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

NIPA2 encodes a possible magnesium transporter.

list all ELISA KIts Gene Name GeneID UniProt
Anti-Human NIPA2 NIPA2 81614 Q8N8Q9
Anti-Mouse NIPA2 NIPA2 93790 Q9JJC8
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More ELISA Kits for NIPA2 Interaction Partners

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

  1. This study primarily reveals that a selective magnesium transporter NIPA2 may play a role in the pathogenesis of CAE (show GJA8 ELISA Kits).

  2. mutations in NIPA2 gene were associated with childhood absence epilepsy (CAE), which indicated that the haploinsufficiency of NIPA2 might be a candidate mechanism underlying the IGE/CAE phenotypes caused by 15q11.2 microdeletions or rare mutations in NIPA2

  3. quantitated mRNA levels of NIPA2, NIPA2,l CYFIP1, and GCP5 in Prader-Willi syndrome and correlated levels with psychological and behavior scales

Mouse (Murine) Non Imprinted in Prader-Willi/Angelman Syndrome 2 (NIPA2) interaction partners

  1. The isolation and characterization of Nipa2 in mouse distal convoluted tubule cells are reported.

NIPA2 Antigen Profile

Antigen Summary

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.

Gene names and symbols associated with NIPA2

  • non imprinted in Prader-Willi/Angelman syndrome 2 (NIPA2) antibody
  • non imprinted in Prader-Willi/Angelman syndrome 2 homolog (human) (Nipa2) antibody
  • 2600017P10Rik antibody
  • 3830408P04Rik antibody
  • AB041581 antibody

Protein level used designations for NIPA2

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

GENE ID SPECIES
81614 Homo sapiens
507430 Bos taurus
93790 Mus musculus
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