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Reconstitution: 25 µL, 50 µL or 0.2 mL double distilled water (DDW), depending on the sample size. The antibody ships as a lyophilized powder at room temperature. Upon arrival, it should be stored at -20C. The reconstituted solution can be stored at 4C for up to 1 week. For longer periods, small aliquots should be stored at -20C. Avoid multiple freezing and thawing. Centrifuge all antibody preparations before use (10000 x g 5 min).
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.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
Protein Aliases: Magnesium transporter NIPA2; non imprinted in Prader-Willi/Angelman syndrome 2 homolog; Non-imprinted in Prader-Willi/Angelman syndrome region protein 2; Non-imprinted in Prader-Willi/Angelman syndrome region protein 2 homolog
Gene Aliases: 2600017P10Rik; 3830408P04Rik; AB041581; MNCb-2146; NIPA2; RGD1306051
UniProt ID: (Human) Q8N8Q9, (Mouse) Q9JJC8
Entrez Gene ID: (Human) 81614, (Mouse) 93790, (Rat) 308667
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