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repli g single cell kit  (Qiagen)


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    Qiagen repli g single cell kit
    Repli G Single Cell Kit, supplied by Qiagen, used in various techniques. Bioz Stars score: 98/100, based on 1593 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/repli+g+single+cell+kit/REPLI-g+Mini+Kit/pm42118245-61-9-13
    Average 98 stars, based on 1593 article reviews
    repli g single cell kit - by Bioz Stars, 2026-10
    98/100 stars

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    Related Articles

    Amplification:

    Article Title: Optimization of Preimplantation Genome Profiling Supports Genomic Selection in Cattle
    Article Snippet: .. Genomic DNA from all MAC-T low-input samples and embryos (23 TE biopsies and 10 arrested embryos) was amplified using the REPLI-g Single Cell Kit (#150343, Qiagen, Mississauga, ON, Canada), which is based on the MDA method. .. In parallel, low-input MAC-T samples were also WGA-amplified using the Single Cell Whole Genome Amplification Kit (#KT110700150, Yikon, Taizhou, Jiangsu, China), which employs the MALBAC method.

    Article Title: Optimization of Preimplantation Genome Profiling Supports Genomic Selection in Cattle.
    Article Snippet: .. Genomic DNA from all MAC-T low-input samples and embryos (23 TE biopsies and 10 arrested embryos) was amplified using the REPLI-g Single Cell Kit (#150343, Qiagen, Mississauga, ON, Canada), which is based on the MDA method. .. In parallel, low-input MAC-T samples were also WGA-amplified using the Single Cell Whole Genome Amplification Kit (#KT110700150, Yikon, Taizhou, Jiangsu, China), which employs the MALBAC method.

    Article Title: Single-cell genomic profiling of antimicrobial resistance in Escherichia coli from the Densu River, Ghana
    Article Snippet: After resuspension of the gel beads in DPBS, the bacterial cells encapsulated in gel beads were lysed by overnight incubation at 40 °C in proteinase K solution (1 mg/mL proteinase K [Promega, Madison, WI] and 0.5% SDS [Wako, Tokyo, Japan] in DPBS). .. Whole-genome amplification was performed using a REPLI-g Single Cell Kit (Qiagen, Hilden, Germany) at 30 °C for 3 h. Genome amplification within the gel beads was confirmed using 1 × SYBR Green I (Thermo Fisher Scientific), and fluorescence-positive gel beads were isolated using a BD FACSMelody Cell Sorter (BD Biosciences) equipped with a 488 nm excitation laser. .. A total of 242 fluorescence-positive gel beads were sorted into a 384-well microplate, and next-generation sequencing libraries were prepared using the QIAseq FX DNA library kit (QIAGEN).

    Single Cell:

    Article Title: Optimization of Preimplantation Genome Profiling Supports Genomic Selection in Cattle
    Article Snippet: .. Genomic DNA from all MAC-T low-input samples and embryos (23 TE biopsies and 10 arrested embryos) was amplified using the REPLI-g Single Cell Kit (#150343, Qiagen, Mississauga, ON, Canada), which is based on the MDA method. .. In parallel, low-input MAC-T samples were also WGA-amplified using the Single Cell Whole Genome Amplification Kit (#KT110700150, Yikon, Taizhou, Jiangsu, China), which employs the MALBAC method.

    Article Title: Optimization of Preimplantation Genome Profiling Supports Genomic Selection in Cattle.
    Article Snippet: .. Genomic DNA from all MAC-T low-input samples and embryos (23 TE biopsies and 10 arrested embryos) was amplified using the REPLI-g Single Cell Kit (#150343, Qiagen, Mississauga, ON, Canada), which is based on the MDA method. .. In parallel, low-input MAC-T samples were also WGA-amplified using the Single Cell Whole Genome Amplification Kit (#KT110700150, Yikon, Taizhou, Jiangsu, China), which employs the MALBAC method.

    Article Title: A discussion on the genus Stigmatomyces sensu lato and the description of two new species from Chile.
    Article Snippet: Taxonomic revisions in mycology often focus on well-studied fungal groups, yet obscure lineages such as Laboulbeniales (Pezizomycotina, Ascomycota) remain underexplored.. Here, we address the taxonomy of Stigmatomyces sensu lato, a diverse genus of obligate biotrophic fungi parasitizing flies (Diptera).. Previous work suggested that Stigmatomyces is paraphyletic, as the well-delineated genus Gloeandromyces was nested within the genus, which resulted in the reinstatement of Appendiculina and Fanniomyces.

    Article Title: From genetic diagnosis to healthy live births: implementing an integrated PGT-M pathway for 21-hydroxylase deficiency.
    Article Snippet: 3 Nyingchi Maternal and Child Health Hospital, Nyingchi, China Abstract Purpose This study aimed to assess the clinical efÏcacy of a comprehensive reproductive management pathway integrating genetic diagnosis, preimplantation genetic testing for monogenic disorders and aneuploid (PGT-M & PGT-A) and prenatal diagnosis for families affected by CYP21A2 variant related 21-hydroxylase deficiency (21-OHD).. Methods We performed a retrospective analysis of three families affected by 21-OHD.. Definitive genetic diagnosis of the CYP21A2 locus was established using Multiplex Ligation-dependent Probe Amplification (MLPA) and Sanger sequencing.

    Article Title: Single-Cell and Tissue-Specific CRISPR Editing Analyses Unveil New Insights to Off-Targets and Translocations
    Article Snippet: .. Whole genome amplification (WGA) of single-cell sorted mESCs was performed using the REPLI-g Single Cell Kit (QIAGEN). ..

    Article Title: Metabolic capacities of large "pillotinaceous" spirochetes from termite guts and their placement among Breznakiellaceae.
    Article Snippet: .. Whole genome amplification (WGA) was performed using the Repli-G Single Cell Kit (150343, QIAGEN) with 30% of the recommended reaction volume and adding SYBR green to a final concentration of 1 μM. ..

    Article Title: Single-cell genomic profiling of antimicrobial resistance in Escherichia coli from the Densu River, Ghana
    Article Snippet: After resuspension of the gel beads in DPBS, the bacterial cells encapsulated in gel beads were lysed by overnight incubation at 40 °C in proteinase K solution (1 mg/mL proteinase K [Promega, Madison, WI] and 0.5% SDS [Wako, Tokyo, Japan] in DPBS). .. Whole-genome amplification was performed using a REPLI-g Single Cell Kit (Qiagen, Hilden, Germany) at 30 °C for 3 h. Genome amplification within the gel beads was confirmed using 1 × SYBR Green I (Thermo Fisher Scientific), and fluorescence-positive gel beads were isolated using a BD FACSMelody Cell Sorter (BD Biosciences) equipped with a 488 nm excitation laser. .. A total of 242 fluorescence-positive gel beads were sorted into a 384-well microplate, and next-generation sequencing libraries were prepared using the QIAseq FX DNA library kit (QIAGEN).

    Article Title: A systematic study of WGA strategies for enhanced STR and SNP genotyping on trace DNA.
    Article Snippet: 2 Shanghai Key Laboratory of Forensic Medicine, Shanghai Forensic Service Platform, Academy of Forensic Science, Shanghai 200063, People’s Republic of China Abstract The robust analysis of trace DNA (≤ 100 pg) remains a persistent challenge in forensic genetics, primarily due to the high failure rates and stochastic effects associated with conventional STR typing at low template quantities.. Although whole genome amplification (WGA) offers a potential solution, its effectiveness and influencing factors in forensic applications still require systematic evaluation.. This study comprehensively evaluated two prominent WGA methods—REPLI-g and MALBAC—for STR and SNP genotyping of trace DNA across a wide input range (0.2441–2000 pg) on both capillary electrophoresis (CE) and targeted next-generation sequencing (NGS).

    Multiple Displacement Amplification:

    Article Title: Optimization of Preimplantation Genome Profiling Supports Genomic Selection in Cattle
    Article Snippet: .. Genomic DNA from all MAC-T low-input samples and embryos (23 TE biopsies and 10 arrested embryos) was amplified using the REPLI-g Single Cell Kit (#150343, Qiagen, Mississauga, ON, Canada), which is based on the MDA method. .. In parallel, low-input MAC-T samples were also WGA-amplified using the Single Cell Whole Genome Amplification Kit (#KT110700150, Yikon, Taizhou, Jiangsu, China), which employs the MALBAC method.

    Article Title: Optimization of Preimplantation Genome Profiling Supports Genomic Selection in Cattle.
    Article Snippet: .. Genomic DNA from all MAC-T low-input samples and embryos (23 TE biopsies and 10 arrested embryos) was amplified using the REPLI-g Single Cell Kit (#150343, Qiagen, Mississauga, ON, Canada), which is based on the MDA method. .. In parallel, low-input MAC-T samples were also WGA-amplified using the Single Cell Whole Genome Amplification Kit (#KT110700150, Yikon, Taizhou, Jiangsu, China), which employs the MALBAC method.

    Article Title: From genetic diagnosis to healthy live births: implementing an integrated PGT-M pathway for 21-hydroxylase deficiency.
    Article Snippet: 3 Nyingchi Maternal and Child Health Hospital, Nyingchi, China Abstract Purpose This study aimed to assess the clinical efÏcacy of a comprehensive reproductive management pathway integrating genetic diagnosis, preimplantation genetic testing for monogenic disorders and aneuploid (PGT-M & PGT-A) and prenatal diagnosis for families affected by CYP21A2 variant related 21-hydroxylase deficiency (21-OHD).. Methods We performed a retrospective analysis of three families affected by 21-OHD.. Definitive genetic diagnosis of the CYP21A2 locus was established using Multiplex Ligation-dependent Probe Amplification (MLPA) and Sanger sequencing.

    Article Title: A systematic study of WGA strategies for enhanced STR and SNP genotyping on trace DNA.
    Article Snippet: 2 Shanghai Key Laboratory of Forensic Medicine, Shanghai Forensic Service Platform, Academy of Forensic Science, Shanghai 200063, People’s Republic of China Abstract The robust analysis of trace DNA (≤ 100 pg) remains a persistent challenge in forensic genetics, primarily due to the high failure rates and stochastic effects associated with conventional STR typing at low template quantities.. Although whole genome amplification (WGA) offers a potential solution, its effectiveness and influencing factors in forensic applications still require systematic evaluation.. This study comprehensively evaluated two prominent WGA methods—REPLI-g and MALBAC—for STR and SNP genotyping of trace DNA across a wide input range (0.2441–2000 pg) on both capillary electrophoresis (CE) and targeted next-generation sequencing (NGS).

    Whole Genome Amplification:

    Article Title: From genetic diagnosis to healthy live births: implementing an integrated PGT-M pathway for 21-hydroxylase deficiency.
    Article Snippet: 3 Nyingchi Maternal and Child Health Hospital, Nyingchi, China Abstract Purpose This study aimed to assess the clinical efÏcacy of a comprehensive reproductive management pathway integrating genetic diagnosis, preimplantation genetic testing for monogenic disorders and aneuploid (PGT-M & PGT-A) and prenatal diagnosis for families affected by CYP21A2 variant related 21-hydroxylase deficiency (21-OHD).. Methods We performed a retrospective analysis of three families affected by 21-OHD.. Definitive genetic diagnosis of the CYP21A2 locus was established using Multiplex Ligation-dependent Probe Amplification (MLPA) and Sanger sequencing.

    Article Title: Single-Cell and Tissue-Specific CRISPR Editing Analyses Unveil New Insights to Off-Targets and Translocations
    Article Snippet: .. Whole genome amplification (WGA) of single-cell sorted mESCs was performed using the REPLI-g Single Cell Kit (QIAGEN). ..

    Article Title: Metabolic capacities of large "pillotinaceous" spirochetes from termite guts and their placement among Breznakiellaceae.
    Article Snippet: .. Whole genome amplification (WGA) was performed using the Repli-G Single Cell Kit (150343, QIAGEN) with 30% of the recommended reaction volume and adding SYBR green to a final concentration of 1 μM. ..

    Article Title: Single-cell genomic profiling of antimicrobial resistance in Escherichia coli from the Densu River, Ghana
    Article Snippet: After resuspension of the gel beads in DPBS, the bacterial cells encapsulated in gel beads were lysed by overnight incubation at 40 °C in proteinase K solution (1 mg/mL proteinase K [Promega, Madison, WI] and 0.5% SDS [Wako, Tokyo, Japan] in DPBS). .. Whole-genome amplification was performed using a REPLI-g Single Cell Kit (Qiagen, Hilden, Germany) at 30 °C for 3 h. Genome amplification within the gel beads was confirmed using 1 × SYBR Green I (Thermo Fisher Scientific), and fluorescence-positive gel beads were isolated using a BD FACSMelody Cell Sorter (BD Biosciences) equipped with a 488 nm excitation laser. .. A total of 242 fluorescence-positive gel beads were sorted into a 384-well microplate, and next-generation sequencing libraries were prepared using the QIAseq FX DNA library kit (QIAGEN).

    Article Title: A systematic study of WGA strategies for enhanced STR and SNP genotyping on trace DNA.
    Article Snippet: 2 Shanghai Key Laboratory of Forensic Medicine, Shanghai Forensic Service Platform, Academy of Forensic Science, Shanghai 200063, People’s Republic of China Abstract The robust analysis of trace DNA (≤ 100 pg) remains a persistent challenge in forensic genetics, primarily due to the high failure rates and stochastic effects associated with conventional STR typing at low template quantities.. Although whole genome amplification (WGA) offers a potential solution, its effectiveness and influencing factors in forensic applications still require systematic evaluation.. This study comprehensively evaluated two prominent WGA methods—REPLI-g and MALBAC—for STR and SNP genotyping of trace DNA across a wide input range (0.2441–2000 pg) on both capillary electrophoresis (CE) and targeted next-generation sequencing (NGS).

    Polymerase Chain Reaction:

    Article Title: From genetic diagnosis to healthy live births: implementing an integrated PGT-M pathway for 21-hydroxylase deficiency.
    Article Snippet: 3 Nyingchi Maternal and Child Health Hospital, Nyingchi, China Abstract Purpose This study aimed to assess the clinical efÏcacy of a comprehensive reproductive management pathway integrating genetic diagnosis, preimplantation genetic testing for monogenic disorders and aneuploid (PGT-M & PGT-A) and prenatal diagnosis for families affected by CYP21A2 variant related 21-hydroxylase deficiency (21-OHD).. Methods We performed a retrospective analysis of three families affected by 21-OHD.. Definitive genetic diagnosis of the CYP21A2 locus was established using Multiplex Ligation-dependent Probe Amplification (MLPA) and Sanger sequencing.

    SYBR Green Assay:

    Article Title: Metabolic capacities of large "pillotinaceous" spirochetes from termite guts and their placement among Breznakiellaceae.
    Article Snippet: .. Whole genome amplification (WGA) was performed using the Repli-G Single Cell Kit (150343, QIAGEN) with 30% of the recommended reaction volume and adding SYBR green to a final concentration of 1 μM. ..

    Article Title: Single-cell genomic profiling of antimicrobial resistance in Escherichia coli from the Densu River, Ghana
    Article Snippet: After resuspension of the gel beads in DPBS, the bacterial cells encapsulated in gel beads were lysed by overnight incubation at 40 °C in proteinase K solution (1 mg/mL proteinase K [Promega, Madison, WI] and 0.5% SDS [Wako, Tokyo, Japan] in DPBS). .. Whole-genome amplification was performed using a REPLI-g Single Cell Kit (Qiagen, Hilden, Germany) at 30 °C for 3 h. Genome amplification within the gel beads was confirmed using 1 × SYBR Green I (Thermo Fisher Scientific), and fluorescence-positive gel beads were isolated using a BD FACSMelody Cell Sorter (BD Biosciences) equipped with a 488 nm excitation laser. .. A total of 242 fluorescence-positive gel beads were sorted into a 384-well microplate, and next-generation sequencing libraries were prepared using the QIAseq FX DNA library kit (QIAGEN).

    Concentration Assay:

    Article Title: Metabolic capacities of large "pillotinaceous" spirochetes from termite guts and their placement among Breznakiellaceae.
    Article Snippet: .. Whole genome amplification (WGA) was performed using the Repli-G Single Cell Kit (150343, QIAGEN) with 30% of the recommended reaction volume and adding SYBR green to a final concentration of 1 μM. ..

    Fluorescence:

    Article Title: Single-cell genomic profiling of antimicrobial resistance in Escherichia coli from the Densu River, Ghana
    Article Snippet: After resuspension of the gel beads in DPBS, the bacterial cells encapsulated in gel beads were lysed by overnight incubation at 40 °C in proteinase K solution (1 mg/mL proteinase K [Promega, Madison, WI] and 0.5% SDS [Wako, Tokyo, Japan] in DPBS). .. Whole-genome amplification was performed using a REPLI-g Single Cell Kit (Qiagen, Hilden, Germany) at 30 °C for 3 h. Genome amplification within the gel beads was confirmed using 1 × SYBR Green I (Thermo Fisher Scientific), and fluorescence-positive gel beads were isolated using a BD FACSMelody Cell Sorter (BD Biosciences) equipped with a 488 nm excitation laser. .. A total of 242 fluorescence-positive gel beads were sorted into a 384-well microplate, and next-generation sequencing libraries were prepared using the QIAseq FX DNA library kit (QIAGEN).

    Isolation:

    Article Title: Single-cell genomic profiling of antimicrobial resistance in Escherichia coli from the Densu River, Ghana
    Article Snippet: After resuspension of the gel beads in DPBS, the bacterial cells encapsulated in gel beads were lysed by overnight incubation at 40 °C in proteinase K solution (1 mg/mL proteinase K [Promega, Madison, WI] and 0.5% SDS [Wako, Tokyo, Japan] in DPBS). .. Whole-genome amplification was performed using a REPLI-g Single Cell Kit (Qiagen, Hilden, Germany) at 30 °C for 3 h. Genome amplification within the gel beads was confirmed using 1 × SYBR Green I (Thermo Fisher Scientific), and fluorescence-positive gel beads were isolated using a BD FACSMelody Cell Sorter (BD Biosciences) equipped with a 488 nm excitation laser. .. A total of 242 fluorescence-positive gel beads were sorted into a 384-well microplate, and next-generation sequencing libraries were prepared using the QIAseq FX DNA library kit (QIAGEN).

    Multiple Annealing and Looping–Based Amplification Cycles:

    Article Title: A systematic study of WGA strategies for enhanced STR and SNP genotyping on trace DNA.
    Article Snippet: 2 Shanghai Key Laboratory of Forensic Medicine, Shanghai Forensic Service Platform, Academy of Forensic Science, Shanghai 200063, People’s Republic of China Abstract The robust analysis of trace DNA (≤ 100 pg) remains a persistent challenge in forensic genetics, primarily due to the high failure rates and stochastic effects associated with conventional STR typing at low template quantities.. Although whole genome amplification (WGA) offers a potential solution, its effectiveness and influencing factors in forensic applications still require systematic evaluation.. This study comprehensively evaluated two prominent WGA methods—REPLI-g and MALBAC—for STR and SNP genotyping of trace DNA across a wide input range (0.2441–2000 pg) on both capillary electrophoresis (CE) and targeted next-generation sequencing (NGS).



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