Gene:  WBSCR22, Human

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

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This gene encodes a protein containing a nuclear localization signal and an S-adenosyl-L-methionine binding motif typical of methyltransferases suggesting that the encoded protein may act on DNA methylation. This gene is deleted in Williams syndrome a multisystem developmental disorder caused by the deletion of contiguous genes at 7q11.23. Alternatively spliced transcript variants have been found. [provided by RefSeq Feb 2011]

PrimePCR™ SYBR® Green Assay: WBSCR22, Human
Williams Beuren syndrome chromosome region 22

Assay Type: SYBR® Green
Assay Design: exonic
Application: Gene Expression
Unique Assay ID: qHsaCED0038645
Info:   Same primer pair as used in probe assay qHsaCEP0041367
List Price:    $146.00
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PrimePCR™ Probe Assay: WBSCR22, Human
Williams Beuren syndrome chromosome region 22

Assay Type: Probe
Assay Design: exonic
Application: Gene Expression
Unique Assay ID: qHsaCEP0041367
List Price:    $214.00
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    Related pathways not available
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