Phone:
+1 877 302 8632
Fax:
+1 888 205 9894 (Toll-free)
E-Mail:
orders@antibodies-online.com

Coagulation Factor IX antibody

This Rabbit Polyclonal antibody specifically detects Coagulation Factor IX in ELISA. It exhibits reactivity toward Human.
Catalog No. ABIN7670576

Quick Overview for Coagulation Factor IX antibody (ABIN7670576)

Target

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

Reactivity

  • 95
  • 35
  • 30
  • 8
  • 7
  • 1
  • 1
  • 1
Human

Host

  • 75
  • 22
  • 9
  • 8
  • 4
  • 1
  • 1
Rabbit

Clonality

  • 96
  • 23
Polyclonal

Conjugate

  • 66
  • 14
  • 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

  • 91
  • 43
  • 39
  • 23
  • 21
  • 13
  • 8
  • 8
  • 7
  • 7
  • 7
  • 5
  • 4
  • 3
  • 3
  • 2
  • 2
  • 1
  • 1
ELISA
  • Purpose

    Factor IX/PTC/F9 Polyclonal Antibody(Capture/Detector)

    Purification

    Antigen Affinity Purification

    Immunogen

    Recombinant Human Factor IX/PTC/F9 protein expressed by Mammalian

    Isotype

    IgG
  • Application Notes

    ELISA Capture 2-8 μg/mL,ELISA Detector 0.1-0.4 μg/mL

    Restrictions

    For Research Use only
  • Concentration

    1 mg/mL

    Buffer

    Sterile PBS , pH 7.4

    Preservative

    Without preservative

    Handling Advice

    Avoid freeze / thaw cycles. This preparation contains no preservatives, thus it should be handled under aseptic conditions.

    Storage

    4 °C,-20 °C

    Storage Comment

    Store at 4°C Valid for 1 month or -20°C Valid for 12 months

    Expiry Date

    12 months
  • Target

    Coagulation Factor IX (F9)

    Alternative Name

    F9

    Background

    HEMB,P19,PTC,THPH8,Christmas Factor,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.

    UniProt

    P00740
You are here:
Chat with us!