acquity beh c-18 column Search Results


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  • 89
    Waters Corporation acquity beh c 18 column
    U ltra-performance liquid chromatography ( UPLC) of ginsenosides in Korean red ginseng–water extract (KRG-WE). UPLC analysis was performed by an <t>ACQUITY</t> <t>BEH</t> <t>C18</t> column (100 mm × 2.1 mm, 1.7 μm; Waters, Milford, MA, USA) at column temperature of 40°C. The binary gradient elution system consisted of 0.001% phosphoric acid in water and 0.001% phosphoric acid in acetonitrile.
    Acquity Beh C 18 Column, supplied by Waters Corporation, used in various techniques. Bioz Stars score: 89/100, based on 814 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/acquity beh c 18 column/product/Waters Corporation
    Average 89 stars, based on 814 article reviews
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    93
    Merck & Co acquity beh c18 column
    U ltra-performance liquid chromatography ( UPLC) of ginsenosides in Korean red ginseng–water extract (KRG-WE). UPLC analysis was performed by an <t>ACQUITY</t> <t>BEH</t> <t>C18</t> column (100 mm × 2.1 mm, 1.7 μm; Waters, Milford, MA, USA) at column temperature of 40°C. The binary gradient elution system consisted of 0.001% phosphoric acid in water and 0.001% phosphoric acid in acetonitrile.
    Acquity Beh C18 Column, supplied by Merck & Co, used in various techniques. Bioz Stars score: 93/100, based on 14 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/acquity beh c18 column/product/Merck & Co
    Average 93 stars, based on 14 article reviews
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    acquity beh c18 column - by Bioz Stars, 2020-08
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    Waters Corporation acquity uplctm beh c18 column
    U ltra-performance liquid chromatography ( UPLC) of ginsenosides in Korean red ginseng–water extract (KRG-WE). UPLC analysis was performed by an <t>ACQUITY</t> <t>BEH</t> <t>C18</t> column (100 mm × 2.1 mm, 1.7 μm; Waters, Milford, MA, USA) at column temperature of 40°C. The binary gradient elution system consisted of 0.001% phosphoric acid in water and 0.001% phosphoric acid in acetonitrile.
    Acquity Uplctm Beh C18 Column, supplied by Waters Corporation, used in various techniques. Bioz Stars score: 88/100, based on 77 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/acquity uplctm beh c18 column/product/Waters Corporation
    Average 88 stars, based on 77 article reviews
    Price from $9.99 to $1999.99
    acquity uplctm beh c18 column - by Bioz Stars, 2020-08
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    93
    Waters Corporation particle acquity beh c18 column
    U ltra-performance liquid chromatography ( UPLC) of ginsenosides in Korean red ginseng–water extract (KRG-WE). UPLC analysis was performed by an <t>ACQUITY</t> <t>BEH</t> <t>C18</t> column (100 mm × 2.1 mm, 1.7 μm; Waters, Milford, MA, USA) at column temperature of 40°C. The binary gradient elution system consisted of 0.001% phosphoric acid in water and 0.001% phosphoric acid in acetonitrile.
    Particle Acquity Beh C18 Column, supplied by Waters Corporation, used in various techniques. Bioz Stars score: 93/100, based on 24 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/particle acquity beh c18 column/product/Waters Corporation
    Average 93 stars, based on 24 article reviews
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    Waters Corporation acquity upc2 beh c18 column
    U ltra-performance liquid chromatography ( UPLC) of ginsenosides in Korean red ginseng–water extract (KRG-WE). UPLC analysis was performed by an <t>ACQUITY</t> <t>BEH</t> <t>C18</t> column (100 mm × 2.1 mm, 1.7 μm; Waters, Milford, MA, USA) at column temperature of 40°C. The binary gradient elution system consisted of 0.001% phosphoric acid in water and 0.001% phosphoric acid in acetonitrile.
    Acquity Upc2 Beh C18 Column, supplied by Waters Corporation, used in various techniques. Bioz Stars score: 94/100, based on 14 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/acquity upc2 beh c18 column/product/Waters Corporation
    Average 94 stars, based on 14 article reviews
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    88
    Waters Corporation acquity beh c18 chromatography column
    U ltra-performance liquid chromatography ( UPLC) of ginsenosides in Korean red ginseng–water extract (KRG-WE). UPLC analysis was performed by an <t>ACQUITY</t> <t>BEH</t> <t>C18</t> column (100 mm × 2.1 mm, 1.7 μm; Waters, Milford, MA, USA) at column temperature of 40°C. The binary gradient elution system consisted of 0.001% phosphoric acid in water and 0.001% phosphoric acid in acetonitrile.
    Acquity Beh C18 Chromatography Column, supplied by Waters Corporation, used in various techniques. Bioz Stars score: 88/100, based on 29 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/acquity beh c18 chromatography column/product/Waters Corporation
    Average 88 stars, based on 29 article reviews
    Price from $9.99 to $1999.99
    acquity beh c18 chromatography column - by Bioz Stars, 2020-08
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    93
    Agilent technologies acquity beh c18 column
    U ltra-performance liquid chromatography ( UPLC) of ginsenosides in Korean red ginseng–water extract (KRG-WE). UPLC analysis was performed by an <t>ACQUITY</t> <t>BEH</t> <t>C18</t> column (100 mm × 2.1 mm, 1.7 μm; Waters, Milford, MA, USA) at column temperature of 40°C. The binary gradient elution system consisted of 0.001% phosphoric acid in water and 0.001% phosphoric acid in acetonitrile.
    Acquity Beh C18 Column, supplied by Agilent technologies, used in various techniques. Bioz Stars score: 93/100, based on 2 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/acquity beh c18 column/product/Agilent technologies
    Average 93 stars, based on 2 article reviews
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    Image Search Results


    U ltra-performance liquid chromatography ( UPLC) of ginsenosides in Korean red ginseng–water extract (KRG-WE). UPLC analysis was performed by an ACQUITY BEH C18 column (100 mm × 2.1 mm, 1.7 μm; Waters, Milford, MA, USA) at column temperature of 40°C. The binary gradient elution system consisted of 0.001% phosphoric acid in water and 0.001% phosphoric acid in acetonitrile.

    Journal: Journal of Ginseng Research

    Article Title: Protective effects of Korean Red Ginseng against sub-acute immobilization stress-induced testicular damage in experimental rats

    doi: 10.1016/j.jgr.2017.09.002

    Figure Lengend Snippet: U ltra-performance liquid chromatography ( UPLC) of ginsenosides in Korean red ginseng–water extract (KRG-WE). UPLC analysis was performed by an ACQUITY BEH C18 column (100 mm × 2.1 mm, 1.7 μm; Waters, Milford, MA, USA) at column temperature of 40°C. The binary gradient elution system consisted of 0.001% phosphoric acid in water and 0.001% phosphoric acid in acetonitrile.

    Article Snippet: The separation was accomplished on an ACQUITY BEH C18 column (100 mm × 2.1 mm, 1.7 μm; Waters) at a column temperature of 40°C.

    Techniques: Liquid Chromatography

    Development of a faster FAHFA analysis method ( a ) Structures of 5-, 9-, and 12-PAHSA and 12-OAHSA. Extracted ion chromatograms showing the retention times of 5-, 9-, and 12-PAHSA and 5-, 9-, 12-OAHSA standards on a Luna C18(2) column (3 µm, 250 × 2.0 mm, Phenomenex) ( b ) and an Acquity UPLC BEH C18 column (1.7 µm, 2.1 mm × 100 mm, Waters) ( c ).

    Journal: Analytical chemistry

    Article Title: A Faster Protocol for Endogenous FAHFA Measurements

    doi: 10.1021/acs.analchem.8b00503

    Figure Lengend Snippet: Development of a faster FAHFA analysis method ( a ) Structures of 5-, 9-, and 12-PAHSA and 12-OAHSA. Extracted ion chromatograms showing the retention times of 5-, 9-, and 12-PAHSA and 5-, 9-, 12-OAHSA standards on a Luna C18(2) column (3 µm, 250 × 2.0 mm, Phenomenex) ( b ) and an Acquity UPLC BEH C18 column (1.7 µm, 2.1 mm × 100 mm, Waters) ( c ).

    Article Snippet: An Acquity UPLC BEH C18 column (1.7 µm, 2.1 mm × 100 mm, Waters) was used for separation of FAHFAs.

    Techniques:

    UPLC-MS-ELSD-PDA analysis of fraction 80679-c9 of Berberis thunbergii . a ELSD chromatogram; b PDA chromatogram; c , d positive and negative ESI–MS TIC chromatograms, respectively; e positive ESI–MS spectra of the compound with a retention time of 2.06 min in the PDA chromatogram; f UV spectra of the compound with a retention time of 2.06 min in PDA chromatogram. UPLC conditions: Acquity UPLC BEH C 18 column (2.1 × 50 mm, 1.7 μm); gradient elution with 0–100 % ACN in 0.1 % HCOOH in 3 min

    Journal: Malaria Journal

    Article Title: Diversity-oriented natural product platform identifies plant constituents targeting Plasmodium falciparum

    doi: 10.1186/s12936-016-1313-7

    Figure Lengend Snippet: UPLC-MS-ELSD-PDA analysis of fraction 80679-c9 of Berberis thunbergii . a ELSD chromatogram; b PDA chromatogram; c , d positive and negative ESI–MS TIC chromatograms, respectively; e positive ESI–MS spectra of the compound with a retention time of 2.06 min in the PDA chromatogram; f UV spectra of the compound with a retention time of 2.06 min in PDA chromatogram. UPLC conditions: Acquity UPLC BEH C 18 column (2.1 × 50 mm, 1.7 μm); gradient elution with 0–100 % ACN in 0.1 % HCOOH in 3 min

    Article Snippet: The progression of compound purification was monitored by using an Agilent 1290 Infinity UHPLC-MS (Agilent Technologies, Santa Clara, CA, USA) and a methanol gradient in 0.05 % formic acid passed through a Waters Acquity BEH C18 column (Waters Corporation, Milford, MA, USA, 150 × 2.1 mm, 1.7-µm particle size).

    Techniques: Mass Spectrometry

    UPLC-MS-ELSD-PDA analysis of fraction 79575-c5 of Eugenia rigida . a ELSD chromatogram; b PDA chromatogram; c and d positive and negative ESI–MS BPI chromatograms, respectively; e , f positive ESI–MS spectra of the compounds with respective retention times of 1.87 and 1.95 min in the PDA chromatogram; g , h negative ESI–MS spectra of the compounds with respective retention times of 1.87 and 1.95 min in the PDA chromatogram; i , j UV spectra of the compounds with respective retention times of 1.87 and 1.95 min in the PDA chromatogram. UPLC conditions: Acquity UPLC BEH C 18 column (2.1 × 50 mm, 1.7 μm); gradient elution with 0–100 % ACN in 0.1 % HCOOH in 3 min

    Journal: Malaria Journal

    Article Title: Diversity-oriented natural product platform identifies plant constituents targeting Plasmodium falciparum

    doi: 10.1186/s12936-016-1313-7

    Figure Lengend Snippet: UPLC-MS-ELSD-PDA analysis of fraction 79575-c5 of Eugenia rigida . a ELSD chromatogram; b PDA chromatogram; c and d positive and negative ESI–MS BPI chromatograms, respectively; e , f positive ESI–MS spectra of the compounds with respective retention times of 1.87 and 1.95 min in the PDA chromatogram; g , h negative ESI–MS spectra of the compounds with respective retention times of 1.87 and 1.95 min in the PDA chromatogram; i , j UV spectra of the compounds with respective retention times of 1.87 and 1.95 min in the PDA chromatogram. UPLC conditions: Acquity UPLC BEH C 18 column (2.1 × 50 mm, 1.7 μm); gradient elution with 0–100 % ACN in 0.1 % HCOOH in 3 min

    Article Snippet: The progression of compound purification was monitored by using an Agilent 1290 Infinity UHPLC-MS (Agilent Technologies, Santa Clara, CA, USA) and a methanol gradient in 0.05 % formic acid passed through a Waters Acquity BEH C18 column (Waters Corporation, Milford, MA, USA, 150 × 2.1 mm, 1.7-µm particle size).

    Techniques: Mass Spectrometry

    UPLC-MS-ELSD-PDA analysis of fraction 80679-c5 of Berberis thunbergii . a ELSD chromatogram; b PDA chromatogram; c , d positive ESI–MS BPI and negative ESI–MS TIC chromatograms, respectively; e – g positive ESI–MS spectra of the compounds with respective retention times of 2.06, 2.18, and 2.23 min in the PDA chromatogram; h , i UV spectra of the compounds with respective retention times of 2.18 and 2.23 min in the PDA chromatogram. UPLC conditions: acquity UPLC BEH C 18 column (2.1 × 50 mm, 1.7 μm); gradient elution with 0–100 % ACN in 0.1 % HCOOH in 3 min

    Journal: Malaria Journal

    Article Title: Diversity-oriented natural product platform identifies plant constituents targeting Plasmodium falciparum

    doi: 10.1186/s12936-016-1313-7

    Figure Lengend Snippet: UPLC-MS-ELSD-PDA analysis of fraction 80679-c5 of Berberis thunbergii . a ELSD chromatogram; b PDA chromatogram; c , d positive ESI–MS BPI and negative ESI–MS TIC chromatograms, respectively; e – g positive ESI–MS spectra of the compounds with respective retention times of 2.06, 2.18, and 2.23 min in the PDA chromatogram; h , i UV spectra of the compounds with respective retention times of 2.18 and 2.23 min in the PDA chromatogram. UPLC conditions: acquity UPLC BEH C 18 column (2.1 × 50 mm, 1.7 μm); gradient elution with 0–100 % ACN in 0.1 % HCOOH in 3 min

    Article Snippet: The progression of compound purification was monitored by using an Agilent 1290 Infinity UHPLC-MS (Agilent Technologies, Santa Clara, CA, USA) and a methanol gradient in 0.05 % formic acid passed through a Waters Acquity BEH C18 column (Waters Corporation, Milford, MA, USA, 150 × 2.1 mm, 1.7-µm particle size).

    Techniques: Mass Spectrometry

    UPLC-MS-ELSD-PDA analysis of fraction 80679-c3 of Berberis thunbergii . a ELSD chromatogram; b PDA chromatogram; c positive ESI–MS TIC chromatogram; d negative ESI–MS TIC chromatogram; e – g positive ESI–MS spectra of the compounds with respective retention times of 0.85, 0.94, and 0.98 min in the PDA chromatogram; h , i negative ESI–MS spectra of the compounds with respective retention times of 0.85 and 0.94 in the PDA chromatogram; j – l UV spectra of the compounds with respective retention times of 0.85, 0.94, and 0.98 min in the PDA chromatogram. UPLC conditions: acquity UPLC BEH C 18 column (2.1 × 50 mm, 1.7 μm); gradient elution with 0– 100 % ACN in 0.1 % HCOOH in 3 min

    Journal: Malaria Journal

    Article Title: Diversity-oriented natural product platform identifies plant constituents targeting Plasmodium falciparum

    doi: 10.1186/s12936-016-1313-7

    Figure Lengend Snippet: UPLC-MS-ELSD-PDA analysis of fraction 80679-c3 of Berberis thunbergii . a ELSD chromatogram; b PDA chromatogram; c positive ESI–MS TIC chromatogram; d negative ESI–MS TIC chromatogram; e – g positive ESI–MS spectra of the compounds with respective retention times of 0.85, 0.94, and 0.98 min in the PDA chromatogram; h , i negative ESI–MS spectra of the compounds with respective retention times of 0.85 and 0.94 in the PDA chromatogram; j – l UV spectra of the compounds with respective retention times of 0.85, 0.94, and 0.98 min in the PDA chromatogram. UPLC conditions: acquity UPLC BEH C 18 column (2.1 × 50 mm, 1.7 μm); gradient elution with 0– 100 % ACN in 0.1 % HCOOH in 3 min

    Article Snippet: The progression of compound purification was monitored by using an Agilent 1290 Infinity UHPLC-MS (Agilent Technologies, Santa Clara, CA, USA) and a methanol gradient in 0.05 % formic acid passed through a Waters Acquity BEH C18 column (Waters Corporation, Milford, MA, USA, 150 × 2.1 mm, 1.7-µm particle size).

    Techniques: Mass Spectrometry