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MEOX2 antibody (AA 201-304) (AbBy Fluor® 750)

The Rabbit Polyclonal anti-MEOX2 antibody has been validated for WB, IF (cc) and IF (p). It is suitable to detect MEOX2 in samples from Human.
Catalog No. ABIN5003248

Quick Overview for MEOX2 antibody (AA 201-304) (AbBy Fluor® 750) (ABIN5003248)

Target

See all MEOX2 Antibodies
MEOX2 (Mesenchyme Homeobox 2 (MEOX2))

Reactivity

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Human

Host

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Rabbit

Clonality

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Polyclonal

Conjugate

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This MEOX2 antibody is conjugated to AbBy Fluor® 750

Application

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Western Blotting (WB), Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p))
  • Binding Specificity

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    AA 201-304

    Predicted Reactivity

    Human,Mouse,Rat,Dog,Cow,Pig,Horse,Chicken,Rabbit

    Purification

    Purified by Protein A.

    Immunogen

    KLH conjugated synthetic peptide derived from human Gax

    Isotype

    IgG
  • Application Notes

    IF(IHC-P) 1:50-200
    IF(IHC-F) 1:50-200
    IF(ICC) 1:50-200

    Restrictions

    For Research Use only
  • Format

    Liquid

    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.

    Expiry Date

    12 months
  • Target

    MEOX2 (Mesenchyme Homeobox 2 (MEOX2))

    Alternative Name

    Gax

    Background

    Synonyms: growth arrest-specic homeobox; Homeobox protein MOX-2; Mesenchyme homeobox 2; mesenchyme homeobox 2-like; Growth arrest-specic homeobox; GAX; growth arrest homeobox transcription factor GAX; mesenchyme homeobox 2; MEOX2_HUMAN.

    Background: This gene encodes a member of a subfamily of non-clustered, diverged, antennapedia-like homeobox-containing genes. The encoded protein may play a role in the regulation of vertebrate limb myogenesis. Mutations in the related mouse protein may be associated with craniofacial and/or skeletal abnormalities, in addition to neurovascular dysfunction observed in Alzheimer's disease.

    Gene ID

    4223
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