PrimePCR™ Probe Assay: RAN, Human

RT

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

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Wet Lab Validated

Assay Information

Technology:   qPCR
Assay Type:   Probe
Application:   Gene Expression
Unique Assay ID:   qHsaCEP0051694
Assay Design:   exonic
Chromosome Location:   12:131357562-131357672question
Amplicon Length:   81
Splice Variants Targeted:   ENST00000543796 ENST00000448750 ENST00000541630 ENST00000392369 ENST00000535090 ENST00000392367 ENST00000254675

Gene Information

RAN (ras-related nuclear protein) is a small GTP binding protein belonging to the RAS superfamily that is essential for the translocation of RNA and proteins through the nuclear pore complex. The RAN protein is also involved in control of DNA synthesis and cell cycle progression. Nuclear localization of RAN requires the presence of regulator of chromosome condensation 1 (RCC1). Mutations in RAN disrupt DNA synthesis. Because of its many functions it is likely that RAN interacts with several other proteins. RAN regulates formation and organization of the microtubule network independently of its role in the nucleus-cytosol exchange of macromolecules. RAN could be a key signaling molecule regulating microtubule polymerization during mitosis. RCC1 generates a high local concentration of RAN-GTP around chromatin which in turn induces the local nucleation of microtubules. RAN is an androgen receptor (AR) coactivator that binds differentially with different lengths of polyglutamine within the androgen receptor. Polyglutamine repeat expansion in the AR is linked to Kennedy's disease (X-linked spinal and bulbar muscular atrophy). RAN coactivation of the AR diminishes with polyglutamine expansion within the AR and this weak coactivation may lead to partial androgen insensitivity during the development of Kennedy's disease. [provided by RefSeq Jul 2008]

Gene Symbol:   RAN
Gene Name:   RAN, member RAS oncogene family
Aliases:   ARA24, Gsp1, TC4
RefSeq:   NC_000012.11 NT_009755.19
Ensembl:   ENSG00000132341
Entrez:   5901
Chromosome Mapping:   12q24.3

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