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cathepsin e substrate  (R&D Systems)


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    R&D Systems cathepsin e substrate
    Cathepsin E Substrate, supplied by R&D Systems, used in various techniques. Bioz Stars score: 93/100, based on 64 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/cathepsin+e+substrate/pm24900778__ml400412x_si_001-118-12-15?v=R%26D+Systems
    Average 93 stars, based on 64 article reviews
    cathepsin e substrate - by Bioz Stars, 2026-07
    93/100 stars

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    cathepsin e substrate  (R&D Systems)
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    Cathepsin E Substrate, supplied by R&D Systems, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    cathepsin d/e substrate  (Enzo Biochem)
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    Impaired lysosomes in TgR and TmR cells A. Immunofluorescence staining showed that LysoTracker red-positive ‘giant vesicular’ compartments were colocalized with LAMP2 and cathepsin D (CTSD) in untreated HT22 WT, TgR and TmR cells. DAPI (blue) was used to stain DNA. Scale bars: 20 μm. Values represent mean ± S.E.M., n = 3 (150–250 cells per group), ∗∗∗p < 0.001. B. Western blotting analysis displayed increases in immature forms of CTSD in TmR cells compared with HT22 WT cells. HSP90 was used as loading control. Values represent mean ± S.E.M., n = 3, ns non-significant, *p < 0.05 compared with the corresponding groups of the WT cells C. Relative cathepsin D/E activity of ER stress-resistant cells was reduced compared to HT22 WT cells. Values represent mean ± S.E.M., n = 3, ∗∗p < 0.01, ∗∗∗p < 0.001. (For interpretation of the references to color in this figure legend, the reader is referred to the Web version of this article.)
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    the cathepsin d/e fluorogenic substrate mca-gkpilffrlk (dnp)-d-arg-nh2 (p-145; 10 mm)  (Enzo Biochem)
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    Impaired lysosomes in TgR and TmR cells A. Immunofluorescence staining showed that LysoTracker red-positive ‘giant vesicular’ compartments were colocalized with LAMP2 and cathepsin D (CTSD) in untreated HT22 WT, TgR and TmR cells. DAPI (blue) was used to stain DNA. Scale bars: 20 μm. Values represent mean ± S.E.M., n = 3 (150–250 cells per group), ∗∗∗p < 0.001. B. Western blotting analysis displayed increases in immature forms of CTSD in TmR cells compared with HT22 WT cells. HSP90 was used as loading control. Values represent mean ± S.E.M., n = 3, ns non-significant, *p < 0.05 compared with the corresponding groups of the WT cells C. Relative cathepsin D/E activity of ER stress-resistant cells was reduced compared to HT22 WT cells. Values represent mean ± S.E.M., n = 3, ∗∗p < 0.01, ∗∗∗p < 0.001. (For interpretation of the references to color in this figure legend, the reader is referred to the Web version of this article.)
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    Impaired lysosomes in TgR and TmR cells A. Immunofluorescence staining showed that LysoTracker red-positive ‘giant vesicular’ compartments were colocalized with LAMP2 and cathepsin D (CTSD) in untreated HT22 WT, TgR and TmR cells. DAPI (blue) was used to stain DNA. Scale bars: 20 μm. Values represent mean ± S.E.M., n = 3 (150–250 cells per group), ∗∗∗p < 0.001. B. Western blotting analysis displayed increases in immature forms of CTSD in TmR cells compared with HT22 WT cells. HSP90 was used as loading control. Values represent mean ± S.E.M., n = 3, ns non-significant, *p < 0.05 compared with the corresponding groups of the WT cells C. Relative cathepsin D/E activity of ER stress-resistant cells was reduced compared to HT22 WT cells. Values represent mean ± S.E.M., n = 3, ∗∗p < 0.01, ∗∗∗p < 0.001. (For interpretation of the references to color in this figure legend, the reader is referred to the Web version of this article.)
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    Impaired lysosomes in TgR and TmR cells A. Immunofluorescence staining showed that LysoTracker red-positive ‘giant vesicular’ compartments were colocalized with LAMP2 and cathepsin D (CTSD) in untreated HT22 WT, TgR and TmR cells. DAPI (blue) was used to stain DNA. Scale bars: 20 μm. Values represent mean ± S.E.M., n = 3 (150–250 cells per group), ∗∗∗p < 0.001. B. Western blotting analysis displayed increases in immature forms of CTSD in TmR cells compared with HT22 WT cells. HSP90 was used as loading control. Values represent mean ± S.E.M., n = 3, ns non-significant, *p < 0.05 compared with the corresponding groups of the WT cells C. Relative cathepsin D/E activity of ER stress-resistant cells was reduced compared to HT22 WT cells. Values represent mean ± S.E.M., n = 3, ∗∗p < 0.01, ∗∗∗p < 0.001. (For interpretation of the references to color in this figure legend, the reader is referred to the Web version of this article.)
    Cathepsin D & E Substrate, supplied by Enzo Biochem, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/cathepsin+e+substrate/pmc09620073__jm2c01336_si_001-376-36-41?v=Enzo+Biochem
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    Impaired lysosomes in TgR and TmR cells A. Immunofluorescence staining showed that LysoTracker red-positive ‘giant vesicular’ compartments were colocalized with LAMP2 and cathepsin D (CTSD) in untreated HT22 WT, TgR and TmR cells. DAPI (blue) was used to stain DNA. Scale bars: 20 μm. Values represent mean ± S.E.M., n = 3 (150–250 cells per group), ∗∗∗p < 0.001. B. Western blotting analysis displayed increases in immature forms of CTSD in TmR cells compared with HT22 WT cells. HSP90 was used as loading control. Values represent mean ± S.E.M., n = 3, ns non-significant, *p < 0.05 compared with the corresponding groups of the WT cells C. Relative cathepsin D/E activity of ER stress-resistant cells was reduced compared to HT22 WT cells. Values represent mean ± S.E.M., n = 3, ∗∗p < 0.01, ∗∗∗p < 0.001. (For interpretation of the references to color in this figure legend, the reader is referred to the Web version of this article.)
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    cathepsin d/e fluorogenic substrate #219360  (Millipore)
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    Millipore cathepsin d/e fluorogenic substrate #219360
    Impaired lysosomes in TgR and TmR cells A. Immunofluorescence staining showed that LysoTracker red-positive ‘giant vesicular’ compartments were colocalized with LAMP2 and cathepsin D (CTSD) in untreated HT22 WT, TgR and TmR cells. DAPI (blue) was used to stain DNA. Scale bars: 20 μm. Values represent mean ± S.E.M., n = 3 (150–250 cells per group), ∗∗∗p < 0.001. B. Western blotting analysis displayed increases in immature forms of CTSD in TmR cells compared with HT22 WT cells. HSP90 was used as loading control. Values represent mean ± S.E.M., n = 3, ns non-significant, *p < 0.05 compared with the corresponding groups of the WT cells C. Relative cathepsin D/E activity of ER stress-resistant cells was reduced compared to HT22 WT cells. Values represent mean ± S.E.M., n = 3, ∗∗p < 0.01, ∗∗∗p < 0.001. (For interpretation of the references to color in this figure legend, the reader is referred to the Web version of this article.)
    Cathepsin D/E Fluorogenic Substrate #219360, supplied by Millipore, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    cathepsin d & e substrate (fluorogenic  (Enzo Biochem)
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    Enzo Biochem cathepsin d & e substrate (fluorogenic
    Key Resource Table
    Cathepsin D & E Substrate (Fluorogenic, supplied by Enzo Biochem, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    synthetic fret cathepsin d/e substrate  (Millipore)
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    Millipore synthetic fret cathepsin d/e substrate
    Key Resource Table
    Synthetic Fret Cathepsin D/E Substrate, supplied by Millipore, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    fluorogenic cathepsin d & e substrate  (Enzo Biochem)
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    Enzo Biochem fluorogenic cathepsin d & e substrate
    Key Resource Table
    Fluorogenic Cathepsin D & E Substrate, supplied by Enzo Biochem, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Image Search Results


    Impaired lysosomes in TgR and TmR cells A. Immunofluorescence staining showed that LysoTracker red-positive ‘giant vesicular’ compartments were colocalized with LAMP2 and cathepsin D (CTSD) in untreated HT22 WT, TgR and TmR cells. DAPI (blue) was used to stain DNA. Scale bars: 20 μm. Values represent mean ± S.E.M., n = 3 (150–250 cells per group), ∗∗∗p < 0.001. B. Western blotting analysis displayed increases in immature forms of CTSD in TmR cells compared with HT22 WT cells. HSP90 was used as loading control. Values represent mean ± S.E.M., n = 3, ns non-significant, *p < 0.05 compared with the corresponding groups of the WT cells C. Relative cathepsin D/E activity of ER stress-resistant cells was reduced compared to HT22 WT cells. Values represent mean ± S.E.M., n = 3, ∗∗p < 0.01, ∗∗∗p < 0.001. (For interpretation of the references to color in this figure legend, the reader is referred to the Web version of this article.)

    Journal: Redox Biology

    Article Title: Adaptive responses of neuronal cells to chronic endoplasmic reticulum (ER) stress

    doi: 10.1016/j.redox.2023.102943

    Figure Lengend Snippet: Impaired lysosomes in TgR and TmR cells A. Immunofluorescence staining showed that LysoTracker red-positive ‘giant vesicular’ compartments were colocalized with LAMP2 and cathepsin D (CTSD) in untreated HT22 WT, TgR and TmR cells. DAPI (blue) was used to stain DNA. Scale bars: 20 μm. Values represent mean ± S.E.M., n = 3 (150–250 cells per group), ∗∗∗p < 0.001. B. Western blotting analysis displayed increases in immature forms of CTSD in TmR cells compared with HT22 WT cells. HSP90 was used as loading control. Values represent mean ± S.E.M., n = 3, ns non-significant, *p < 0.05 compared with the corresponding groups of the WT cells C. Relative cathepsin D/E activity of ER stress-resistant cells was reduced compared to HT22 WT cells. Values represent mean ± S.E.M., n = 3, ∗∗p < 0.01, ∗∗∗p < 0.001. (For interpretation of the references to color in this figure legend, the reader is referred to the Web version of this article.)

    Article Snippet: Cathepsin D/E substrate , Enzo Life Sciences , BML-P145 , Cathepsin D/E substrate.

    Techniques: Immunofluorescence, Staining, Western Blot, Activity Assay

    Journal: Redox Biology

    Article Title: Adaptive responses of neuronal cells to chronic endoplasmic reticulum (ER) stress

    doi: 10.1016/j.redox.2023.102943

    Figure Lengend Snippet:

    Article Snippet: Cathepsin D/E substrate , Enzo Life Sciences , BML-P145 , Cathepsin D/E substrate.

    Techniques: Protease Inhibitor, Transduction

    Journal: Cell chemical biology

    Article Title: Regulation of Autophagic Flux by the 20S Proteasome

    doi: 10.1016/j.chembiol.2019.07.002

    Figure Lengend Snippet: Key Resource Table

    Article Snippet: Cathepsin D & E substrate (fluorogenic) , Enzo Life Sciences , Cat# BML-P145–0001.

    Techniques: Recombinant, Transfection, Magnetic Beads, SYBR Green Assay, BIA-KA, Immunofluorescence, Cell Viability Assay, Plasmid Preparation, Software