lightcycler 480 sw 1 5 1 (Roche)
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99
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Roche
lightcycler 480 sw 1 5 1
Lightcycler 480 Sw 1 5 1, supplied by Roche, used in various techniques. Bioz Stars score: 99/100, based on 6 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/lightcycler+480+sw+1+5/LightCycler+480+System/pm41985846-141-20-18
Average 99 stars, based on 6 article reviews
Lightcycler 480 Sw 1 5 1, supplied by Roche, used in various techniques. Bioz Stars score: 99/100, based on 6 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/lightcycler+480+sw+1+5/LightCycler+480+System/pm41985846-141-20-18
Average 99 stars, based on 6 article reviews
lightcycler 480 sw 1 5 1 - by Bioz Stars,
2026-09
99/100 stars
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Software:Article Title: The myosin motor domain-containing chitin synthase PdChsVII is required for development, cell wall integrity and virulence in the citrus postharvest pathogen Penicillium digitatum. Article Snippet: .. The quantification cycle point (Ct) was obtained using the software Article Title: The type of carbon source not the growth rate it supports can determine diauxie in Saccharomyces cerevisiae Article Snippet: .. We used the manufacturer’s software (Roche Article Title: Penicilliumdigitatum MFS transporters can display different roles during pathogen-fruit interaction. Article Snippet: Major facilitator superfamily (MFS) comprises a large family of fungal transporters.. In this work four Penicillium digitatum MFS transporters named PdMFS2–5 were identified and functionally characterized through gene elimination and gene overexpression with aim of unveil the similarities and differences among members of the same family during pathogen-fruit interaction.. Fungal mutants in which each of the MFS transporters were individually deleted, displayed a clear effect on their infective capacity during citrus fruit infection especially in two of them. Article Title: Involvement of Penicillium digitatum PdSUT1 in fungicide sensitivity and virulence during citrus fruit infection. Article Snippet: Oligos SUT14-SUT15 were used for the PdSUT1 gene, and genes coding for fungal β-tubulin (qTubF-qTubR), ribosomal protein 28S (q28SF-q28SR) and histone H3 (qH3F-qH3R) were simultaneously used as independent reference genes (Table 1). .. The quantification cycle point (Cq) was obtained using the software Article Title: Rapid screening for sickle cell disease by polymerase chain reaction-high resolution melting analysis. Article Snippet: .. HRM analysis was performed using the software Real-time Polymerase Chain Reaction:Article Title: In vitro model of human subcutaneous adipocyte spheroids for studying mitochondrial dysfunction and mitochondria activating compounds Article Snippet: RT-qPCR was conducted according to the manufacturer’s protocol with SYBR Green Master Mix (K0252, Thermo Fisher Scientific) and the template amount used was 2 ng per well. .. The amount of mitochondrial CYTB , DLOOP and 16S as well as genomic HBB , APP and B2M were analysed using LightCycler® 480 System (Roche Diagnostics AG, Basel, Switzerland) combined with Maestro Software:Article Title: In vitro model of human subcutaneous adipocyte spheroids for studying mitochondrial dysfunction and mitochondria activating compounds Article Snippet: RT-qPCR was conducted according to the manufacturer’s protocol with SYBR Green Master Mix (K0252, Thermo Fisher Scientific) and the template amount used was 2 ng per well. .. The amount of mitochondrial CYTB , DLOOP and 16S as well as genomic HBB , APP and B2M were analysed using LightCycler® 480 System (Roche Diagnostics AG, Basel, Switzerland) combined with Functional Assay:Article Title: Microbes mediating the sulfur cycle in the Atlantic Ocean and their link to chemolithoautotrophy. Article Snippet: The extraction was performed using the Ultraclean soil DNA isolation kit (Mobio) following the manufacturer’s protocol. .. q-PCR was used to evaluate the abundance of two cbbM genes encoding the RuBisCO form II, subsequently named cbbM65 and cbbM68 according to the primer sets used (Swan et al., 2011), and the aprA gene encoding the alpha subunit of APS. cbbM65 and cbbM68 cover the two main clusters of cbbM (rubisco form II) (Swan et al., 2011), and were specifically developed for q-PCR. q-PCR was conducted in triplicate for all functional genes on a |