The protein encoded by this gene is a cyclic nucleotide phosphodiesterase (PDE) that catalyzes the hydrolysis of the second messenger cAMP. The encoded protein, which does not hydrolyze cGMP, is resistant to several PDE inhibitors. Defects in this gene are a cause of autosomal dominant striatal degeneration (ADSD). Several transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, Jul 2010]
SKU | Test Kits | Buffer | Dye Color | Order Now |
---|---|---|---|---|
PDE8B-20-RE | 20 (40 μL) | 200 μL | Request Pricing | |
PDE8B-20-OR | 20 (40 μL) | 200 μL | Request Pricing | |
PDE8B-20-GO | 20 (40 μL) | 200 μL | Request Pricing | |
PDE8B-20-GR | 20 (40 μL) | 200 μL | Request Pricing | |
PDE8B-20-AQ | 20 (40 μL) | 200 μL | Request Pricing |
The protein encoded by this gene is a cyclic nucleotide phosphodiesterase (PDE) that catalyzes the hydrolysis of the second messenger cAMP. The encoded protein, which does not hydrolyze cGMP, is resistant to several PDE inhibitors. Defects in this gene are a cause of autosomal dominant striatal degeneration (ADSD). Several transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, Jul 2010]
Gene Symbol : PDE8B
Gene Name : Phosphodiesterase 8B
Chromosome : CHR 5: 771,802,51-774,282,55
Locus : 5q13.3
Alt. Genes : HIPK3
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