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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
$608.40
Plus shipping costs $50.00
0.1 mL
Shipping to: United States
Delivery in 6 to 8 Business Days

Quick Overview for IRF6 antibody (ABIN2723803)

Target

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

Reactivity

  • 81
  • 61
  • 49
  • 13
  • 8
  • 8
  • 8
  • 6
  • 6
  • 6
  • 6
  • 6
  • 4
  • 4
  • 2
  • 1
Human, Rat, Dog

Host

  • 74
  • 8
  • 1
Mouse

Clonality

  • 58
  • 25
Monoclonal

Conjugate

  • 36
  • 5
  • 4
  • 4
  • 4
  • 4
  • 4
  • 4
  • 3
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This IRF6 antibody is un-conjugated

Application

  • 57
  • 23
  • 17
  • 15
  • 13
  • 6
  • 5
  • 5
  • 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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