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FOXC1 antibody (AA 392-554)

This Rabbit Polyclonal antibody specifically detects FOXC1 in WB, ELISA and IF. It exhibits reactivity toward Human.
Catalog No. ABIN7874618
$625.62
Plus shipping costs $50.00
100 μg
Shipping to: United States
Delivery in 2 to 4 Business Days

Quick Overview for FOXC1 antibody (AA 392-554) (ABIN7874618)

Target

See all FOXC1 Antibodies
FOXC1 (Forkhead Box C1 (FOXC1))

Reactivity

  • 53
  • 41
  • 19
  • 4
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
Human

Host

  • 63
  • 2
  • 1
Rabbit

Clonality

  • 55
  • 11
Polyclonal

Conjugate

  • 32
  • 7
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 2
  • 1
  • 1
  • 1
  • 1
This FOXC1 antibody is un-conjugated

Application

  • 46
  • 22
  • 12
  • 10
  • 9
  • 6
  • 4
  • 3
  • 2
  • 1
  • 1
  • 1
  • 1
Western Blotting (WB), ELISA, Immunofluorescence (IF)
  • Binding Specificity

    • 8
    • 6
    • 5
    • 3
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 392-554

    Purpose

    FOXC1 Antibody

    Purification

    Affinity purified

    Immunogen

    A human recombinant protein (amino acids T392-F554) was used as the immunogen for the FOXC1 antibody.

    Isotype

    IgG
  • Application Notes

    Optimal dilution of the FOXC1 antibody should be determined by the researcher.

    Restrictions

    For Research Use only
  • Format

    Lyophilized

    Buffer

    0.5 mg/mL if reconstituted with 0.2 mL sterile DI water

    Storage

    4 °C,-20 °C

    Storage Comment

    After reconstitution, the FOXC1 antibody can be stored for up to one month at 4oC. For long-term, aliquot and store at -20oC. Avoid repeated freezing and thawing.
  • Target

    FOXC1 (Forkhead Box C1 (FOXC1))

    Alternative Name

    FOXC1

    Background

    Forkhead box C1, also known as FOXC1, is a protein which in humans is encoded by the FOXC1 gene. It is mapped to 6p25.3. This gene belongs to the forkhead family of transcription factors which is characterized by a distinct DNA-binding forkhead domain. The specific function of this gene has not yet been determined, however, it has been shown to play a role in the regulation of embryonic and ocular development. Mutations in this gene cause various glaucoma phenotypes including primary congenital glaucoma, autosomal dominant iridogoniodysgenesis anomaly, and Axenfeld-Rieger anomaly.

    UniProt

    Q12948

    Pathways

    Chromatin Binding, Glycosaminoglycan Metabolic Process
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