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rtl-plus buffer  (Qiagen)


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    Structured Review

    Qiagen rtl-plus buffer
    Rtl Plus Buffer, supplied by Qiagen, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/rtl+plus+buffer/rtl+plus+buffer/pmc10998374-43-11-13
    Average 90 stars, based on 1 article reviews
    rtl-plus buffer - by Bioz Stars, 2026-10
    90/100 stars

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    Related Articles

    Derivative Assay:

    Article Title: Multiomic QTL mapping reveals phenotypic complexity of GWAS loci and prioritizes putative causal variants.
    Article Snippet: Harvesting of material for molecular assays. (1) At D15, 107 PPCs derived from 106 iPSC clones from 106 individuals, pellets were collected and frozen in RTL plus buffer (Qiagen) for the RNA-seq assay. (2) At D15, 109 PPCs derived from 108 iPSC clones from 108 individuals were collected and frozen as nuclear pellets for the ATAC-seq assay. (3) H3K27ac ChIP-seq assay was not performed for the PPCs, however, we have frozen samples, and this dataset could be added in the future. .. Harvesting of material for molecular assays. (1) At D15, 107 PPCs derived from 106 iPSC clones from 106 individuals, pellets were collected and frozen in RTL plus buffer (Qiagen) for the RNA-seq assay. (2) At D15, 109 PPCs derived from 108 iPSC clones from 108 individuals were collected and frozen as nuclear pellets for the ATAC-seq assay. (3) H3K27ac ChIP-seq assay was not performed for the PPCs, however, we have frozen samples, and this dataset could be added in the future. ..

    Article Title: Complex regulatory networks influence pluripotent cell state transitions in human iPSCs.
    Article Snippet: Emerging hiPSC colonies were manually picked after Day 21 and maintained on Matrigel (BD Corning) with mTeSR1 medium (Stem Cell Technologies). .. Multiple independently established hiPSC clones (i.e. referred to as lines) were derived from each individual, which were cultured typically to passage 12, and at least ten stock vials were frozen from each cell line. hiPSC pellets collected from each cell line were frozen in RTL plus buffer (Qiagen) and used for total RNA isolation. ..

    Article Title: Complex regulatory networks influence pluripotent cell state transitions in human iPSCs
    Article Snippet: Emerging hiPSC colonies were manually picked after Day 21 and maintained on Matrigel (BD Corning) with mTeSR1 medium (Stem Cell Technologies). .. Multiple independently established hiPSC clones (i.e. referred to as lines) were derived from each individual, which were cultured typically to passage 12, and at least ten stock vials were frozen from each cell line. hiPSC pellets collected from each cell line were frozen in RTL plus buffer (Qiagen) and used for total RNA isolation. ..

    Article Title: Multiomic QTL mapping reveals phenotypic complexity of GWAS loci and prioritizes putative causal variants
    Article Snippet: Stained cells were acquired using BD FACSCanto II system (BD Biosciences) and the fraction of cTnT-positive cells were calculated using FlowJo software version 10.2. .. Harvesting of material for molecular assays. (1) At D0 of the CVPC differentiation, 142 iPSC lines from 129 individuals were collected and frozen as nuclear pellets for the ATAC-seq assay∗∗. (2) At D0 of the CVPC differentiation, 43 iPSC lines from 41 individuals were collected and frozen as nuclear pellets for the H3K27ac ChIP-seq assay∗∗. (3) At D25, 178 CVPCs derived from 147 iPSC clones from 137 individuals, pellets were collected and frozen in RTL plus buffer (Qiagen) for the RNA-seq assay. (4) At D25, 140 CVPCs derived from 132 iPSC clones from 124 individuals were collected and frozen as nuclear pellets for the ATAC-seq assay. (5) At D25, 101 CVPCs derived from 97 iPSC clones from 96 individuals were collected and cross-linked for the H3K27ac ChIP-seq assay. ..

    Clone Assay:

    Article Title: Multiomic QTL mapping reveals phenotypic complexity of GWAS loci and prioritizes putative causal variants.
    Article Snippet: Harvesting of material for molecular assays. (1) At D15, 107 PPCs derived from 106 iPSC clones from 106 individuals, pellets were collected and frozen in RTL plus buffer (Qiagen) for the RNA-seq assay. (2) At D15, 109 PPCs derived from 108 iPSC clones from 108 individuals were collected and frozen as nuclear pellets for the ATAC-seq assay. (3) H3K27ac ChIP-seq assay was not performed for the PPCs, however, we have frozen samples, and this dataset could be added in the future. .. Harvesting of material for molecular assays. (1) At D15, 107 PPCs derived from 106 iPSC clones from 106 individuals, pellets were collected and frozen in RTL plus buffer (Qiagen) for the RNA-seq assay. (2) At D15, 109 PPCs derived from 108 iPSC clones from 108 individuals were collected and frozen as nuclear pellets for the ATAC-seq assay. (3) H3K27ac ChIP-seq assay was not performed for the PPCs, however, we have frozen samples, and this dataset could be added in the future. ..

    Article Title: Complex regulatory networks influence pluripotent cell state transitions in human iPSCs.
    Article Snippet: Emerging hiPSC colonies were manually picked after Day 21 and maintained on Matrigel (BD Corning) with mTeSR1 medium (Stem Cell Technologies). .. Multiple independently established hiPSC clones (i.e. referred to as lines) were derived from each individual, which were cultured typically to passage 12, and at least ten stock vials were frozen from each cell line. hiPSC pellets collected from each cell line were frozen in RTL plus buffer (Qiagen) and used for total RNA isolation. ..

    Article Title: Complex regulatory networks influence pluripotent cell state transitions in human iPSCs
    Article Snippet: Emerging hiPSC colonies were manually picked after Day 21 and maintained on Matrigel (BD Corning) with mTeSR1 medium (Stem Cell Technologies). .. Multiple independently established hiPSC clones (i.e. referred to as lines) were derived from each individual, which were cultured typically to passage 12, and at least ten stock vials were frozen from each cell line. hiPSC pellets collected from each cell line were frozen in RTL plus buffer (Qiagen) and used for total RNA isolation. ..

    Article Title: Multiomic QTL mapping reveals phenotypic complexity of GWAS loci and prioritizes putative causal variants
    Article Snippet: Stained cells were acquired using BD FACSCanto II system (BD Biosciences) and the fraction of cTnT-positive cells were calculated using FlowJo software version 10.2. .. Harvesting of material for molecular assays. (1) At D0 of the CVPC differentiation, 142 iPSC lines from 129 individuals were collected and frozen as nuclear pellets for the ATAC-seq assay∗∗. (2) At D0 of the CVPC differentiation, 43 iPSC lines from 41 individuals were collected and frozen as nuclear pellets for the H3K27ac ChIP-seq assay∗∗. (3) At D25, 178 CVPCs derived from 147 iPSC clones from 137 individuals, pellets were collected and frozen in RTL plus buffer (Qiagen) for the RNA-seq assay. (4) At D25, 140 CVPCs derived from 132 iPSC clones from 124 individuals were collected and frozen as nuclear pellets for the ATAC-seq assay. (5) At D25, 101 CVPCs derived from 97 iPSC clones from 96 individuals were collected and cross-linked for the H3K27ac ChIP-seq assay. ..

    RNA Sequencing:

    Article Title: Multiomic QTL mapping reveals phenotypic complexity of GWAS loci and prioritizes putative causal variants.
    Article Snippet: Harvesting of material for molecular assays. (1) At D15, 107 PPCs derived from 106 iPSC clones from 106 individuals, pellets were collected and frozen in RTL plus buffer (Qiagen) for the RNA-seq assay. (2) At D15, 109 PPCs derived from 108 iPSC clones from 108 individuals were collected and frozen as nuclear pellets for the ATAC-seq assay. (3) H3K27ac ChIP-seq assay was not performed for the PPCs, however, we have frozen samples, and this dataset could be added in the future. .. Harvesting of material for molecular assays. (1) At D15, 107 PPCs derived from 106 iPSC clones from 106 individuals, pellets were collected and frozen in RTL plus buffer (Qiagen) for the RNA-seq assay. (2) At D15, 109 PPCs derived from 108 iPSC clones from 108 individuals were collected and frozen as nuclear pellets for the ATAC-seq assay. (3) H3K27ac ChIP-seq assay was not performed for the PPCs, however, we have frozen samples, and this dataset could be added in the future. ..

    Article Title: Multiomic QTL mapping reveals phenotypic complexity of GWAS loci and prioritizes putative causal variants
    Article Snippet: Stained cells were acquired using BD FACSCanto II system (BD Biosciences) and the fraction of cTnT-positive cells were calculated using FlowJo software version 10.2. .. Harvesting of material for molecular assays. (1) At D0 of the CVPC differentiation, 142 iPSC lines from 129 individuals were collected and frozen as nuclear pellets for the ATAC-seq assay∗∗. (2) At D0 of the CVPC differentiation, 43 iPSC lines from 41 individuals were collected and frozen as nuclear pellets for the H3K27ac ChIP-seq assay∗∗. (3) At D25, 178 CVPCs derived from 147 iPSC clones from 137 individuals, pellets were collected and frozen in RTL plus buffer (Qiagen) for the RNA-seq assay. (4) At D25, 140 CVPCs derived from 132 iPSC clones from 124 individuals were collected and frozen as nuclear pellets for the ATAC-seq assay. (5) At D25, 101 CVPCs derived from 97 iPSC clones from 96 individuals were collected and cross-linked for the H3K27ac ChIP-seq assay. ..

    Article Title: Multiomic QTL mapping reveals phenotypic complexity of GWAS loci and prioritizes putative causal variants
    Article Snippet: .. Harvesting of material for molecular assays. (1) At P12, for 220 iPSC lines from 220 individuals, pellets were collected and frozen in RTL plus buffer (Qiagen) for the RNA-seq assay. (2) iPSC nuclear pellets for the ATAC-seq and H3K27ac ChIP-seq assays were collected at D0 of the CVPC differentiation protocol (see below: CVPC differentiation ). ..

    Chromatin Immunoprecipitation:

    Article Title: Multiomic QTL mapping reveals phenotypic complexity of GWAS loci and prioritizes putative causal variants.
    Article Snippet: Harvesting of material for molecular assays. (1) At D15, 107 PPCs derived from 106 iPSC clones from 106 individuals, pellets were collected and frozen in RTL plus buffer (Qiagen) for the RNA-seq assay. (2) At D15, 109 PPCs derived from 108 iPSC clones from 108 individuals were collected and frozen as nuclear pellets for the ATAC-seq assay. (3) H3K27ac ChIP-seq assay was not performed for the PPCs, however, we have frozen samples, and this dataset could be added in the future. .. Harvesting of material for molecular assays. (1) At D15, 107 PPCs derived from 106 iPSC clones from 106 individuals, pellets were collected and frozen in RTL plus buffer (Qiagen) for the RNA-seq assay. (2) At D15, 109 PPCs derived from 108 iPSC clones from 108 individuals were collected and frozen as nuclear pellets for the ATAC-seq assay. (3) H3K27ac ChIP-seq assay was not performed for the PPCs, however, we have frozen samples, and this dataset could be added in the future. ..

    Article Title: Multiomic QTL mapping reveals phenotypic complexity of GWAS loci and prioritizes putative causal variants
    Article Snippet: Stained cells were acquired using BD FACSCanto II system (BD Biosciences) and the fraction of cTnT-positive cells were calculated using FlowJo software version 10.2. .. Harvesting of material for molecular assays. (1) At D0 of the CVPC differentiation, 142 iPSC lines from 129 individuals were collected and frozen as nuclear pellets for the ATAC-seq assay∗∗. (2) At D0 of the CVPC differentiation, 43 iPSC lines from 41 individuals were collected and frozen as nuclear pellets for the H3K27ac ChIP-seq assay∗∗. (3) At D25, 178 CVPCs derived from 147 iPSC clones from 137 individuals, pellets were collected and frozen in RTL plus buffer (Qiagen) for the RNA-seq assay. (4) At D25, 140 CVPCs derived from 132 iPSC clones from 124 individuals were collected and frozen as nuclear pellets for the ATAC-seq assay. (5) At D25, 101 CVPCs derived from 97 iPSC clones from 96 individuals were collected and cross-linked for the H3K27ac ChIP-seq assay. ..

    Article Title: Multiomic QTL mapping reveals phenotypic complexity of GWAS loci and prioritizes putative causal variants
    Article Snippet: .. Harvesting of material for molecular assays. (1) At P12, for 220 iPSC lines from 220 individuals, pellets were collected and frozen in RTL plus buffer (Qiagen) for the RNA-seq assay. (2) iPSC nuclear pellets for the ATAC-seq and H3K27ac ChIP-seq assays were collected at D0 of the CVPC differentiation protocol (see below: CVPC differentiation ). ..

    Cell Culture:

    Article Title: Complex regulatory networks influence pluripotent cell state transitions in human iPSCs.
    Article Snippet: Emerging hiPSC colonies were manually picked after Day 21 and maintained on Matrigel (BD Corning) with mTeSR1 medium (Stem Cell Technologies). .. Multiple independently established hiPSC clones (i.e. referred to as lines) were derived from each individual, which were cultured typically to passage 12, and at least ten stock vials were frozen from each cell line. hiPSC pellets collected from each cell line were frozen in RTL plus buffer (Qiagen) and used for total RNA isolation. ..

    Article Title: Complex regulatory networks influence pluripotent cell state transitions in human iPSCs
    Article Snippet: Emerging hiPSC colonies were manually picked after Day 21 and maintained on Matrigel (BD Corning) with mTeSR1 medium (Stem Cell Technologies). .. Multiple independently established hiPSC clones (i.e. referred to as lines) were derived from each individual, which were cultured typically to passage 12, and at least ten stock vials were frozen from each cell line. hiPSC pellets collected from each cell line were frozen in RTL plus buffer (Qiagen) and used for total RNA isolation. ..

    Isolation:

    Article Title: Complex regulatory networks influence pluripotent cell state transitions in human iPSCs.
    Article Snippet: Emerging hiPSC colonies were manually picked after Day 21 and maintained on Matrigel (BD Corning) with mTeSR1 medium (Stem Cell Technologies). .. Multiple independently established hiPSC clones (i.e. referred to as lines) were derived from each individual, which were cultured typically to passage 12, and at least ten stock vials were frozen from each cell line. hiPSC pellets collected from each cell line were frozen in RTL plus buffer (Qiagen) and used for total RNA isolation. ..

    Article Title: Complex regulatory networks influence pluripotent cell state transitions in human iPSCs
    Article Snippet: Emerging hiPSC colonies were manually picked after Day 21 and maintained on Matrigel (BD Corning) with mTeSR1 medium (Stem Cell Technologies). .. Multiple independently established hiPSC clones (i.e. referred to as lines) were derived from each individual, which were cultured typically to passage 12, and at least ten stock vials were frozen from each cell line. hiPSC pellets collected from each cell line were frozen in RTL plus buffer (Qiagen) and used for total RNA isolation. ..

    other:

    Article Title: Multiomic QTL mapping reveals phenotypic complexity of GWAS loci and prioritizes putative causal variants.
    Article Snippet: CVPC differentiation As previously described in detail,90 to generate CVPCs, we used a small molecule cardiac differentiation protocol.91 The 25-day differentiation protocol consisted of four phases. (1) Expansion of iPSC: One vial of each iPSC line was thawed intomTeSR1medium containing 10 mMROCK Inhibitor (Sigma) and plated on one well of a 6-well plate coated overnight with matrigel.

    Article Title: Single-cell profiling reveals transcriptome dynamics during bovine oocyte growth
    Article Snippet: Measured oocytes were snap-frozen in 4 μL PBS + 4 μL RTL-Plus buffer (Qiagen) in 0.2 mL PCR microtubes.



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