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T-Box 22 antibody (AA 21-120) (HRP)

This Rabbit Polyclonal antibody specifically detects T-Box 22 in WB, ELISA, IHC (p) and IHC (fro). It exhibits reactivity toward Mouse.
Catalog No. ABIN7092378

Quick Overview for T-Box 22 antibody (AA 21-120) (HRP) (ABIN7092378)

Target

See all T-Box 22 (TBX22) Antibodies
T-Box 22 (TBX22)

Reactivity

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  • 18
  • 4
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  • 2
  • 2
  • 2
  • 1
Mouse

Host

  • 37
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Rabbit

Clonality

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Polyclonal

Conjugate

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  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
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  • 1
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This T-Box 22 antibody is conjugated to HRP

Application

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Western Blotting (WB), ELISA, Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Immunohistochemistry (Frozen Sections) (IHC (fro))
  • Binding Specificity

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    • 1
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    AA 21-120

    Cross-Reactivity

    Mouse

    Purification

    Purified by Protein A.

    Immunogen

    KLH conjugated synthetic peptide derived from mouse TBX22

    Isotype

    IgG
  • Application Notes

    WB 1:300-5000
    IHC-P 1:200-400
    IHC-F 1:100-500

    Restrictions

    For Research Use only
  • Concentration

    1 μg/μL

    Buffer

    Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.

    Preservative

    ProClin

    Precaution of Use

    This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

    Storage

    -20 °C

    Storage Comment

    Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.
  • Target

    T-Box 22 (TBX22)

    Alternative Name

    TBX22

    Background

    Synonyms: ABERS, CLPA, CPX, D230020M15Rik, dJ795G23.1, T box 22, T box protein 22, T box transcription factor TBX22, T-box protein 22, T-box transcription factor TBX22, Tbx22, TBX22_MOUSE, TBXX.

    Background: This gene is a member of a phylogenetically conserved family of genes that share a common DNA-binding domain, the T-box. T-box genes encode transcription factors involved in the regulation of developmental processes. Mutations in this gene have been associated with the inherited X-linked disorder, Cleft palate with ankyloglossia, and it is believed to play a major role in human palatogenesis. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]

    Gene ID

    245572

    UniProt

    Q8K402
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