C21orf25 Polyclonal Antibody, Biotin Conjugated

The smallest of the human chromosomes, 21 makes up about 1.5% of the human genome. Chromosome 21 contains nearly 300 genes and 47 million base pairs. Down syndrome, also known as trisomy 21, is the disease most commonly associated with chromosome 21. Alzheimer's disease, Jervell and Lange-Nielsen syndrome and amyotrophic lateral sclerosis are also associated with chromosome 21. Translocations are found to occur between chromosome 21 and 8, and chromosome 21 and 12, in certain leukemias. C2CD2 is an 696 amino acid protien that is secreted. The C2CD2 gene product has been provisionally designated C2CD2 pending further characterization.

C2 calcium-dependent domain containing 2; C2 domain containing protein 2; C21orf25; C21orf258; C2CD2; Chromosome 21 open reading frame 25; MGC71445; TMEM24-like; TMEM24L; CU025_HUMAN.