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Rabbit anti-Human F9 Polyclonal Antibody

The antibody against F9 was raised in rabbit using the Recombinant Human Coagulation factor IX protein (144-239AA) as the immunogen. This antibody exists as a non-conjugated isotype IgG, purified by protein G with a purity greater than 95%. This antibody has been validated on ELISA, IHC, IF.

ADC-14032A

The antibody against F9 was raised in rabbit using the Recombinant Human Coagulation factor IX protein (144-239AA) as the immunogen. This antibody exists as a non-conjugated isotype IgG, purified by protein G with a purity greater than 95%. This antibody has been validated on ELISA, IHC, IF.

$299.00

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Specifications


Cat.No ADC-14032A ClonalityPolyclonal
Host SpeciesRabbitTarget NameF9
FormLiquidSpecies ReactivityHuman
IsotypeIgGStorage Buffer0.01M PBS, 0.03% Proclin 300; Constituents: 50% Glycerol, PH 7.4
Purification Method>95%, Protein G purifiedConjugateNon-conjugated
ApplicationELISA, IF, IHCStorageUpon receipt

Immunogen Information


Immunogen DescriptionRecombinant Human Coagulation factor IX protein (144-239AA)Target SpeciesHuman
Immunogen SequenceComplete sequences for the immunogen, target protein, and peptides are available upon request.Uniprot IDP00740
Background Information
  • Uniprot Id

    P00740

  • Target Species

    Human

  • Target Name

    F9

  • Target Full Name

    Coagulation factor IX

  • Target Function

    Factor IX is a vitamin K-dependent plasma protein that participates in the intrinsic pathway of blood coagulation by converting factor X to its active form in the presence of Ca(2+) ions, phospholipids, and factor VIIIa.

  • Target Involvement

    Hemophilia B (HEMB); Thrombophilia, X-linked, due to factor IX defect (THPH8)

  • Target Subcellular Location

    Secreted.

  • Target Protein Families

    Peptidase S1 family

  • Target Tissue Specificity

    Detected in blood plasma (at protein level). Synthesized primarily in the liver and secreted in plasma.

  • Target Research Area

    Cardiovascular

  • Target Synonyms

    Christmas Disease; Christmas factor; Coagulant factor IX; Coagulation factor 9; Coagulation factor IX; Coagulation factor IXa heavy chain; F9; FA9_HUMAN; Factor 9; Factor IX Deficiency; FactorIX; FIX; Haemophilia B; HEMB; MGC129641; MGC129642; P19; Plasma Thromboplastic Component; Plasma thromboplastin component; PTC

  • Target Background

    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. Alternative splicing results in multiple transcript variants encoding different isoforms that may undergo similar proteolytic processing.

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