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IRF6 antibody

This Rabbit Monoclonal antibody specifically detects IRF6 in WB. It exhibits reactivity toward Human.
Catalog No. ABIN7881248
$625.62
Plus shipping costs $50.00
100 μL
Shipping to: United States
Delivery in 2 to 4 Business Days

Quick Overview for IRF6 antibody (ABIN7881248)

Target

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

Reactivity

  • 82
  • 61
  • 49
  • 13
  • 8
  • 8
  • 8
  • 6
  • 6
  • 6
  • 6
  • 6
  • 4
  • 4
  • 2
  • 1
Human

Host

  • 75
  • 8
  • 1
Rabbit

Clonality

  • 58
  • 26
Monoclonal

Conjugate

  • 37
  • 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

  • 58
  • 23
  • 18
  • 15
  • 13
  • 6
  • 5
  • 5
  • 1
  • 1
Western Blotting (WB)

Clone

GHD-9
  • Purpose

    IRF6 Antibody / Interferon Regulatory Factor 6

    Purification

    Affinity purified

    Immunogen

    A synthetic peptide specific to human IRF6 was used as the immunogen for the IRF6 antibody.

    Isotype

    IgG
  • Application Notes

    Optimal dilution of the IRF6 antibody should be determined by the researcher.

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    Antibody in PBS with 0.02 % sodium azide, 50 % glycerol and 0.4-0.5 mg/mL BSA

    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

    Storage Comment

    Store the IRF6 antibody at -20oC.
  • Target

    IRF6 (Interferon Regulatory Factor 6 (IRF6))

    Alternative Name

    IRF6

    Background

    The IRF6 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. [RefSeq]

    UniProt

    O14896
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