SYBR Green qPCR primers for detecting human MAGEL2 (MAGE family member L2) gene expression by real-time PCR. Each set comes with primer sequences and reaction conditions.
Human MAGEL2 qPCR Primer Set – MAGE family member L2
Also known as: NDNL1, PWLS, SHFYNG, nM15
About this gene: Prader-Willi syndrome 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.
Gene details: NCBI Gene ID: 54551; HGNC ID: HGNC:6814; UniProt: Q9UJ55; RefSeq (MANE Select): NM_019066.5; Chromosome location: 15q11.2
What you get: Primers are provided as a 40 µl solution containing both primers at a final concentration of 50 µM in 10 mM Tris-HCl (pH 7.5), 0.1 mM EDTA. Dilute with H2O as needed prior to use. This amount is sufficient for 1,000 PCR reactions of 20 µl, assuming a final primer concentration of 0.1 µM.
Browse all Human PCR Primer Sets.