Gene:  BBS10, Human

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

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This gene is a member of the Bardet-Biedl syndrome (BBS) gene family. Bardet-Biedl syndrome is an autosomal recessive disorder characterized by progressive retinal degeneration obesity polydactyly renal malformation and mental retardation. The proteins encoded by BBS gene family members are structurally diverse and the similar phenotypes exhibited by mutations in BBS gene family members is likely due to their shared roles in cilia formation and function. Many BBS proteins localize to the basal bodies ciliary axonemes and pericentriolar regions of cells. BBS proteins may also be involved in intracellular trafficking via microtubule-related transport. The protein encoded by this gene is likely not a ciliary protein but rather has distant sequence homology to type II chaperonins. As a molecular chaperone this protein may affect the folding or stability of other ciliary or basal body proteins. Inhibition of this protein's expression impairs ciliogenesis in preadipocytes. Mutations in this gene cause Bardet-Biedl syndrome type 10. [provided by RefSeq Jan 2010]

PrimePCR™ SYBR® Green Assay: BBS10, Human
Bardet-Biedl syndrome 10

Assay Type: SYBR® Green
Assay Design: exonic
Application: Gene Expression
Unique Assay ID: qHsaCED0047395
Info:   Same primer pair as used in probe assay qHsaCEP0054655
List Price:    $174.00
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PrimePCR™ SYBR® Green Assay: BBS10, Human
Bardet-Biedl syndrome 10

Assay Type: SYBR® Green
Assay Design: Exon-exon junction
Application: Gene Expression
Unique Assay ID: qHsaCJD0034583
Info:   Recommended - best coverage
List Price:    $174.00
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PrimePCR™ Probe Assay: BBS10, Human
Bardet-Biedl syndrome 10

Assay Type: Probe
Assay Design: exonic
Application: Gene Expression
Unique Assay ID: qHsaCEP0054655
List Price:    $255.00
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