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PITX2 antibody

This anti-PITX2 antibody is a Rabbit Polyclonal antibody detecting PITX2 in WB and ELISA. Suitable for Human and Rat.
Catalog No. ABIN7000423

Quick Overview for PITX2 antibody (ABIN7000423)

Target

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

Reactivity

  • 50
  • 6
  • 4
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
Human, Rat

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
  • Characteristics

    Polyclonal Antibody

    Purification

    Affinity purification

    Immunogen

    Recombinant protein of human PITX2

    Isotype

    IgG
  • Application Notes

    WB 1:500-1:2000

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    0.4 mg/mL

    Buffer

    PBS with 0.05 % sodium azide and 50 % glycerol, PH7.4

    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

    -20 °C

    Storage Comment

    Store at -20°C. Avoid 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.

    Molecular Weight

    35 kDa

    UniProt

    Q99697

    Pathways

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