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FOXE3 antibody (AA 87-114)

This Rabbit Polyclonal antibody specifically detects FOXE3 in WB. It exhibits reactivity toward Human.
Catalog No. ABIN656110

Quick Overview for FOXE3 antibody (AA 87-114) (ABIN656110)

Target

See all FOXE3 Antibodies
FOXE3 (Forkhead Box E3 (FOXE3))

Reactivity

  • 29
  • 13
  • 13
  • 1
Human

Host

  • 29
Rabbit

Clonality

  • 29
Polyclonal

Conjugate

  • 13
  • 3
  • 3
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This FOXE3 antibody is un-conjugated

Application

  • 18
  • 17
  • 4
  • 2
  • 2
  • 1
  • 1
  • 1
Western Blotting (WB)

Clone

RB32214
  • Binding Specificity

    • 6
    • 6
    • 5
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 87-114

    Predicted Reactivity

    M

    Purification

    This antibody is purified through a protein A column, followed by peptide affinity purification.

    Immunogen

    This FOXE3 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 87-114 amino acids from the Central region of human FOXE3.

    Isotype

    Ig Fraction
  • Application Notes

    WB: 1:1000

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    Purified polyclonal antibody supplied in PBS with 0.09 % (W/V) 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,-20 °C

    Storage Comment

    Maintain refrigerated at 2-8 °C for up to 6 months. For long term storage store at -20 °C in small aliquots to prevent freeze-thaw cycles.

    Expiry Date

    6 months
  • Target

    FOXE3 (Forkhead Box E3 (FOXE3))

    Alternative Name

    FOXE3

    Background

    This intronless gene belongs to the forkhead family of transcription factors, which is characterized by a distinct forkhead domain. The protein encoded functions as a lens-specific transcription factor and plays an important role in vertebrate lens formation. Mutations in this gene are associated with anterior segment mesenchymal dysgenesis and congenital primary aphakia.

    Molecular Weight

    33234

    Gene ID

    2301

    NCBI Accession

    NP_036318

    UniProt

    Q13461
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