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universal genomic dna purification mini spin kit  (Beyotime)


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    Structured Review

    Beyotime universal genomic dna purification mini spin kit
    Universal Genomic Dna Purification Mini Spin Kit, supplied by Beyotime, used in various techniques. Bioz Stars score: 99/100, based on 121 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/universal+genomic+dna+purification+mini+spin+kit/Universal+Genomic+DNA+Purification+Mini+Spin+Kit/pm41995456-246-5-12
    Average 99 stars, based on 121 article reviews
    universal genomic dna purification mini spin kit - by Bioz Stars, 2026-09
    99/100 stars

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    Related Articles

    Isolation:

    Article Title: Ginsenoside Rg1 delays the senescence of adipose-derived stem cells: network pharmacology and experimental validation.
    Article Snippet: .. Genomic DNA from ADSCs was isolated using the Universal Genomic DNA Purification Mini Spin Kit (cat. no. D0063; Beyotime, China) and adjusted to 5 ng/μL. ..

    Article Title: Ginsenoside Rg1 delays the senescence of adipose-derived stem cells: network pharmacology and experimental validation
    Article Snippet: Stained cells were imaged on an inverted microscope (Leica, Germany), and positive cells were counted in four random fields per well. .. Genomic DNA from ADSCs was isolated using the Universal Genomic DNA Purification Mini Spin Kit (cat. no. D0063; Beyotime, China) and adjusted to 5 ng/μL. ..

    Article Title: Anti-alcoholism drug disulfiram inhibits PANoptosis by blocking mitochondrial permeabilization in macrophages
    Article Snippet: .. DNA was isolated from the cytosolic fraction using a Universal Genomic DNA Purification Mini Spin kit (D0063, Beyotime). .. Quantitative PCR (qPCR) was employed to measure mtDNA using TB Green Premix Ex Taq (Tli RNaseH Plus) (RR420A, Takara, Dalian, China) on a CFX96 Real-Time PCR Detection System (Bio-Rad, Hercules, CA, USA). mtDNA was quantified by qPCR using primers specific for COX-1 (encoding cytochrome c oxidase 1), and the mitochondrial D-loop region.

    Article Title: An ADAR2-mimic base editor for efficient C-to-U RNA editing in vivo.
    Article Snippet: C-to-U RNA editing tools face several challenges, including concurrent DNA mutations and the large-size anchoring domains associated with immunogenicity due to their microbial origin.. To overcome these limitations, here we present AMBER (ADAR2mimic base editor for RNA), which emulates the mode of natural adenosine deaminase acting on RNA (ADAR) for C-to-U RNA editing.. AMBER exhibited robust editing efficiency across many different targets in diverse cell lines, and demonstrated strong efficacy in a mouse model. Our findings establish AMBER as a promising therapeutic tool for repairing T-to-C mutations, offering great potential for the treatment of genetic diseases.

    DNA Purification:

    Article Title: Ginsenoside Rg1 delays the senescence of adipose-derived stem cells: network pharmacology and experimental validation.
    Article Snippet: .. Genomic DNA from ADSCs was isolated using the Universal Genomic DNA Purification Mini Spin Kit (cat. no. D0063; Beyotime, China) and adjusted to 5 ng/μL. ..

    Article Title: Splicing factor SC35 inhibits Nosema bombycis proliferation by regulating the alternative splicing of Bmupp1.
    Article Snippet: Alternative splicing is a crucial mechanism in higher eukaryotes that enhances the structural complexity of the transcriptome and augments protein functional diversity.. The regulation of alternative splicing is governed by splicing factors, which influence disease development by modulating this process.. Pebrine disease, caused by Nosema bombycis (N. bombycis) infection, is a significant disease affecting the sericulture industry.

    Article Title: Ginsenoside Rg1 delays the senescence of adipose-derived stem cells: network pharmacology and experimental validation
    Article Snippet: Stained cells were imaged on an inverted microscope (Leica, Germany), and positive cells were counted in four random fields per well. .. Genomic DNA from ADSCs was isolated using the Universal Genomic DNA Purification Mini Spin Kit (cat. no. D0063; Beyotime, China) and adjusted to 5 ng/μL. ..

    Article Title: DNA methylation-mediated silencing of MEOX1 promotes glycolysis and immune evasion in colorectal cancer cells through inhibition of GLP2R transcription.
    Article Snippet: .. Universal genomic DNA purification Mini Spin Kit (D0063, Beyotime) was used to extract genomic DNA from CRC cells and NCM460 cells. ..

    Article Title: Anti-alcoholism drug disulfiram inhibits PANoptosis by blocking mitochondrial permeabilization in macrophages
    Article Snippet: .. DNA was isolated from the cytosolic fraction using a Universal Genomic DNA Purification Mini Spin kit (D0063, Beyotime). .. Quantitative PCR (qPCR) was employed to measure mtDNA using TB Green Premix Ex Taq (Tli RNaseH Plus) (RR420A, Takara, Dalian, China) on a CFX96 Real-Time PCR Detection System (Bio-Rad, Hercules, CA, USA). mtDNA was quantified by qPCR using primers specific for COX-1 (encoding cytochrome c oxidase 1), and the mitochondrial D-loop region.

    Article Title: An ADAR2-mimic base editor for efficient C-to-U RNA editing in vivo.
    Article Snippet: C-to-U RNA editing tools face several challenges, including concurrent DNA mutations and the large-size anchoring domains associated with immunogenicity due to their microbial origin.. To overcome these limitations, here we present AMBER (ADAR2mimic base editor for RNA), which emulates the mode of natural adenosine deaminase acting on RNA (ADAR) for C-to-U RNA editing.. AMBER exhibited robust editing efficiency across many different targets in diverse cell lines, and demonstrated strong efficacy in a mouse model. Our findings establish AMBER as a promising therapeutic tool for repairing T-to-C mutations, offering great potential for the treatment of genetic diseases.

    Article Title: GRWD1 enhances HSV-1 replication by facilitating nuclear egress.
    Article Snippet: A reverse transcription (RT) system (Promega) was used to synthesize cDNA. .. Total DNA was extracted with Universal Genomic DNA Purification Mini Spin Kit (Beyotime). .. SYBR green PCR mix (CWBiotech) and a real-time PCR system (Roche 480) were used for quantitative RT-PCR.

    Article Title: Laser‐Scanning Infrared‐Raman‐Fluorescence Microscopy for Metabolic Flux Imaging in Living Organisms
    Article Snippet: .. Genomic DNA was extracted using universal genomic DNA purification mini spin kit (Beyotime, D0063), and proteins were extracted using RIPA buffer. ..

    RNA Extraction:

    Article Title: An ADAR2-mimic base editor for efficient C-to-U RNA editing in vivo.
    Article Snippet: C-to-U RNA editing tools face several challenges, including concurrent DNA mutations and the large-size anchoring domains associated with immunogenicity due to their microbial origin.. To overcome these limitations, here we present AMBER (ADAR2mimic base editor for RNA), which emulates the mode of natural adenosine deaminase acting on RNA (ADAR) for C-to-U RNA editing.. AMBER exhibited robust editing efficiency across many different targets in diverse cell lines, and demonstrated strong efficacy in a mouse model. Our findings establish AMBER as a promising therapeutic tool for repairing T-to-C mutations, offering great potential for the treatment of genetic diseases.

    DNA Extraction:

    Article Title: An ADAR2-mimic base editor for efficient C-to-U RNA editing in vivo.
    Article Snippet: C-to-U RNA editing tools face several challenges, including concurrent DNA mutations and the large-size anchoring domains associated with immunogenicity due to their microbial origin.. To overcome these limitations, here we present AMBER (ADAR2mimic base editor for RNA), which emulates the mode of natural adenosine deaminase acting on RNA (ADAR) for C-to-U RNA editing.. AMBER exhibited robust editing efficiency across many different targets in diverse cell lines, and demonstrated strong efficacy in a mouse model. Our findings establish AMBER as a promising therapeutic tool for repairing T-to-C mutations, offering great potential for the treatment of genetic diseases.



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