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FOXD4L1 antibody (N-Term)

This anti-FOXD4L1 antibody is a Rabbit Polyclonal antibody detecting FOXD4L1 in WB and FACS. Suitable for Human.
Catalog No. ABIN655284

Quick Overview for FOXD4L1 antibody (N-Term) (ABIN655284)

Target

See all FOXD4L1 Antibodies
FOXD4L1 (Forkhead Box D4-Like 1 (FOXD4L1))

Reactivity

  • 15
  • 3
  • 1
  • 1
  • 1
Human

Host

  • 14
  • 2
Rabbit

Clonality

  • 15
  • 1
Polyclonal

Conjugate

  • 11
  • 1
  • 1
  • 1
  • 1
  • 1
This FOXD4L1 antibody is un-conjugated

Application

  • 16
  • 10
  • 8
  • 2
  • 2
  • 1
Western Blotting (WB), Flow Cytometry (FACS)

Clone

RB28484
  • Binding Specificity

    • 8
    • 4
    • 2
    • 1
    • 1
    • 1
    AA 1-30, N-Term

    Purification

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

    Immunogen

    This FX4L1 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 1-30 amino acids from the N-terminal region of human FX4L1.

    Isotype

    Ig Fraction
  • Application Notes

    WB: 1:1000. FC: 1:10~50

    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

    FOXD4L1 (Forkhead Box D4-Like 1 (FOXD4L1))

    Alternative Name

    FX4L1

    Background

    This gene is a member of the forkhead/winged-helix (FOX) family of transcription factors with highly conserved FOX DNA-binding domains. Members of the FOX family of transcription factors are regulators of embryogenesis and may play a role in human cancer. This gene lies in a region of chromosome 2 that surrounds the site where two ancestral chromosomes fused to form human chromosome 2. This region is duplicated elsewhere in the human genome, primarily in subtelomeric and pericentromeric locations, thus mutiple copies of this gene have been found.

    Gene ID

    200350

    NCBI Accession

    NP_036316

    UniProt

    Q9NU39
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