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ml 141  (MedChemExpress)


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    Structured Review

    MedChemExpress ml 141
    Ml 141, supplied by MedChemExpress, used in various techniques. Bioz Stars score: 95/100, based on 42 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/ml+141/ML141/pmc12020991-217-4-12
    Average 95 stars, based on 42 article reviews
    ml 141 - by Bioz Stars, 2026-10
    95/100 stars

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    Related Articles

    other:

    Article Title: In vivo investigation of PEDV transmission via nasal infection: mechanisms of CD4 + T-cell-mediated intestinal infection
    Article Snippet: CT7758 (HY-70073), Y-27632 (HY-10071), ML-141 (HY-12755), and IPA3 (HY-15663) were purchased from MCE (New Jersey, USA).

    Article Title: In vivo investigation of PEDV transmission via nasal infection: mechanisms of CD4 + T-cell-mediated intestinal infection.
    Article Snippet: CT7758 (HY-70073), Y-27632 (HY-10071), ML-141 (HY-12755), and IPA3 (HY-15663) were purchased from MCE (New Jersey, USA).



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    Tocris ml141
    CD13-mediated FAK/Src/IQGAP1/ARF6 signaling promotes protrusion formation. ( a ) Treatment with inhibitors of major actin-organizing proteins such as FAK (FAK14; 20 μM), Src (PP2; 10 μM) or Cdc42 <t>(ML141;</t> 20 μM) significantly inhibits protrusion formation in WT KSCs, indicating that these proteins are critical for regulating actin cytoskeletal proteins in the formation of protrusions. ( b ). Representative images showing IQGAP1 or ARF6 (green) and phalloidin (actin; red) staining under CM or crosslinking (mAb 452; 1.8 µg/mL) conditions. ( c - d ) Quantification of Pearson Correlation Coefficient (PCC) between IQGAP1 and phalloidin ( c ) and ARF6 and phalloidin ( d ) staining following treatment with either CM or mAb 452. Treatment with mAb 452 significantly increased the correlation between IQGAP1 and phalloidin as well as ARF6 and phalloidin at the membrane. Data are represented as mean ± standard error and consists of at least three independent experiments with at least 5–10 images taken per treatment condition. *p < 0.05.
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    Tocris l3000015 ml141 tocris
    CD13-mediated FAK/Src/IQGAP1/ARF6 signaling promotes protrusion formation. ( a ) Treatment with inhibitors of major actin-organizing proteins such as FAK (FAK14; 20 μM), Src (PP2; 10 μM) or Cdc42 <t>(ML141;</t> 20 μM) significantly inhibits protrusion formation in WT KSCs, indicating that these proteins are critical for regulating actin cytoskeletal proteins in the formation of protrusions. ( b ). Representative images showing IQGAP1 or ARF6 (green) and phalloidin (actin; red) staining under CM or crosslinking (mAb 452; 1.8 µg/mL) conditions. ( c - d ) Quantification of Pearson Correlation Coefficient (PCC) between IQGAP1 and phalloidin ( c ) and ARF6 and phalloidin ( d ) staining following treatment with either CM or mAb 452. Treatment with mAb 452 significantly increased the correlation between IQGAP1 and phalloidin as well as ARF6 and phalloidin at the membrane. Data are represented as mean ± standard error and consists of at least three independent experiments with at least 5–10 images taken per treatment condition. *p < 0.05.
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    Image Search Results


    CD13-mediated FAK/Src/IQGAP1/ARF6 signaling promotes protrusion formation. ( a ) Treatment with inhibitors of major actin-organizing proteins such as FAK (FAK14; 20 μM), Src (PP2; 10 μM) or Cdc42 (ML141; 20 μM) significantly inhibits protrusion formation in WT KSCs, indicating that these proteins are critical for regulating actin cytoskeletal proteins in the formation of protrusions. ( b ). Representative images showing IQGAP1 or ARF6 (green) and phalloidin (actin; red) staining under CM or crosslinking (mAb 452; 1.8 µg/mL) conditions. ( c - d ) Quantification of Pearson Correlation Coefficient (PCC) between IQGAP1 and phalloidin ( c ) and ARF6 and phalloidin ( d ) staining following treatment with either CM or mAb 452. Treatment with mAb 452 significantly increased the correlation between IQGAP1 and phalloidin as well as ARF6 and phalloidin at the membrane. Data are represented as mean ± standard error and consists of at least three independent experiments with at least 5–10 images taken per treatment condition. *p < 0.05.

    Journal: Scientific Reports

    Article Title: CD13 activation assembles phosphoinositide (PI) signaling complexes to regulate the actin cytoskeleton

    doi: 10.1038/s41598-026-35022-6

    Figure Lengend Snippet: CD13-mediated FAK/Src/IQGAP1/ARF6 signaling promotes protrusion formation. ( a ) Treatment with inhibitors of major actin-organizing proteins such as FAK (FAK14; 20 μM), Src (PP2; 10 μM) or Cdc42 (ML141; 20 μM) significantly inhibits protrusion formation in WT KSCs, indicating that these proteins are critical for regulating actin cytoskeletal proteins in the formation of protrusions. ( b ). Representative images showing IQGAP1 or ARF6 (green) and phalloidin (actin; red) staining under CM or crosslinking (mAb 452; 1.8 µg/mL) conditions. ( c - d ) Quantification of Pearson Correlation Coefficient (PCC) between IQGAP1 and phalloidin ( c ) and ARF6 and phalloidin ( d ) staining following treatment with either CM or mAb 452. Treatment with mAb 452 significantly increased the correlation between IQGAP1 and phalloidin as well as ARF6 and phalloidin at the membrane. Data are represented as mean ± standard error and consists of at least three independent experiments with at least 5–10 images taken per treatment condition. *p < 0.05.

    Article Snippet: ML141 , 20 μM , Tocris; 4266.

    Techniques: Staining, Membrane