the cyan fluorescent protein (cfp) expression plasmid (TaKaRa)
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TaKaRa
the cyan fluorescent protein (cfp) expression plasmid
The Cyan Fluorescent Protein (Cfp) Expression Plasmid, supplied by TaKaRa, used in various techniques. Bioz Stars score: 94/100, based on 23 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/the+cyan+fluorescent+protein+(cfp)+expression+plasmid/pLVX-AmCyan1-C1+Vector/pmc11054720-38-1-9
Average 94 stars, based on 23 article reviews
The Cyan Fluorescent Protein (Cfp) Expression Plasmid, supplied by TaKaRa, used in various techniques. Bioz Stars score: 94/100, based on 23 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/the+cyan+fluorescent+protein+(cfp)+expression+plasmid/pLVX-AmCyan1-C1+Vector/pmc11054720-38-1-9
Average 94 stars, based on 23 article reviews
the cyan fluorescent protein (cfp) expression plasmid - by Bioz Stars,
2026-10
94/100 stars
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Imaging:Article Title: Dissecting the pathogenic mechanisms of mutations in the pore region of the human cone photoreceptor cyclic nucleotide-gated channel. Article Snippet: For calcium imaging and patch clamp measurements, the cells were cotransfected with the cyan fluorescent protein (CFP) expression vector pECFP-C1 (Clontech, Mountain View, CA) to distinguish transfected from untransfected cells. Article Title: Functional analysis of human CNGA3 mutations associated with colour blindness suggests impaired surface expression of channel mutants A3(R427C) and A3(R563C). Article Snippet: Mutations in the CNGA3 gene have been associated with complete and incomplete forms of total colour blindness (achromatopsia), a disorder characterized by reduced visual acuity, lack of colour discrimination, photophobia and nystagmus.. CNGA3 encodes the A-subunit of the cone photoreceptor cyclic nucleotide-gated (CNG) channel, an essential component of the phototransduction cascade.. Here we report the identification of three new CNGA3 mutations in patients with achromatopsia. Article Title: Homozygous missense variant in the human CNGA3 channel causes cone-rod dystrophy Article Snippet: For Expressing:Article Title: Dissecting the pathogenic mechanisms of mutations in the pore region of the human cone photoreceptor cyclic nucleotide-gated channel. Article Snippet: For calcium imaging and patch clamp measurements, the cells were cotransfected with the cyan fluorescent protein (CFP) expression vector pECFP-C1 (Clontech, Mountain View, CA) to distinguish transfected from untransfected cells. Article Title: Functional analysis of human CNGA3 mutations associated with colour blindness suggests impaired surface expression of channel mutants A3(R427C) and A3(R563C). Article Snippet: Mutations in the CNGA3 gene have been associated with complete and incomplete forms of total colour blindness (achromatopsia), a disorder characterized by reduced visual acuity, lack of colour discrimination, photophobia and nystagmus.. CNGA3 encodes the A-subunit of the cone photoreceptor cyclic nucleotide-gated (CNG) channel, an essential component of the phototransduction cascade.. Here we report the identification of three new CNGA3 mutations in patients with achromatopsia. Article Title: Homozygous missense variant in the human CNGA3 channel causes cone-rod dystrophy Article Snippet: For Plasmid Preparation:Article Title: Dissecting the pathogenic mechanisms of mutations in the pore region of the human cone photoreceptor cyclic nucleotide-gated channel. Article Snippet: For calcium imaging and patch clamp measurements, the cells were cotransfected with the cyan fluorescent protein (CFP) expression vector pECFP-C1 (Clontech, Mountain View, CA) to distinguish transfected from untransfected cells. Article Title: Functional analysis of human CNGA3 mutations associated with colour blindness suggests impaired surface expression of channel mutants A3(R427C) and A3(R563C). Article Snippet: Mutations in the CNGA3 gene have been associated with complete and incomplete forms of total colour blindness (achromatopsia), a disorder characterized by reduced visual acuity, lack of colour discrimination, photophobia and nystagmus.. CNGA3 encodes the A-subunit of the cone photoreceptor cyclic nucleotide-gated (CNG) channel, an essential component of the phototransduction cascade.. Here we report the identification of three new CNGA3 mutations in patients with achromatopsia. Article Title: Homozygous missense variant in the human CNGA3 channel causes cone-rod dystrophy Article Snippet: For Transfection:Article Title: Dissecting the pathogenic mechanisms of mutations in the pore region of the human cone photoreceptor cyclic nucleotide-gated channel. Article Snippet: For calcium imaging and patch clamp measurements, the cells were cotransfected with the cyan fluorescent protein (CFP) expression vector pECFP-C1 (Clontech, Mountain View, CA) to distinguish transfected from untransfected cells. Article Title: Functional analysis of human CNGA3 mutations associated with colour blindness suggests impaired surface expression of channel mutants A3(R427C) and A3(R563C). Article Snippet: Mutations in the CNGA3 gene have been associated with complete and incomplete forms of total colour blindness (achromatopsia), a disorder characterized by reduced visual acuity, lack of colour discrimination, photophobia and nystagmus.. CNGA3 encodes the A-subunit of the cone photoreceptor cyclic nucleotide-gated (CNG) channel, an essential component of the phototransduction cascade.. Here we report the identification of three new CNGA3 mutations in patients with achromatopsia. Article Title: Homozygous missense variant in the human CNGA3 channel causes cone-rod dystrophy Article Snippet: For Patch Clamp:Article Title: Dissecting the pathogenic mechanisms of mutations in the pore region of the human cone photoreceptor cyclic nucleotide-gated channel. Article Snippet: For calcium imaging and patch clamp measurements, the cells were cotransfected with the cyan fluorescent protein (CFP) expression vector pECFP-C1 (Clontech, Mountain View, CA) to distinguish transfected from untransfected cells. Article Title: Functional analysis of human CNGA3 mutations associated with colour blindness suggests impaired surface expression of channel mutants A3(R427C) and A3(R563C). Article Snippet: Mutations in the CNGA3 gene have been associated with complete and incomplete forms of total colour blindness (achromatopsia), a disorder characterized by reduced visual acuity, lack of colour discrimination, photophobia and nystagmus.. CNGA3 encodes the A-subunit of the cone photoreceptor cyclic nucleotide-gated (CNG) channel, an essential component of the phototransduction cascade.. Here we report the identification of three new CNGA3 mutations in patients with achromatopsia. Article Title: Homozygous missense variant in the human CNGA3 channel causes cone-rod dystrophy Article Snippet: For |