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Rod cGMP-specific 3',5'-cyclic phosphodiesterase

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This protein participates in processes of transmission and amplification of the visual signal.

Below are the list of possible Rod cGMP-specific 3',5'-cyclic phosphodiesterase products. If you cannot find the target and/or product is not available in our catalog, please click here to contact us and request the product or submit your request for custom elisa kit production, custom recombinant protein production or custom antibody production. Custom ELISA Kits, Recombinant Proteins and Antibodies can be designed, manufactured and produced according to the researcher's specifications.
 

Rod cGMP-specific 3',5'-cyclic phosphodiesterase subunit alpha

 Rod cGMP-specific 3',5'-cyclic phosphodiesterase subunit alpha ELISA Kit
 Rod cGMP-specific 3',5'-cyclic phosphodiesterase subunit alpha Recombinant
 Rod cGMP-specific 3',5'-cyclic phosphodiesterase subunit alpha Antibody
Also known as Rod cGMP-specific 3',5'-cyclic phosphodiesterase subunit alpha (GMP-PDE alpha).
This protein participates in processes of transmission and amplification of the visual signal.
 PDE6A ELISA Kit
 PDE6A Recombinant
 PDE6A Antibody
 PDEA ELISA Kit
 PDEA Recombinant
 PDEA Antibody
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Rod cGMP-specific 3',5'-cyclic phosphodiesterase subunit beta

 Rod cGMP-specific 3',5'-cyclic phosphodiesterase subunit beta ELISA Kit
 Rod cGMP-specific 3',5'-cyclic phosphodiesterase subunit beta Recombinant
 Rod cGMP-specific 3',5'-cyclic phosphodiesterase subunit beta Antibody
Also known as Rod cGMP-specific 3',5'-cyclic phosphodiesterase subunit beta (GMP-PDE beta).
PDE6B: This protein participates in processes of transmission and amplification of the visual signal. Necessary for the formation of a functional phosphodiesterase holoenzyme. Defects in PDE6B are the cause of retinitis pigmentosa type 40 (RP40). RP40 is a retinal dystrophy belonging to the group of pigmentary retinopathies. Retinitis pigmentosa is characterized by retinal pigment deposits visible on fundus examination and primary loss of rod photoreceptor cells followed by secondary loss of cone pho
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toreceptors. Patients typically have night vision blindness and loss of midperipheral visual field. As their condition progresses, they lose their far peripheral visual field and eventually central vision as well. Defects in PDE6B are a cause of congenital stationary night blindness autosomal dominant type 2 (CSNBAD2); also known as congenital stationary night blindness Rambusch type. Congenital stationary night blindness is a non-progressive retinal disorder characterized by impaired night vision. Belongs to the cyclic nucleotide phosphodiesterase family. 2 isoforms of the human protein are produced by alternative splicing.

Protein type: EC 3.1.4.35; Phosphodiesterase

Cellular Component: photoreceptor outer segment

Molecular Function: 3',5'-cyclic-GMP phosphodiesterase activity

Biological Process: cytosolic calcium ion homeostasis; detection of light stimulus; GMP metabolic process; retina development in camera-type eye
 Pde6b ELISA Kit
 Pde6b Recombinant
 Pde6b Antibody
 Mpb ELISA Kit
 Mpb Recombinant
 Mpb Antibody
 Pdeb ELISA Kit
 Pdeb Recombinant
 Pdeb Antibody
 rd ELISA Kit
 rd Recombinant
 rd Antibody
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Proteins Root Name Listing
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