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8 1e7 s lysosome associated membrane protein 2 lamp2  (Developmental Studies Hybridoma Bank)


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    Developmental Studies Hybridoma Bank 8 1e7 s lysosome associated membrane protein 2 lamp2
    8 1e7 S Lysosome Associated Membrane Protein 2 Lamp2, supplied by Developmental Studies Hybridoma Bank, used in various techniques. Bioz Stars score: 94/100, based on 43 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/8 1e7 s lysosome associated membrane protein 2 lamp2/product/Developmental Studies Hybridoma Bank
    Average 94 stars, based on 43 article reviews
    8 1e7 s lysosome associated membrane protein 2 lamp2 - by Bioz Stars, 2026-03
    94/100 stars

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    (A) Confocal microscopic analysis of lysosomes stained by LysoTracker Red in PC3/Doc cells exposed to 1 μM St-N or St-C for the indicated times. (B) Flow cytometric analysis of lysosomes stained with LysoTracker, and the relative ratio of geometric LysoTracker Red fluorescence. * P < 0.05, ** P < 0.01. (C) Electron micrographs showing lysosomal swelling induced by St-N. (D) ASM activities in lysates from the vehicle or St-N-treated PC3/Doc cells. * P < 0.05. (E) Western blotting analysis of LAMP1, <t>LAMP2,</t> CTSB, CTSD, p62, and LC3B in PC3/Doc cells after St-N treatment for different times. (F) Heatmap of the relative mRNA levels [logarithm value (base2)] of various cathepsins, LAMPs, and LC3B in St-N-treated PC3/Doc cells as determined by RT-qPCR. GAPDH served as an internal control. (G) Western blotting analysis of the active CTSB of lysosomal and cytosolic fractions in PC3/Doc cells treated with St-N. LAMP1 served as a lysosomal marker. (H) CTSB activity of lysosomal and cytosolic fractions was measured after subcellular fractionation of St-N-treated PC3/Doc cells. * P < 0.05.
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    (A) Confocal microscopic analysis of lysosomes stained by LysoTracker Red in PC3/Doc cells exposed to 1 μM St-N or St-C for the indicated times. (B) Flow cytometric analysis of lysosomes stained with LysoTracker, and the relative ratio of geometric LysoTracker Red fluorescence. * P < 0.05, ** P < 0.01. (C) Electron micrographs showing lysosomal swelling induced by St-N. (D) ASM activities in lysates from the vehicle or St-N-treated PC3/Doc cells. * P < 0.05. (E) Western blotting analysis of LAMP1, LAMP2, CTSB, CTSD, p62, and LC3B in PC3/Doc cells after St-N treatment for different times. (F) Heatmap of the relative mRNA levels [logarithm value (base2)] of various cathepsins, LAMPs, and LC3B in St-N-treated PC3/Doc cells as determined by RT-qPCR. GAPDH served as an internal control. (G) Western blotting analysis of the active CTSB of lysosomal and cytosolic fractions in PC3/Doc cells treated with St-N. LAMP1 served as a lysosomal marker. (H) CTSB activity of lysosomal and cytosolic fractions was measured after subcellular fractionation of St-N-treated PC3/Doc cells. * P < 0.05.

    Journal: PLOS ONE

    Article Title: St-N, a novel alkaline derivative of stevioside, reverses docetaxel resistance by targeting lysosomes in vitro and in vivo

    doi: 10.1371/journal.pone.0316268

    Figure Lengend Snippet: (A) Confocal microscopic analysis of lysosomes stained by LysoTracker Red in PC3/Doc cells exposed to 1 μM St-N or St-C for the indicated times. (B) Flow cytometric analysis of lysosomes stained with LysoTracker, and the relative ratio of geometric LysoTracker Red fluorescence. * P < 0.05, ** P < 0.01. (C) Electron micrographs showing lysosomal swelling induced by St-N. (D) ASM activities in lysates from the vehicle or St-N-treated PC3/Doc cells. * P < 0.05. (E) Western blotting analysis of LAMP1, LAMP2, CTSB, CTSD, p62, and LC3B in PC3/Doc cells after St-N treatment for different times. (F) Heatmap of the relative mRNA levels [logarithm value (base2)] of various cathepsins, LAMPs, and LC3B in St-N-treated PC3/Doc cells as determined by RT-qPCR. GAPDH served as an internal control. (G) Western blotting analysis of the active CTSB of lysosomal and cytosolic fractions in PC3/Doc cells treated with St-N. LAMP1 served as a lysosomal marker. (H) CTSB activity of lysosomal and cytosolic fractions was measured after subcellular fractionation of St-N-treated PC3/Doc cells. * P < 0.05.

    Article Snippet: The primary antibodies used were as follows: cathepsin B (CTSB; cat. no. 12216-1-AP; Proteintech, Wuhan, China), Microtubule-associated protein 1 light chain 3 beta (LC3B; cat. no. NB100-2220; Novus Biologicals, Littleton, CO, USA), lysosome-associated membrane protein 1 (LAMP1; cat. no. 21997-1-AP; Proteintech), lysosome-associated membrane protein 2 (LAMP2; cat. no. 66301-1-Ig; Proteintech), p62/SQSTM1 (cat. no. sc-28359; Santa Cruz Biotechnology, Dallas, TX, USA), tubulin alpha 1b (TUBA1B; cat. No. 11224-1-AP; Proteintech), cathepsin D (CTSD; cat. No. 21327-1-AP; Proteintech), poly (ADP-ribose) polymerase 1 (PARP1; cat. No. 80174-1-RR; Proteintech), β-actin (ACTB; cat. No. 60008-1-Ig; Proteintech), and glyceraldehyde-3-phosphate dehydrogenase (GAPDH; cat. no. sc-365062; Santa Cruz Biotechnology).

    Techniques: Staining, Fluorescence, Western Blot, Quantitative RT-PCR, Control, Marker, Activity Assay, Fractionation

    (A–D) Body weights (A, B) and tumor sizes (C, D) were measured every 2 days after the indicated treatment including 5 mg/kg Doc, 30 mg/kg St-N, or a combination of 30 mg/kg St-N and 5 mg/kg Doc. * P < 0.05, ** P < 0.01 and *** P < 0.001. (E) Tumor weights were determined at the time of sacrifice. * P < 0.05, ** P < 0.01 and *** P < 0.001. (F) Tumors from different groups are shown. (G) Ki67 staining of the indicated treated groups. Scale bar: 50 μm. (H) Effect of St-N on CTSB, p62, LC3B, and LAMP2 expression in RM-1/Doc homografts determined by western blotting. Representative patterns and the corresponding histograms were displayed. * P < 0.05, ** P < 0.01 compared with the vehicle control. (I) Effect of St-N on ASM activities in lysates from RM-1/Doc homografts. *** P < 0.001.

    Journal: PLOS ONE

    Article Title: St-N, a novel alkaline derivative of stevioside, reverses docetaxel resistance by targeting lysosomes in vitro and in vivo

    doi: 10.1371/journal.pone.0316268

    Figure Lengend Snippet: (A–D) Body weights (A, B) and tumor sizes (C, D) were measured every 2 days after the indicated treatment including 5 mg/kg Doc, 30 mg/kg St-N, or a combination of 30 mg/kg St-N and 5 mg/kg Doc. * P < 0.05, ** P < 0.01 and *** P < 0.001. (E) Tumor weights were determined at the time of sacrifice. * P < 0.05, ** P < 0.01 and *** P < 0.001. (F) Tumors from different groups are shown. (G) Ki67 staining of the indicated treated groups. Scale bar: 50 μm. (H) Effect of St-N on CTSB, p62, LC3B, and LAMP2 expression in RM-1/Doc homografts determined by western blotting. Representative patterns and the corresponding histograms were displayed. * P < 0.05, ** P < 0.01 compared with the vehicle control. (I) Effect of St-N on ASM activities in lysates from RM-1/Doc homografts. *** P < 0.001.

    Article Snippet: The primary antibodies used were as follows: cathepsin B (CTSB; cat. no. 12216-1-AP; Proteintech, Wuhan, China), Microtubule-associated protein 1 light chain 3 beta (LC3B; cat. no. NB100-2220; Novus Biologicals, Littleton, CO, USA), lysosome-associated membrane protein 1 (LAMP1; cat. no. 21997-1-AP; Proteintech), lysosome-associated membrane protein 2 (LAMP2; cat. no. 66301-1-Ig; Proteintech), p62/SQSTM1 (cat. no. sc-28359; Santa Cruz Biotechnology, Dallas, TX, USA), tubulin alpha 1b (TUBA1B; cat. No. 11224-1-AP; Proteintech), cathepsin D (CTSD; cat. No. 21327-1-AP; Proteintech), poly (ADP-ribose) polymerase 1 (PARP1; cat. No. 80174-1-RR; Proteintech), β-actin (ACTB; cat. No. 60008-1-Ig; Proteintech), and glyceraldehyde-3-phosphate dehydrogenase (GAPDH; cat. no. sc-365062; Santa Cruz Biotechnology).

    Techniques: Staining, Expressing, Western Blot, Control