cid, Aznar: Molecular analyses in hemophilia B families: identification of six new mutations in the factor IX gene. in Haematologica 2003 (PubMed)
    Show all 5 references for ABIN2004307

  2. Mouse (Murine) Coagulation Factor IX Protein expressed in Human Cells - ABIN2007714 : Onay, Kavakli, Kilinç, Gürgey, Aktu?lu, Kemahli, Ozbek, Ca?layan: Molecular pathology of haemophilia B in Turkish patients: identification of a large deletion and 33 independent point mutations. in British journal of haematology 2003 (PubMed)
    Show all 4 references for ABIN2007714

More Proteins for Coagulation Factor IX (F9) Interaction Partners

Human Coagulation Factor IX (F9) interaction partners

  1. Differentiation studies demonstrated osteogenic (but not chondrogenic or adipogenic) differentiation capability and efficient FIX secretion of the enclosed MSCs in the fibronectin (show FN1 Proteins)-alginate suspension culture.

  2. Selective disruption of exosite-mediated regulation of factor IX by heparin and antithrombin (show SERPINC1 Proteins) can be achieved with preserved or enhanced thrombin (show F2 Proteins) generation capacity.

  3. Describe inhibition of tissue factor:factor VIIa-catalyzed factor IX and factor X activation by TFPI (show TFPI Proteins) and TFPI (show TFPI Proteins) constructs.

  4. Activatable bioengineered FIX molecules with FVIII (show F8 Proteins)-independent activity might be a promising tool for improving hemophilia A treatment, especially for patients with inhibitors.

  5. Data suggest that Gly317 plays role in normal catalytic function for FIX/FIXa (show ETFB Proteins) in the clotting cascade; mutations in Gly317 (G317R, G317E) result in variable severity of bleeding in hemophilia B patients.

  6. 11 FIX gene mutations (8 point mutations, 2 small deletions/insertions, and 1 large deletion), including two novel mutations (exon6 c.687-695, del 9 mer (show MERTK Proteins) and c.460-461, ins (show INS Proteins) T) were found.

  7. All four domains of FIXa (show ETFB Proteins) wrap across FVIIIa that spans the co-factor binding surface of A2, A3 and C1 domains.

  8. Thrombin (show F2 Proteins)-mediated, TAFI (show CPB2 Proteins)-dependent down-regulation of fibrinolysis provides new clues for explaining the heightened thrombotic risk in subjects carrying the FIX-Padua mutation.

  9. the glycan at 1810 is not involved in FVIII (show F8 Proteins) cofactor function, and that Phe-1816 of region 1811-1818 contributes to FIXa (show ETFB Proteins) binding. Both regions 1803-1810 and 1811-1818 contribute to FVIIIa stability.

  10. The allosteric mechanism of activation of antithrombin (show SERPINC1 Proteins) as an inhibitor of factor IXa and factor Xa (show F10 Proteins): heparin-independent full activation through mutations adjacent to helix D.

Mouse (Murine) Coagulation Factor IX (F9) interaction partners

  1. structural features within residues of the 39-loop contribute to the resistance of FIXa (show ETFB Proteins) to inhibition by plasma inhibitors ZPI (show SERPINA10 Proteins) and TFPI (show TFPI Proteins).

  2. hnRNP A3 is a major liver nuclear protein binding to age related increase element of the factor IX gene.

  3. functional role of binding of F9 to collagen IV (show COL4 Proteins) in hemostasis.

  4. FIX and FXI (show F11 Proteins) deficiency cause similar effects in the carotid artery injury model

  5. 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 (show LDLR Proteins)-related protein (show LRP1 Proteins)

  6. Mice lacking plasminogen (show PLG Proteins) and fIX (Plg (show PLG Proteins)(-/-)/fIX-/-) have lower mortality at age 6 months than Plg (show PLG Proteins)(-/-)/fIX+/+ mice

  7. important role for Lyn (show LYN Proteins) in VWF (show VWF Proteins)/GPIb-IX-induced integrin activation mediated via the cGMP signaling pathway independently of TXA2 synthesis and also indicate that Lyn (show LYN Proteins) is critically important in GPIb-IX-mediated activation of the cGMP pathway

  8. the heparin-binding exosite of factor IXa is a critical regulator of plasma thrombin (show F2 Proteins) generation and venous thrombosis

Cow (Bovine) Coagulation Factor IX (F9) interaction partners

  1. structural features within residues of the 39-loop contribute to the resistance of FIXa (show ETFB Proteins) to inhibition by plasma inhibitors ZPI (show SERPINA10 Proteins) and TFPI (show TFPI Proteins).

  2. Mg2 (show MCOLN1 Proteins)+ ions are required to maintain native conformation and in vivo function of factor IX gamma-carboxyglutamic acid domain

Coagulation Factor IX (F9) Protein Profile

Protein Summary

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.

Gene names and symbols associated with Coagulation Factor IX Proteins (F9)

  • coagulation factor IXa (f9a)
  • coagulation factor 9 (f9)
  • coagulation factor IX (CpipJ_CPIJ003776)
  • coagulation factor IX (CpipJ_CPIJ009129)
  • coagulation factor IX (CpipJ_CPIJ013063)
  • coagulation factor IX (CpipJ_CPIJ013624)
  • coagulation factor IX (Tsp_01441)
  • Coagulation factor IX (fa9)
  • coagulation factor IX (F9)
  • AW111646 protein
  • Cf-9 protein
  • Cf9 protein
  • f9 protein
  • FIX protein
  • FIXA protein
  • HEMB protein
  • P19 protein
  • PTC protein
  • THPH8 protein
  • zgc:109775 protein

Protein level used designations for Coagulation Factor IX Proteins (F9)

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

GENE ID SPECIES
359826 Danio rerio
496659 Xenopus (Silurana) tropicalis
6035113 Culex quinquefasciatus
6041549 Culex quinquefasciatus
6046266 Culex quinquefasciatus
6047200 Culex quinquefasciatus
10911295 Trichinella spiralis
100049721 Xenopus laevis
100380442 Salmo salar
100398468 Callithrix jacchus
2158 Homo sapiens
14071 Mus musculus
24946 Rattus norvegicus
280688 Bos taurus
100009113 Oryctolagus cuniculus
100135464 Cavia porcellus
397518 Sus scrofa
493973 Felis catus
374258 Gallus gallus
404015 Canis lupus familiaris
443316 Ovis aries
465887 Pan troglodytes
Selected quality suppliers for Coagulation Factor IX Proteins (F9)
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