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tianmicrobe pathogen dna kit  (tiangen biotech co)


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    tiangen biotech co tianmicrobe pathogen dna kit
    Tianmicrobe Pathogen Dna Kit, supplied by tiangen biotech co, used in various techniques. Bioz Stars score: 99/100, based on 3 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/pathogen/TIANMicrobe+Pathogen+DNA+Kit/pm39857726-65-32-36
    Average 99 stars, based on 3 article reviews
    tianmicrobe pathogen dna kit - by Bioz Stars, 2026-10
    99/100 stars

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    Related Articles

    Extraction:

    Article Title: Comparative Analysis of Microbial Detection in Traditional Culture Versus Metagenomic Next-Generation Sequencing in Patients with Periprosthetic Joint Infection: A Prospective Observational Study
    Article Snippet: .. Genomic DNA (gDNA) extraction was performed using the TIANMicrobe Pathogen DNA Kit (TIANGEN BIOTECH, Beijing, China) according to the manufacturer’s instructions. .. The total gDNA was quantified using the Qubit dsDNA HS Assay Kit on a Qubit 4.0 Fluorometer (Thermo Scientific, Waltham, MA, USA) [ ].

    Article Title: Comparative Analysis of Microbial Detection in Traditional Culture Versus Metagenomic Next-Generation Sequencing in Patients with Periprosthetic Joint Infection: A Prospective Observational Study.
    Article Snippet: .. Genomic DNA (gDNA) extraction was performed using the TIANMicrobe Pathogen DNA Kit (TIANGEN BIOTECH, Beijing, China) according to the manufacturer’s instructions. .. The total gDNA was quantified using the Qubit dsDNA HS Assay Kit on a Qubit 4.0 Fluorometer (Thermo Scientific, Waltham, MA, USA) [12].

    Article Title: Investigating the Pulmonary Host Response of Acinetobacter baumannii Infection-Associated Pneumonia by Metagenomic Next-Generation Sequencing
    Article Snippet: The tube was placed on a FastPrep-24 5G instrument (MP Biomedicals, Santa Ana, CA, USA) at a speed of 10 m/s for 25 min. .. Subsequently, the supernatant (200 μL) was transferred to a new 1.5 mL tube following high-speed centrifugation at 8000× g for 1 min for further DNA extraction. gDNA extraction was performed using the TIANMicrobe Pathogen DNA Kit (Tiangen Biotech, Beijing, China) following the manufacturer’s instructions. .. The total gDNA was quantified using the Qubit dsDNA HS Assay Kit on a Qubit 4.0 Fluorometer (Thermo Fisher Scientific.

    Article Title: Investigating the Pulmonary Host Response of Acinetobacter baumannii Infection-Associated Pneumonia by Metagenomic Next-Generation Sequencing.
    Article Snippet: The tube was placed on a FastPrep-24 5G instrument (MP Biomedicals, Santa Ana, CA, USA) at a speed of 10 m/s for 25 min. .. Subsequently, the supernatant (200 μL) was transferred to a new 1.5 mL tube following high-speed centrifugation at 8000× g for 1 min for further DNA extraction. gDNA extraction was performed using the TIANMicrobe Pathogen DNA Kit (Tiangen Biotech, Beijing, China) following the manufacturer’s instructions. .. The total gDNA was Biomedicines 2025, 13, 142 5 of 14 quantified using the Qubit dsDNA HS Assay Kit on a Qubit 4.0 Fluorometer (Thermo Fisher Scientific.

    Centrifugation:

    Article Title: Investigating the Pulmonary Host Response of Acinetobacter baumannii Infection-Associated Pneumonia by Metagenomic Next-Generation Sequencing
    Article Snippet: The tube was placed on a FastPrep-24 5G instrument (MP Biomedicals, Santa Ana, CA, USA) at a speed of 10 m/s for 25 min. .. Subsequently, the supernatant (200 μL) was transferred to a new 1.5 mL tube following high-speed centrifugation at 8000× g for 1 min for further DNA extraction. gDNA extraction was performed using the TIANMicrobe Pathogen DNA Kit (Tiangen Biotech, Beijing, China) following the manufacturer’s instructions. .. The total gDNA was quantified using the Qubit dsDNA HS Assay Kit on a Qubit 4.0 Fluorometer (Thermo Fisher Scientific.

    Article Title: Investigating the Pulmonary Host Response of Acinetobacter baumannii Infection-Associated Pneumonia by Metagenomic Next-Generation Sequencing.
    Article Snippet: The tube was placed on a FastPrep-24 5G instrument (MP Biomedicals, Santa Ana, CA, USA) at a speed of 10 m/s for 25 min. .. Subsequently, the supernatant (200 μL) was transferred to a new 1.5 mL tube following high-speed centrifugation at 8000× g for 1 min for further DNA extraction. gDNA extraction was performed using the TIANMicrobe Pathogen DNA Kit (Tiangen Biotech, Beijing, China) following the manufacturer’s instructions. .. The total gDNA was Biomedicines 2025, 13, 142 5 of 14 quantified using the Qubit dsDNA HS Assay Kit on a Qubit 4.0 Fluorometer (Thermo Fisher Scientific.

    DNA Extraction:

    Article Title: Investigating the Pulmonary Host Response of Acinetobacter baumannii Infection-Associated Pneumonia by Metagenomic Next-Generation Sequencing
    Article Snippet: The tube was placed on a FastPrep-24 5G instrument (MP Biomedicals, Santa Ana, CA, USA) at a speed of 10 m/s for 25 min. .. Subsequently, the supernatant (200 μL) was transferred to a new 1.5 mL tube following high-speed centrifugation at 8000× g for 1 min for further DNA extraction. gDNA extraction was performed using the TIANMicrobe Pathogen DNA Kit (Tiangen Biotech, Beijing, China) following the manufacturer’s instructions. .. The total gDNA was quantified using the Qubit dsDNA HS Assay Kit on a Qubit 4.0 Fluorometer (Thermo Fisher Scientific.

    Article Title: Investigating the Pulmonary Host Response of Acinetobacter baumannii Infection-Associated Pneumonia by Metagenomic Next-Generation Sequencing.
    Article Snippet: The tube was placed on a FastPrep-24 5G instrument (MP Biomedicals, Santa Ana, CA, USA) at a speed of 10 m/s for 25 min. .. Subsequently, the supernatant (200 μL) was transferred to a new 1.5 mL tube following high-speed centrifugation at 8000× g for 1 min for further DNA extraction. gDNA extraction was performed using the TIANMicrobe Pathogen DNA Kit (Tiangen Biotech, Beijing, China) following the manufacturer’s instructions. .. The total gDNA was Biomedicines 2025, 13, 142 5 of 14 quantified using the Qubit dsDNA HS Assay Kit on a Qubit 4.0 Fluorometer (Thermo Fisher Scientific.



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    Functional characterization of Latilactobacillus curvatus NBL2305 as probiotics and postbiotics. a Schematic illustration of the preparation procedure for postbiotics derived from L. curvatus NBL2305. b Phylogenetic tree based on 16S rRNA gene sequences showing the taxonomic position of strain NBL2305 among closely related Latilactobacillus species. c – e Survival of the strain under salt tolerance and simulated gastrointestinal conditions, including simulated gastric and intestinal fluids. f Antibiotic susceptibility profile of L. curvatus NBL2305 against commonly used antibiotics. g Effects of probiotic cells and postbiotic preparations on HT-29 cell viability. h Adhesion ability of L. curvatus NBL2305 to HT-29 cells, expressed as percentage adhesion. i Antimicrobial activity of the postbiotic preparation against six fish pathogens, including <t>Edwardsiella</t> <t>tarda</t> , Flexibacter japonensis , Vibrio anguillarum , Photobacterium damselae subsp. damselae , Streptococcus iniae , and Vibrio harveyi , evaluated using an agar diffusion assay and expressed as inhibition zone diameter (mm). j Antioxidant activities of the postbiotic supernatant determined by DPPH, ABTS, SOD, TAC, and FRAP assays. Data are presented as mean ± SD, and statistical significance was determined using Student’s t -test ( P < 0.05)
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    Image Search Results


    Functional characterization of Latilactobacillus curvatus NBL2305 as probiotics and postbiotics. a Schematic illustration of the preparation procedure for postbiotics derived from L. curvatus NBL2305. b Phylogenetic tree based on 16S rRNA gene sequences showing the taxonomic position of strain NBL2305 among closely related Latilactobacillus species. c – e Survival of the strain under salt tolerance and simulated gastrointestinal conditions, including simulated gastric and intestinal fluids. f Antibiotic susceptibility profile of L. curvatus NBL2305 against commonly used antibiotics. g Effects of probiotic cells and postbiotic preparations on HT-29 cell viability. h Adhesion ability of L. curvatus NBL2305 to HT-29 cells, expressed as percentage adhesion. i Antimicrobial activity of the postbiotic preparation against six fish pathogens, including Edwardsiella tarda , Flexibacter japonensis , Vibrio anguillarum , Photobacterium damselae subsp. damselae , Streptococcus iniae , and Vibrio harveyi , evaluated using an agar diffusion assay and expressed as inhibition zone diameter (mm). j Antioxidant activities of the postbiotic supernatant determined by DPPH, ABTS, SOD, TAC, and FRAP assays. Data are presented as mean ± SD, and statistical significance was determined using Student’s t -test ( P < 0.05)

    Journal: Journal of Animal Science and Biotechnology

    Article Title: Postbiotics enhance immune competence in black rockfish ( Sebastes schlegelii ): linking innate immunity, apoptosis, and resistance to bacterial infection

    doi: 10.1186/s40104-026-01502-y

    Figure Lengend Snippet: Functional characterization of Latilactobacillus curvatus NBL2305 as probiotics and postbiotics. a Schematic illustration of the preparation procedure for postbiotics derived from L. curvatus NBL2305. b Phylogenetic tree based on 16S rRNA gene sequences showing the taxonomic position of strain NBL2305 among closely related Latilactobacillus species. c – e Survival of the strain under salt tolerance and simulated gastrointestinal conditions, including simulated gastric and intestinal fluids. f Antibiotic susceptibility profile of L. curvatus NBL2305 against commonly used antibiotics. g Effects of probiotic cells and postbiotic preparations on HT-29 cell viability. h Adhesion ability of L. curvatus NBL2305 to HT-29 cells, expressed as percentage adhesion. i Antimicrobial activity of the postbiotic preparation against six fish pathogens, including Edwardsiella tarda , Flexibacter japonensis , Vibrio anguillarum , Photobacterium damselae subsp. damselae , Streptococcus iniae , and Vibrio harveyi , evaluated using an agar diffusion assay and expressed as inhibition zone diameter (mm). j Antioxidant activities of the postbiotic supernatant determined by DPPH, ABTS, SOD, TAC, and FRAP assays. Data are presented as mean ± SD, and statistical significance was determined using Student’s t -test ( P < 0.05)

    Article Snippet: The pathogenic bacterium E. tarda (ATCC 15947) was obtained from the Korean Collection for Type Cultures (KCTC, Korea).

    Techniques: Functional Assay, Probiotics, Derivative Assay, Activity Assay, Diffusion-based Assay, Inhibition

    Effects of dietary postbiotic supplementation on growth performance, physiological parameters, and disease resistance in juvenile black rockfish ( Sebastes schlegelii ). The control group (CON) was fed a basal diet, whereas the POST group received a diet supplemented with postbiotics derived from Latilactobacillus curvatus NBL2305. a Growth performance, feed utilization, and somatic indices after an 8-week feeding trial, including weight gain (WG), specific growth rate (SGR), survival rate (SR), feed conversion ratio (FCR), protein efficiency ratio (PER), hepatosomatic index (HSI), viscerosomatic index (VSI), and condition factor (CF) ( n = 15). b Serum biochemical parameters, including total protein (TP), triglycerides (TG), glucose (GLU), total cholesterol (TCHO), alanine aminotransferase (ALT), and aspartate aminotransferase (AST) ( n = 5). c Non-specific immune parameters in serum ( n = 5). d Digestive enzyme activities measured in intestinal tissue ( n = 5). e Experimental design of the feeding and challenge trial, in which fish were fed the experimental diets for 8 weeks (T1) followed by a bacterial challenge test (T2) with Edwardsiella tarda . f Kaplan–Meier survival curves of juvenile rockfish following E. tarda challenge ( n = 15). Data are presented as mean ± SD. Statistical significance was determined using Student’s t -test, with differences indicated as * P < 0.05, ** P < 0.01, and *** P < 0.001. CON, control group; POST, postbiotic-supplemented group

    Journal: Journal of Animal Science and Biotechnology

    Article Title: Postbiotics enhance immune competence in black rockfish ( Sebastes schlegelii ): linking innate immunity, apoptosis, and resistance to bacterial infection

    doi: 10.1186/s40104-026-01502-y

    Figure Lengend Snippet: Effects of dietary postbiotic supplementation on growth performance, physiological parameters, and disease resistance in juvenile black rockfish ( Sebastes schlegelii ). The control group (CON) was fed a basal diet, whereas the POST group received a diet supplemented with postbiotics derived from Latilactobacillus curvatus NBL2305. a Growth performance, feed utilization, and somatic indices after an 8-week feeding trial, including weight gain (WG), specific growth rate (SGR), survival rate (SR), feed conversion ratio (FCR), protein efficiency ratio (PER), hepatosomatic index (HSI), viscerosomatic index (VSI), and condition factor (CF) ( n = 15). b Serum biochemical parameters, including total protein (TP), triglycerides (TG), glucose (GLU), total cholesterol (TCHO), alanine aminotransferase (ALT), and aspartate aminotransferase (AST) ( n = 5). c Non-specific immune parameters in serum ( n = 5). d Digestive enzyme activities measured in intestinal tissue ( n = 5). e Experimental design of the feeding and challenge trial, in which fish were fed the experimental diets for 8 weeks (T1) followed by a bacterial challenge test (T2) with Edwardsiella tarda . f Kaplan–Meier survival curves of juvenile rockfish following E. tarda challenge ( n = 15). Data are presented as mean ± SD. Statistical significance was determined using Student’s t -test, with differences indicated as * P < 0.05, ** P < 0.01, and *** P < 0.001. CON, control group; POST, postbiotic-supplemented group

    Article Snippet: The pathogenic bacterium E. tarda (ATCC 15947) was obtained from the Korean Collection for Type Cultures (KCTC, Korea).

    Techniques: Control, Derivative Assay, Tissue