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OTX2 antibody (AA 1-204)

This Rabbit Polyclonal antibody specifically detects OTX2 in WB. It exhibits reactivity toward Human.
Catalog No. ABIN5027412

Quick Overview for OTX2 antibody (AA 1-204) (ABIN5027412)

Target

See all OTX2 Antibodies
OTX2 (Orthodenticle Homeobox 2 (OTX2))

Reactivity

  • 41
  • 29
  • 15
  • 5
  • 5
  • 5
  • 5
  • 5
  • 4
  • 4
  • 4
  • 4
  • 4
  • 3
  • 2
  • 1
  • 1
  • 1
  • 1
Human

Host

  • 53
  • 4
Rabbit

Clonality

  • 51
  • 6
Polyclonal

Conjugate

  • 30
  • 4
  • 3
  • 3
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This OTX2 antibody is un-conjugated

Application

  • 41
  • 21
  • 14
  • 13
  • 13
  • 5
  • 5
  • 5
  • 3
  • 3
  • 2
  • 1
  • 1
Western Blotting (WB)
  • Binding Specificity

    • 15
    • 7
    • 4
    • 3
    • 3
    • 3
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 1-204

    Purification

    Protein A Chromatography

    Immunogen

    A partial length recombinant Otx2 protein (amino acids 1-204) was used as the immunogen for this antibody.

    Isotype

    IgG
  • Application Notes

    WB: 2-4 μg/mL

    Restrictions

    For Research Use only
  • Concentration

    0.5 mg/mL

    Buffer

    PBS containing 0.05 % BSA, PH 7.4

    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

    Store the antibody at 4°C, stable for 6 months. For long-term storage, store at -20°C. Avoid repeated freeze and thaw cycles.
  • Target

    OTX2 (Orthodenticle Homeobox 2 (OTX2))

    Alternative Name

    Otx2

    Background

    Otx2 encodes a transcription factor that plays a critical role in craniofacial development and anterior brain morphogenesis. Otx2 homologs in model organisms are expressed in a complex spatial, temporal, and gradient-specific manner that is required for correct antero-posterior patterning and craniofacial development. Otx2 mutations are associated with severe ocular phenotypes and central nervous system abnormalities such as seizures, short stature and developmental delay, CPHD (Combined Pituitary Hormone Deficiency), structural abnormalities of the pituitary gland and early onset retinal dystrophy.

    Molecular Weight

    32 kDa

    Gene ID

    5015

    UniProt

    P32243

    Pathways

    Dopaminergic Neurogenesis
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