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Bioteke Corporation fecal genome dna extraction kit
Fecal Genome Dna Extraction Kit, supplied by Bioteke Corporation, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/extraction+kit/dna+extraction+fecal+genome+kit/pmc13264189-161-9-15
Average 86 stars, based on 1 article reviews
fecal genome dna extraction kit - by Bioz Stars, 2026-10
86/100 stars

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Related Articles

Recombinase Polymerase Amplification:

Article Title: Isothermal recombinase polymerase amplification based diagnostics for female genital schistosomiasis and human papillomavirus: a review of combined molecular diagnostic opportunities
Article Snippet: .. An RPA assay targeting HPV 16 and 18 individually achieved a clinical sensitivity of 97.6–98.5% and specificity of 100% when tested on 335 liquid-based cytology samples extracted using a commercial extraction kit (Viral genomic DNA Extraction Kit) (Bioteke, China) (Ma et al., ). ..

Article Title: Isothermal Recombinase Polymerase Amplification based diagnostics for Female Genital Schistosomiasis and Human Papillomavirus: A Review of Combined Molecular Diagnostic Opportunities
Article Snippet: .. An RPA assay targeting HPV 16 and 18 individually achieved a clinical sensitivity of 97.6-98.5% and specificity of 100% when tested on 335 liquid-based cytology samples extracted using a commercial extraction kit (Viral genomic DNA Extraction Kit) (Bioteke, China) (Ma et al., 2017). ..

Extraction:

Article Title: Isothermal recombinase polymerase amplification based diagnostics for female genital schistosomiasis and human papillomavirus: a review of combined molecular diagnostic opportunities
Article Snippet: .. An RPA assay targeting HPV 16 and 18 individually achieved a clinical sensitivity of 97.6–98.5% and specificity of 100% when tested on 335 liquid-based cytology samples extracted using a commercial extraction kit (Viral genomic DNA Extraction Kit) (Bioteke, China) (Ma et al., ). ..

Article Title: Potential mechanism of enhanced anaerobic degradation of high concentration phenol-containing wastewater by hazardous waste fly ash with high iron content: Direct interspecies electron transport pathway
Article Snippet: Micron-grade high iron-containing fly ash (MHIFA)—a processed hazardous waste containing Fe3O4—was added to an up-flow anaerobic sludge blanket reactor to improve the removal performance of high concentration phenol-containing wastewater.. The chemical oxygen demand and total phenol removal efficiency with MHIFA were 72.13% and 81.83%, respectively.. Moreover, MHIFA addition increased the contents of coenzyme F420 and extracellular polymeric substances, as well as higher electron transport system activity in activated sludge.

Article Title: Low-carbon electro-assisted biological treatment of fluoronitrobenzene with DFT-guided cathodes and RSM optimization
Article Snippet: The global pursuit of carbon neutrality demands sustainable technologies for treating recalcitrant wastewater pollutants.. This study presents a high-performance electro-assisted biological treatment system for fluoronitrobenzene degradation selected stainless-steel cathode.. Density functional theory calculations revealed its superior performance: strong pollutant chemisorption and rapid interfacial electron transfer at the SS surface.

Article Title: Association between functional polymorphisms in the flanking region of miR-143/145 and risk of papillary thyroid carcinoma
Article Snippet: .. Genomic DNA was isolated from ethylene diamine tetraacetic acid-anticoagulated peripheral blood using an extraction kit (Bioteke, Beijing, China). ..

Article Title: Mesenchymal Stromal Cells Suppress Hippocampal Neuron Autophagy Stress Induced by Hypoxic-Ischemic Brain Damage: The Possible Role of Endogenous IL-6 Secretion
Article Snippet: The injured neurons were placed in Transwell inserts (Millipore, USA) for separate coculture with either (1) neural basal medium as a control or (2) MSCs subjected to the different treatments described above. .. After 12 h and 24 h, total protein was extracted using an extraction kit (BioTeke, China). ..

Article Title: Light irradiation with different wavelmengths modifies the quality traits and monoterpenes biosynthesis of postharvest grape berries during the shelf life
Article Snippet: .. Under liquid nitrogen protection, 1 g of grape skins were sampled in triplicate from each treatment for total RNA extraction by an extraction kit (Bioteke, Beijing, China). .. After measuring the quality and concentration of the purified RNA, reverse transcription of first-strand cDNA was performed using a cDNA synthesis kit (TransGen Biotech, Beijing, China).

Article Title: Isothermal Recombinase Polymerase Amplification based diagnostics for Female Genital Schistosomiasis and Human Papillomavirus: A Review of Combined Molecular Diagnostic Opportunities
Article Snippet: .. An RPA assay targeting HPV 16 and 18 individually achieved a clinical sensitivity of 97.6-98.5% and specificity of 100% when tested on 335 liquid-based cytology samples extracted using a commercial extraction kit (Viral genomic DNA Extraction Kit) (Bioteke, China) (Ma et al., 2017). ..

Article Title: Association of MBL2 gene polymorphisms and MBL levels with dilated cardiomyopathy in a Chinese Han population.
Article Snippet: .. Genomic DNA was extracted from leukocytes by an extraction kit according to the manufacturer’s instructions (Bioteke Corporation, Beijing, China). ..

DNA Extraction:

Article Title: Isothermal recombinase polymerase amplification based diagnostics for female genital schistosomiasis and human papillomavirus: a review of combined molecular diagnostic opportunities
Article Snippet: .. An RPA assay targeting HPV 16 and 18 individually achieved a clinical sensitivity of 97.6–98.5% and specificity of 100% when tested on 335 liquid-based cytology samples extracted using a commercial extraction kit (Viral genomic DNA Extraction Kit) (Bioteke, China) (Ma et al., ). ..

Article Title: Isothermal Recombinase Polymerase Amplification based diagnostics for Female Genital Schistosomiasis and Human Papillomavirus: A Review of Combined Molecular Diagnostic Opportunities
Article Snippet: .. An RPA assay targeting HPV 16 and 18 individually achieved a clinical sensitivity of 97.6-98.5% and specificity of 100% when tested on 335 liquid-based cytology samples extracted using a commercial extraction kit (Viral genomic DNA Extraction Kit) (Bioteke, China) (Ma et al., 2017). ..

Isolation:

Article Title: Association between functional polymorphisms in the flanking region of miR-143/145 and risk of papillary thyroid carcinoma
Article Snippet: .. Genomic DNA was isolated from ethylene diamine tetraacetic acid-anticoagulated peripheral blood using an extraction kit (Bioteke, Beijing, China). ..

RNA Extraction:

Article Title: Light irradiation with different wavelmengths modifies the quality traits and monoterpenes biosynthesis of postharvest grape berries during the shelf life
Article Snippet: .. Under liquid nitrogen protection, 1 g of grape skins were sampled in triplicate from each treatment for total RNA extraction by an extraction kit (Bioteke, Beijing, China). .. After measuring the quality and concentration of the purified RNA, reverse transcription of first-strand cDNA was performed using a cDNA synthesis kit (TransGen Biotech, Beijing, China).



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Optimization of RPA primers and CRISPR/Cas12a detection for the Mycoplasma bovis uvrC gene. (A) Schematic of p‐uvrC generation by restriction cloning of a 558‐bp uvrC fragment, which was used as the standard <t>DNA</t> template. (B) Screening of eight RPA primer pairs (PP1–PP8) targeting uvrC; PP3–PP8 produced strong, specific amplicons, and target amplification was also detected in DNA from M. bovis ‐positive bison lung. (C) Sequence of three CRISPR guide RNAs (gRNA1–gRNA3) designed within the amplified uvrC region adjacent to 5′‐TTTG‐3′ PAM sites. (D) Comparison of Cas12a fluorescence kinetics showed that all three guides detected uvrC, with gRNA3 producing the fastest and strongest signal. (E) Optimization of ssDNA‐FQ reporter concentration identified 0.75 μM as the best condition for visual detection with minimal background, although maximal fluorescence was reached at 5 μM. (F) All guide RNA combinations produced detectable fluorescence with similar kinetics, although gRNA2 + 3 and gRNA1 + 2 + 3 showed slightly faster onset.
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Optimization of RPA primers and CRISPR/Cas12a detection for the Mycoplasma bovis uvrC gene. (A) Schematic of p‐uvrC generation by restriction cloning of a 558‐bp uvrC fragment, which was used as the standard <t>DNA</t> template. (B) Screening of eight RPA primer pairs (PP1–PP8) targeting uvrC; PP3–PP8 produced strong, specific amplicons, and target amplification was also detected in DNA from M. bovis ‐positive bison lung. (C) Sequence of three CRISPR guide RNAs (gRNA1–gRNA3) designed within the amplified uvrC region adjacent to 5′‐TTTG‐3′ PAM sites. (D) Comparison of Cas12a fluorescence kinetics showed that all three guides detected uvrC, with gRNA3 producing the fastest and strongest signal. (E) Optimization of ssDNA‐FQ reporter concentration identified 0.75 μM as the best condition for visual detection with minimal background, although maximal fluorescence was reached at 5 μM. (F) All guide RNA combinations produced detectable fluorescence with similar kinetics, although gRNA2 + 3 and gRNA1 + 2 + 3 showed slightly faster onset.
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Image Search Results


Journal: iScience

Article Title: Tregs transduced with a Ro60-reactive TCR have increased immunosuppressive functions in Sjögren’s disease

doi: 10.1016/j.isci.2026.117642

Figure Lengend Snippet:

Article Snippet: Genomic DNA Extraction Kit , New England Biolabs , Cat No. T3010L.

Techniques: Isolation, Cell Isolation, DNA Extraction, Quantitation Assay, Plasmid Preparation, Extraction, Recombinant, Expressing, Software

Journal: iScience

Article Title: Tregs transduced with a Ro60-reactive TCR have increased immunosuppressive functions in Sjögren’s disease

doi: 10.1016/j.isci.2026.117642

Figure Lengend Snippet:

Article Snippet: DNA Plasmid Extraction Kit , Qiagen , Cat No. 27104.

Techniques: Isolation, Cell Isolation, DNA Extraction, Quantitation Assay, Plasmid Preparation, Extraction, Recombinant, Expressing, Software

Journal: iScience

Article Title: Targeting mutant NPM1-expressing AML with T cell receptor-like antibodies

doi: 10.1016/j.isci.2026.117630

Figure Lengend Snippet:

Article Snippet: Non-toxic Plasmid Large Extraction Kit , TianGen , Cat# DP117.

Techniques: Cell-Signaling, Purification, Recombinant, Sequencing, Control, Plasmid Preparation, Extraction, Transfection, Bicinchoninic Acid Protein Assay, Conjugation Assay, Staining, Enzyme-linked Immunosorbent Assay, Software

Optimization of RPA primers and CRISPR/Cas12a detection for the Mycoplasma bovis uvrC gene. (A) Schematic of p‐uvrC generation by restriction cloning of a 558‐bp uvrC fragment, which was used as the standard DNA template. (B) Screening of eight RPA primer pairs (PP1–PP8) targeting uvrC; PP3–PP8 produced strong, specific amplicons, and target amplification was also detected in DNA from M. bovis ‐positive bison lung. (C) Sequence of three CRISPR guide RNAs (gRNA1–gRNA3) designed within the amplified uvrC region adjacent to 5′‐TTTG‐3′ PAM sites. (D) Comparison of Cas12a fluorescence kinetics showed that all three guides detected uvrC, with gRNA3 producing the fastest and strongest signal. (E) Optimization of ssDNA‐FQ reporter concentration identified 0.75 μM as the best condition for visual detection with minimal background, although maximal fluorescence was reached at 5 μM. (F) All guide RNA combinations produced detectable fluorescence with similar kinetics, although gRNA2 + 3 and gRNA1 + 2 + 3 showed slightly faster onset.

Journal: MicrobiologyOpen

Article Title: Synergistic Integration of Recombinase Polymerase Amplification and CRISPR–Cas12a Enables High‐Sensitivity Detection of Mycoplasma bovis

doi: 10.1002/mbo3.70435

Figure Lengend Snippet: Optimization of RPA primers and CRISPR/Cas12a detection for the Mycoplasma bovis uvrC gene. (A) Schematic of p‐uvrC generation by restriction cloning of a 558‐bp uvrC fragment, which was used as the standard DNA template. (B) Screening of eight RPA primer pairs (PP1–PP8) targeting uvrC; PP3–PP8 produced strong, specific amplicons, and target amplification was also detected in DNA from M. bovis ‐positive bison lung. (C) Sequence of three CRISPR guide RNAs (gRNA1–gRNA3) designed within the amplified uvrC region adjacent to 5′‐TTTG‐3′ PAM sites. (D) Comparison of Cas12a fluorescence kinetics showed that all three guides detected uvrC, with gRNA3 producing the fastest and strongest signal. (E) Optimization of ssDNA‐FQ reporter concentration identified 0.75 μM as the best condition for visual detection with minimal background, although maximal fluorescence was reached at 5 μM. (F) All guide RNA combinations produced detectable fluorescence with similar kinetics, although gRNA2 + 3 and gRNA1 + 2 + 3 showed slightly faster onset.

Article Snippet: The target band was excised and purified using the Monarch DNA Gel Extraction Kit (New England Biolabs).

Techniques: CRISPR, Cloning, Screening, Produced, Amplification, Sequencing, Comparison, Fluorescence, Concentration Assay