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NIPA2 产品

(Non Imprinted in Prader-Willi/Angelman Syndrome 2 (NIPA2))

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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].

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NIPA2 抗体

High quality antibodies with extensive validation data.

Recommended NIPA2 抗体

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Recommended NIPA2 蛋白

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Cat. No. ABIN3103444
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Synonyms and alternative names related to NIPA2

non imprinted in Prader-Willi/Angelman syndrome 2 (NIPA2), non imprinted in Prader-Willi/Angelman syndrome 2 (Nipa2), non imprinted in Prader-Willi/Angelman syndrome 2 (human) (nipa2), non imprinted in Prader-Willi/Angelman syndrome 2 homolog (human) (Nipa2), 2600017P10Rik, 3830408P04Rik, AB041581, fb72g02, RGD1306051, wu:fb72g02, zgc:66088

Protein level used designations for NIPA2

  • magnesium transporter NIPA2
  • non-imprinted in Prader-Willi/Angelman syndrome 2
  • non-imprinted in Prader-Willi/Angelman syndrome region protein 2
  • non-imprinted in Prader-Willi/Angelman syndrome region protein 2 homolog
  • non imprinted in Prader-Willi/Angelman syndrome 2 homolog
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