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Description
GDPGP1/C15orf58 Polyclonal Antibody, Cy5 Conjugated. ? Target Background: Encoding more than 700 genes, chromosome 15 is made up of approximately 106 million base pairs and is about 3% of the human genome. Angelman and Prader-Willi syndromes are associated with loss of function or deletion of genes in the 15q11-q13 region. In the case of Angelman syndrome, this loss is due to inactivity of the maternal 15q11-q13 encoded UBE3A gene in the brain by either chromosomal deletion or mutation. In cases of Prader-Willi syndrome, there is a partial or complete deletion of this
Immunogen
KLH conjugated synthetic peptide derived from human GDPGP1/C15orf58