mcherry cdna (TaKaRa)
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TaKaRa
mcherry cdna
Mcherry Cdna, supplied by TaKaRa, used in various techniques. Bioz Stars score: 96/100, based on 3286 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/mcherry+c1/pmCherry-C1+Vector/pm41565995-276-20-26
Average 96 stars, based on 3286 article reviews
Mcherry Cdna, supplied by TaKaRa, used in various techniques. Bioz Stars score: 96/100, based on 3286 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/mcherry+c1/pmCherry-C1+Vector/pm41565995-276-20-26
Average 96 stars, based on 3286 article reviews
mcherry cdna - by Bioz Stars,
2026-09
96/100 stars
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Related Articles
Plasmid Preparation:Article Title: Rho GTPase activity crosstalk mediated by Arhgef11 and Arhgef12 coordinates cell protrusion-retraction cycles Article Snippet: .. The plasmid coding for mCherry fused to β-actin, driven by the Ubiquitin-C promotor (mCherry-actin-Ub) was generated in two steps: 1. Article Title: Use of miR-18b for prevention, treatment, or diagnosis of muscle disease and neuromuscular disease Article Snippet: .. The amplified Mctp1 PCR product was cloned into Article Title: Programmable RNA base editing with photoactivatable CRISPR-Cas13 Article Snippet: .. The constructs were generated using Gibson assembly, and DNA fragments corresponding to N351-pMag, nMagHigh1-C352, nMagHigh1-C350, EGFP-N1 (Takara), and Ubiquitin Proteomics:Article Title: Rho GTPase activity crosstalk mediated by Arhgef11 and Arhgef12 coordinates cell protrusion-retraction cycles Article Snippet: .. The plasmid coding for mCherry fused to β-actin, driven by the Ubiquitin-C promotor (mCherry-actin-Ub) was generated in two steps: 1. Generated:Article Title: Rho GTPase activity crosstalk mediated by Arhgef11 and Arhgef12 coordinates cell protrusion-retraction cycles Article Snippet: .. The plasmid coding for mCherry fused to β-actin, driven by the Ubiquitin-C promotor (mCherry-actin-Ub) was generated in two steps: 1. Article Title: Programmable RNA base editing with photoactivatable CRISPR-Cas13 Article Snippet: .. The constructs were generated using Gibson assembly, and DNA fragments corresponding to N351-pMag, nMagHigh1-C352, nMagHigh1-C350, EGFP-N1 (Takara), and Amplification:Article Title: Rho GTPase activity crosstalk mediated by Arhgef11 and Arhgef12 coordinates cell protrusion-retraction cycles Article Snippet: .. The plasmid coding for mCherry fused to β-actin, driven by the Ubiquitin-C promotor (mCherry-actin-Ub) was generated in two steps: 1. Article Title: API5 Phosphorylation Promotes Antiviral Immunity by Inhibiting Degradation of Cytosolic RNA Sensor RLRs. Article Snippet: .. Construction of Plasmids and Transfection: DNA fragments encoding full-length gene were amplified from HEK293T cells and individually subcloned into the following expression vectors: pCMV-Myc-N (635 689, Clontech), pCMV-Flag-N (635 689, Clontech), pEGFP-C3 (6082-1, Clontech), Article Title: API5 Phosphorylation Promotes Antiviral Immunity by Inhibiting Degradation of Cytosolic RNA Sensor RLRs Article Snippet: .. DNA fragments encoding full‐length gene were amplified from HEK293T cells and individually subcloned into the following expression vectors: pCMV‐Myc‐N (635 689, Clontech), pCMV‐Flag‐N (635 689, Clontech), pEGFP‐C3 (6082‐1, Clontech), Article Title: Use of miR-18b for prevention, treatment, or diagnosis of muscle disease and neuromuscular disease Article Snippet: .. The amplified Mctp1 PCR product was cloned into Transfection:Article Title: API5 Phosphorylation Promotes Antiviral Immunity by Inhibiting Degradation of Cytosolic RNA Sensor RLRs. Article Snippet: .. Construction of Plasmids and Transfection: DNA fragments encoding full-length gene were amplified from HEK293T cells and individually subcloned into the following expression vectors: pCMV-Myc-N (635 689, Clontech), pCMV-Flag-N (635 689, Clontech), pEGFP-C3 (6082-1, Clontech), Expressing:Article Title: API5 Phosphorylation Promotes Antiviral Immunity by Inhibiting Degradation of Cytosolic RNA Sensor RLRs. Article Snippet: .. Construction of Plasmids and Transfection: DNA fragments encoding full-length gene were amplified from HEK293T cells and individually subcloned into the following expression vectors: pCMV-Myc-N (635 689, Clontech), pCMV-Flag-N (635 689, Clontech), pEGFP-C3 (6082-1, Clontech), Article Title: API5 Phosphorylation Promotes Antiviral Immunity by Inhibiting Degradation of Cytosolic RNA Sensor RLRs Article Snippet: .. DNA fragments encoding full‐length gene were amplified from HEK293T cells and individually subcloned into the following expression vectors: pCMV‐Myc‐N (635 689, Clontech), pCMV‐Flag‐N (635 689, Clontech), pEGFP‐C3 (6082‐1, Clontech), Article Title: KCNH6 Potassium Channel Regulates Assembling of Mitochondrial Complex I and Promotes Insulin Secretion in Islet Beta Cells Article Snippet: Mitochondrial glucose metabolism is critical for glucosestimulated insulin secretion and glucose homeostasis in pancreatic β cells.. We previously showed that KCNH6, a voltagedependent potassium (Kv) channel, participated regulation of insulin secretion in pancreatic β cells, however, its role in mitochondrial metabolism remains unclear.. Since we recently found that KCNH6 distributed in mitochondria, in this study, we investigated the role of KCNH6 in regulating mitochondrial function in pancreatic β cells by using a β cellspecific knockout (KCNH6βKO) mouse model. Proteomics analysis of islets indicated that multiple proteins involved in mitochondrial metabolism were dysregulated in islets of KCNH6βKO mice. Polymerase Chain Reaction:Article Title: The conformation of FOXM1 homodimers in vivo is crucial for regulating transcriptional activities Article Snippet: The cDNA fragments of FOXM1 NRD or TAD were PCR amplified from pCMV-FOXM1b (#SC128214, OriGene) using the respective primer pairs ( ) and Phusion High-Fidelity PCR Kit (#F553, Thermo Scientific TM ). .. The resulting PCR products were digested with EcoRI-HF (#R3101, NEW ENGLAND BioLabs) and BamHI (#R3136, NEW ENGLAND BioLabs), and then ligated into Article Title: Use of miR-18b for prevention, treatment, or diagnosis of muscle disease and neuromuscular disease Article Snippet: .. The amplified Mctp1 PCR product was cloned into Clone Assay:Article Title: Use of miR-18b for prevention, treatment, or diagnosis of muscle disease and neuromuscular disease Article Snippet: .. The amplified Mctp1 PCR product was cloned into Construct:Article Title: Use of miR-18b for prevention, treatment, or diagnosis of muscle disease and neuromuscular disease Article Snippet: .. The amplified Mctp1 PCR product was cloned into Article Title: Programmable RNA base editing with photoactivatable CRISPR-Cas13 Article Snippet: .. The constructs were generated using Gibson assembly, and DNA fragments corresponding to N351-pMag, nMagHigh1-C352, nMagHigh1-C350, EGFP-N1 (Takara), and |
