FRAS1 Related Extracellular Matrix Protein 1 (FREM1)

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QBRICK; TILRR; C9orf143; C9orf145; C9orf154

FRAS1 Related Extracellular Matrix Protein 1 (FREM1)
The mouse and human FREM1 proteins contain an N-terminal signal peptide, 12 chondroitin sulfate proteoglycan (CSPG) repeats, a calcium-binding loop similar to those of sodium-calcium exchangers , and a C-terminal C-type lectin domain. FREM1 also has sites for N- and O-glycosylation. FREM1 shares significant similarity with FRAS1, particularly through the CSPG repeats, but FREM1 lacks additional domains found in FRAS1. In situ hybridization and immunohistochemical analysis detected wide Frem1 expression during mouse embryonic development in the dermis and in a number of differentiating epidermal structures, such as mammary and meibomian glands, teeth, and hair follicles. Expression appeared in regions of epithelial-mesenchymal interaction and epidermal remodeling.

Organism species: Homo sapiens (Human)

CATALOG NO. PRODUCT NAME APPLICATIONS
Proteins n/a Recombinant FRAS1 Related Extracellular Matrix Protein 1 (FREM1) Recombinant Protein Customized Service Offer
Antibodies n/a Monoclonal Antibody to FRAS1 Related Extracellular Matrix Protein 1 (FREM1) Monoclonal Antibody Customized Service Offer
n/a Polyclonal Antibody to FRAS1 Related Extracellular Matrix Protein 1 (FREM1) Polyclonal Antibody Customized Service Offer
Assay Kits n/a CLIA Kit for FRAS1 Related Extracellular Matrix Protein 1 (FREM1) CLIA Kit Customized Service Offer
n/a ELISA Kit for FRAS1 Related Extracellular Matrix Protein 1 (FREM1) ELISA Kit Customized Service Offer

Organism species: Mus musculus (Mouse)

CATALOG NO. PRODUCT NAME APPLICATIONS
Proteins n/a Recombinant FRAS1 Related Extracellular Matrix Protein 1 (FREM1) Recombinant Protein Customized Service Offer
Antibodies n/a Monoclonal Antibody to FRAS1 Related Extracellular Matrix Protein 1 (FREM1) Monoclonal Antibody Customized Service Offer
n/a Polyclonal Antibody to FRAS1 Related Extracellular Matrix Protein 1 (FREM1) Polyclonal Antibody Customized Service Offer
Assay Kits n/a CLIA Kit for FRAS1 Related Extracellular Matrix Protein 1 (FREM1) CLIA Kit Customized Service Offer
n/a ELISA Kit for FRAS1 Related Extracellular Matrix Protein 1 (FREM1) ELISA Kit Customized Service Offer

Organism species: Rattus norvegicus (Rat)

CATALOG NO. PRODUCT NAME APPLICATIONS
Proteins n/a Recombinant FRAS1 Related Extracellular Matrix Protein 1 (FREM1) Recombinant Protein Customized Service Offer
Antibodies n/a Monoclonal Antibody to FRAS1 Related Extracellular Matrix Protein 1 (FREM1) Monoclonal Antibody Customized Service Offer
n/a Polyclonal Antibody to FRAS1 Related Extracellular Matrix Protein 1 (FREM1) Polyclonal Antibody Customized Service Offer
Assay Kits n/a CLIA Kit for FRAS1 Related Extracellular Matrix Protein 1 (FREM1) CLIA Kit Customized Service Offer
n/a ELISA Kit for FRAS1 Related Extracellular Matrix Protein 1 (FREM1) ELISA Kit Customized Service Offer
  1. "Identification of a novel cell-adhesive protein spatiotemporally expressed in the basement membrane of mouse developing hair follicle."Exp. Cell Res. 306:9-23(2005) [PubMed] [Europe PMC] [Abstract]
  2. "Complete sequencing and characterization of 21,243 full-length human cDNAs." Nat. Genet. 36:40-45(2004) [PubMed] [Europe PMC] [Abstract]
  3. "The full-ORF clone resource of the German cDNA consortium."BMC Genomics 8:399-399(2007) [PubMed] [Europe PMC] [Abstract]
  4. "DNA sequence and analysis of human chromosome 9." Nature 429:369-374(2004) [PubMed] [Europe PMC] [Abstract]
  5. "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]
  6. "FREM1 mutations cause bifid nose, renal agenesis, and anorectal malformations syndrome."Am. J. Hum. Genet. 85:414-418(2009) [PubMed] [Europe PMC] [Abstract]
  7. "Manitoba-oculo-tricho-anal (MOTA) syndrome is caused by mutations in FREM1." J. Med. Genet. 48:375-382(2011) [PubMed] [Europe PMC] [Abstract]
  8. "Heterozygous mutations of FREM1 are associated with an increased risk of isolated metopic craniosynostosis in humans and mice." PLoS Genet. 7:E1002278-E1002278(2011) [PubMed] [Europe PMC] [Abstract]