Also recognizes the two published isoforms of CNGA3.
Immunogen
synthetic peptide corresponding to amino acids 594-611 of rat CNGA3. Mouse is 15/18 residues identical.
application
Anti-Cyclic Nucleotide-Gated Cation Channel A3 (CNGA3) antibody produced in rabbit is suitable for western blotting at a dilution of 1:200 using rat brain membranes.
Biochem/physiol Actions
Cyclic nucleotide-gated cation channel alpha-3 is a protein encoded by the CNGA3 gene in humans. It is also referred as CNG3, ACHM2, CCNC1, CCNCa, CNCG3 and CCNCalpha. A cyclic nucleotide-gated (CNG) channel serves as essential target for sensory transduction in retinal photoreceptors and olfactory receptor cells. CNGA3 subunits specify the arrangement of subunits containing L633P and other mutations which leads to interact between channel subunits or intersubunit. Its mutations are the most common cause of cone-rod dystrophies and achromatopsia.
Physical form
Lyophilized from phosphate buffered saline, pH 7.4, 1% BSA, and 0.05% sodium azide.
American journal of physiology. Cell physiology, 305(2), C147-C159 (2013-04-05)
Cyclic nucleotide-gated (CNG) channels are critical for sensory transduction in retinal photoreceptors and olfactory receptor cells; their activity is modulated by phosphoinositides (PIPn) such as phosphatidylinositol 4,5-bisphosphate (PIP2) and phosphatidylinositol 3,4,5-trisphosphate (PIP3). An achromatopsia-associated mutation in cone photoreceptor CNGA3, L633P
Mutations in CNGA3 are the most common cause of achromatopsia and cone-rod dystrophies. To identify CNGA3 mutations in patients with cone dystrophies or Leber congenital amaurosis. Clinical data and genomic DNA in 267 Chinese probands from 138 families with cone
Cyclic nucleotide-gated (CNG) channels are crucial for visual and olfactory transductions. These channels are tetramers and in their native forms are composed of A and B subunits, with a stoichiometry thought to be 2A:2B (refs 6, 7). Here we report
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