Cancer Associated Nucleoprotein (CANP)

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FAM111B; Family With Sequence Similarity 111 Member B

Cancer Associated Nucleoprotein (CANP)
CANP mRNA was expressed fetal liver and in various adult and fetal tissues, but the mRNA levels were very low in adult livers. CANP is developmentally regulated during liver development and downregulated during the liver development and maturation, as well as during the differentiation of HepG2 cells. Southern blot analysis did not show amplificatin of CANP gene at 11q12. CANP mRNA was overexpressed in 160 (74%) of 216 unifocal primary HCCs. CANP overexpression did not correlate with tumor grade, tumor stage and early tumor recurrence of HCC after hepatecomy. CANP mRNA overexpression is an early event during the growth of HCC. The 293T CANP stable cell showed more rapid cell growth than the controls and exhibited more colonies on 0.35% soft agar. 293T CANP stable transfectants developed tumor in NOD/SCID mice.

Organism species: Homo sapiens (Human)

CATALOG NO. PRODUCT NAME APPLICATIONS
Proteins n/a Recombinant Cancer Associated Nucleoprotein (CANP) Recombinant Protein Customized Service Offer
Antibodies n/a Monoclonal Antibody to Cancer Associated Nucleoprotein (CANP) Monoclonal Antibody Customized Service Offer
n/a Polyclonal Antibody to Cancer Associated Nucleoprotein (CANP) Polyclonal Antibody Customized Service Offer
Assay Kits n/a CLIA Kit for Cancer Associated Nucleoprotein (CANP) CLIA Kit Customized Service Offer
n/a ELISA Kit for Cancer Associated Nucleoprotein (CANP) ELISA Kit Customized Service Offer
  1. "Complete sequencing and characterization of 21,243 full-length human cDNAs." Nat. Genet. 36:40-45(2004) [PubMed] [Europe PMC] [Abstract]
  2. "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]
  3. "N-terminal acetylome analyses and functional insights of the N-terminal acetyltransferase NatB."Proc. Natl. Acad. Sci. U.S.A. 109:12449-12454(2012) [PubMed] [Europe PMC] [Abstract]
  4. "Mutations in FAM111B cause hereditary fibrosing poikiloderma with tendon contracture, myopathy, and pulmonary fibrosis." Am. J. Hum. Genet. 93:1100-1107(2013) [PubMed] [Europe PMC] [Abstract]