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384 well bio rad qpcr clear plate  (Bio-Rad)


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    Structured Review

    Bio-Rad 384 well bio rad qpcr clear plate

    384 Well Bio Rad Qpcr Clear Plate, supplied by Bio-Rad, used in various techniques. Bioz Stars score: 94/100, based on 51 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/384 well bio rad qpcr clear plate/product/Bio-Rad
    Average 94 stars, based on 51 article reviews
    384 well bio rad qpcr clear plate - by Bioz Stars, 2026-02
    94/100 stars

    Images

    1) Product Images from "Protocol for single-cell isolation and genome amplification of environmental microbial eukaryotes for genomic analysis"

    Article Title: Protocol for single-cell isolation and genome amplification of environmental microbial eukaryotes for genomic analysis

    Journal: STAR Protocols

    doi: 10.1016/j.xpro.2021.100968


    Figure Legend Snippet:

    Techniques Used: Recombinant, SYBR Green Assay, Amplification, Purification, Software, Sequencing, Sterility, Suction Filtration, Transferring, Real-time Polymerase Chain Reaction, Microscopy



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    Image Search Results


    Journal: STAR Protocols

    Article Title: Protocol for single-cell isolation and genome amplification of environmental microbial eukaryotes for genomic analysis

    doi: 10.1016/j.xpro.2021.100968

    Figure Lengend Snippet:

    Article Snippet: Verify under the microscope that the desired organism was sorted and the cleanliness of the enrichment. g. Insert the single-cell clean (10–15 min UV sterilized in the Stratalinker 2400) 384-well Bio Rad qPCR clear plate, into the plate holder∗.

    Techniques: Recombinant, SYBR Green Assay, Amplification, Purification, Software, Sequencing, Sterility, Suction Filtration, Transferring, Real-time Polymerase Chain Reaction, Microscopy

    Figure 1. CFX plate loading scheme. Shown is the pipetting strategy for the transfer of extracted RNA from the 96-well elution plate to the 384-well qPCR plate using a 12-channel pipette in order to run a full plate RT-qPCR experiment that includes 88 samples measured with three primer/probe sets like N1 (blue), N2 (orange) and RP (purple). Four dilutions (105, 104, 103, and 102 copies) of the RNA control as well as two no-template control reactions (NTC) for each primer/probe set are included.

    Journal: Viruses

    Article Title: Processing Hundreds of SARS-CoV-2 Samples with an In-House PCR-Based Method without Robotics.

    doi: 10.3390/v13091712

    Figure Lengend Snippet: Figure 1. CFX plate loading scheme. Shown is the pipetting strategy for the transfer of extracted RNA from the 96-well elution plate to the 384-well qPCR plate using a 12-channel pipette in order to run a full plate RT-qPCR experiment that includes 88 samples measured with three primer/probe sets like N1 (blue), N2 (orange) and RP (purple). Four dilutions (105, 104, 103, and 102 copies) of the RNA control as well as two no-template control reactions (NTC) for each primer/probe set are included.

    Article Snippet: The RT-qPCR reactions were set up in an optical 384-well plate (Bio-Rad, Hercules, CA, USA, #HSP3865) on ice and sealed with adhesive optical clear qPCR plate seals (Bio-Rad, #MSB1001), briefly mixed and centrifuged for 2 min at 2000× g. The RT-qPCR run was performed using a CFX384 Real-Time System type C1000 thermocycler (Bio-Rad) with the following thermal conditions: 25 ◦C for 2 min, Viruses 2021, 13, 1712 5 of 16 50 ◦C for 20 min, 95 ◦C for 3 min and 45 cycles of 95 ◦C for 15 s and 58 ◦C for 10 s including a plate read to detect for the FAM/Cy5/HEX signal, depending on the probes used.

    Techniques: Transferring, Quantitative RT-PCR, Control