NIPA2 rabbit pAb - 50 μL
This gene encodes a possible magnesium transporter. This gene is located adjacent to the imprinted domain in the Prader-Willi syndrome deletion region of chromosome 15. Alternate splicing results in multiple transcript variants. Pseudogenes of this gene are found on chromosomes 3, 7 and 21. [provided by RefSeq, May 2010],
Distributed by Gentaur

View the Technical Datasheet of the product below

View the Technical Datasheet of the product below
Votre snippet dynamique sera affiché ici... Ce message est affiché parce que vous n'avez pas défini le filtre et le modèle à utiliser.