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Coagulation Factor IX antibody

This anti-Coagulation Factor IX antibody is a Mouse Monoclonal antibody detecting Coagulation Factor IX in WB, IHC (p) and EIA. Suitable for Human.
Catalog No. ABIN951594

Quick Overview for Coagulation Factor IX antibody (ABIN951594)

Target

See all Coagulation Factor IX (F9) Antibodies
Coagulation Factor IX (F9)

Reactivity

  • 100
  • 37
  • 31
  • 9
  • 8
  • 2
  • 1
  • 1
Human

Host

  • 83
  • 25
  • 9
  • 8
  • 4
  • 1
  • 1
Mouse

Clonality

  • 103
  • 27
Monoclonal

Conjugate

  • 76
  • 15
  • 9
  • 7
  • 4
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This Coagulation Factor IX antibody is un-conjugated

Application

  • 100
  • 48
  • 45
  • 31
  • 28
  • 13
  • 8
  • 8
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  • 7
  • 6
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  • 4
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  • 3
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  • 2
  • 1
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Western Blotting (WB), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Enzyme Immunoassay (EIA)

Clone

13F42-F6
  • Specificity

    Recognises Factor IX

    Purification

    Protein G Chromatography

    Immunogen

    Full length native protein (purified) (Human).

    Isotype

    IgG1
  • Application Notes

    Optimal working dilution should be determined by the investigator.

    Restrictions

    For Research Use only
  • Concentration

    3.5 mg/mL

    Buffer

    0.05 M Sodium Phosphate, 0.5 M NaCl, 1 mM EDTA, pH 6.6

    Handling Advice

    Avoid repeated freezing and thawing.

    Storage

    -80 °C

    Storage Comment

    Store at -70 °C.
  • Target

    Coagulation Factor IX (F9)

    Background

    Coagulation Factor IX (F9) 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.Synonyms: Christmas factor, PTC, Plasma thromboplastin component

    Gene ID

    2158

    NCBI Accession

    NP_000124

    UniProt

    P00740
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