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Invitrogen
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Product is shipped at room temperature as a lyophilized powder and should be stored at -20 °C upon receipt. Reconstitution: add 50 µL of deionized water.
Nipa2 encodes a protein that acts as a selective Mg(2+) transporter. The Nipa2 gene encodes a possible magnesium transporter, and is located adjacent to the imprinted domain in the Prader-Willi syndrome deletion region of chromosome 15. Alternate splicing of the Nipa2 gene results in multiple transcript variants. Pseudogenes of the Nipa2 gene are found on chromosomes 3, 7 and 21. Diseases associated with NIPA2 include Angelman Syndrome and Prader-Willi Syndrome.
仅用于科研。不用于诊断过程。未经明确授权不得转售。