Gene:  MAGEL2, Human

PrimePCR Primer Assays for Real-Time PCR oligo primer pair gene expression assay target

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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]

PrimePCR™ SYBR® Green Assay: MAGEL2, Human
MAGE-like 2

Assay Type: SYBR® Green
Assay Design: Exonic
Application: Gene Expression
Unique Assay ID: qHsaCED0034524
Info:   Recommended - best specificity
List Price:    $188.00
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PrimePCR™ SYBR® Green Assay: MAGEL2, Human
MAGE-like 2

Assay Type: SYBR® Green
Assay Design: exonic
Application: Gene Expression
Unique Assay ID: qHsaCED0048875
Info:   Same primer pair as used in probe assay qHsaCEP0056135
List Price:    $188.00
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PrimePCR™ Probe Assay: MAGEL2, Human
MAGE-like 2

Assay Type: Probe
Assay Design: exonic
Application: Gene Expression
Unique Assay ID: qHsaCEP0056135
List Price:    $278.00
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    Related pathways not available
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