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FOXC1 antibody (AA 375-425)

The Rabbit Polyclonal anti-FOXC1 antibody has been validated for WB, IP and IHC (fp). It is suitable to detect FOXC1 in samples from Human.
Catalog No. ABIN7453631
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$495.55
$583.00
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Quick Overview for FOXC1 antibody (AA 375-425) (ABIN7453631)

Target

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

Reactivity

  • 51
  • 41
  • 19
  • 4
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
Human

Host

  • 61
  • 2
  • 1
Rabbit

Clonality

  • 54
  • 10
Polyclonal

Conjugate

  • 30
  • 7
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 2
  • 1
  • 1
  • 1
  • 1
This FOXC1 antibody is un-conjugated

Application

  • 44
  • 22
  • 11
  • 10
  • 10
  • 6
  • 4
  • 4
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Western Blotting (WB), Immunoprecipitation (IP), Immunohistochemistry (Formalin-fixed Paraffin-embedded Sections) (IHC (fp))
  • Binding Specificity

    • 8
    • 6
    • 5
    • 3
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 375-425

    Purpose

    Rabbit anti-FOXC1 Antibody, Affinity Purified

    Purification

    Affinity Purified

    Immunogen

    between AA 375 and 425

    Isotype

    IgG
  • Application Notes

    IHC: 1:100 - 1:500. Epitope retrieval with citrate buffer pH 6.0 is recommended for FFPE tissue sections.

    IP: 2 - 10 μg/mg lysate

    WB: 1:2,000 - 1:10,000

    Restrictions

    For Research Use only
  • Concentration

    200 μg/mL

    Buffer

    Tris-buffered Saline containing 0.1 % BSA and 0.09 % Sodium Azide

    Preservative

    Sodium azide

    Precaution of Use

    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

    Storage

    4 °C

    Expiry Date

    12 months
  • Target

    FOXC1 (Forkhead Box C1 (FOXC1))

    Alternative Name

    FOXC1

    Background

    Background: Forkhead box C1 (FOXC1) belongs to the forkhead family of transcription factors which is characterized by a distinct DNA-binding forkhead domain. The specific function of FOXC1 has not yet been determined, however, the gene has been shown to play a role in the regulation of embryonic and ocular development. Mutations in the FOXC1 gene cause various glaucoma phenotypes including primary congenital glaucoma, autosomal dominant iridogoniodysgenesis anomaly, and Axenfeld-Rieger anomaly.[taken from NCBI Entrez Gene (Gene ID: 2296)].

    Gene ID

    2296

    NCBI Accession

    NP_001444

    UniProt

    Q12948

    Pathways

    Chromatin Binding, Glycosaminoglycan Metabolic Process
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