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    Agilent technologies hplc elsd
    Identification of AA as the active ingredient in crude and bran-processed Atractylodes lancea . Model: SDS model rats group; M + Crude: SDS model rats administrated with crude AL extraction; M + Bran-processed: SDS model rats administrated with BAL extraction. (A) <t>HPLC-ELSD</t> chromatogram of the 50% EtOH extraction from AL (black) and BAL (red), the content of AA increased by 191.22% in the bran-processed Atractylodes lancea . (B) and (C) Comparison of the intestinal propulsion rate and GAS in SDS rats treated with crude and bran-processed Atractylodes lancea extracts. (D) 3D structure of AA. Data represented mean ± SD. Results are expressed as the mean ± SD from at least three independent experiments. * p
    Hplc Elsd, supplied by Agilent technologies, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Average 94 stars, based on 1 article reviews
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    hplc elsd - by Bioz Stars, 2021-06
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    Identification of AA as the active ingredient in crude and bran-processed Atractylodes lancea . Model: SDS model rats group; M + Crude: SDS model rats administrated with crude AL extraction; M + Bran-processed: SDS model rats administrated with BAL extraction. (A) HPLC-ELSD chromatogram of the 50% EtOH extraction from AL (black) and BAL (red), the content of AA increased by 191.22% in the bran-processed Atractylodes lancea . (B) and (C) Comparison of the intestinal propulsion rate and GAS in SDS rats treated with crude and bran-processed Atractylodes lancea extracts. (D) 3D structure of AA. Data represented mean ± SD. Results are expressed as the mean ± SD from at least three independent experiments. * p

    Journal: Frontiers in Pharmacology

    Article Title: Treatment of Spleen-Deficiency Syndrome With Atractyloside A From Bran-Processed Atractylodes lancea by Protection of the Intestinal Mucosal Barrier

    doi: 10.3389/fphar.2020.583160

    Figure Lengend Snippet: Identification of AA as the active ingredient in crude and bran-processed Atractylodes lancea . Model: SDS model rats group; M + Crude: SDS model rats administrated with crude AL extraction; M + Bran-processed: SDS model rats administrated with BAL extraction. (A) HPLC-ELSD chromatogram of the 50% EtOH extraction from AL (black) and BAL (red), the content of AA increased by 191.22% in the bran-processed Atractylodes lancea . (B) and (C) Comparison of the intestinal propulsion rate and GAS in SDS rats treated with crude and bran-processed Atractylodes lancea extracts. (D) 3D structure of AA. Data represented mean ± SD. Results are expressed as the mean ± SD from at least three independent experiments. * p

    Article Snippet: HPLC-ELSD analysis was performed using an Agilent-1260 system coupled to a Welch HPLC C18 column (4.6 mm × 250 mm, 5 μm) maintained at 30 °C (injection volume, 20 μL).

    Techniques: High Performance Liquid Chromatography

    The set-up for collecting the fraction with an ELSD. The splitter is the grey segment connected below the HPLC column (high-flow and low-flow outlets are denoted); the black circle represents a UV detector monitoring salicin (for comparison purposes).

    Journal: Molecules

    Article Title: Feasibility of Fraction Collection in HPLC Systems with Evaporative Light Scattering Detector: Analysis of Pectinatella magnifica

    doi: 10.3390/molecules21111495

    Figure Lengend Snippet: The set-up for collecting the fraction with an ELSD. The splitter is the grey segment connected below the HPLC column (high-flow and low-flow outlets are denoted); the black circle represents a UV detector monitoring salicin (for comparison purposes).

    Article Snippet: A YL9100 HPLC system (Young Lin, Anyang, Korea) connected to an ELSD (Agilent Technologies, Santa Clara, CA, USA) was used.

    Techniques: High Performance Liquid Chromatography, Flow Cytometry