NIPA2

gene product
SLC57A2
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]
More gene data

Antibodies

 

Filters

Application

Antibodypedia Validation Initiative

Validation method

Reference

Provider

Host

Reactivity

Antibody type

Conjugate

Antibody

  or   Clear
Enhanced validation
Enhanced validation
Supportive data in Antibodypedia
Data presented on provider website
Data in Antibodypedia (inconclusive)
Validated within AVI
Eligible for validation within AVI
40 antibodies from 16 providers.

Antibody properties

General

Applications

or Cancel
Antibody
Acris Antibodies GmbH
1 antibody
Novus Biologicals
3 antibodies
antibodies-online
11 antibodies
Atlas Antibodies
2 antibodies
Invitrogen Antibodies
4 antibodies
Aviva Systems Biology
1 antibody
GeneTex
1 antibody
Boster Biological Technology
1 antibody
Biorbyt
6 antibodies
LifeSpan BioSciences, Inc.
4 antibodies
OriGene
1 antibody
ProSci
1 antibody
Leading Biology
1 antibody
Creative Diagnostics
1 antibody
Abnova Corporation
1 antibody
Sigma-Aldrich
1 antibody