Tissue expression
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Protein structure

MAGEL2

MAGE family member L2
NDNL1, nM15 
Prader-Willi syndrome (PWS) is caused by the loss of expression of imprinted genes in chromosome 15q11-q13 region. Affected individuals exhibit neonatal hypotonia, developmental delay, and childhood-onset obesity. Necdin (NDN), a gene involved in the terminal differentiation of neurons, localizes to this region of the genome and has been implicated as one of the genes responsible for the etiology of PWS. This gene is structurally similar to NDN, is also localized to the PWS chromosomal region, and is paternally imprinted, suggesting a possible role for it in PWS. [provided by RefSeq, Oct 2010]
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103 antibodies from 13 providers.

Antibody properties

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AntibodyRefsTypeWBELICCIPIHCFC
antibodies-online
47 antibodies
ABIN28406292Polyclonal
ABIN2445258Polyclonal
Abnova Corporation
2 antibodies
PAB47612Polyclonal
H00054551-B01PPolyclonal
Biorbyt
6 antibodies
orb1274675Polyclonal
orb1276698Polyclonal
Cusabio Biotech Co., Ltd
2 antibodies
CSB-PA013771Polyclonal
CSB-PA277591Polyclonal
LS-B864Polyclonal
LS-C403315Polyclonal
OriGene
3 antibodies
TA342770Polyclonal
TA351378Polyclonal
Invitrogen Antibodies
2 antibodies
PA5-70460Polyclonal
BS-6828RPolyclonal
Aviva Systems Biology
1 antibody
ARP59891_P050Polyclonal
ProSci
1 antibody
49-693Polyclonal
Abbexa
3 antibodies
abx210993Polyclonal
abx339677Polyclonal
bs-6828RPolyclonal
bs-6828R-A350Polyclonal
MyBioSource
1 antibody
MBS2519833Polyclonal
RayBiotech, Inc.
1 antibody
119-11867Polyclonal