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sv40pa n500r phusion high fidelity pcr master mix  (New England Biolabs)


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    Structured Review

    New England Biolabs sv40pa n500r phusion high fidelity pcr master mix
    In PCR #1, a 500 bp test sequence and 225 bp <t>SV40PA</t> sequence are added to the same reaction to form a test sequence-SV40PA combined construct. In PCR #2, the PCR #1 product and a 600 bp CMV Promoter are added to the same reaction to form the full minigene construct. Overlapping, homologous regions of these gene fragments allow for assembly to occur.
    Sv40pa N500r Phusion High Fidelity Pcr Master Mix, supplied by New England Biolabs, used in various techniques. Bioz Stars score: 99/100, based on 805 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/gc+buffer/Phusion+High-Fidelity+PCR+Master+Mix+with+GC+Buffer/pmc06054316-615-25-34
    Average 99 stars, based on 805 article reviews
    sv40pa n500r phusion high fidelity pcr master mix - by Bioz Stars, 2026-11
    99/100 stars

    Images

    1) Product Images from "In vivo and In vitro methods to identify DNA sequence variants that alter RNA Splicing"

    Article Title: In vivo and In vitro methods to identify DNA sequence variants that alter RNA Splicing

    Journal: Current protocols in human genetics

    doi: 10.1002/cphg.60

    In PCR #1, a 500 bp test sequence and 225 bp SV40PA sequence are added to the same reaction to form a test sequence-SV40PA combined construct. In PCR #2, the PCR #1 product and a 600 bp CMV Promoter are added to the same reaction to form the full minigene construct. Overlapping, homologous regions of these gene fragments allow for assembly to occur.
    Figure Legend Snippet: In PCR #1, a 500 bp test sequence and 225 bp SV40PA sequence are added to the same reaction to form a test sequence-SV40PA combined construct. In PCR #2, the PCR #1 product and a 600 bp CMV Promoter are added to the same reaction to form the full minigene construct. Overlapping, homologous regions of these gene fragments allow for assembly to occur.

    Techniques Used: Sequencing, Construct

    gBlocks and other primers used in laboratory protocols
    Figure Legend Snippet: gBlocks and other primers used in laboratory protocols

    Techniques Used: Sequencing, Multiplexing, Amplification

    PCR #1 set up. Repeat for as many gBlocks as are required.
    Figure Legend Snippet: PCR #1 set up. Repeat for as many gBlocks as are required.

    Techniques Used: Concentration Assay, Sequencing, Construct

    15 lanes containing independent PCR #1 products are shown. Each band is approximately 650-700 bp in size, and represents an individual test sequence (500 bp) attached to a SV40PA signal (225 bp). Note that products seem to be migrating to the same positions in pairs, as would be expected with reference and alternate containing test sequences that have identical lengths.
    Figure Legend Snippet: 15 lanes containing independent PCR #1 products are shown. Each band is approximately 650-700 bp in size, and represents an individual test sequence (500 bp) attached to a SV40PA signal (225 bp). Note that products seem to be migrating to the same positions in pairs, as would be expected with reference and alternate containing test sequences that have identical lengths.

    Techniques Used: Sequencing

    PCR #2 set up. Repeat for as many gBlocks as are required.
    Figure Legend Snippet: PCR #2 set up. Repeat for as many gBlocks as are required.

    Techniques Used: Concentration Assay

    Amplification of CMVp-N500
    Figure Legend Snippet: Amplification of CMVp-N500

    Techniques Used: Amplification, Concentration Assay, Sequencing

    Related Articles

    Amplification:

    Article Title: How Bacterial Growth-Phase Reshapes Synthetic Gene Circuit Function
    Article Snippet: DNA oligos and genes were ordered using the Oligo Rapid Service from Azenta Life Sciences. .. DNA fragments to be assembled were amplified by PCR using Phusion High-Fidelity PCR Master Mix with GC Buffer (NEB, M0532S). ..

    Article Title: Yupingfeng powder attenuates influenza A virus induced lung injury via gut microbiota-dependent modulation of branched-chain amino acid metabolism and macrophage polarization
    Article Snippet: .. PCR amplification was performed using barcode-specific primers, Phusion High-Fidelity PCR Master Mix with GC Buffer, and efficient high-fidelity enzymes (New England Biolabs, Beijing, China). .. SMRT Bell libraries were constructed, and sequencing was performed on the PacBio platform by Novogene Co., Ltd. (Beijing, China) following standard protocols.

    Article Title: Analysis of rumen fermentation, bacterial diversity and blood biochemical parameters in sheep fed with cotton straw and different roughage combinations
    Article Snippet: .. The polymerase chain reaction (PCR) amplification used specific barcoded primers: forward primer 338F (5′-ACTCCTACGGGAGGCAGCAG-3′) and reverse primer 806R (5′-GGACTACHVGGGTWTCTAAT-3′) with the Phusion High-Fidelity PCR master mix with GC buffer (New England Biolabs). ..

    Article Title: Comparative Analysis of the EF-1α Intergenic Region in Babesia divergens Isolates: Insights into TA Repeat Variation and Potential Regulatory Implications
    Article Snippet: All primers were designed using the Primer QuestTM Tool ( https://www.idtdna.com/pages/tools/primerquest , accessed on 9 May 2023) ( ). .. PCR amplification was carried out using Phusion ® High-Fidelity PCR Master Mix with GC Buffer (M0532S; New England Biolabs, Ipswich, MA, USA). ..

    Article Title: Soil Fertility Differences and Bacterial and Fungal Community Variation Among Subtropical Forest Stands Dominated by Different Tree Species
    Article Snippet: .. PCR amplification was performed using barcode-tagged primers and Phusion HighFidelity PCR Master Mix with GC Buffer (New England Biolabs, Ipswich, MA, USA). .. PCR products were checked by agarose gel electrophoresis, and qualified amplicons were purified using a Qiagen Gel Extraction Kit (Qiagen, Hilden, Germany).

    Article Title: Comparative Analysis of the EF-1α Intergenic Region in Babesia divergens Isolates: Insights into TA Repeat Variation and Potential Regulatory Implications.
    Article Snippet: All primers were designed using the Primer QuestTM Tool (https://www.idtdna.com/ pages/tools/primerquest, accessed on 9 May 2023) (Table S1 and Figure S4). .. PCR amplification was carried out using Phusion® High-Fidelity PCR Master Mix with GC Buffer (M0532S; New England Biolabs, Ipswich, MA, USA). ..

    Polymerase Chain Reaction:

    Article Title: How Bacterial Growth-Phase Reshapes Synthetic Gene Circuit Function
    Article Snippet: DNA oligos and genes were ordered using the Oligo Rapid Service from Azenta Life Sciences. .. DNA fragments to be assembled were amplified by PCR using Phusion High-Fidelity PCR Master Mix with GC Buffer (NEB, M0532S). ..

    Article Title: Yupingfeng powder attenuates influenza A virus induced lung injury via gut microbiota-dependent modulation of branched-chain amino acid metabolism and macrophage polarization
    Article Snippet: .. PCR amplification was performed using barcode-specific primers, Phusion High-Fidelity PCR Master Mix with GC Buffer, and efficient high-fidelity enzymes (New England Biolabs, Beijing, China). .. SMRT Bell libraries were constructed, and sequencing was performed on the PacBio platform by Novogene Co., Ltd. (Beijing, China) following standard protocols.

    Article Title: Analysis of rumen fermentation, bacterial diversity and blood biochemical parameters in sheep fed with cotton straw and different roughage combinations
    Article Snippet: .. The polymerase chain reaction (PCR) amplification used specific barcoded primers: forward primer 338F (5′-ACTCCTACGGGAGGCAGCAG-3′) and reverse primer 806R (5′-GGACTACHVGGGTWTCTAAT-3′) with the Phusion High-Fidelity PCR master mix with GC buffer (New England Biolabs). ..

    Article Title: Comparative Analysis of the EF-1α Intergenic Region in Babesia divergens Isolates: Insights into TA Repeat Variation and Potential Regulatory Implications
    Article Snippet: All primers were designed using the Primer QuestTM Tool ( https://www.idtdna.com/pages/tools/primerquest , accessed on 9 May 2023) ( ). .. PCR amplification was carried out using Phusion ® High-Fidelity PCR Master Mix with GC Buffer (M0532S; New England Biolabs, Ipswich, MA, USA). ..

    Article Title: Soil Fertility Differences and Bacterial and Fungal Community Variation Among Subtropical Forest Stands Dominated by Different Tree Species
    Article Snippet: .. PCR amplification was performed using barcode-tagged primers and Phusion HighFidelity PCR Master Mix with GC Buffer (New England Biolabs, Ipswich, MA, USA). .. PCR products were checked by agarose gel electrophoresis, and qualified amplicons were purified using a Qiagen Gel Extraction Kit (Qiagen, Hilden, Germany).

    Article Title: Taxonomic shifts in bacterial communities of mine tailings suggest persistence of chemolithotrophic traits under oligotrophic and metal-rich conditions
    Article Snippet: .. PCR reactions were performed with Phusion High-Fidelity PCR Master Mix (New England Biolabs, Ipswich, MA) and GC Buffer under the following conditions: initial denaturation at 94 °C for 3 min (1 cycle), followed by 35 cycles of 94 °C for 45 s, 50 °C for 60 s, and 72 °C for 90 s, with a final extension at 72 °C for 10 min. PCR products were purified using the Qiagen gel extraction kit (Qiagen, Hilden, Germany) and sequenced on the Illumina MiSeq platform with a v3 chemistry kit. ..

    Article Title: Comparative Analysis of the EF-1α Intergenic Region in Babesia divergens Isolates: Insights into TA Repeat Variation and Potential Regulatory Implications.
    Article Snippet: All primers were designed using the Primer QuestTM Tool (https://www.idtdna.com/ pages/tools/primerquest, accessed on 9 May 2023) (Table S1 and Figure S4). .. PCR amplification was carried out using Phusion® High-Fidelity PCR Master Mix with GC Buffer (M0532S; New England Biolabs, Ipswich, MA, USA). ..

    Gas Chromatography:

    Article Title: How Bacterial Growth-Phase Reshapes Synthetic Gene Circuit Function
    Article Snippet: DNA oligos and genes were ordered using the Oligo Rapid Service from Azenta Life Sciences. .. DNA fragments to be assembled were amplified by PCR using Phusion High-Fidelity PCR Master Mix with GC Buffer (NEB, M0532S). ..

    Article Title: Yupingfeng powder attenuates influenza A virus induced lung injury via gut microbiota-dependent modulation of branched-chain amino acid metabolism and macrophage polarization
    Article Snippet: .. PCR amplification was performed using barcode-specific primers, Phusion High-Fidelity PCR Master Mix with GC Buffer, and efficient high-fidelity enzymes (New England Biolabs, Beijing, China). .. SMRT Bell libraries were constructed, and sequencing was performed on the PacBio platform by Novogene Co., Ltd. (Beijing, China) following standard protocols.

    Article Title: Analysis of rumen fermentation, bacterial diversity and blood biochemical parameters in sheep fed with cotton straw and different roughage combinations
    Article Snippet: .. The polymerase chain reaction (PCR) amplification used specific barcoded primers: forward primer 338F (5′-ACTCCTACGGGAGGCAGCAG-3′) and reverse primer 806R (5′-GGACTACHVGGGTWTCTAAT-3′) with the Phusion High-Fidelity PCR master mix with GC buffer (New England Biolabs). ..

    Article Title: Soil Fertility Differences and Bacterial and Fungal Community Variation Among Subtropical Forest Stands Dominated by Different Tree Species
    Article Snippet: .. PCR amplification was performed using barcode-tagged primers and Phusion HighFidelity PCR Master Mix with GC Buffer (New England Biolabs, Ipswich, MA, USA). .. PCR products were checked by agarose gel electrophoresis, and qualified amplicons were purified using a Qiagen Gel Extraction Kit (Qiagen, Hilden, Germany).

    Article Title: Taxonomic shifts in bacterial communities of mine tailings suggest persistence of chemolithotrophic traits under oligotrophic and metal-rich conditions
    Article Snippet: .. PCR reactions were performed with Phusion High-Fidelity PCR Master Mix (New England Biolabs, Ipswich, MA) and GC Buffer under the following conditions: initial denaturation at 94 °C for 3 min (1 cycle), followed by 35 cycles of 94 °C for 45 s, 50 °C for 60 s, and 72 °C for 90 s, with a final extension at 72 °C for 10 min. PCR products were purified using the Qiagen gel extraction kit (Qiagen, Hilden, Germany) and sequenced on the Illumina MiSeq platform with a v3 chemistry kit. ..

    Purification:

    Article Title: Taxonomic shifts in bacterial communities of mine tailings suggest persistence of chemolithotrophic traits under oligotrophic and metal-rich conditions
    Article Snippet: .. PCR reactions were performed with Phusion High-Fidelity PCR Master Mix (New England Biolabs, Ipswich, MA) and GC Buffer under the following conditions: initial denaturation at 94 °C for 3 min (1 cycle), followed by 35 cycles of 94 °C for 45 s, 50 °C for 60 s, and 72 °C for 90 s, with a final extension at 72 °C for 10 min. PCR products were purified using the Qiagen gel extraction kit (Qiagen, Hilden, Germany) and sequenced on the Illumina MiSeq platform with a v3 chemistry kit. ..

    Gel Extraction:

    Article Title: Taxonomic shifts in bacterial communities of mine tailings suggest persistence of chemolithotrophic traits under oligotrophic and metal-rich conditions
    Article Snippet: .. PCR reactions were performed with Phusion High-Fidelity PCR Master Mix (New England Biolabs, Ipswich, MA) and GC Buffer under the following conditions: initial denaturation at 94 °C for 3 min (1 cycle), followed by 35 cycles of 94 °C for 45 s, 50 °C for 60 s, and 72 °C for 90 s, with a final extension at 72 °C for 10 min. PCR products were purified using the Qiagen gel extraction kit (Qiagen, Hilden, Germany) and sequenced on the Illumina MiSeq platform with a v3 chemistry kit. ..



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