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IRF6 antibody

This anti-IRF6 antibody is a Rabbit Monoclonal antibody detecting IRF6 in WB, IF and IP. Suitable for Human.
Catalog No. ABIN3017589
-15% Promotion 2026
$1,143.25
$1,345.00
save $201.75 (-15 %)
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Quick Overview for IRF6 antibody (ABIN3017589)

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

Host

  • 74
  • 8
  • 1
Rabbit

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), Immunofluorescence (IF), Immunoprecipitation (IP)
  • Cross-Reactivity

    Human, Mouse, Rat

    Characteristics

    Monoclonal Antibodies

    Purification

    Affinity purification

    Immunogen

    A synthesized peptide derived from human IRF6

    Isotype

    IgG
  • Application Notes

    WB,1:500 - 1:2000,IF,1:50 - 1:200,IP,1:50 - 1:200

    Restrictions

    For Research Use only
  • Buffer

    PBS with 0.02 % sodium azide,0.05 % BSA,50 % glycerol, pH 7.3.

    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 at -20°C. Avoid freeze / thaw cycles.
  • 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.[provided by RefSeq, May 2011],LPS, OFC6, PIT, PPS, PPS1, VWS, VWS1,Cell Intrinsic Innate Immunity Signaling Pathway,Cytokines,Cytokines_Interferons,Embryonic Stem Cells,Epigenetics & Nuclear Signaling,Immunology & Inflammation,Stem Cells,Transcription Factors,IRF6

    Molecular Weight

    53 kDa

    Gene ID

    3664

    UniProt

    O14896
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