Gene:  BBS2, 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 severe pigmentary retinopathy 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 forms a multiprotein BBSome complex with six other BBS proteins.[provided by RefSeq Jan 2009]

PrimePCR™ SYBR® Green Assay: BBS2, Human
Bardet-Biedl syndrome 2

Assay Type: SYBR® Green
Assay Design: exonic
Application: Gene Expression
Unique Assay ID: qHsaCED0044075
Info:   Recommended - best coverage; Same primer pair as used in probe assay qHsaCEP0051337
List Price:    $174.00
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PrimePCR™ SYBR® Green Assay: BBS2, Human
Bardet-Biedl syndrome 2

Assay Type: SYBR® Green
Assay Design: Intron-spanning
Application: Gene Expression
Unique Assay ID: qHsaCID0015912
List Price:    $174.00
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PrimePCR™ Probe Assay: BBS2, Human
Bardet-Biedl syndrome 2

Assay Type: Probe
Assay Design: exonic
Application: Gene Expression
Unique Assay ID: qHsaCEP0051337
List Price:    $255.00
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