GUC1A rabbit pAb
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GUC1A rabbit pAb
Background :
This gene encodes an enzyme that plays a role in the recovery of retinal photoreceptors from photobleaching. This enzyme promotes the activity of retinal guanylyl cyclase-1 (GC1) at low calcium concentrations and inhibits GC1 at high calcium concentrations. Mutations in this gene can cause cone dystrophy 3 and code-rod dystrophy 14. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2016]Description :
This gene encodes an enzyme that plays a role in the recovery of retinal photoreceptors from photobleaching. This enzyme promotes the activity of retinal guanylyl cyclase-1 (GC1) at low calcium concentrations and inhibits GC1 at high calcium concentrations. Mutations in this gene can cause cone dystrophy 3 and code-rod dystrophy 14. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jan 2016],UniProt :
P43080Swiss Prot :
P43080Reactivity :
Human; MouseImmunogen :
Synthesized peptide derived from human GUC1A AA range: 63-113Target :
GUC1AClonality :
PolyclonalSource :
RabbitApplications :
WBConcentration :
1 mg/mlDilution :
WB 1:500-2000Buffer :
-20°C/1 yearStorage Conditions :
-20°C/1 yearFragment :
IgGSubcellular Location :
Membrane; Lipid-anchor . Photoreceptor inner segment . Cell projection, cilium, photoreceptor outer segment . Present at higher levels in cone than in rod outer segments (PubMed:9620085) . Subcellular location is not affected by light or dark conditions. .Gene ID (Human) :
2978

