7188543

PITX2 Polyclonal Antibody, Active Motif™

Rabbit Polyclonal Antibody

Manufacturer: Fischer Scientific

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Antigen

PITX2

Applications

Western Blot

Conjugate

Unconjugated

Host Species

Rabbit

Target Species

Human

Gene Accession No.

Q99697

Gene ID (Entrez)

5308

Immunogen

This PITX2 antibody was raised against a peptide within the N-terminal region of human PITX2.

Primary or Secondary

Primary

Content And Storage

-20°C, Avoid Freeze/Thaw Cycles

Gene

PITX2

Concentration

Lot-Specific

Classification

Polyclonal

Form

Liquid

Regulatory Status

RUO

Formulation

PBS with 30% glycerol and 0.035% sodium azide; pH 7.5

Gene Alias

9430085M16Rik; all1-responsive gene 1; ALL1-responsive protein ARP1; ARP1; BOS_6374; Brx1; BRX1 homeoprotein; Brx1b; Homeobox protein PITX2; homeodomain transcription factor 2; IDG2; IGDS; IGDS2; IHG2; IRID2; Munc30; Orthodenticle-like homeobox 2; Otlx2; paired like homeodomain 2; paired-like homeodomain 1; paired-like homeodomain 2; paired-like homeodomain transcription factor 1; Paired-like homeodomain transcription factor 2; Paired-like homeodomain transcription factor Munc 30; Pituitary homeobox 2; PITX1; PITX2; Pitx-2; Pitx2c; Ptx2; RGS; RIEG; RIEG bicoid-related homeobox transcription factor; rieg bicoid-related homeobox transcription factor 1; RIEG1; rPtx2; RS; S a 1 glycoprotein; S a1glycoprotein; S alpha 1 glycoprotein; S a 1 glycoprotein; S a1glycoprotein; Solurshin

Gene Symbols

PITX2

Isotype

IgG

Purification Method

Antigen affinity chromatography

Product Type

Antibody

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Description

  • Pilx2 is a member of the RIEG/PITX homeobox family, which is in the bicoid class of homeodomain proteins
  • This protein acts as a transcription factor and regulates procollagen lysyl hydroxylase gene expression
  • It 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 protein 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.