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MEOX2 antibody (AA 164-192)

This Rabbit Polyclonal antibody specifically detects MEOX2 in WB, IF and IHC (p). It exhibits reactivity toward Human.
Catalog No. ABIN1537918

Quick Overview for MEOX2 antibody (AA 164-192) (ABIN1537918)

Target

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

Reactivity

  • 55
  • 23
  • 21
  • 6
  • 5
  • 5
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  • 4
  • 3
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  • 2
  • 2
  • 1
Human

Host

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Rabbit

Clonality

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Polyclonal

Conjugate

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  • 4
  • 4
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  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
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This MEOX2 antibody is un-conjugated

Application

  • 43
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  • 13
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  • 3
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  • 1
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Western Blotting (WB), Immunofluorescence (IF), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))

Clone

RB38441
  • Binding Specificity

    • 15
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    AA 164-192

    Predicted Reactivity

    M, Rat

    Purification

    This antibody is purified through a protein A column, followed by peptide affinity purification.

    Immunogen

    This MEOX2 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 164-192 amino acids from the Central region of human MEOX2.

    Isotype

    Ig Fraction
  • Application Notes

    IF: 1:10~50. WB: 1:2000. IHC-P-Leica: 1:500. IHC-P-Leica: 1:500

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    Purified polyclonal antibody supplied in PBS with 0.09 % (W/V) 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

    4 °C,-20 °C

    Storage Comment

    MEOX2 Antibody (Center) can be refrigerated at 2-8 °C for up to 6 months. For long term storage, keep at -20 °C.

    Expiry Date

    6 months
  • Target

    MEOX2 (Mesenchyme Homeobox 2 (MEOX2))

    Alternative Name

    MEOX2

    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.

    Molecular Weight

    33594

    Gene ID

    4223

    NCBI Accession

    NP_005915

    UniProt

    P50222
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