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IRF6 antibody

This Mouse Monoclonal antibody specifically detects IRF6 in WB, IHC, IF and FACS. It exhibits reactivity toward Human, Rat and Dog.
Catalog No. ABIN2723803

Quick Overview for IRF6 antibody (ABIN2723803)

Target

See all IRF6 Antibodies
IRF6 (Interferon Regulatory Factor 6 (IRF6))

Reactivity

  • 74
  • 53
  • 39
  • 13
  • 9
  • 8
  • 8
  • 6
  • 6
  • 6
  • 6
  • 6
  • 4
  • 4
  • 2
  • 1
Human, Rat, Dog

Host

  • 68
  • 8
  • 1
Mouse

Clonality

  • 62
  • 15
Monoclonal

Conjugate

  • 39
  • 4
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This IRF6 antibody is un-conjugated

Application

  • 52
  • 16
  • 14
  • 9
  • 8
  • 8
  • 5
  • 4
  • 1
  • 1
Western Blotting (WB), Immunohistochemistry (IHC), Immunofluorescence (IF), Flow Cytometry (FACS)

Clone

2C10
  • Characteristics

    Homo sapiens interferon regulatory factor 6 (IRF6), transcript variant 1

    Purification

    Purified from mouse ascites fluids by affinity chromatography

    Immunogen

    Full length human recombinant protein of human IRF6(NP_006138) produced in HEK293T cell.

    Isotype

    IgG1
  • Application Notes

    WB 1:500~2000, IHC 1:150, IF 1:100, FLOW 1:100,

    Comment

    The concentration of the product may vary between diferrent lots.

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    0.5-1.0 mg/mL

    Buffer

    PBS (PH 7.3) containing 1 % BSA, 50 % glycerol and 0.02 % 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

    -20 °C
  • Target

    IRF6 (Interferon Regulatory Factor 6 (IRF6))

    Alternative Name

    IRF6

    Background

    This gene encodes a member of the interferon regulatory transcription factor (IRF) family. Family members share a highly-conserved N-terminal helix-turn-helix DNA-binding domain and a less conserved C-terminal protein-binding domain. The encoded protein may be a transcriptional activator. Mutations in this gene can cause van der Woude syndrome and popliteal pterygium syndrome. Mutations in this gene are also associated with non-syndromic orofacial cleft type 6. Alternate splicing results in multiple transcript variants.

    Molecular Weight

    52.9 kDa

    Gene ID

    3664

    NCBI Accession

    NM_006147

    HGNC

    3664
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