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Chromosome 15 is one of the 23 pairs of chromosomes in humans. People normally have two copies of this chromosome. Chromosome 15 spans about 106 million base pairs (the building material of DNA) and represents between 3% and 3.5% of the total DNA in cells.
A type of blood cancer known as acute promyelocytic leukemia is caused by a rearrangement (translocation) of genetic material between chromosomes 15 and 17. This translocation, written as t(15;17), fuses part of the PML gene from chromosome 15 with part of the RARA gene from chromosome 17. This mutation is acquired during a person's lifetime and is present only in certain cells. This type of genetic change, called a somatic mutation, is not inherited.
A type of blood cancer known as acute promyelocytic leukemia is caused by a rearrangement (translocation) of genetic material between chromosomes 15 and 17. This translocation, written as t(15;17), fuses part of the PML gene from chromosome 15 with part of the RARA gene from chromosome 17. This mutation is acquired during a person's lifetime and is present only in certain cells. This type of genetic change, called a somatic mutation, is not inherited.
Organism species: Homo sapiens (Human)
| CATALOG NO. | PRODUCT NAME | APPLICATIONS | |
| Proteins | n/a | Recombinant ST20 Antisense Gene Protein 1 (ST20-AS1) | Recombinant Protein Customized Service Offer |
| Antibodies | n/a | Monoclonal Antibody to ST20 Antisense Gene Protein 1 (ST20-AS1) | Monoclonal Antibody Customized Service Offer |
| n/a | Polyclonal Antibody to ST20 Antisense Gene Protein 1 (ST20-AS1) | Polyclonal Antibody Customized Service Offer | |
| Assay Kits | n/a | CLIA Kit for ST20 Antisense Gene Protein 1 (ST20-AS1) | CLIA Kit Customized Service Offer |
| n/a | ELISA Kit for ST20 Antisense Gene Protein 1 (ST20-AS1) | ELISA Kit Customized Service Offer |
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- "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]