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NIPA2 Polyclonal Antibody, Invitrogen™
Rabbit Polyclonal Antibody
Brand: Invitrogen PA567168
This item is not returnable.
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Description
Immunogen sequence: LESLPVSFRKD EKAMNGNLSN MYEVLNNNEE S Highest antigen sequence identity to the following orthologs - mouse 88%, rat 88%.
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.Specifications
NIPA2 | |
Polyclonal | |
Unconjugated | |
NIPA2 | |
2600017P10Rik; 3830408P04Rik; AB041581; Magnesium transporter NIPA2; MNCb-2146; Nipa2; non imprinted in Prader-Willi/Angelman syndrome 2; non imprinted in Prader-Willi/Angelman syndrome 2 homolog; non imprinted in Prader-Willi/Angelman syndrome 2 homolog (human); non-imprinted in Prader-Willi/Angelman syndrome region protein 2; Non-imprinted in Prader-Willi/Angelman syndrome region protein 2 homolog; RGD1306051 | |
Rabbit | |
Antigen affinity chromatography | |
RUO | |
81614 | |
Store at 4°C short term. For long term storage, store at -20°C, avoiding freeze/thaw cycles. | |
Liquid |
Immunocytochemistry | |
0.3 mg/mL | |
PBS with 40% glycerol and 0.02% sodium azide; pH 7.2 | |
Q8N8Q9 | |
NIPA2 | |
Recombinant Human NIPA2 | |
100 μL | |
Primary | |
Human | |
Antibody | |
IgG |
For Research Use Only