mturquoise2 cdna (Addgene inc)
Addgene inc is a verified supplier 
93
Structured Review
Addgene inc
mturquoise2 cdna
Mturquoise2 Cdna, supplied by Addgene inc, used in various techniques. Bioz Stars score: 93/100, based on 17 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/mturquoise2+cdna/pPalmitoyl-mTurquoise2+(Plasmid+%2336209)/bio_rxiv__64898__2026__03__24__713949-135-2-10
Average 93 stars, based on 17 article reviews
Mturquoise2 Cdna, supplied by Addgene inc, used in various techniques. Bioz Stars score: 93/100, based on 17 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/mturquoise2+cdna/pPalmitoyl-mTurquoise2+(Plasmid+%2336209)/bio_rxiv__64898__2026__03__24__713949-135-2-10
Average 93 stars, based on 17 article reviews
mturquoise2 cdna - by Bioz Stars,
2026-09
93/100 stars
Images
Related Articles
Construct:Article Title: Loss of intracellular ATP affects axoplasmic viscosity and pathological protein aggregation in mammalian neurons. Article Snippet: Cells were cultured in neural differentiation medium (Neurobasal medium, #A3582901, Thermo Fisher Scientific), GlutaMAX (#35050061, Thermo Fisher Scientific), Primocin, 0.1 mM nonessential amino acids, and 1% N2 supplement, supplemented with 2% B27 (#A3653401, Thermo Fisher Scientific), 25 μM glutamate (#G5889, Sigma- Aldrich), ascorbic acid (0.4 μg/ ml), glial- derived neurotrophic factor (10 ng/ml; #450- 10, PeproTech), and ciliary neurotrophic factor (10 ng/ml; #450- 13, PeproTech). hMNs were allowed to differentiate and mature for 2 to 3 weeks before experiments. cDNA constructs and transfection cGFP pCAG- AcGFP (45), vesicular glutamate transporters pCAGVenus- VGLUT2 (46), pCAG- mTurquoise2- RIM1, GW1- PercevalHR (#49082, Addgene), and pCAG- FusionRed constructs were transfected into mouse neurons by electroporation (Neon Electroporation System, Thermo Fisher Scientific) before plating, as described previously (46). .. Briefly, the pCAG- mTurquoise2- RIM1 was constructed by cloning RIM1 cDNA (#100064122, DNAFORM) and Article Title: Loss of intracellular ATP affects axoplasmic viscosity and pathological protein aggregation in mammalian neurons Article Snippet: cGFP pCAG-AcGFP , vesicular glutamate transporters pCAG-Venus-VGLUT2 , pCAG-mTurquoise2-RIM1, GW1-PercevalHR (#49082, Addgene), and pCAG-FusionRed constructs were transfected into mouse neurons by electroporation (Neon Electroporation System, Thermo Fisher Scientific) before plating, as described previously ( ). .. Briefly, the pCAG-mTurquoise2-RIM1 was constructed by cloning RIM1 cDNA (#100064122, DNAFORM) and Cloning:Article Title: Loss of intracellular ATP affects axoplasmic viscosity and pathological protein aggregation in mammalian neurons. Article Snippet: Cells were cultured in neural differentiation medium (Neurobasal medium, #A3582901, Thermo Fisher Scientific), GlutaMAX (#35050061, Thermo Fisher Scientific), Primocin, 0.1 mM nonessential amino acids, and 1% N2 supplement, supplemented with 2% B27 (#A3653401, Thermo Fisher Scientific), 25 μM glutamate (#G5889, Sigma- Aldrich), ascorbic acid (0.4 μg/ ml), glial- derived neurotrophic factor (10 ng/ml; #450- 10, PeproTech), and ciliary neurotrophic factor (10 ng/ml; #450- 13, PeproTech). hMNs were allowed to differentiate and mature for 2 to 3 weeks before experiments. cDNA constructs and transfection cGFP pCAG- AcGFP (45), vesicular glutamate transporters pCAGVenus- VGLUT2 (46), pCAG- mTurquoise2- RIM1, GW1- PercevalHR (#49082, Addgene), and pCAG- FusionRed constructs were transfected into mouse neurons by electroporation (Neon Electroporation System, Thermo Fisher Scientific) before plating, as described previously (46). .. Briefly, the pCAG- mTurquoise2- RIM1 was constructed by cloning RIM1 cDNA (#100064122, DNAFORM) and Article Title: Loss of intracellular ATP affects axoplasmic viscosity and pathological protein aggregation in mammalian neurons Article Snippet: cGFP pCAG-AcGFP , vesicular glutamate transporters pCAG-Venus-VGLUT2 , pCAG-mTurquoise2-RIM1, GW1-PercevalHR (#49082, Addgene), and pCAG-FusionRed constructs were transfected into mouse neurons by electroporation (Neon Electroporation System, Thermo Fisher Scientific) before plating, as described previously ( ). .. Briefly, the pCAG-mTurquoise2-RIM1 was constructed by cloning RIM1 cDNA (#100064122, DNAFORM) and Derivative Assay:Article Title: Intravital imaging uncovers remodelling of humanised bone marrow-like niches Article Snippet: .. Briefly, the Plasmid Preparation:Article Title: Intravital imaging uncovers remodelling of humanised bone marrow-like niches Article Snippet: .. Briefly, the |