PrimePCR™ ddPCR™ Expression Probe Assay: CLN5, Human

PrimePCR

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 qHsaCEP0050205; exonic

 
Fluorophore:   FAM
List Price:    $207.00
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Assay Information

Technology:   ddPCR
Assay Type:   Probe
Application:   Gene Expression
Unique Assay ID:   dHsaCPE5033866
Chromosome Location:   13:77576438-77576587question
Amplicon Length:   120

Gene Information

This gene is one of eight which have been associated with neuronal ceroid lipofuscinoses (NCL). Also referred to as Batten disease NCL comprises a class of autosomal recessive neurodegenerative disorders affecting children. The genes responsible likely encode proteins involved in the degradation of post-translationally modified proteins in lysosomes. The primary defect in NCL disorders is thought to be associated with lysosomal storage function.[provided by RefSeq Oct 2008]

Gene Symbol:   CLN5
Gene Name:   ceroid-lipofuscinosis, neuronal 5
Aliases:   FLJ90628, NCL
RefSeq:   NC_000013.10 NG_009064.1 NT_024524.14
Ensembl:   ENSG00000102805
Entrez:   1203
UniGene:   Hs.30213
Chromosome Mapping:   13q21.1-q32

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