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GUCY2D encodes a retina-specific guanylate cyclase, which is a member of the membrane guanylyl cyclase family. Additionally we are shipping Guanylate Cyclase 2D, Membrane (Retina-Specific) Proteins (7) and many more products for this protein.
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Human Polyclonal GUCY2D Primary Antibody for WB - ABIN493348
Birdsall, Hulme: Biochemical studies on muscarinic acetylcholine receptors. in Journal of neurochemistry 1976
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Human Polyclonal GUCY2D Primary Antibody for EIA, FACS - ABIN952663
Silva, Blanton, Parrado, Melo, Morato, Reis, Dias, Castro, Vasconcelos, Goddard, Barreto, Reis, Teixeira: Dengue hemorrhagic fever is associated with polymorphisms in JAK1. in European journal of human genetics : EJHG 2010
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Two novel mutations causing phenotypic LCA (show CLTA Antibodies) and Alstrom syndrome in Saudi patients from consanguineous families expand the genotypic spectrum of congenital retinal dystrophies.
Data suggest that GCAP1 (guanylate cyclase activator 1A (show GUCA1A Antibodies); Mg2 (show MUC7 Antibodies)+ vs. Ca2 (show CA2 Antibodies)+) exhibits conformational changes in Ca2 (show CA2 Antibodies)+ switch helix that are important in activation of RetGC1; myristoylation of GCAP1 (show GUCA1A Antibodies) is important as well in attaining activator conformation.
Gc1s/Gc1s phenotype variant of DBP (show GC Antibodies) and the unbound fraction of plasma RBP4 (show POLR2D Antibodies) may be considered as factors related with the incidence, and possibly the risk, of IR in CHC (show CLTC Antibodies) patients.
Guanylate cyclase signaling pathway is down regulated in the pathogenesis of inflammatory bowel diseases.
Studies indicate that mutations in retinal guanylate cylase-1 (GUCY2D) are associated with a leading cause of recessive Leber congenital amaurosis (LCA1).
The GUCY2D mutations were frequent in Chinese families with autosomal dominant cone or cone-rod dystrophies. All mutations were found in exon 13.
Dimerization domain of RETGC1 is an essential part of GCAP1 (show GUCA1A Antibodies) and GCAP2 (show GUCA1B Antibodies) binding interface.
The GCAP1 and GCAP2 binding site(s) overlaps within the kinase homology and/or dimerization domains of retinal GC1.
Cardiac fibrosis and the endogenous natriuretic peptide system were evaluated in end-stage heart failure to assess the anti-fibrotic actions of the dual GC-A (show NPR1 Antibodies)/-B activator.
A deletion mutation in the GUCY2D gene is associated with Leber congenital amaurosis in a consanguineous Pakistani family.
The findings define a new regulatory mechanism of the ROS-GC system that affects visual transduction and is likely to affect the course of retinal diseases caused by cGMP toxicity.
The coexpression of ROS-GC1 and its activators in spermatozoa suggests that the Ca(2+)-modulated ROS-GC1 transduction system may be a part of the fertilization machinery
Mg(2 (show MCOLN1 Antibodies)+) binding to GCAPs is critical for setting the actual dynamic range of RetGC regulation by GCAPs at physiological levels of free Ca(2 (show CA2 Antibodies)+)
The Tyr965-Asn981 region of rod outer segment membrane guanylate cyclase type 1 (ROS-GC1) houses both the structural and functional components that mediate guanylate cyclase activating protein type 2 (GCAP2 (show GUCA1B Antibodies)) regulation.
This gene encodes a retina-specific guanylate cyclase, which is a member of the membrane guanylyl cyclase family. Like other membrane guanylyl cyclases, this enzyme has a hydrophobic amino-terminal signal sequence followed by a large extracellular domain, a single membrane spanning domain, a kinase homology domain, and a guanylyl cyclase catalytic domain. In contrast to other membrane guanylyl cyclases, this enzyme is not activated by natriuretic peptides. Mutations in this gene result in Leber congenital amaurosis and cone-rod dystrophy-6 diseases.
, cone rod dystrophy 6
, guanylate cyclase 2D, retinal
, retinal guanylyl cyclase 1
, rod outer segment membrane guanylate cyclase
, guanylate cyclase E