PrimePCR™ ddPCR™ Expression Probe Assay: WBSCR22, Human


ddPCR probe assay designed for gene expression analysis. Probe assays consist of unlabeled PCR primers and a dual labeled fluorescent probe.

Info:   FAM; Same primer pair and probe as used in qPCR assay qHsaCEP0041367; exonic

Fluorophore:   FAM
List Price:    $207.00
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Assay Information

Technology:   ddPCR
Assay Type:   Probe
Application:   Gene Expression
Unique Assay ID:   dHsaCPE5031566
Chromosome Location:   7:73112162-73112254question
Amplicon Length:   63

Gene Information

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]

Gene Symbol:   WBSCR22
Gene Name:   Williams Beuren syndrome chromosome region 22
Aliases:   FLJ44236, HASJ4442, HUSSY-3, MGC19709, MGC2022, MGC5140, PP3381, WBMT
RefSeq:   NG_013360.1 NC_000007.13 NT_007933.15
Ensembl:   ENSG00000071462
Entrez:   114049
UniGene:   Hs.647063
Chromosome Mapping:   -

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