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ventricular cardiomyocyte cell line ac16  (ATCC)
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ATCC ventricular cardiomyocyte cell line ac16
Ventricular Cardiomyocyte Cell Line Ac16, supplied by ATCC, used in various techniques. Bioz Stars score: 97/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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human ventricular cardiomyocytes ac16  (Merck & Co)
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A fraction of DPP3 is transported via EVs and upregulated during septic shock in humans (A) Western blot qualitative analysis of cluster of differentiation 63 (CD63) at 26 KD (bottom), heat shock protein 70 (HSC70) at 73 KD (middle), and DPP3 at 83 KD (above), in protein extracts of EVs derived from bone marrow supernatant (BM SN) from Ctrl mice (left) and ISO mice (right). DPP3 activity (U/L) in large (lEVs) and small (sEVs) EVs derived from (B) plasma of control mice (Ctrl) ( n = 6) and isoproterenol-treated mice (ISO) ( n = 5), or from (C) BM SN of Ctrl ( n = 6) and ISO mice ( n = 6). (D) DPP3 activity in lEVs and sEVs derived from BM SN of WT mice injected with bone marrow cells from Dpp3-KO (WT BM KO ) and Dpp3-KO mice injected with bone marrow cells from WT mice (KO BM WT ) ( n = 5) for each. (E) Quantification of Nano track analysis (NTA) results of plasma derived-lEVs and sEVs concentration (vesicle/ml) in healthy individuals ( n = 7), septic shock (SS) ( n = 6) and cardiogenic shock (CS) patients ( n = 5). (F) DPP3 activity (U/L) in lEVs and sEVs derived from plasma of healthy individuals ( n = 8) and septic shock (SS) patients ( n = 6). (G) DPP3 activity (U/L) in lEVs and sEVs derived from plasma of healthy individuals ( n = 8) and cardiogenic shock (CS) patients ( n = 11). DPP3 activity (U/L) in lEVs and sEVs derived from cell culture supernatant of (H) human cardiomyocytes <t>AC16</t> ( n = 6) and (I) human monocytes THP-1 ( n = 2). In all bars, data are presented as mean ± standard error of the mean (SEM). Comparisons were made by Multiple Mann-Whitney tests in B, C, F, and G, and by two-way ANOVA in D and E. Significance was presented as follows (∗ p < 0.05, ∗∗ p < 0.01, and ns for non-significant differences).
Human Ventricular Cardiomyocytes Ac16, supplied by Merck & Co, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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human ventricular cardiomyocytes ac16 - by Bioz Stars, 2026-09
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ac16 human ventricular cardiomyocyte  (Merck & Co)
86
Merck & Co ac16 human ventricular cardiomyocyte
A fraction of DPP3 is transported via EVs and upregulated during septic shock in humans (A) Western blot qualitative analysis of cluster of differentiation 63 (CD63) at 26 KD (bottom), heat shock protein 70 (HSC70) at 73 KD (middle), and DPP3 at 83 KD (above), in protein extracts of EVs derived from bone marrow supernatant (BM SN) from Ctrl mice (left) and ISO mice (right). DPP3 activity (U/L) in large (lEVs) and small (sEVs) EVs derived from (B) plasma of control mice (Ctrl) ( n = 6) and isoproterenol-treated mice (ISO) ( n = 5), or from (C) BM SN of Ctrl ( n = 6) and ISO mice ( n = 6). (D) DPP3 activity in lEVs and sEVs derived from BM SN of WT mice injected with bone marrow cells from Dpp3-KO (WT BM KO ) and Dpp3-KO mice injected with bone marrow cells from WT mice (KO BM WT ) ( n = 5) for each. (E) Quantification of Nano track analysis (NTA) results of plasma derived-lEVs and sEVs concentration (vesicle/ml) in healthy individuals ( n = 7), septic shock (SS) ( n = 6) and cardiogenic shock (CS) patients ( n = 5). (F) DPP3 activity (U/L) in lEVs and sEVs derived from plasma of healthy individuals ( n = 8) and septic shock (SS) patients ( n = 6). (G) DPP3 activity (U/L) in lEVs and sEVs derived from plasma of healthy individuals ( n = 8) and cardiogenic shock (CS) patients ( n = 11). DPP3 activity (U/L) in lEVs and sEVs derived from cell culture supernatant of (H) human cardiomyocytes <t>AC16</t> ( n = 6) and (I) human monocytes THP-1 ( n = 2). In all bars, data are presented as mean ± standard error of the mean (SEM). Comparisons were made by Multiple Mann-Whitney tests in B, C, F, and G, and by two-way ANOVA in D and E. Significance was presented as follows (∗ p < 0.05, ∗∗ p < 0.01, and ns for non-significant differences).
Ac16 Human Ventricular Cardiomyocyte, supplied by Merck & Co, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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human ventricular cardiomyocytes ac 16 cells  (ATCC)
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ATCC human ventricular cardiomyocytes ac 16 cells
A fraction of DPP3 is transported via EVs and upregulated during septic shock in humans (A) Western blot qualitative analysis of cluster of differentiation 63 (CD63) at 26 KD (bottom), heat shock protein 70 (HSC70) at 73 KD (middle), and DPP3 at 83 KD (above), in protein extracts of EVs derived from bone marrow supernatant (BM SN) from Ctrl mice (left) and ISO mice (right). DPP3 activity (U/L) in large (lEVs) and small (sEVs) EVs derived from (B) plasma of control mice (Ctrl) ( n = 6) and isoproterenol-treated mice (ISO) ( n = 5), or from (C) BM SN of Ctrl ( n = 6) and ISO mice ( n = 6). (D) DPP3 activity in lEVs and sEVs derived from BM SN of WT mice injected with bone marrow cells from Dpp3-KO (WT BM KO ) and Dpp3-KO mice injected with bone marrow cells from WT mice (KO BM WT ) ( n = 5) for each. (E) Quantification of Nano track analysis (NTA) results of plasma derived-lEVs and sEVs concentration (vesicle/ml) in healthy individuals ( n = 7), septic shock (SS) ( n = 6) and cardiogenic shock (CS) patients ( n = 5). (F) DPP3 activity (U/L) in lEVs and sEVs derived from plasma of healthy individuals ( n = 8) and septic shock (SS) patients ( n = 6). (G) DPP3 activity (U/L) in lEVs and sEVs derived from plasma of healthy individuals ( n = 8) and cardiogenic shock (CS) patients ( n = 11). DPP3 activity (U/L) in lEVs and sEVs derived from cell culture supernatant of (H) human cardiomyocytes <t>AC16</t> ( n = 6) and (I) human monocytes THP-1 ( n = 2). In all bars, data are presented as mean ± standard error of the mean (SEM). Comparisons were made by Multiple Mann-Whitney tests in B, C, F, and G, and by two-way ANOVA in D and E. Significance was presented as follows (∗ p < 0.05, ∗∗ p < 0.01, and ns for non-significant differences).
Human Ventricular Cardiomyocytes Ac 16 Cells, supplied by ATCC, used in various techniques. Bioz Stars score: 97/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/ventricular+cardiomyocytes+ac16/AC16/pm40436014-659-9-25
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human ventricular cardiomyocytes ac 16 cells - by Bioz Stars, 2026-09
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human ventricular cardiomyocyte cell line  (ATCC)
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ATCC human ventricular cardiomyocyte cell line
A fraction of DPP3 is transported via EVs and upregulated during septic shock in humans (A) Western blot qualitative analysis of cluster of differentiation 63 (CD63) at 26 KD (bottom), heat shock protein 70 (HSC70) at 73 KD (middle), and DPP3 at 83 KD (above), in protein extracts of EVs derived from bone marrow supernatant (BM SN) from Ctrl mice (left) and ISO mice (right). DPP3 activity (U/L) in large (lEVs) and small (sEVs) EVs derived from (B) plasma of control mice (Ctrl) ( n = 6) and isoproterenol-treated mice (ISO) ( n = 5), or from (C) BM SN of Ctrl ( n = 6) and ISO mice ( n = 6). (D) DPP3 activity in lEVs and sEVs derived from BM SN of WT mice injected with bone marrow cells from Dpp3-KO (WT BM KO ) and Dpp3-KO mice injected with bone marrow cells from WT mice (KO BM WT ) ( n = 5) for each. (E) Quantification of Nano track analysis (NTA) results of plasma derived-lEVs and sEVs concentration (vesicle/ml) in healthy individuals ( n = 7), septic shock (SS) ( n = 6) and cardiogenic shock (CS) patients ( n = 5). (F) DPP3 activity (U/L) in lEVs and sEVs derived from plasma of healthy individuals ( n = 8) and septic shock (SS) patients ( n = 6). (G) DPP3 activity (U/L) in lEVs and sEVs derived from plasma of healthy individuals ( n = 8) and cardiogenic shock (CS) patients ( n = 11). DPP3 activity (U/L) in lEVs and sEVs derived from cell culture supernatant of (H) human cardiomyocytes <t>AC16</t> ( n = 6) and (I) human monocytes THP-1 ( n = 2). In all bars, data are presented as mean ± standard error of the mean (SEM). Comparisons were made by Multiple Mann-Whitney tests in B, C, F, and G, and by two-way ANOVA in D and E. Significance was presented as follows (∗ p < 0.05, ∗∗ p < 0.01, and ns for non-significant differences).
Human Ventricular Cardiomyocyte Cell Line, supplied by ATCC, used in various techniques. Bioz Stars score: 97/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/ventricular+cardiomyocytes+ac16/AC16/pmc12208340-61-0-7
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human ventricular cardiomyocyte cell line - by Bioz Stars, 2026-09
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cell lines human ventricular cardiomyocyte cell line ac16 atcc cat crl 3568  (ATCC)
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ATCC cell lines human ventricular cardiomyocyte cell line ac16 atcc cat crl 3568
A fraction of DPP3 is transported via EVs and upregulated during septic shock in humans (A) Western blot qualitative analysis of cluster of differentiation 63 (CD63) at 26 KD (bottom), heat shock protein 70 (HSC70) at 73 KD (middle), and DPP3 at 83 KD (above), in protein extracts of EVs derived from bone marrow supernatant (BM SN) from Ctrl mice (left) and ISO mice (right). DPP3 activity (U/L) in large (lEVs) and small (sEVs) EVs derived from (B) plasma of control mice (Ctrl) ( n = 6) and isoproterenol-treated mice (ISO) ( n = 5), or from (C) BM SN of Ctrl ( n = 6) and ISO mice ( n = 6). (D) DPP3 activity in lEVs and sEVs derived from BM SN of WT mice injected with bone marrow cells from Dpp3-KO (WT BM KO ) and Dpp3-KO mice injected with bone marrow cells from WT mice (KO BM WT ) ( n = 5) for each. (E) Quantification of Nano track analysis (NTA) results of plasma derived-lEVs and sEVs concentration (vesicle/ml) in healthy individuals ( n = 7), septic shock (SS) ( n = 6) and cardiogenic shock (CS) patients ( n = 5). (F) DPP3 activity (U/L) in lEVs and sEVs derived from plasma of healthy individuals ( n = 8) and septic shock (SS) patients ( n = 6). (G) DPP3 activity (U/L) in lEVs and sEVs derived from plasma of healthy individuals ( n = 8) and cardiogenic shock (CS) patients ( n = 11). DPP3 activity (U/L) in lEVs and sEVs derived from cell culture supernatant of (H) human cardiomyocytes <t>AC16</t> ( n = 6) and (I) human monocytes THP-1 ( n = 2). In all bars, data are presented as mean ± standard error of the mean (SEM). Comparisons were made by Multiple Mann-Whitney tests in B, C, F, and G, and by two-way ANOVA in D and E. Significance was presented as follows (∗ p < 0.05, ∗∗ p < 0.01, and ns for non-significant differences).
Cell Lines Human Ventricular Cardiomyocyte Cell Line Ac16 Atcc Cat Crl 3568, supplied by ATCC, used in various techniques. Bioz Stars score: 97/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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cell lines human ventricular cardiomyocyte cell line ac16 atcc cat crl 3568 - by Bioz Stars, 2026-09
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ac16 human ventricular cardiomyocytes  (Merck & Co)
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A fraction of DPP3 is transported via EVs and upregulated during septic shock in humans (A) Western blot qualitative analysis of cluster of differentiation 63 (CD63) at 26 KD (bottom), heat shock protein 70 (HSC70) at 73 KD (middle), and DPP3 at 83 KD (above), in protein extracts of EVs derived from bone marrow supernatant (BM SN) from Ctrl mice (left) and ISO mice (right). DPP3 activity (U/L) in large (lEVs) and small (sEVs) EVs derived from (B) plasma of control mice (Ctrl) ( n = 6) and isoproterenol-treated mice (ISO) ( n = 5), or from (C) BM SN of Ctrl ( n = 6) and ISO mice ( n = 6). (D) DPP3 activity in lEVs and sEVs derived from BM SN of WT mice injected with bone marrow cells from Dpp3-KO (WT BM KO ) and Dpp3-KO mice injected with bone marrow cells from WT mice (KO BM WT ) ( n = 5) for each. (E) Quantification of Nano track analysis (NTA) results of plasma derived-lEVs and sEVs concentration (vesicle/ml) in healthy individuals ( n = 7), septic shock (SS) ( n = 6) and cardiogenic shock (CS) patients ( n = 5). (F) DPP3 activity (U/L) in lEVs and sEVs derived from plasma of healthy individuals ( n = 8) and septic shock (SS) patients ( n = 6). (G) DPP3 activity (U/L) in lEVs and sEVs derived from plasma of healthy individuals ( n = 8) and cardiogenic shock (CS) patients ( n = 11). DPP3 activity (U/L) in lEVs and sEVs derived from cell culture supernatant of (H) human cardiomyocytes <t>AC16</t> ( n = 6) and (I) human monocytes THP-1 ( n = 2). In all bars, data are presented as mean ± standard error of the mean (SEM). Comparisons were made by Multiple Mann-Whitney tests in B, C, F, and G, and by two-way ANOVA in D and E. Significance was presented as follows (∗ p < 0.05, ∗∗ p < 0.01, and ns for non-significant differences).
Ac16 Human Ventricular Cardiomyocytes, supplied by Merck & Co, 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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ac16 human ventricular cardiomyocytes  (Merck KGaA)
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Merck KGaA ac16 human ventricular cardiomyocytes
A fraction of DPP3 is transported via EVs and upregulated during septic shock in humans (A) Western blot qualitative analysis of cluster of differentiation 63 (CD63) at 26 KD (bottom), heat shock protein 70 (HSC70) at 73 KD (middle), and DPP3 at 83 KD (above), in protein extracts of EVs derived from bone marrow supernatant (BM SN) from Ctrl mice (left) and ISO mice (right). DPP3 activity (U/L) in large (lEVs) and small (sEVs) EVs derived from (B) plasma of control mice (Ctrl) ( n = 6) and isoproterenol-treated mice (ISO) ( n = 5), or from (C) BM SN of Ctrl ( n = 6) and ISO mice ( n = 6). (D) DPP3 activity in lEVs and sEVs derived from BM SN of WT mice injected with bone marrow cells from Dpp3-KO (WT BM KO ) and Dpp3-KO mice injected with bone marrow cells from WT mice (KO BM WT ) ( n = 5) for each. (E) Quantification of Nano track analysis (NTA) results of plasma derived-lEVs and sEVs concentration (vesicle/ml) in healthy individuals ( n = 7), septic shock (SS) ( n = 6) and cardiogenic shock (CS) patients ( n = 5). (F) DPP3 activity (U/L) in lEVs and sEVs derived from plasma of healthy individuals ( n = 8) and septic shock (SS) patients ( n = 6). (G) DPP3 activity (U/L) in lEVs and sEVs derived from plasma of healthy individuals ( n = 8) and cardiogenic shock (CS) patients ( n = 11). DPP3 activity (U/L) in lEVs and sEVs derived from cell culture supernatant of (H) human cardiomyocytes <t>AC16</t> ( n = 6) and (I) human monocytes THP-1 ( n = 2). In all bars, data are presented as mean ± standard error of the mean (SEM). Comparisons were made by Multiple Mann-Whitney tests in B, C, F, and G, and by two-way ANOVA in D and E. Significance was presented as follows (∗ p < 0.05, ∗∗ p < 0.01, and ns for non-significant differences).
Ac16 Human Ventricular Cardiomyocytes, supplied by Merck KGaA, 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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ac16 human ventricular cardiomyocyte cell line  (iCell Bioscience Inc)
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A fraction of DPP3 is transported via EVs and upregulated during septic shock in humans (A) Western blot qualitative analysis of cluster of differentiation 63 (CD63) at 26 KD (bottom), heat shock protein 70 (HSC70) at 73 KD (middle), and DPP3 at 83 KD (above), in protein extracts of EVs derived from bone marrow supernatant (BM SN) from Ctrl mice (left) and ISO mice (right). DPP3 activity (U/L) in large (lEVs) and small (sEVs) EVs derived from (B) plasma of control mice (Ctrl) ( n = 6) and isoproterenol-treated mice (ISO) ( n = 5), or from (C) BM SN of Ctrl ( n = 6) and ISO mice ( n = 6). (D) DPP3 activity in lEVs and sEVs derived from BM SN of WT mice injected with bone marrow cells from Dpp3-KO (WT BM KO ) and Dpp3-KO mice injected with bone marrow cells from WT mice (KO BM WT ) ( n = 5) for each. (E) Quantification of Nano track analysis (NTA) results of plasma derived-lEVs and sEVs concentration (vesicle/ml) in healthy individuals ( n = 7), septic shock (SS) ( n = 6) and cardiogenic shock (CS) patients ( n = 5). (F) DPP3 activity (U/L) in lEVs and sEVs derived from plasma of healthy individuals ( n = 8) and septic shock (SS) patients ( n = 6). (G) DPP3 activity (U/L) in lEVs and sEVs derived from plasma of healthy individuals ( n = 8) and cardiogenic shock (CS) patients ( n = 11). DPP3 activity (U/L) in lEVs and sEVs derived from cell culture supernatant of (H) human cardiomyocytes <t>AC16</t> ( n = 6) and (I) human monocytes THP-1 ( n = 2). In all bars, data are presented as mean ± standard error of the mean (SEM). Comparisons were made by Multiple Mann-Whitney tests in B, C, F, and G, and by two-way ANOVA in D and E. Significance was presented as follows (∗ p < 0.05, ∗∗ p < 0.01, and ns for non-significant differences).
Ac16 Human Ventricular Cardiomyocyte Cell Line, supplied by iCell Bioscience Inc, 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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ac16 human ventricular cardiomyocyte cell line - by Bioz Stars, 2026-09
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A fraction of DPP3 is transported via EVs and upregulated during septic shock in humans (A) Western blot qualitative analysis of cluster of differentiation 63 (CD63) at 26 KD (bottom), heat shock protein 70 (HSC70) at 73 KD (middle), and DPP3 at 83 KD (above), in protein extracts of EVs derived from bone marrow supernatant (BM SN) from Ctrl mice (left) and ISO mice (right). DPP3 activity (U/L) in large (lEVs) and small (sEVs) EVs derived from (B) plasma of control mice (Ctrl) ( n = 6) and isoproterenol-treated mice (ISO) ( n = 5), or from (C) BM SN of Ctrl ( n = 6) and ISO mice ( n = 6). (D) DPP3 activity in lEVs and sEVs derived from BM SN of WT mice injected with bone marrow cells from Dpp3-KO (WT BM KO ) and Dpp3-KO mice injected with bone marrow cells from WT mice (KO BM WT ) ( n = 5) for each. (E) Quantification of Nano track analysis (NTA) results of plasma derived-lEVs and sEVs concentration (vesicle/ml) in healthy individuals ( n = 7), septic shock (SS) ( n = 6) and cardiogenic shock (CS) patients ( n = 5). (F) DPP3 activity (U/L) in lEVs and sEVs derived from plasma of healthy individuals ( n = 8) and septic shock (SS) patients ( n = 6). (G) DPP3 activity (U/L) in lEVs and sEVs derived from plasma of healthy individuals ( n = 8) and cardiogenic shock (CS) patients ( n = 11). DPP3 activity (U/L) in lEVs and sEVs derived from cell culture supernatant of (H) human cardiomyocytes AC16 ( n = 6) and (I) human monocytes THP-1 ( n = 2). In all bars, data are presented as mean ± standard error of the mean (SEM). Comparisons were made by Multiple Mann-Whitney tests in B, C, F, and G, and by two-way ANOVA in D and E. Significance was presented as follows (∗ p < 0.05, ∗∗ p < 0.01, and ns for non-significant differences).

Journal: iScience

Article Title: Crosstalk between circulating DPP3 and immune cells in the context of cardio-systemic stress

doi: 10.1016/j.isci.2026.115114

Figure Lengend Snippet: A fraction of DPP3 is transported via EVs and upregulated during septic shock in humans (A) Western blot qualitative analysis of cluster of differentiation 63 (CD63) at 26 KD (bottom), heat shock protein 70 (HSC70) at 73 KD (middle), and DPP3 at 83 KD (above), in protein extracts of EVs derived from bone marrow supernatant (BM SN) from Ctrl mice (left) and ISO mice (right). DPP3 activity (U/L) in large (lEVs) and small (sEVs) EVs derived from (B) plasma of control mice (Ctrl) ( n = 6) and isoproterenol-treated mice (ISO) ( n = 5), or from (C) BM SN of Ctrl ( n = 6) and ISO mice ( n = 6). (D) DPP3 activity in lEVs and sEVs derived from BM SN of WT mice injected with bone marrow cells from Dpp3-KO (WT BM KO ) and Dpp3-KO mice injected with bone marrow cells from WT mice (KO BM WT ) ( n = 5) for each. (E) Quantification of Nano track analysis (NTA) results of plasma derived-lEVs and sEVs concentration (vesicle/ml) in healthy individuals ( n = 7), septic shock (SS) ( n = 6) and cardiogenic shock (CS) patients ( n = 5). (F) DPP3 activity (U/L) in lEVs and sEVs derived from plasma of healthy individuals ( n = 8) and septic shock (SS) patients ( n = 6). (G) DPP3 activity (U/L) in lEVs and sEVs derived from plasma of healthy individuals ( n = 8) and cardiogenic shock (CS) patients ( n = 11). DPP3 activity (U/L) in lEVs and sEVs derived from cell culture supernatant of (H) human cardiomyocytes AC16 ( n = 6) and (I) human monocytes THP-1 ( n = 2). In all bars, data are presented as mean ± standard error of the mean (SEM). Comparisons were made by Multiple Mann-Whitney tests in B, C, F, and G, and by two-way ANOVA in D and E. Significance was presented as follows (∗ p < 0.05, ∗∗ p < 0.01, and ns for non-significant differences).

Article Snippet: Human ventricular cardiomyocytes (AC16) , Merck , SCC109.

Techniques: Western Blot, Derivative Assay, Activity Assay, Clinical Proteomics, Control, Injection, Concentration Assay, Cell Culture, MANN-WHITNEY