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PITX2 antibody (AA 42-71)

This Rabbit Polyclonal antibody specifically detects PITX2 in WB and ELISA. It exhibits reactivity toward Human.
Catalog No. ABIN3032140

Quick Overview for PITX2 antibody (AA 42-71) (ABIN3032140)

Target

See all PITX2 Antibodies
PITX2 (Paired-Like Homeodomain 2 (PITX2))

Reactivity

  • 50
  • 6
  • 5
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
Human

Host

  • 42
  • 8
  • 1
Rabbit

Clonality

  • 45
  • 6
Polyclonal

Conjugate

  • 28
  • 5
  • 3
  • 3
  • 3
  • 3
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This PITX2 antibody is un-conjugated

Application

  • 39
  • 27
  • 9
  • 5
  • 4
  • 1
  • 1
  • 1
Western Blotting (WB), ELISA
  • Binding Specificity

    • 9
    • 7
    • 7
    • 6
    • 5
    • 3
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 42-71

    Purification

    Antigen affinity purified

    Immunogen

    A portion of amino acids 42-71 from the human protein was used as the immunogen for this PITX2 antibody.

    Isotype

    Ig Fraction
  • Application Notes

    Titration of the PITX2 antibody may be required due to differences in protocols and secondary/substrate sensitivity.\. Western blot: 1:1000

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    In 1X PBS, pH 7.4, with 0.09 % 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

    -20 °C

    Storage Comment

    Aliquot the PITX2 antibody and store frozen at -20°C or colder. Avoid repeated freeze-thaw cycles.
  • Target

    PITX2 (Paired-Like Homeodomain 2 (PITX2))

    Alternative Name

    PITX2

    Background

    This gene encodes a member of the RIEG/PITX homeobox family, which is in the bicoid class of homeodomain proteins. The encoded protein acts as a transcription factor and regulates procollagen lysyl hydroxylase gene expression. This protein plays a role in the terminal differentiation of somatotroph and lactotroph cell phenotypes, is involved in the development of the eye, tooth and abdominal organs, and acts as a transcriptional regulator involved in basal and hormone-regulated activity of prolactin. Mutations in this gene are associated with Axenfeld-Rieger syndrome, iridogoniodysgenesis syndrome, and sporadic cases of Peters anomaly. A similar protein in other vertebrates is involved in the determination of left-right asymmetry during development. Alternatively spliced transcript variants encoding distinct isoforms have been described.

    UniProt

    Q99697

    Pathways

    Retinoic Acid Receptor Signaling Pathway, Regulation of Muscle Cell Differentiation, Skeletal Muscle Fiber Development
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