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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 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.)
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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the cathepsin d/e fluorogenic substrate mca-gkpilffrlk (dnp)-d-arg-nh2 (p-145; 10 mm)  (Enzo Biochem)
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Enzo Biochem the cathepsin d/e fluorogenic substrate mca-gkpilffrlk (dnp)-d-arg-nh2 (p-145; 10 mm)
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.)
The Cathepsin D/E Fluorogenic Substrate Mca Gkpilffrlk (Dnp) D Arg Nh2 (P 145; 10 Mm), 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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the cathepsin d/e fluorogenic substrate mca-gkpilffrlk (dnp)-d-arg-nh2 (p-145; 10 mm) - by Bioz Stars, 2026-08
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fluorogenic cathepsin d/e substrate (7-methoxycoumarin-4-yl)acetyl-gkpilf ~ frlk(2,4dinitrophenyl)-d-r-nh2  (Millipore)
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Millipore fluorogenic cathepsin d/e substrate (7-methoxycoumarin-4-yl)acetyl-gkpilf ~ frlk(2,4dinitrophenyl)-d-r-nh2
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.)
Fluorogenic Cathepsin D/E Substrate (7 Methoxycoumarin 4 Yl)acetyl Gkpilf ~ Frlk(2,4dinitrophenyl) D R Nh2, 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 (7-methoxycoumarin-4-yl)acetyl-gkpilf ~ frlk(2,4dinitrophenyl)-d-r-nh2 - by Bioz Stars, 2026-08
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cathepsin d & e substrate  (Enzo Biochem)
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Enzo Biochem cathepsin d & e substrate
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
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cathepsin d & e substrate (fluorogenic)  (Enzo Biochem)
90
Enzo Biochem cathepsin d & e substrate (fluorogenic)
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 (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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cathepsin d & e substrate (fluorogenic) - by Bioz Stars, 2026-08
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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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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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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