NIPA2 rabbit pAb
Ref. EK-ES14491
50µl | 188.00 € | ||
100µl | 316.00 € |
Product Information
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],
Chemical properties
Technical inquiry about: EK-ES14491 NIPA2 rabbit pAb
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