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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

Quick Overview for FOXC1 antibody (AA 375-425) (ABIN7453631)

Target

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

Reactivity

  • 51
  • 34
  • 19
  • 4
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
Human

Host

  • 54
  • 2
  • 1
Rabbit

Clonality

  • 56
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Polyclonal

Conjugate

  • 31
  • 7
  • 3
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
This FOXC1 antibody is un-conjugated

Application

  • 38
  • 22
  • 12
  • 10
  • 8
  • 4
  • 4
  • 3
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Western Blotting (WB), Immunoprecipitation (IP), Immunohistochemistry (Formalin-fixed Paraffin-embedded Sections) (IHC (fp))
  • Binding Specificity

    • 8
    • 6
    • 6
    • 3
    • 3
    • 3
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
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    • 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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