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PITX2 antibody (AA 1-100)

The Rabbit Polyclonal anti-PITX2 antibody has been validated for WB. It is suitable to detect PITX2 in samples from Human.
Catalog No. ABIN3015652

Quick Overview for PITX2 antibody (AA 1-100) (ABIN3015652)

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
  • 28
  • 9
  • 5
  • 4
  • 1
  • 1
  • 1
Western Blotting (WB)
  • Binding Specificity

    • 9
    • 8
    • 7
    • 6
    • 5
    • 3
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 1-100

    Sequence

    MNCMKGPLHL EHRAAGTKLS AVSSSSCHHP QPLAMASVLA PGQPRSLDSS KHRLEVHTIS DTSSPEAAEK DKSQQGKNED VGAEDPSKKK RQRRQRTHFT

    Cross-Reactivity

    Human, Mouse, Rat

    Characteristics

    Polyclonal Antibodies

    Immunogen

    A synthetic peptide corresponding to a sequence within amino acids 1-100 of human PITX2 (NP_000316.2).

    Isotype

    IgG
  • Application Notes

    WB,1:500 - 1:2000

    Restrictions

    For Research Use only
  • Buffer

    PBS with 0.02 % sodium azide,50 % glycerol, pH 7.3.

    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.,PITX2,ARP1,ASGD4,Brx1,IDG2,IGDS,IGDS2,IHG2,IRID2,Otlx2,PTX2,RGS,RIEG,RIEG1,RS,Epigenetics & Nuclear Signaling,Transcription Factors,Cell Biology & Developmental Biology,Cardiovascular,Heart,Cardiogenesis,PITX2

    Molecular Weight

    30 kDa/35 kDa

    Gene ID

    5308

    UniProt

    Q99697

    Pathways

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