NIPA2 rabbit pAb - ES14491

NIPA2 rabbit pAb

Sizes: 50μL, 100μL

Catalogue Numbers: ES14491-50, ES14491-100

Citations, Manuals and MSDS Available upon request.

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 are found on chromosomes 3, 7 and 21.[provided by RefSeq, May 2010],

Source: Rabbit

Applications: WB

Dilution: WB 1: 500-2000

Reactivity: Human; Mouse

Immunogen: Synthesized peptide derived from human NIPA2 AA range: 175-225

Storage and Stability: -20°C/1 year

Clonality: Polyclonal

Isotype: IgG

Concentration: 1 mg/ml

Human Gene ID: 81614

Human SWISS Prot NO: Q8N8Q9

Subcellular Location: Cell membrane; Multi-pass membrane protein. Early endosome. Recruited to the cell membrane in response to low extracellular magnesium.

Research Use Only