MAGEL2 polyclonal, anti-human

Background:
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.

Synonyms: PWLS, nM15, NDNL1

Cellular Location: Nucleus Cytoplasm

Immunogen:
A synthetic peptide of human MAGEL2

Gene Symbol: MAGEL2

Gene ID: 54551

Swiss prot: Q9UJ55

Calculated MW: 59 kDa

Recommended dilution:
WB 1:200-1000

Purity:
Affinity purification

Storage Buffer:
Buffer: PBS with 0.03% Proclin300, 50% glycerol, pH7.3.

Storage:
Store at -20℃. Avoid freeze / thaw cycles.