dapi staining solution (Sangon Biotech)
86
Structured Review
Sangon Biotech
dapi staining solution
Dapi Staining Solution, supplied by Sangon Biotech, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/dapi+solution/dapi+solution+staining/pm42123883-145-2-5
Average 86 stars, based on 1 article reviews
Dapi Staining Solution, supplied by Sangon Biotech, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/dapi+solution/dapi+solution+staining/pm42123883-145-2-5
Average 86 stars, based on 1 article reviews
dapi staining solution - by Bioz Stars,
2026-10
86/100 stars
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Staining:Article Title: Enterohemorrhagic Escherichia coli senses colonic oxygen availability to modulate its virulence and colonization Article Snippet: .. Article Title: An Immune Microenvironment-Integrated Intestinal-on-a-Chip Model for Investigating Immunopathogenesis in Inflammatory Bowel Disease. Article Snippet: .. Finally, add Article Title: The calcium ion channel protein TRPML is indispensable to the reproduction of Nilaparvata lugens and the transovarial transmission of its yeast-like symbionts. Article Snippet: The secondary antibody was a goat anti-rabbit IgG antibody conjugated with Dylight 488 fluorescent dye (Abbkine, Atlanta, GA, USA). .. Nuclei were stained with Article Title: Harnessing the yeast nucleus for the efficient production of valuable monoterpenes. Article Snippet: Subcellular engineering emerges as a pivotal strategy to amplify terpene production in yeast cell factories.. The yeast nucleus, which shares acetyl-CoA pool with the cytosol and maintains nuclear membrane integrity during mitosis, offers unique compartmentalization capabilities.. Despite these attributes, there is a notable absence of research harnessing the potential of the yeast nucleus for subcellular engineering. Article Title: An Immune Microenvironment-Integrated Intestinal-on-a-Chip Model for Investigating Immunopathogenesis in Inflammatory Bowel Disease Article Snippet: .. Finally, add Article Title: TRIM47 Regulates Energy Metabolism via Glycolytic Reprogramming to Drive Hepatocellular Carcinoma Progression and Represents an Efficient Therapeutic Target Article Snippet: Meanwhile, experimental cells were seeded in confocal dishes (Thermo Fisher Scientific, USA) at a density of 20%–30% and cultured overnight in a sugar‐free medium. .. The cells were subsequently incubated in glucose‐free DMEM containing 20 μ m 2‐NBDG (Thermo Fisher Scientific, USA) for 2 h. After being washed with PBS, the cells were fixed with 4% paraformaldehyde, and a Article Title: Rapid detection of Streptococcus agalactiae in tilapia using RPA-PfAgo detection systems Article Snippet: Streptococcus agalactiae (GBS), a leading tilapia pathogen, causes high mortality with frequent asymptomatic infections, complicating early detection.. The study focused on GBS and employed recombinase polymerase amplification (RPA) technology in conjunction with Pyrococcus furiosus Argonaute (PfAgo) to establish real-time fluorescent RPA-PfAgo (RPA-PfAgo-RTF) and lateral flow strip-based RPA-PfAgo assay (RPA-PfAgo-LFD).. The conserved cfb gene was selected for the design and screening of primers, gDNAs, and molecular beacons. other:Article Title: Deciphering OCT4A-dose-dependent transcriptional profiles associated with tumorigenic potential in somatic cancer cells. Article Snippet: Thereafter, cells were incubated with anti-OCT4A (Cell Signaling Technology 2890S) at 4°C overnight. Incubation:Article Title: TRIM47 Regulates Energy Metabolism via Glycolytic Reprogramming to Drive Hepatocellular Carcinoma Progression and Represents an Efficient Therapeutic Target Article Snippet: Meanwhile, experimental cells were seeded in confocal dishes (Thermo Fisher Scientific, USA) at a density of 20%–30% and cultured overnight in a sugar‐free medium. .. The cells were subsequently incubated in glucose‐free DMEM containing 20 μ m 2‐NBDG (Thermo Fisher Scientific, USA) for 2 h. After being washed with PBS, the cells were fixed with 4% paraformaldehyde, and a Polymerase Chain Reaction:Article Title: Rapid detection of Streptococcus agalactiae in tilapia using RPA-PfAgo detection systems Article Snippet: Streptococcus agalactiae (GBS), a leading tilapia pathogen, causes high mortality with frequent asymptomatic infections, complicating early detection.. The study focused on GBS and employed recombinase polymerase amplification (RPA) technology in conjunction with Pyrococcus furiosus Argonaute (PfAgo) to establish real-time fluorescent RPA-PfAgo (RPA-PfAgo-RTF) and lateral flow strip-based RPA-PfAgo assay (RPA-PfAgo-LFD).. The conserved cfb gene was selected for the design and screening of primers, gDNAs, and molecular beacons. Plasmid Preparation:Article Title: Rapid detection of Streptococcus agalactiae in tilapia using RPA-PfAgo detection systems Article Snippet: Streptococcus agalactiae (GBS), a leading tilapia pathogen, causes high mortality with frequent asymptomatic infections, complicating early detection.. The study focused on GBS and employed recombinase polymerase amplification (RPA) technology in conjunction with Pyrococcus furiosus Argonaute (PfAgo) to establish real-time fluorescent RPA-PfAgo (RPA-PfAgo-RTF) and lateral flow strip-based RPA-PfAgo assay (RPA-PfAgo-LFD).. The conserved cfb gene was selected for the design and screening of primers, gDNAs, and molecular beacons. DNA Extraction:Article Title: Rapid detection of Streptococcus agalactiae in tilapia using RPA-PfAgo detection systems Article Snippet: Streptococcus agalactiae (GBS), a leading tilapia pathogen, causes high mortality with frequent asymptomatic infections, complicating early detection.. The study focused on GBS and employed recombinase polymerase amplification (RPA) technology in conjunction with Pyrococcus furiosus Argonaute (PfAgo) to establish real-time fluorescent RPA-PfAgo (RPA-PfAgo-RTF) and lateral flow strip-based RPA-PfAgo assay (RPA-PfAgo-LFD).. The conserved cfb gene was selected for the design and screening of primers, gDNAs, and molecular beacons. |
