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l-ascorbic acid 2-phosphate  (MedChemExpress)


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    Structured Review

    MedChemExpress l-ascorbic acid 2-phosphate
    L Ascorbic Acid 2 Phosphate, supplied by MedChemExpress, used in various techniques. Bioz Stars score: 94/100, based on 12 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/acid+2+phosphate/L-Ascorbic+acid+2-phosphate/custom%40hy-103701%4010%2E1016%2Fj%2Ephymed%2E2026%2E158567
    Average 94 stars, based on 12 article reviews
    l-ascorbic acid 2-phosphate - by Bioz Stars, 2026-09
    94/100 stars

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    other:

    Article Title: Targeted Inhibition of CD74 + Macrophages by Luteolin via CEBPB/P65 Signaling Ameliorates Osteoarthritis Progression
    Article Snippet: The tissue explants were then placed in a culture medium composed of DMEM supplemented with 1% Insulin‐Transferrin‐Selenium (ITS, MCE, HY‐150287, USA), 50 μg mL −1 L‐proline (MCE, HY‐Y0252, USA), 0.1 μ m dexamethasone (MCE, HY‐14648, USA), 0.9 m m sodium pyruvate (Gibco, 11360‐070, USA), and 50 μg mL −1 ascorbic acid 2‐phosphate (MCE, HY‐103701, USA).

    Article Title: Mitochondrial Imaging and Transcriptome Analysis of Bone Mesenchymal Stem Cells During Osteogenesis Under Different Culture Conditions
    Article Snippet: Once the cells reached 90% confluence, the growth medium was replaced with osteogenic induction medium consisting of α-MEM, 10% FBS, 10 mM β-glycerophosphate (MCE, Monmouth Junction, NJ, USA), 50 μg/mL L-ascorbic acid 2-phosphate (MCE, Monmouth Junction, NJ, USA), and 100 nM dexamethasone (MCE, Monmouth Junction, NJ, USA).

    Article Title: Ugonin P facilitates chondrogenic properties in chondrocytes by inhibiting miR-3074-5p production: implications for the treatment of arthritic disorders
    Article Snippet: This medium consisted of growth medium supplemented with 1% Insulin-Transferrin-Selenium solution (1 mg/mL insulin, 0.55 mg/mL transferrin, 0.67 mg/mL sodium selenite) (Gibco, Cat. No. 41400045) and 50 μg/mL L-ascorbic acid 2-phosphate (MCE, Cat. No. HY-103701).

    Article Title: Targeted Inhibition of CD74 + Macrophages by Luteolin via CEBPB/P65 Signaling Ameliorates Osteoarthritis Progression.
    Article Snippet: The tissue explants were then placed in a culture medium composed of DMEM supplemented with 1% Insulin-TransferrinSelenium (ITS, MCE, HY-150287, USA), 50 μg mL−1 L-proline (MCE, HYY0252, USA), 0.1 μm dexamethasone (MCE, HY-14648, USA), 0.9 mm sodium pyruvate (Gibco, 11360-070, USA), and 50 μg mL−1 ascorbic acid 2-phosphate (MCE, HY-103701, USA).



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    (A) Representative images of Sirius Red-stained MSC sheets after 10 days of in vitro culture in L-ascorbic <t>acid-2-phosphate.</t> (B) Quantification of eluted Sirius Red dye from MSC sheets (n=6). Significance was calculated using a one-way ANOVA with a Tukey’s post-hoc test. (C) Representative SEM images of MSC sheets demonstrating vesicle-like structures on cells and ECM fibers. Potential MBV are indicated with white arrows.
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    (A) Representative images of Sirius Red-stained MSC sheets after 10 days of in vitro culture in L-ascorbic <t>acid-2-phosphate.</t> (B) Quantification of eluted Sirius Red dye from MSC sheets (n=6). Significance was calculated using a one-way ANOVA with a Tukey’s post-hoc test. (C) Representative SEM images of MSC sheets demonstrating vesicle-like structures on cells and ECM fibers. Potential MBV are indicated with white arrows.
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    (A) Representative images of Sirius Red-stained MSC sheets after 10 days of in vitro culture in L-ascorbic <t>acid-2-phosphate.</t> (B) Quantification of eluted Sirius Red dye from MSC sheets (n=6). Significance was calculated using a one-way ANOVA with a Tukey’s post-hoc test. (C) Representative SEM images of MSC sheets demonstrating vesicle-like structures on cells and ECM fibers. Potential MBV are indicated with white arrows.
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    (A) Representative images of Sirius Red-stained MSC sheets after 10 days of in vitro culture in L-ascorbic <t>acid-2-phosphate.</t> (B) Quantification of eluted Sirius Red dye from MSC sheets (n=6). Significance was calculated using a one-way ANOVA with a Tukey’s post-hoc test. (C) Representative SEM images of MSC sheets demonstrating vesicle-like structures on cells and ECM fibers. Potential MBV are indicated with white arrows.
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    (A) Representative images of Sirius Red-stained MSC sheets after 10 days of in vitro culture in L-ascorbic <t>acid-2-phosphate.</t> (B) Quantification of eluted Sirius Red dye from MSC sheets (n=6). Significance was calculated using a one-way ANOVA with a Tukey’s post-hoc test. (C) Representative SEM images of MSC sheets demonstrating vesicle-like structures on cells and ECM fibers. Potential MBV are indicated with white arrows.
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    Image Search Results


    (A) Representative images of Sirius Red-stained MSC sheets after 10 days of in vitro culture in L-ascorbic acid-2-phosphate. (B) Quantification of eluted Sirius Red dye from MSC sheets (n=6). Significance was calculated using a one-way ANOVA with a Tukey’s post-hoc test. (C) Representative SEM images of MSC sheets demonstrating vesicle-like structures on cells and ECM fibers. Potential MBV are indicated with white arrows.

    Journal: bioRxiv

    Article Title: Defining characteristics of mesenchymal stem cell-derived matrix-bound nanovesicles compared to conditioned culture medium extracellular vesicles

    doi: 10.64898/2026.05.05.722048

    Figure Lengend Snippet: (A) Representative images of Sirius Red-stained MSC sheets after 10 days of in vitro culture in L-ascorbic acid-2-phosphate. (B) Quantification of eluted Sirius Red dye from MSC sheets (n=6). Significance was calculated using a one-way ANOVA with a Tukey’s post-hoc test. (C) Representative SEM images of MSC sheets demonstrating vesicle-like structures on cells and ECM fibers. Potential MBV are indicated with white arrows.

    Article Snippet: Two days later, normal growth medium was supplemented with 50 μM L-ascorbic acid-2-phosphate sesquimagnesium salt hydrate (Tokyo Chemical Industry, A2521) to induce cell-driven extracellular matrix deposition in vitro and cells were cultured for an additional 10 days.

    Techniques: Staining, In Vitro