Gene:  DFNB31, Human

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

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This gene is thought to function in the organization and stabilization of sterocilia elongation and actin cystoskeletal assembly based on studies of the related mouse gene. Mutations in this gene have been associated with autosomal recessive non-syndromic deafness and Usher Syndrome. Alternative splicing of this gene results in multiple transcript variants encoding different isoforms.[provided by RefSeq Mar 2010]

PrimePCR™ SYBR® Green Assay: DFNB31, Human
deafness, autosomal recessive 31

Assay Type: SYBR® Green
Assay Design: exonic
Application: Gene Expression
Unique Assay ID: qHsaCED0042683
Info:   Same primer pair as used in probe assay qHsaCEP0049945
List Price:    $174.00
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PrimePCR™ SYBR® Green Assay: DFNB31, Human
deafness, autosomal recessive 31

Assay Type: SYBR® Green
Assay Design: Intron-spanning
Application: Gene Expression
Unique Assay ID: qHsaCID0006488
List Price:    $174.00
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PrimePCR™ Probe Assay: DFNB31, Human
deafness, autosomal recessive 31

Assay Type: Probe
Assay Design: exonic
Application: Gene Expression
Unique Assay ID: qHsaCEP0049945
List Price:    $255.00
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    Related pathways not available
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