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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 |
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Products
Antibodies
(4)
Type
Primary
(4)
Target
NIPA2
(4)
Reactivity
Human
(4)
Mouse
(3)
Rat
(3)
Chicken
(3)
Chimpanzee
(3)
Dog
(3)
Gibbon
(3)
Horse
(3)
Orangutan
(3)
Pig
(3)
Rabbit
(3)
Zebrafish
(3)
Application
WB
(4)
Host
rabbit
(4)
Isotype
IgG
(4)
Clonality
polyclonal pc
(4)
Format
Biotin Conjugated
(1)
FITC Conjugated
(1)
HRP Conjugated
(1)
Unconjugated
(1)
Epitope
aa180-229
(4)
Publications
No
(4)
NIPA2 Rabbit anti-Human Polyclonal (aa180-229) Antibody
Human
WB
Unconjugated
100 µl/$424
NIPA2 Rabbit anti-Human Polyclonal (aa180-229) (HRP) Antibody
Chicken, Zebrafish, Rat, Rabbit, Mouse, Dog, Pig, Horse, Orangutan, Gibbon, Human, Chimpanzee
WB
HRP Conjugated
100 µl/$469
NIPA2 Rabbit anti-Human Polyclonal (aa180-229) (Biotin) Antibody
Chicken, Zebrafish, Rat, Rabbit, Mouse, Dog, Pig, Horse, Orangutan, Gibbon, Human, Chimpanzee
WB
Biotin Conjugated
100 µl/$469
NIPA2 Rabbit anti-Human Polyclonal (aa180-229) (FITC) Antibody
Chicken, Zebrafish, Rat, Rabbit, Mouse, Dog, Pig, Horse, Orangutan, Gibbon, Human, Chimpanzee
WB
FITC Conjugated
100 µl/$469
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