lightcycler 96 application software (Roche)
Roche manufactures this product 
99
Structured Review
Roche
lightcycler 96 application software
Lightcycler 96 Application Software, 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+96+application+software/LightCycler+480+System/pm41348853-104-11-15
Average 99 stars, based on 6 article reviews
Lightcycler 96 Application Software, 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+96+application+software/LightCycler+480+System/pm41348853-104-11-15
Average 99 stars, based on 6 article reviews
lightcycler 96 application software - by Bioz Stars,
2026-09
99/100 stars
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Amplification:Article Title: Reversing transgene silencing via targeted chromatin editing Article Snippet: .. Melt curve analysis was performed to verify a single amplification product, and the Article Title: Analog epigenetic memory revealed by targeted chromatin editing Article Snippet: The qPCRs were performed using Power SYBR Green PCR Master Mix (Applied Biosystems) and primers in using a LightCycler 96 (Roche). .. Melt curves were used to confirm a single amplification product and the Software:Article Title: Reversing transgene silencing via targeted chromatin editing Article Snippet: .. Melt curve analysis was performed to verify a single amplification product, and the Article Title: Development and validation of a quantitative real-time PCR assay for the enumeration of Clostridium sporogenes in NaCl- and nitrite-reduced meat products. Article Snippet: .. To analyse the raw data of each PCR run and create standard curves, the Article Title: Development and validation of a quantitative real-time PCR assay for the enumeration of Clostridium sporogenes in NaCl- and nitrite-reduced meat products. Article Snippet: PLOS One | https://doi.org/10.1371/journal.pone.0337645 December 5, 2025 6 / 16 To exclude cross-contamination and to ensure the PCR reaction was conducted properly, a negative control with 2 μL nuclease-free water (Qiagen GmbH) as template and a positive control with 2 ng DNA of C. sporogenes DSM 795 were included in each PCR run. .. The raw data of each PCR run were analysed using the Article Title: Development and validation of a quantitative real-time PCR assay for the enumeration of Clostridium sporogenes in NaCl- and nitrite-reduced meat products Article Snippet: .. To analyse the raw data of each PCR run and create standard curves, the Article Title: Analog epigenetic memory revealed by targeted chromatin editing Article Snippet: The qPCRs were performed using Power SYBR Green PCR Master Mix (Applied Biosystems) and primers in using a LightCycler 96 (Roche). .. Melt curves were used to confirm a single amplification product and the Article Title: Article Snippet: .. The obtained qPCR data were analyzed using the Article Title: Development and validation of a quantitative real-time PCR assay for the enumeration of Clostridium sporogenes in NaCl- and nitrite-reduced meat products Article Snippet: To exclude cross-contamination and to ensure the PCR reaction was conducted properly, a negative control with 2 μL nuclease-free water (Qiagen GmbH) as template and a positive control with 2 ng DNA of C. sporogenes DSM 795 were included in each PCR run. .. The raw data of each PCR run were analysed using the Article Title: Uncovering the Pathogenic Mechanisms of Cronobacter turicensis: A Dual Transcriptomics Study Using a Zebrafish Larvae Model. Article Snippet: .. Data were analyzed using the Polymerase Chain Reaction:Article Title: Development and validation of a quantitative real-time PCR assay for the enumeration of Clostridium sporogenes in NaCl- and nitrite-reduced meat products. Article Snippet: .. To analyse the raw data of each PCR run and create standard curves, the Article Title: Development and validation of a quantitative real-time PCR assay for the enumeration of Clostridium sporogenes in NaCl- and nitrite-reduced meat products. Article Snippet: PLOS One | https://doi.org/10.1371/journal.pone.0337645 December 5, 2025 6 / 16 To exclude cross-contamination and to ensure the PCR reaction was conducted properly, a negative control with 2 μL nuclease-free water (Qiagen GmbH) as template and a positive control with 2 ng DNA of C. sporogenes DSM 795 were included in each PCR run. .. The raw data of each PCR run were analysed using the Article Title: Development and validation of a quantitative real-time PCR assay for the enumeration of Clostridium sporogenes in NaCl- and nitrite-reduced meat products Article Snippet: .. To analyse the raw data of each PCR run and create standard curves, the Article Title: Development and validation of a quantitative real-time PCR assay for the enumeration of Clostridium sporogenes in NaCl- and nitrite-reduced meat products Article Snippet: To exclude cross-contamination and to ensure the PCR reaction was conducted properly, a negative control with 2 μL nuclease-free water (Qiagen GmbH) as template and a positive control with 2 ng DNA of C. sporogenes DSM 795 were included in each PCR run. .. The raw data of each PCR run were analysed using the Real-time Polymerase Chain Reaction:Article Title: Article Snippet: .. The obtained qPCR data were analyzed using the |