A18398
Size
  • 50ul
  • 100ul
Price
  • $129
  • $229
Qty
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Product description

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 a

Source
Rabbit
Applications
WB
Reactivity
Human, Mouse
Dilution
WB 1：500-2000
Storage
-20°C/1 year
Specificity
This antibody detects endogenous levels of NIPA2 at Human/Mouse
Source/Purification
The antibody was affinity-purified from rabbit serum by affinity-chromatography using specific immunogen.
Immunogen
Synthesized peptide derived from human NIPA2
Uniprot No
Q8N8Q9
Form
Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
Clonality
Polyclonal
Background
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 a
Other
Gene_name: NIPA2 ; Protein_name: NIPA2; Expression:
Mol.Wt (Da)
40 kD
Concentration
1 mg/ml

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