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Receptor Transporter Protein 5 (RTP5)

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C2orf85; CXXC11; Z3CXXC5; Chromosome 2 Open Reading Frame 85; CXXC-type zinc finger protein 11; 3CxxC-type zinc finger protein 5

Receptor Transporter Protein 5 (RTP5)
CCC W299
HGNC 26585
UniProt Q14D33
Chromosome 2 is one of the 23 pairs of chromosomes in humans. People normally have two copies of this chromosome. Chromosome 2 is the second largest human chromosome, spanning more than 237 million base pairs (the building material of DNA) and representing almost 8% of the total DNA in cells.
Identifying genes on each chromosome is an active area of genetic research. Because researchers use different approaches to predict the number of genes on each chromosome, the estimated number of genes varies. Chromosome 2 likely contains 1,491 genes, including those of the HOXD homeobox gene cluster.Human chromosome 2 is widely accepted to be a result of an end-to-end fusion of two ancestral chromosomes.

Organism species: Homo sapiens (Human)

CATALOG NO. PRODUCT NAME APPLICATIONS
Proteins n/a Recombinant Receptor Transporter Protein 5 (RTP5) Recombinant Protein Customized Service Offer
Antibodies n/a Monoclonal Antibody to Receptor Transporter Protein 5 (RTP5) Monoclonal Antibody Customized Service Offer
n/a Polyclonal Antibody to Receptor Transporter Protein 5 (RTP5) Polyclonal Antibody Customized Service Offer
Assay Kits n/a CLIA Kit for Receptor Transporter Protein 5 (RTP5) CLIA Kit Customized Service Offer
n/a ELISA Kit for Receptor Transporter Protein 5 (RTP5) 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. "Generation and annotation of the DNA sequences of human chromosomes 2 and 4." Nature 434:724-731(2005) [PubMed] [Europe PMC] [Abstract]
  3. "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]
  4. "Diagnostic exome sequencing in persons with severe intellectual disability."N. Engl. J. Med. 367:1921-1929(2012) [PubMed] [Europe PMC] [Abstract]