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PITX2 anticorps

Cet anticorps anti-PITX2 est un anticorps Lapin Polyclonal détectant PITX2 dans WB et ELISA. Adapté pour Humain et Rat.
N° du produit ABIN7000423

Aperçu rapide pour PITX2 anticorps (ABIN7000423)

Antigène

Voir toutes PITX2 Anticorps
PITX2 (Paired-Like Homeodomain 2 (PITX2))

Reactivité

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

Hôte

  • 42
  • 8
  • 1
Lapin

Clonalité

  • 45
  • 6
Polyclonal

Conjugué

  • 28
  • 5
  • 3
  • 3
  • 3
  • 3
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Cet anticorp PITX2 est non-conjugé

Application

  • 39
  • 27
  • 9
  • 5
  • 4
  • 1
  • 1
  • 1
Western Blotting (WB), ELISA
  • Attributs du produit

    Polyclonal Antibody

    Purification

    Affinity purification

    Immunogène

    Recombinant protein of human PITX2

    Isotype

    IgG
  • Indications d'application

    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

    Agent conservateur

    Sodium azide

    Précaution d'utilisation

    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

    Stock

    -20 °C

    Stockage commentaire

    Store at -20°C. Avoid freeze / thaw cycles.
  • Antigène

    PITX2 (Paired-Like Homeodomain 2 (PITX2))

    Autre désignation

    PITX2

    Sujet

    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.

    Poids moléculaire

    35 kDa

    UniProt

    Q99697

    Pathways

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