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NIPA2
non imprinted in Prader-Willi/Angelman syndrome 2
NIPA2 is 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 Name: | non imprinted in Prader-Willi/Angelman syndrome 2 |
| Synonyms: | NIPA2, Magnesium transporter NIPA2 |
| Target Sequences: | Q8N8Q9 Q8N8Q9 |
☰ Filters
Products
Proteins
(8)
Type
Over-Expression Lysate
(8)
Target
NIPA2
(8)
Publications
No
(8)
Tag
Myc-DDK (Flag)
(8)
Species
Human
(4)
Source
293T Cells
(4)
HEK 293 Cells
(4)
293T Cells
Myc-DDK (Flag)
39 kDa
20 µg/$150
293T Cells
Myc-DDK (Flag)
39 kDa
20 µg/$150
293T Cells
Myc-DDK (Flag)
39 kDa
20 µg/$150
293T Cells
Myc-DDK (Flag)
37.4 kDa
20 µg/$150
HEK 293 Cells
Myc-DDK (Flag)
37.4 kDa
100 µg/$494
HEK 293 Cells
Myc-DDK (Flag)
39 kDa
100 µg/$494
HEK 293 Cells
Myc-DDK (Flag)
39 kDa
100 µg/$494
HEK 293 Cells
Myc-DDK (Flag)
39 kDa
100 µg/$494
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