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    Eiken Chemical loopamp real time turbidimeter
    Different temperatures of the LAMP reaction for detection of NDM-1. Turbidity was monitored by a <t>Loopamp</t> real-time turbidimeter at 400 nm every 6 s.
    Loopamp Real Time Turbidimeter, supplied by Eiken Chemical, 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/result/loopamp real time turbidimeter/product/Eiken Chemical
    Average 86 stars, based on 1 article reviews
    Price from $9.99 to $1999.99
    loopamp real time turbidimeter - by Bioz Stars, 2021-06
    86/100 stars
      Buy from Supplier

    86
    Eiken Chemical real time turbidimeter
    Different temperatures of the LAMP reaction for detection of NDM-1. Turbidity was monitored by a <t>Loopamp</t> real-time turbidimeter at 400 nm every 6 s.
    Real Time Turbidimeter, supplied by Eiken Chemical, 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/result/real time turbidimeter/product/Eiken Chemical
    Average 86 stars, based on 1 article reviews
    Price from $9.99 to $1999.99
    real time turbidimeter - by Bioz Stars, 2021-06
    86/100 stars
      Buy from Supplier

    86
    Teramecs Co Ltd loopamp real time turbidimeter
    Different temperatures of the LAMP reaction for detection of NDM-1. Turbidity was monitored by a <t>Loopamp</t> real-time turbidimeter at 400 nm every 6 s.
    Loopamp Real Time Turbidimeter, supplied by Teramecs Co Ltd, 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/result/loopamp real time turbidimeter/product/Teramecs Co Ltd
    Average 86 stars, based on 1 article reviews
    Price from $9.99 to $1999.99
    loopamp real time turbidimeter - by Bioz Stars, 2021-06
    86/100 stars
      Buy from Supplier

    86
    Eiken Chemical loopamp realtime turbidimeter
    Different temperatures at which the LAMP reaction detected K. pneumoniae . Turbidity was monitored every 6 s with a <t>Loopamp</t> <t>Realtime</t> Turbidimeter at 650 nm.
    Loopamp Realtime Turbidimeter, supplied by Eiken Chemical, 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/result/loopamp realtime turbidimeter/product/Eiken Chemical
    Average 86 stars, based on 1 article reviews
    Price from $9.99 to $1999.99
    loopamp realtime turbidimeter - by Bioz Stars, 2021-06
    86/100 stars
      Buy from Supplier

    Image Search Results


    Different temperatures of the LAMP reaction for detection of NDM-1. Turbidity was monitored by a Loopamp real-time turbidimeter at 400 nm every 6 s.

    Journal: Journal of Clinical Microbiology

    Article Title: Sensitive and Rapid Detection of the New Delhi Metallo-Beta-Lactamase Gene by Loop-Mediated Isothermal Amplification

    doi: 10.1128/JCM.06647-11

    Figure Lengend Snippet: Different temperatures of the LAMP reaction for detection of NDM-1. Turbidity was monitored by a Loopamp real-time turbidimeter at 400 nm every 6 s.

    Article Snippet: For monitoring of turbidity , real-time amplification by the LAMP assay was monitored through spectrophotometric analysis by recording the optical density at 400 nm every 6 s with the help of a Loopamp real-time turbidimeter (LA-230; Eiken Chemical Co., Ltd., Tochigi, Japan).

    Techniques:

    Detection of the bla NDM-1 gene in simulated sputum samples (A), simulated urine samples (B), and simulated fecal samples (C) by a Loopamp real-time turbidimeter at 400 nm every 6 s. The concentration of pure genomic DNA extracted from A. baumannii XM in each simulated sputum sample is shown.

    Journal: Journal of Clinical Microbiology

    Article Title: Sensitive and Rapid Detection of the New Delhi Metallo-Beta-Lactamase Gene by Loop-Mediated Isothermal Amplification

    doi: 10.1128/JCM.06647-11

    Figure Lengend Snippet: Detection of the bla NDM-1 gene in simulated sputum samples (A), simulated urine samples (B), and simulated fecal samples (C) by a Loopamp real-time turbidimeter at 400 nm every 6 s. The concentration of pure genomic DNA extracted from A. baumannii XM in each simulated sputum sample is shown.

    Article Snippet: For monitoring of turbidity , real-time amplification by the LAMP assay was monitored through spectrophotometric analysis by recording the optical density at 400 nm every 6 s with the help of a Loopamp real-time turbidimeter (LA-230; Eiken Chemical Co., Ltd., Tochigi, Japan).

    Techniques: Concentration Assay

    Specificity of the LAMP reaction for detection of bla NDM-1 . Turbidity was monitored by a Loopamp real-time turbidimeter at 400 nm every 6 s. Amplification was performed at 65°C for 65 min. Lines: 1, negative control (double-distilled water); 2, A. baumannii XM; 3, A. baumannii H949; 4, A. baumannii F398; 5, A. baumannii B260; 6, A. baumannii H18; 7, S. sonnei 2531; 8, S. flexneri 4536; 9, S. enterica serotype Enteritidis 50326-1; 10, V. carchariae 5732; 11, S. enterica serotype Paratyphi 86423; 12, enteroinvasive E. coli 44825; 13, enterotoxigenic E. coli 44824; 14, enteropathogenic E. coli 2348; and 15, V. parahaemolyticus 5474.

    Journal: Journal of Clinical Microbiology

    Article Title: Sensitive and Rapid Detection of the New Delhi Metallo-Beta-Lactamase Gene by Loop-Mediated Isothermal Amplification

    doi: 10.1128/JCM.06647-11

    Figure Lengend Snippet: Specificity of the LAMP reaction for detection of bla NDM-1 . Turbidity was monitored by a Loopamp real-time turbidimeter at 400 nm every 6 s. Amplification was performed at 65°C for 65 min. Lines: 1, negative control (double-distilled water); 2, A. baumannii XM; 3, A. baumannii H949; 4, A. baumannii F398; 5, A. baumannii B260; 6, A. baumannii H18; 7, S. sonnei 2531; 8, S. flexneri 4536; 9, S. enterica serotype Enteritidis 50326-1; 10, V. carchariae 5732; 11, S. enterica serotype Paratyphi 86423; 12, enteroinvasive E. coli 44825; 13, enterotoxigenic E. coli 44824; 14, enteropathogenic E. coli 2348; and 15, V. parahaemolyticus 5474.

    Article Snippet: For monitoring of turbidity , real-time amplification by the LAMP assay was monitored through spectrophotometric analysis by recording the optical density at 400 nm every 6 s with the help of a Loopamp real-time turbidimeter (LA-230; Eiken Chemical Co., Ltd., Tochigi, Japan).

    Techniques: Amplification, Negative Control

    Comparison of sensitivity between the LAMP reaction and PCR for detection of the bla NDM-1 gene. The pure genomic DNA extracted from A. baumannii XM was diluted in a serial 10-fold dilution. Both LAMP reactions (A and B) and PCRs (C) were carried out in duplicate for each dilution point. Tubes and lanes: 1, 1,070 ng/μl; 2, 107.0 ng/μl; 3, 10.70 ng/μl; 4, 1.070 ng/μl; 5, 107.0 pg/μl; 6, 10.70 pg/μl; 7, 1.070 pg/μl; 8, 0.107 pg/μl. (A) Turbidity was monitored by a Loopamp real-time turbidimeter at 400 nm every 6 s; (B) 1 μl of fluorescent detection reagent was added to 25 μl of LAMP reaction mixture before the LAMP reaction; (C) the PCR products were analyzed by 2% agarose gel electrophoresis and stained with ethidium bromide.

    Journal: Journal of Clinical Microbiology

    Article Title: Sensitive and Rapid Detection of the New Delhi Metallo-Beta-Lactamase Gene by Loop-Mediated Isothermal Amplification

    doi: 10.1128/JCM.06647-11

    Figure Lengend Snippet: Comparison of sensitivity between the LAMP reaction and PCR for detection of the bla NDM-1 gene. The pure genomic DNA extracted from A. baumannii XM was diluted in a serial 10-fold dilution. Both LAMP reactions (A and B) and PCRs (C) were carried out in duplicate for each dilution point. Tubes and lanes: 1, 1,070 ng/μl; 2, 107.0 ng/μl; 3, 10.70 ng/μl; 4, 1.070 ng/μl; 5, 107.0 pg/μl; 6, 10.70 pg/μl; 7, 1.070 pg/μl; 8, 0.107 pg/μl. (A) Turbidity was monitored by a Loopamp real-time turbidimeter at 400 nm every 6 s; (B) 1 μl of fluorescent detection reagent was added to 25 μl of LAMP reaction mixture before the LAMP reaction; (C) the PCR products were analyzed by 2% agarose gel electrophoresis and stained with ethidium bromide.

    Article Snippet: For monitoring of turbidity , real-time amplification by the LAMP assay was monitored through spectrophotometric analysis by recording the optical density at 400 nm every 6 s with the help of a Loopamp real-time turbidimeter (LA-230; Eiken Chemical Co., Ltd., Tochigi, Japan).

    Techniques: Polymerase Chain Reaction, Agarose Gel Electrophoresis, Staining

    Different temperatures at which the LAMP reaction detected K. pneumoniae . Turbidity was monitored every 6 s with a Loopamp Realtime Turbidimeter at 650 nm.

    Journal: Frontiers in Microbiology

    Article Title: Survey and rapid detection of Klebsiella pneumoniae in clinical samples targeting the rcsA gene in Beijing, China

    doi: 10.3389/fmicb.2015.00519

    Figure Lengend Snippet: Different temperatures at which the LAMP reaction detected K. pneumoniae . Turbidity was monitored every 6 s with a Loopamp Realtime Turbidimeter at 650 nm.

    Article Snippet: Real-time changes in turbidity were monitored with spectrophotometric analysis by recording the optical density (650 nm) every 6 s with a Loopamp Realtime Turbidimeter (LA-320c; Eiken Chemical Co., Ltd).

    Techniques:

    LAMP results for K. pneumoniae isolates from clinical samples. (A) Turbidity was monitored every 6 s using a Loopamp Realtime Turbidimeter at 650 nm. (B) The results were visualized by the addition of 1 μl of fluorescent detection reagent to the 25 μl LAMP reaction mixture before the LAMP reaction. 1, Negative control (double-distilled water); 2, positive control ( K. pneumoniae ATCC BAA-2146); 3, K. pneumoniae WJ-48; 4, K. pneumoniae WJ-50; 5, K. pneumoniae WJ-51; 6, K. pneumoniae WJ-52; 7, K. pneumoniae WJ-53; 8, K. pneumoniae WJ-57; 9, K. pneumoniae WJ-58; 10, K. pneumoniae WJ-60; 11, K. pneumoniae WJ-61; 12, K. pneumoniae WJ-64; 13, K. pneumoniae WJ-65; 14, K. pneumoniae WJ-66; 15, K. pneumoniae WJ-68; 16, K. pneumoniae 301-052; 17, K. pneumoniae 301-207; 18, K. pneumoniae 301-263; 19, K. pneumoniae 301-432; 20, K. pneumoniae 301-416; 21, K. pneumoniae 301-323; 22, K. pneumoniae 301-365; 23, K. pneumoniae 301-282; 24, K. pneumoniae 301-406; 25, K. pneumoniae 301-158; 26, K. pneumoniae 307-206; 27, K. pneumoniae 307-082; 28, K. pneumoniae 307-429; 29, K. pneumoniae 307-095; 30, K. pneumoniae 307-003; 31, K. pneumoniae 307-030; 32, K. pneumoniae 307-194; 33, K. pneumoniae 307-356; 34, K. pneumoniae 307-235.

    Journal: Frontiers in Microbiology

    Article Title: Survey and rapid detection of Klebsiella pneumoniae in clinical samples targeting the rcsA gene in Beijing, China

    doi: 10.3389/fmicb.2015.00519

    Figure Lengend Snippet: LAMP results for K. pneumoniae isolates from clinical samples. (A) Turbidity was monitored every 6 s using a Loopamp Realtime Turbidimeter at 650 nm. (B) The results were visualized by the addition of 1 μl of fluorescent detection reagent to the 25 μl LAMP reaction mixture before the LAMP reaction. 1, Negative control (double-distilled water); 2, positive control ( K. pneumoniae ATCC BAA-2146); 3, K. pneumoniae WJ-48; 4, K. pneumoniae WJ-50; 5, K. pneumoniae WJ-51; 6, K. pneumoniae WJ-52; 7, K. pneumoniae WJ-53; 8, K. pneumoniae WJ-57; 9, K. pneumoniae WJ-58; 10, K. pneumoniae WJ-60; 11, K. pneumoniae WJ-61; 12, K. pneumoniae WJ-64; 13, K. pneumoniae WJ-65; 14, K. pneumoniae WJ-66; 15, K. pneumoniae WJ-68; 16, K. pneumoniae 301-052; 17, K. pneumoniae 301-207; 18, K. pneumoniae 301-263; 19, K. pneumoniae 301-432; 20, K. pneumoniae 301-416; 21, K. pneumoniae 301-323; 22, K. pneumoniae 301-365; 23, K. pneumoniae 301-282; 24, K. pneumoniae 301-406; 25, K. pneumoniae 301-158; 26, K. pneumoniae 307-206; 27, K. pneumoniae 307-082; 28, K. pneumoniae 307-429; 29, K. pneumoniae 307-095; 30, K. pneumoniae 307-003; 31, K. pneumoniae 307-030; 32, K. pneumoniae 307-194; 33, K. pneumoniae 307-356; 34, K. pneumoniae 307-235.

    Article Snippet: Real-time changes in turbidity were monitored with spectrophotometric analysis by recording the optical density (650 nm) every 6 s with a Loopamp Realtime Turbidimeter (LA-320c; Eiken Chemical Co., Ltd).

    Techniques: Negative Control, Positive Control

    Five sets of primers were used to amplify the target gene under the same conditions . Turbidity was monitored every 6 s with a Loopamp Realtime Turbidimeter at 650 nm.

    Journal: Frontiers in Microbiology

    Article Title: Survey and rapid detection of Klebsiella pneumoniae in clinical samples targeting the rcsA gene in Beijing, China

    doi: 10.3389/fmicb.2015.00519

    Figure Lengend Snippet: Five sets of primers were used to amplify the target gene under the same conditions . Turbidity was monitored every 6 s with a Loopamp Realtime Turbidimeter at 650 nm.

    Article Snippet: Real-time changes in turbidity were monitored with spectrophotometric analysis by recording the optical density (650 nm) every 6 s with a Loopamp Realtime Turbidimeter (LA-320c; Eiken Chemical Co., Ltd).

    Techniques:

    Specificity of the LAMP reaction in detecting K. pneumoniae . (A) Turbidity was monitored every 6 s using a Loopamp Realtime Turbidimeter at 650 nm. (B) The results were visualized by the addition of 1 μl of fluorescent detection reagent to the 25 μl LAMP reaction mixture before the LAMP reaction. Amplification was performed at 61°C for 60 min. 1, positive control ( K. pneumoniae ATCC BAA-2146); 2, negative control (double-distilled water); 3, Klebsiella oxytoca ATCC 700324; 4, Klebsiella rhinoscleromatis CMCC 46111; 5, Citrobacter freundii CMCC 48001; 6, Enterobacter aerogenes ATCC 13048; 7, Enterobacter cloacae ATCC 13047; 8, Proteus mirabilis CMCC 49005; 9, Proteus vulgaris CMCC 49027; 10, Serratia marcescens ATCC 14756; 11, Morganella morganii ATCC 25830; 12, Streptococcus pneumoniae 112-07; 13, Mycobacterium tuberculosis 005; 14, Pseudomonas aeruginosa D104; 15, Haemophilus influenza ATCC 49247; 16, Yersinia enterocolitica 027; 17, Yersinia pestis 2638; 18, Bacillus tularense 3450; 19, Vibrio cholera 3802; 20, Salmonella aberdeen 9264; 21, Neisseria meningitides CMCC 29022; 22, Staphylococcus aureus 2740; 23, Pseudomonas pseudomallei 029; 24, Salmonella typhimurium 4030; 25, Corynebacterium diphtheriae CMCC 38001; 26, Bacillus megatherium 4623; 27, Stenotrophomonas maltophilia K279a; 28, Legionella pneumophila 9135; 29, Acinetobacter baumannii 12101; 30, enteroinvasive E. coli 44825; 31, enterotoxigenic E. coli 44824; 32, enteropathogenic E. coli 2348.

    Journal: Frontiers in Microbiology

    Article Title: Survey and rapid detection of Klebsiella pneumoniae in clinical samples targeting the rcsA gene in Beijing, China

    doi: 10.3389/fmicb.2015.00519

    Figure Lengend Snippet: Specificity of the LAMP reaction in detecting K. pneumoniae . (A) Turbidity was monitored every 6 s using a Loopamp Realtime Turbidimeter at 650 nm. (B) The results were visualized by the addition of 1 μl of fluorescent detection reagent to the 25 μl LAMP reaction mixture before the LAMP reaction. Amplification was performed at 61°C for 60 min. 1, positive control ( K. pneumoniae ATCC BAA-2146); 2, negative control (double-distilled water); 3, Klebsiella oxytoca ATCC 700324; 4, Klebsiella rhinoscleromatis CMCC 46111; 5, Citrobacter freundii CMCC 48001; 6, Enterobacter aerogenes ATCC 13048; 7, Enterobacter cloacae ATCC 13047; 8, Proteus mirabilis CMCC 49005; 9, Proteus vulgaris CMCC 49027; 10, Serratia marcescens ATCC 14756; 11, Morganella morganii ATCC 25830; 12, Streptococcus pneumoniae 112-07; 13, Mycobacterium tuberculosis 005; 14, Pseudomonas aeruginosa D104; 15, Haemophilus influenza ATCC 49247; 16, Yersinia enterocolitica 027; 17, Yersinia pestis 2638; 18, Bacillus tularense 3450; 19, Vibrio cholera 3802; 20, Salmonella aberdeen 9264; 21, Neisseria meningitides CMCC 29022; 22, Staphylococcus aureus 2740; 23, Pseudomonas pseudomallei 029; 24, Salmonella typhimurium 4030; 25, Corynebacterium diphtheriae CMCC 38001; 26, Bacillus megatherium 4623; 27, Stenotrophomonas maltophilia K279a; 28, Legionella pneumophila 9135; 29, Acinetobacter baumannii 12101; 30, enteroinvasive E. coli 44825; 31, enterotoxigenic E. coli 44824; 32, enteropathogenic E. coli 2348.

    Article Snippet: Real-time changes in turbidity were monitored with spectrophotometric analysis by recording the optical density (650 nm) every 6 s with a Loopamp Realtime Turbidimeter (LA-320c; Eiken Chemical Co., Ltd).

    Techniques: Amplification, Positive Control, Negative Control

    Comparison of the sensitivities of the LAMP reaction and conventional PCR in detecting the rcsA gene of K. pneumoniae . Pure genomic DNA extracted from K. pneumoniae ATCC BAA-2146 was serially diluted 10-fold. (A) Turbidity was monitored every 6 s with a Loopamp Realtime Turbidimeter at 650 nm. (B) The reaction result was detected visually by the addition of 1 μl of fluorescent detection reagent to the 25 μl LAMP reaction mixture before the LAMP reaction. (C) PCR products were separated by 2% agarose gel electrophoresis and stained with ethidium bromide. Amplification was performed at 61°C for 60 min. 1, negative control (double-distilled water); 2, 115.0 ng/μl; 3, 11.5 ng/μl; 4, 1.15 ng/μl; 5, 115.0 pg/μl; 6, 11.5 pg/μl; 7, 1.15 pg/μl; 8, 0.115 pg/μl; 9, 0.0115 pg/μl.

    Journal: Frontiers in Microbiology

    Article Title: Survey and rapid detection of Klebsiella pneumoniae in clinical samples targeting the rcsA gene in Beijing, China

    doi: 10.3389/fmicb.2015.00519

    Figure Lengend Snippet: Comparison of the sensitivities of the LAMP reaction and conventional PCR in detecting the rcsA gene of K. pneumoniae . Pure genomic DNA extracted from K. pneumoniae ATCC BAA-2146 was serially diluted 10-fold. (A) Turbidity was monitored every 6 s with a Loopamp Realtime Turbidimeter at 650 nm. (B) The reaction result was detected visually by the addition of 1 μl of fluorescent detection reagent to the 25 μl LAMP reaction mixture before the LAMP reaction. (C) PCR products were separated by 2% agarose gel electrophoresis and stained with ethidium bromide. Amplification was performed at 61°C for 60 min. 1, negative control (double-distilled water); 2, 115.0 ng/μl; 3, 11.5 ng/μl; 4, 1.15 ng/μl; 5, 115.0 pg/μl; 6, 11.5 pg/μl; 7, 1.15 pg/μl; 8, 0.115 pg/μl; 9, 0.0115 pg/μl.

    Article Snippet: Real-time changes in turbidity were monitored with spectrophotometric analysis by recording the optical density (650 nm) every 6 s with a Loopamp Realtime Turbidimeter (LA-320c; Eiken Chemical Co., Ltd).

    Techniques: Polymerase Chain Reaction, Agarose Gel Electrophoresis, Staining, Amplification, Negative Control