PROP Paired Like Homeobox Protein 1 (PROP1)

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Prophet Of Pit1,Paired Like Homeodomain Transcription Factor; Pituitary-specific homeodomain factor

PROP Paired Like Homeobox Protein 1 (PROP1)
PROP1 has both DNA-binding and transcriptional activation ability. Its expression leads to ontogenesis of pituitary gonadotropes, as well as somatotropes, lactotropes, and caudomedial thyrotropes. Inactivating mutations in PROP1 result in deficiencies of luteinizing hormone (LH), follicle-stimulating hormone (FSH), growth hormone (GH), prolactin (PRL), and thyroid-stimulating hormone (TSH). PROP1 mRNA is expressed in the developing pituitary gland before PIT1 mRNA expression and maximum expression are observed at e12.0. After e14.5, PROP1 mRNA expression rapidly decreases, and only trace amounts of mRNA are detectable in adult mouse pituitary.Human PROP1 transcripts were detected in normal adult pituitary by Northern blot analysis, and in all pituitary adenomas examined by RT-PCR analysis.

Organism species: Homo sapiens (Human)

CATALOG NO. PRODUCT NAME APPLICATIONS
Proteins n/a Recombinant PROP Paired Like Homeobox Protein 1 (PROP1) Recombinant Protein Customized Service Offer
Antibodies n/a Monoclonal Antibody to PROP Paired Like Homeobox Protein 1 (PROP1) Monoclonal Antibody Customized Service Offer
n/a Polyclonal Antibody to PROP Paired Like Homeobox Protein 1 (PROP1) Polyclonal Antibody Customized Service Offer
Assay Kits n/a CLIA Kit for PROP Paired Like Homeobox Protein 1 (PROP1) CLIA Kit Customized Service Offer
n/a ELISA Kit for PROP Paired Like Homeobox Protein 1 (PROP1) ELISA Kit Customized Service Offer

Organism species: Mus musculus (Mouse)

CATALOG NO. PRODUCT NAME APPLICATIONS
Proteins n/a Recombinant PROP Paired Like Homeobox Protein 1 (PROP1) Recombinant Protein Customized Service Offer
Antibodies n/a Monoclonal Antibody to PROP Paired Like Homeobox Protein 1 (PROP1) Monoclonal Antibody Customized Service Offer
n/a Polyclonal Antibody to PROP Paired Like Homeobox Protein 1 (PROP1) Polyclonal Antibody Customized Service Offer
Assay Kits n/a CLIA Kit for PROP Paired Like Homeobox Protein 1 (PROP1) CLIA Kit Customized Service Offer
n/a ELISA Kit for PROP Paired Like Homeobox Protein 1 (PROP1) ELISA Kit Customized Service Offer

Organism species: Rattus norvegicus (Rat)

CATALOG NO. PRODUCT NAME APPLICATIONS
Proteins n/a Recombinant PROP Paired Like Homeobox Protein 1 (PROP1) Recombinant Protein Customized Service Offer
Antibodies n/a Monoclonal Antibody to PROP Paired Like Homeobox Protein 1 (PROP1) Monoclonal Antibody Customized Service Offer
n/a Polyclonal Antibody to PROP Paired Like Homeobox Protein 1 (PROP1) Polyclonal Antibody Customized Service Offer
Assay Kits n/a CLIA Kit for PROP Paired Like Homeobox Protein 1 (PROP1) CLIA Kit Customized Service Offer
n/a ELISA Kit for PROP Paired Like Homeobox Protein 1 (PROP1) ELISA Kit Customized Service Offer
  1. "Human Prop-1: cloning, mapping, genomic structure. Mutations in familial combined pituitary hormone deficiency."FEBS Lett. 437:216-220(1998) [PubMed] [Europe PMC] [Abstract]
  2. "Mutations in PROP1 cause familial combined pituitary hormone deficiency."Nat. Genet. 18:147-149(1998) [PubMed] [Europe PMC] [Abstract]
  3. "The DNA sequence and comparative analysis of human chromosome 5." Nature 431:268-274(2004) [PubMed] [Europe PMC] [Abstract]
  4. "The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC)."Genome Res. 14:2121-2127(2004) [PubMed] [Europe PMC] [Abstract]
  5. "Phenotypic variability in familial combined pituitary hormone deficiency caused by a PROP1 gene mutation resulting in the substitution of Arg-->Cys at codon 120 (R120C)."J. Clin. Endocrinol. Metab. 83:3727-3734(1998) [PubMed] [Europe PMC] [Abstract]
  6. "Combined pituitary hormone deficiency caused by a novel mutation of a highly conserved residue (F88S) in the homeodomain of PROP-1."J. Clin. Endocrinol. Metab. 85:2779-2785(2000) [PubMed] [Europe PMC] [Abstract]
  7. "PROP1 gene screening in patients with multiple pituitary hormone deficiency reveals two sites of hypermutability and a high incidence of corticotroph deficiency."J. Clin. Endocrinol. Metab. 86:4529-4535(2001) [PubMed] [Europe PMC] [Abstract]
  8. "Familial combined pituitary hormone deficiency due to a novel mutation R99Q in the hot spot region of Prophet of Pit-1 presenting as constitutional growth delay."J. Clin. Endocrinol. Metab. 88:38-44(2003) [PubMed] [Europe PMC] [Abstract]
  9. "A familial form of congenital hypopituitarism due to a PROP1 mutation in a large kindred: phenotypic and in vitro functional studies."J. Clin. Endocrinol. Metab. 89:5779-5786(2004) [PubMed] [Europe PMC] [Abstract]
  10. "Molecular analysis of novel PROP1 mutations associated with combined pituitary hormone deficiency (CPHD)."Clin. Endocrinol. (Oxf.) 70:96-103(2009) [PubMed] [Europe PMC] [Abstract]