NIPA2 Antibodies

AND NIPA2 ELISA kits, NIPA2 Proteins

Many biological assays use antibodies to detect NIPA2, such as Western Blot (WB), ELISA, Flow Cytometry, Immunocytochemistry (IHC). These antibodies can be polyclonal or monoclonal, and react with NIPA2 in Human, Mouse, Rat, and many other animal samples. Boster Bio use mainly mouse and rabbit to develop NIPA2 antibodies...

We validate the specificity of these antibodies to NIPA2 by testing them on tissues known to express NIPA2 positively and negatively. Browse below to find the NIPA2 antibody that suites your experiment. We have 1 of these antibodies and many publications and validation images.

If you cannot find antibodies that fit your needs, contact us for making custom antibodies. We have a full suite of custom antibody services covering from research to diagnostic and therapeutic applications.

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NIPA2 Infographic by Boster Bio

All NIPA2 Products

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NIPA2 (NM_030922) Human Over-expression Lysate

NIPA2 Human Over-expression Lysates NM_001008860

Human

$628
Cat # LS081614
20 µg, 100 µg

NIPA2 Overview

Facts about Magnesium transporter NIPA2.

NIPA2 3D structure. Source: alphafold

Magnesium transporter NIPA2 (NIPA2)

Acts as a selective Mg(2+) transporter.
.

Gene Information

Human
Gene Name:	NIPA2
Uniprot:	Q8N8Q9
Entrez:	81614

Family

Belongs to:

NIPA family

Alternative Names

magnesium transporter NIPA2; MGC5466; non imprinted in Prader-Willi/Angelman syndrome 2

Molecular Weight

Mass (kDA):
39.185 kDA

Genomic Context


Human

Location:	15q11.2
Sequence:	15; NC_000015.10 (22838641..22868384)

Tissue Specificity

Widely expressed.

Subcellular Localizations

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

Diseases

Prader-willi Syndrome
Angelman Syndrome
Muscle Hypotonia
Nervousness
Ataxia
Chromosome Breakage
Microdeletion 15q11.2
Haploinsufficiency
Mental Disorders
Hypogonadism
Cytogenetic Abnormality

Speech Disorders
Speech Impairment
Obsessive-compulsive Disorder
Autistic Disorder
Obesity

Pathways

Transport
Methylation
Transposition
System Development
Nervous System Development
Central Nervous System Development

PTMs

Methylation

For details, visit:
bosterbio.com/bosterbio-gene-info-cards/NIPA2

References

PMID: 14508708 by Chai J.-H., et al. Identification of four highly conserved genes between breakpoint hotspots BP1 and BP2 of the Prader-Willi/Angelman syndromes deletion region that have undergone evolutionary transposition mediated by flanking duplicons.