Gene:  PEX12, Human

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

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This gene belongs to the peroxin-12 family. Peroxins (PEXs) are proteins that are essential for the assembly of functional peroxisomes. The peroxisome biogenesis disorders (PBDs) are a group of genetically heterogeneous autosomal recessive lethal diseases characterized by multiple defects in peroxisome function. The peroxisomal biogenesis disorders are a heterogeneous group with at least 14 complementation groups and with more than 1 phenotype being observed in cases falling into particular complementation groups. Although the clinical features of PBD patients vary cells from all PBD patients exhibit a defect in the import of one or more classes of peroxisomal matrix proteins into the organelle. Defects in this gene are a cause of Zellweger syndrome (ZWS). [provided by RefSeq Oct 2008]

PrimePCR™ SYBR® Green Assay: PEX12, Human
peroxisomal biogenesis factor 12

Assay Type: SYBR® Green
Assay Design: exonic
Application: Gene Expression
Unique Assay ID: qHsaCED0043242
Info:   Same primer pair as used in probe assay qHsaCEP0050504
List Price:    $142.00
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PrimePCR™ SYBR® Green Assay: PEX12, Human
peroxisomal biogenesis factor 12

Assay Type: SYBR® Green
Assay Design: Intron-spanning
Application: Gene Expression
Unique Assay ID: qHsaCID0011639
List Price:    $142.00
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PrimePCR™ Probe Assay: PEX12, Human
peroxisomal biogenesis factor 12

Assay Type: Probe
Assay Design: exonic
Application: Gene Expression
Unique Assay ID: qHsaCEP0050504
List Price:    $208.00
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    Related pathways not available
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