Gene:  SLC26A4, Human

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

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Mutations in this gene are associated with Pendred syndrome the most common form of syndromic deafness an autosomal-recessive disease. It is highly homologous to the SLC26A3 gene; they have similar genomic structures and this gene is located 3' of the SLC26A3 gene. The encoded protein has homology to sulfate transporters. [provided by RefSeq Jul 2008]

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PrimePCR™ SYBR® Green Assay: SLC26A4, Human
solute carrier family 26, member 4

Assay Type: SYBR® Green
Assay Design: Exonic
Application: Gene Expression
Unique Assay ID: qHsaCED0007795
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PrimePCR™ SYBR® Green Assay: SLC26A4, Human
solute carrier family 26, member 4

Assay Type: SYBR® Green
Assay Design: exonic
Application: Gene Expression
Unique Assay ID: qHsaCED0042627
Info:   Recommended - best efficiency; Same primer pair as used in probe assay qHsaCEP0049889
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PrimePCR™ Probe Assay: SLC26A4, Human
solute carrier family 26, member 4

Assay Type: Probe
Assay Design: exonic
Application: Gene Expression
Unique Assay ID: qHsaCEP0049889
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PrimePCR™ ddPCR™ Expression EvaGreen® Assay: SLC26A4, Human
solute carrier family 26, member 4

Assay Type: EvaGreen
Application: Gene Expression
Unique Assay ID: dHsaEG5003766
Info:   EG; Same primer pair as used in qPCR assay qHsaCED0007795; Exonic
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PrimePCR™ ddPCR™ Expression EvaGreen® Assay: SLC26A4, Human
solute carrier family 26, member 4

Assay Type: EvaGreen
Application: Gene Expression
Unique Assay ID: dHsaEG5007480
Info:   EG; Same primer pair as used in qPCR assay qHsaCED0042627; exonic
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PrimePCR™ ddPCR™ Expression Probe Assay: SLC26A4, Human
solute carrier family 26, member 4

Assay Type: Probe
Application: Gene Expression
Unique Assay ID: dHsaCPE5033272
Info:   FAM; Same primer pair and probe as used in qPCR assay qHsaCEP0049889; exonic
 
Fluorophore:   FAM
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PrimePCR™ ddPCR™ Expression Probe Assay: SLC26A4, Human
solute carrier family 26, member 4

Assay Type: Probe
Application: Gene Expression
Unique Assay ID: dHsaCPE5033273
Info:   HEX; Same primer pair and probe as used in qPCR assay qHsaCEP0049889; exonic
 
Fluorophore:   HEX
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PrimePCR™ ddPCR™ Mutation Assay:SLC26A4 p.V650V, Human
solute carrier family 26, member 4

Assay Type: Probe
Application: Mutation Detection in silico design
Unique Assay ID: dHsaIS2504396
Info:   69nt amplicon; exonic; in silico
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PrimePCR™ ddPCR™ Mutation Assay:SLC26A4 WT for p.V650V, Human
solute carrier family 26, member 4

Assay Type: Probe
Application: Mutation Detection in silico design
Unique Assay ID: dHsaIS2504397
Info:   69nt amplicon; exonic; in silico
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    Related pathways not available
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