PrimePCR™ ddPCR™ Expression Probe Assay: SLC25A19, Human


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

Info:   HEX; Same primer pair and probe as used in qPCR assay qHsaCIP0028031; Intron-spanning

Fluorophore:   HEX
List Price:    $201.00
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Assay Information

Technology:   ddPCR
Assay Type:   Probe
Application:   Gene Expression
Unique Assay ID:   dHsaCPE5050003
Chromosome Location:   17:73273519-73274355question
Amplicon Length:   139

Gene Information

This gene encodes a mitochondrial protein that is a member of the solute carrier family. Although this protein was initially thought to be the mitochondrial deoxynucleotide carrier involved in the uptake of deoxynucleotides into the matrix of the mitochondria further studies have demonstrated that this protein instead functions as the mitochondrial thiamine pyrophosphate carrier which transports thiamine pyrophosphates into mitochondria. Mutations in this gene cause microcephaly Amish type a metabolic disease that results in severe congenital microcephaly severe 2-ketoglutaric aciduria and death within the first year. Multiple alternatively spliced variants encoding the same protein have been identified for this gene. [provided by RefSeq Jul 2008]

Gene Symbol:   SLC25A19
Gene Name:   solute carrier family 25 (mitochondrial thiamine pyrophosphate carrier), member 19
Aliases:   DNC, MCPHA, MUP1, TPC
RefSeq:   NC_000017.10 NT_010783.15 NG_008274.1
Ensembl:   ENSG00000125454
Entrez:   60386
UniGene:   Hs.514470
Chromosome Mapping:   17q25.3

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