turner model 20e luminometer Search Results


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Turner Designs turner model 20e luminometer
Turner Model 20e Luminometer, supplied by Turner Designs, 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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Promega turner luminometer td-20e
Turner Luminometer Td 20e, supplied by Promega, 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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Turner Td 20e Luminometer, supplied by Molecular Dynamics 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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Luminometer 96 Well Plate Reader Turner Designs 20e, supplied by Turner Designs, 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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Turner Td 20e Luminometer, supplied by Jencons 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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Millipore 20e
(A) Diagram of the Drosophila testis. Around 10 GSCs (3 shown, pink) are attached to the hub. GSCs divide asymmetrically to produce daughter gonialblasts (GB) that are displaced from the hub. GBs go on to form spermatogonial cysts. Fusomes (red) are spherical in GSCs and branched in spermatogonia. Approximately 2 CySCs (blue) flank each GSC and contact the hub with cytoplasmic extensions. CySCs divide to produce cyst cell daughters; two envelop each GB and its descendants. (B) Diagram of the Drosophila ecdysone pathway. <t>20E</t> (blue dots) activates this pathway by binding to a heterodimer composed of EcR and USP. Both EcR and USP contain a LBD that can bind 20E and a DBD that can recognize the EcRE and regulate downstream gene expression (pink dots). (C–E) Testes from adult y w flies stained with germline marker anti-Vasa (red), DNA stain DAPI (blue), and antibodies (green) against: (C) USP (hub and CySC lineage); (D) EcR (CySC lineage); or (E) ecdysone signaling target Br (CySC lineage). Insets show green channel alone. (F) Diagram of the GAL4-EcR reporter construct, which is composed of the LBD from EcR fused to the DBD from Gal4 and is under control of the hsp-70 promoter. When expressed at low levels, this reporter shows where the pathway can be activated: in the presence of 20E and EcR’s binding partners, Gal4 is activated and induces expression of UAS-lacZ or UAS-GFP (green dots). A similar GAL4-usp construct (not shown) is activated by ecdysone and USP’s binding partners. (G) Late 3rd instar larval testis carrying the GAL4-EcR reporter and stained with DAPI (blue), anti-Vasa (red), and anti-GFP (green). Without 20E feeding, endogenous 20E drives GFP expression in the larval hub and CySC lineage. Inset shows green channel alone. (H–J) Adult testes stained with DAPI (blue), somatic cell marker anti-Tj (red), and anti-lacZ (green). Without 20E feeding (H), adult testes carrying the Gal4-EcR reporter (or Gal4-usp reporter, not shown) do not express lacZ. After adult flies carrying the Gal4-EcR reporter (I) or Gal4-usp reporter (J) are fed 1 mM 20E overnight, testes express lacZ in the hub and CySC lineage. Hub, asterisk or arrow; CySC lineage cells, arrowhead. Scale bar in J, for all panels, = 20 µm.
20e, 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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Biophytis 20e bio101
<t>20-hydroxyecdysone</t> <t>(20E;</t> β-ecdysone; crustecdysone; ecdysterone; <t>BIO101;</t> CAS 5289-74-7; IUPAC 2β,3β,14α,20 R ,22 R ,25-hexahydroxy-5β-cholest-7-en-6-one).
20e Bio101, supplied by Biophytis, 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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20e  (Takeda)
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Takeda 20e
<t>20-hydroxyecdysone</t> <t>(20E;</t> β-ecdysone; crustecdysone; ecdysterone; <t>BIO101;</t> CAS 5289-74-7; IUPAC 2β,3β,14α,20 R ,22 R ,25-hexahydroxy-5β-cholest-7-en-6-one).
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Biolog Inc api zym kit
<t>20-hydroxyecdysone</t> <t>(20E;</t> β-ecdysone; crustecdysone; ecdysterone; <t>BIO101;</t> CAS 5289-74-7; IUPAC 2β,3β,14α,20 R ,22 R ,25-hexahydroxy-5β-cholest-7-en-6-one).
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Image Search Results


(A) Diagram of the Drosophila testis. Around 10 GSCs (3 shown, pink) are attached to the hub. GSCs divide asymmetrically to produce daughter gonialblasts (GB) that are displaced from the hub. GBs go on to form spermatogonial cysts. Fusomes (red) are spherical in GSCs and branched in spermatogonia. Approximately 2 CySCs (blue) flank each GSC and contact the hub with cytoplasmic extensions. CySCs divide to produce cyst cell daughters; two envelop each GB and its descendants. (B) Diagram of the Drosophila ecdysone pathway. 20E (blue dots) activates this pathway by binding to a heterodimer composed of EcR and USP. Both EcR and USP contain a LBD that can bind 20E and a DBD that can recognize the EcRE and regulate downstream gene expression (pink dots). (C–E) Testes from adult y w flies stained with germline marker anti-Vasa (red), DNA stain DAPI (blue), and antibodies (green) against: (C) USP (hub and CySC lineage); (D) EcR (CySC lineage); or (E) ecdysone signaling target Br (CySC lineage). Insets show green channel alone. (F) Diagram of the GAL4-EcR reporter construct, which is composed of the LBD from EcR fused to the DBD from Gal4 and is under control of the hsp-70 promoter. When expressed at low levels, this reporter shows where the pathway can be activated: in the presence of 20E and EcR’s binding partners, Gal4 is activated and induces expression of UAS-lacZ or UAS-GFP (green dots). A similar GAL4-usp construct (not shown) is activated by ecdysone and USP’s binding partners. (G) Late 3rd instar larval testis carrying the GAL4-EcR reporter and stained with DAPI (blue), anti-Vasa (red), and anti-GFP (green). Without 20E feeding, endogenous 20E drives GFP expression in the larval hub and CySC lineage. Inset shows green channel alone. (H–J) Adult testes stained with DAPI (blue), somatic cell marker anti-Tj (red), and anti-lacZ (green). Without 20E feeding (H), adult testes carrying the Gal4-EcR reporter (or Gal4-usp reporter, not shown) do not express lacZ. After adult flies carrying the Gal4-EcR reporter (I) or Gal4-usp reporter (J) are fed 1 mM 20E overnight, testes express lacZ in the hub and CySC lineage. Hub, asterisk or arrow; CySC lineage cells, arrowhead. Scale bar in J, for all panels, = 20 µm.

Journal: Developmental biology

Article Title: Steroid Signaling Promotes Stem Cell Maintenance in the Drosophila Testis

doi: 10.1016/j.ydbio.2014.07.016

Figure Lengend Snippet: (A) Diagram of the Drosophila testis. Around 10 GSCs (3 shown, pink) are attached to the hub. GSCs divide asymmetrically to produce daughter gonialblasts (GB) that are displaced from the hub. GBs go on to form spermatogonial cysts. Fusomes (red) are spherical in GSCs and branched in spermatogonia. Approximately 2 CySCs (blue) flank each GSC and contact the hub with cytoplasmic extensions. CySCs divide to produce cyst cell daughters; two envelop each GB and its descendants. (B) Diagram of the Drosophila ecdysone pathway. 20E (blue dots) activates this pathway by binding to a heterodimer composed of EcR and USP. Both EcR and USP contain a LBD that can bind 20E and a DBD that can recognize the EcRE and regulate downstream gene expression (pink dots). (C–E) Testes from adult y w flies stained with germline marker anti-Vasa (red), DNA stain DAPI (blue), and antibodies (green) against: (C) USP (hub and CySC lineage); (D) EcR (CySC lineage); or (E) ecdysone signaling target Br (CySC lineage). Insets show green channel alone. (F) Diagram of the GAL4-EcR reporter construct, which is composed of the LBD from EcR fused to the DBD from Gal4 and is under control of the hsp-70 promoter. When expressed at low levels, this reporter shows where the pathway can be activated: in the presence of 20E and EcR’s binding partners, Gal4 is activated and induces expression of UAS-lacZ or UAS-GFP (green dots). A similar GAL4-usp construct (not shown) is activated by ecdysone and USP’s binding partners. (G) Late 3rd instar larval testis carrying the GAL4-EcR reporter and stained with DAPI (blue), anti-Vasa (red), and anti-GFP (green). Without 20E feeding, endogenous 20E drives GFP expression in the larval hub and CySC lineage. Inset shows green channel alone. (H–J) Adult testes stained with DAPI (blue), somatic cell marker anti-Tj (red), and anti-lacZ (green). Without 20E feeding (H), adult testes carrying the Gal4-EcR reporter (or Gal4-usp reporter, not shown) do not express lacZ. After adult flies carrying the Gal4-EcR reporter (I) or Gal4-usp reporter (J) are fed 1 mM 20E overnight, testes express lacZ in the hub and CySC lineage. Hub, asterisk or arrow; CySC lineage cells, arrowhead. Scale bar in J, for all panels, = 20 µm.

Article Snippet: 20E feeding experiment 20E (Sigma-Aldrich) was dissolved in 10% ethanol to prepare a 25 mM stock solution.

Techniques: Binding Assay, Expressing, Staining, Marker, Construct

(A) Diagram showing how Gal4-EcR or Gal4-usp can act as dominant negative constructs (20E “sponges”): when expressed at high levels, they bind with endogenous receptors, compete for endogenous 20E and reduce its effective concentration, thus preventing endogenous EcR or USP from functioning normally (Hackney et al. 2007). (B–D) Testes from adult flies carrying Gal4-EcR stained with anti-Vasa (red), DAPI (blue), anti-Zfh1 (green; CySCs and their immediate daughters), anti-Hts/1B1 (white; fusomes), and anti-Arm (white; hub cells). Before overexpression (B), testes look normal; after heat-shock induced overexpression of Gal4-EcR(C), GSCs and CySCs are lost; feeding 20E to adult flies rescues the loss (D). Scale bar in D, for B-D, = 20 µm. (E) Bar graphs showing number of GSCs or Zfh1-positive cells per testis for this experiment. Data are represented as mean ± standard error of the mean (SEM). ** P-value < 0.005; *** P-value < 0.0005.

Journal: Developmental biology

Article Title: Steroid Signaling Promotes Stem Cell Maintenance in the Drosophila Testis

doi: 10.1016/j.ydbio.2014.07.016

Figure Lengend Snippet: (A) Diagram showing how Gal4-EcR or Gal4-usp can act as dominant negative constructs (20E “sponges”): when expressed at high levels, they bind with endogenous receptors, compete for endogenous 20E and reduce its effective concentration, thus preventing endogenous EcR or USP from functioning normally (Hackney et al. 2007). (B–D) Testes from adult flies carrying Gal4-EcR stained with anti-Vasa (red), DAPI (blue), anti-Zfh1 (green; CySCs and their immediate daughters), anti-Hts/1B1 (white; fusomes), and anti-Arm (white; hub cells). Before overexpression (B), testes look normal; after heat-shock induced overexpression of Gal4-EcR(C), GSCs and CySCs are lost; feeding 20E to adult flies rescues the loss (D). Scale bar in D, for B-D, = 20 µm. (E) Bar graphs showing number of GSCs or Zfh1-positive cells per testis for this experiment. Data are represented as mean ± standard error of the mean (SEM). ** P-value < 0.005; *** P-value < 0.0005.

Article Snippet: 20E feeding experiment 20E (Sigma-Aldrich) was dissolved in 10% ethanol to prepare a 25 mM stock solution.

Techniques: Dominant Negative Mutation, Construct, Concentration Assay, Staining, Over Expression

20-hydroxyecdysone (20E; β-ecdysone; crustecdysone; ecdysterone; BIO101; CAS 5289-74-7; IUPAC 2β,3β,14α,20 R ,22 R ,25-hexahydroxy-5β-cholest-7-en-6-one).

Journal: Biomedicines

Article Title: 20-Hydroxyecdysone, from Plant Extracts to Clinical Use: Therapeutic Potential for the Treatment of Neuromuscular, Cardio-Metabolic and Respiratory Diseases

doi: 10.3390/biomedicines9050492

Figure Lengend Snippet: 20-hydroxyecdysone (20E; β-ecdysone; crustecdysone; ecdysterone; BIO101; CAS 5289-74-7; IUPAC 2β,3β,14α,20 R ,22 R ,25-hexahydroxy-5β-cholest-7-en-6-one).

Article Snippet: It is proposed that RAS balance could be restored in COVID-19 patients through Mas1 activation downstream of ACE2 activity, with 20E (BIO101), a non-peptidic Mas receptor (Mas1) activator developed by Biophytis ( ).

Techniques:

Selected examples of ecdysteroid-rich medicinal plants and their traditional uses. The names of ecdysteroids are underlined (see www.ecdybase.org for structures, accessed on 1 April 2021). Note that it is not established that all the reported biological activities are due totally or partly to the presence of ecdysteroids.

Journal: Biomedicines

Article Title: 20-Hydroxyecdysone, from Plant Extracts to Clinical Use: Therapeutic Potential for the Treatment of Neuromuscular, Cardio-Metabolic and Respiratory Diseases

doi: 10.3390/biomedicines9050492

Figure Lengend Snippet: Selected examples of ecdysteroid-rich medicinal plants and their traditional uses. The names of ecdysteroids are underlined (see www.ecdybase.org for structures, accessed on 1 April 2021). Note that it is not established that all the reported biological activities are due totally or partly to the presence of ecdysteroids.

Article Snippet: It is proposed that RAS balance could be restored in COVID-19 patients through Mas1 activation downstream of ACE2 activity, with 20E (BIO101), a non-peptidic Mas receptor (Mas1) activator developed by Biophytis ( ).

Techniques:

Summary of the literature concerning 20E’s pharmacological effects in mammals.

Journal: Biomedicines

Article Title: 20-Hydroxyecdysone, from Plant Extracts to Clinical Use: Therapeutic Potential for the Treatment of Neuromuscular, Cardio-Metabolic and Respiratory Diseases

doi: 10.3390/biomedicines9050492

Figure Lengend Snippet: Summary of the literature concerning 20E’s pharmacological effects in mammals.

Article Snippet: It is proposed that RAS balance could be restored in COVID-19 patients through Mas1 activation downstream of ACE2 activity, with 20E (BIO101), a non-peptidic Mas receptor (Mas1) activator developed by Biophytis ( ).

Techniques:

( A ) The effects of 20E (0.01–10 μM) on protein synthesis in C2C12 cells, showing the anabolic effect of 20E on optimal value for 1 µM 20E. C2C12 cells were grown on 24-well plates at a density of 30,000 cells/well in 0.5 mL of growth medium (Dulbecco’s Modified Eagle Medium (DMEM) 4.5 g/L glucose supplemented with 10% fetal bovine serum). Twenty-four hours after plating, the differentiation induction into multinucleated myotubes was carried out, and after 5 days, cells were pre-incubated in Krebs medium 1 h at 37 °C before being incubated in DMEM media without serum for 2.5 h in the presence of [ 3 H]-Leucine (5 µCi/mL) and DMSO (control condition) or IGF-1 (100 ng/mL) or 20E (0.01–0.1–1–10 µM). At the end of incubation, supernatants were discarded and cells were lysed in 0.1 N NaOH for 30 min. The cell soluble fraction-associated radioactivity was then counted and protein was quantified using the Lowry method (after ). ( B ) Effects of dexamethasone (Dexa 6 = 10 −6 M, Dexa 5 = 10 −5 M), IGF-1 (10 ng/mL), and 20E (10 −6 M) on the diameter of C2C12 myotubes. Four- to six-day-old myotubes were incubated for 48 h with test chemicals, and were fixed and photographed by glutaraldehyde-induced autofluorescence. *: p = < 0.05; **: p = 0.01. (redrawn and modified from ).

Journal: Biomedicines

Article Title: 20-Hydroxyecdysone, from Plant Extracts to Clinical Use: Therapeutic Potential for the Treatment of Neuromuscular, Cardio-Metabolic and Respiratory Diseases

doi: 10.3390/biomedicines9050492

Figure Lengend Snippet: ( A ) The effects of 20E (0.01–10 μM) on protein synthesis in C2C12 cells, showing the anabolic effect of 20E on optimal value for 1 µM 20E. C2C12 cells were grown on 24-well plates at a density of 30,000 cells/well in 0.5 mL of growth medium (Dulbecco’s Modified Eagle Medium (DMEM) 4.5 g/L glucose supplemented with 10% fetal bovine serum). Twenty-four hours after plating, the differentiation induction into multinucleated myotubes was carried out, and after 5 days, cells were pre-incubated in Krebs medium 1 h at 37 °C before being incubated in DMEM media without serum for 2.5 h in the presence of [ 3 H]-Leucine (5 µCi/mL) and DMSO (control condition) or IGF-1 (100 ng/mL) or 20E (0.01–0.1–1–10 µM). At the end of incubation, supernatants were discarded and cells were lysed in 0.1 N NaOH for 30 min. The cell soluble fraction-associated radioactivity was then counted and protein was quantified using the Lowry method (after ). ( B ) Effects of dexamethasone (Dexa 6 = 10 −6 M, Dexa 5 = 10 −5 M), IGF-1 (10 ng/mL), and 20E (10 −6 M) on the diameter of C2C12 myotubes. Four- to six-day-old myotubes were incubated for 48 h with test chemicals, and were fixed and photographed by glutaraldehyde-induced autofluorescence. *: p = < 0.05; **: p = 0.01. (redrawn and modified from ).

Article Snippet: It is proposed that RAS balance could be restored in COVID-19 patients through Mas1 activation downstream of ACE2 activity, with 20E (BIO101), a non-peptidic Mas receptor (Mas1) activator developed by Biophytis ( ).

Techniques: Modification, Incubation, Control, Radioactivity

Dose-dependent inhibition of myostatin gene expression in C2C12 cells by 20E. C2C12 mouse myoblasts were differentiated for 6 days into myotubes. They were then treated for 6 h with concentrations of 20E ranging from 0.001 to 10 μM. Myostatin gene expression was detected by qRT-PCR. Results are shown as means ± standard error of the mean (SEM) ().

Journal: Biomedicines

Article Title: 20-Hydroxyecdysone, from Plant Extracts to Clinical Use: Therapeutic Potential for the Treatment of Neuromuscular, Cardio-Metabolic and Respiratory Diseases

doi: 10.3390/biomedicines9050492

Figure Lengend Snippet: Dose-dependent inhibition of myostatin gene expression in C2C12 cells by 20E. C2C12 mouse myoblasts were differentiated for 6 days into myotubes. They were then treated for 6 h with concentrations of 20E ranging from 0.001 to 10 μM. Myostatin gene expression was detected by qRT-PCR. Results are shown as means ± standard error of the mean (SEM) ().

Article Snippet: It is proposed that RAS balance could be restored in COVID-19 patients through Mas1 activation downstream of ACE2 activity, with 20E (BIO101), a non-peptidic Mas receptor (Mas1) activator developed by Biophytis ( ).

Techniques: Inhibition, Gene Expression, Quantitative RT-PCR

Effect of 20E on mice fed a high-fat diet (HF), when compared to mice fed a low-fat diet (LF). The animals received either pure 20E (50 mg/kg/day) or the same amount of 20E as a quinoa extract (Q). Panel ( A ) shows the impact on the mass of epididymal adipose tissue (*** p < 0.01 when compared to LF; ## p < 0.01 and ### p < 0.001 when compared to HF) and panel ( B ) shows the effect on adipocyte diameter (reproduced, with permission, from ).

Journal: Biomedicines

Article Title: 20-Hydroxyecdysone, from Plant Extracts to Clinical Use: Therapeutic Potential for the Treatment of Neuromuscular, Cardio-Metabolic and Respiratory Diseases

doi: 10.3390/biomedicines9050492

Figure Lengend Snippet: Effect of 20E on mice fed a high-fat diet (HF), when compared to mice fed a low-fat diet (LF). The animals received either pure 20E (50 mg/kg/day) or the same amount of 20E as a quinoa extract (Q). Panel ( A ) shows the impact on the mass of epididymal adipose tissue (*** p < 0.01 when compared to LF; ## p < 0.01 and ### p < 0.001 when compared to HF) and panel ( B ) shows the effect on adipocyte diameter (reproduced, with permission, from ).

Article Snippet: It is proposed that RAS balance could be restored in COVID-19 patients through Mas1 activation downstream of ACE2 activity, with 20E (BIO101), a non-peptidic Mas receptor (Mas1) activator developed by Biophytis ( ).

Techniques:

20E reduction of myostatin gene expression in C2C12 cells (differentiated for 6 days into myotubules) is mediated by binding to receptor sites on the external surface of the cells. The histogram compares the activities of IGF-1 (100 nM) and 20E (10 μM) with those of conjugates of 20E covalently bound to protein (HSA or BSA) through different C-atoms (C-2 and C-22-hemisuccinates or C-6 [6-carboxymethoxime]), all at nominal 10 μM hapten concentration. BSA bovine serum albumin; HSA: human serum albumin; error bars = standard error of the mean [ , ].

Journal: Biomedicines

Article Title: 20-Hydroxyecdysone, from Plant Extracts to Clinical Use: Therapeutic Potential for the Treatment of Neuromuscular, Cardio-Metabolic and Respiratory Diseases

doi: 10.3390/biomedicines9050492

Figure Lengend Snippet: 20E reduction of myostatin gene expression in C2C12 cells (differentiated for 6 days into myotubules) is mediated by binding to receptor sites on the external surface of the cells. The histogram compares the activities of IGF-1 (100 nM) and 20E (10 μM) with those of conjugates of 20E covalently bound to protein (HSA or BSA) through different C-atoms (C-2 and C-22-hemisuccinates or C-6 [6-carboxymethoxime]), all at nominal 10 μM hapten concentration. BSA bovine serum albumin; HSA: human serum albumin; error bars = standard error of the mean [ , ].

Article Snippet: It is proposed that RAS balance could be restored in COVID-19 patients through Mas1 activation downstream of ACE2 activity, with 20E (BIO101), a non-peptidic Mas receptor (Mas1) activator developed by Biophytis ( ).

Techniques: Gene Expression, Binding Assay, Concentration Assay

Diagrammatic representation of the proposed mode of action of 20E in the regulation of protein synthesis in C2C12 muscle cells in vitro ().

Journal: Biomedicines

Article Title: 20-Hydroxyecdysone, from Plant Extracts to Clinical Use: Therapeutic Potential for the Treatment of Neuromuscular, Cardio-Metabolic and Respiratory Diseases

doi: 10.3390/biomedicines9050492

Figure Lengend Snippet: Diagrammatic representation of the proposed mode of action of 20E in the regulation of protein synthesis in C2C12 muscle cells in vitro ().

Article Snippet: It is proposed that RAS balance could be restored in COVID-19 patients through Mas1 activation downstream of ACE2 activity, with 20E (BIO101), a non-peptidic Mas receptor (Mas1) activator developed by Biophytis ( ).

Techniques: In Vitro

Time-course of the distribution of radioactivity in the stomach/intestine/feces in mice after the oral application of [1α,2α- 3 H 2 ]20E. Note the logarithmic scale for abscissa. Each value is a mean of 2 animals. Note the plateau of small intestine content that is best explained by an entero-hepatic cycle and consistent with the prolonged concentration of radioactivity in bile as observed by Wu et al. (reproduced, with permission, from ).

Journal: Biomedicines

Article Title: 20-Hydroxyecdysone, from Plant Extracts to Clinical Use: Therapeutic Potential for the Treatment of Neuromuscular, Cardio-Metabolic and Respiratory Diseases

doi: 10.3390/biomedicines9050492

Figure Lengend Snippet: Time-course of the distribution of radioactivity in the stomach/intestine/feces in mice after the oral application of [1α,2α- 3 H 2 ]20E. Note the logarithmic scale for abscissa. Each value is a mean of 2 animals. Note the plateau of small intestine content that is best explained by an entero-hepatic cycle and consistent with the prolonged concentration of radioactivity in bile as observed by Wu et al. (reproduced, with permission, from ).

Article Snippet: It is proposed that RAS balance could be restored in COVID-19 patients through Mas1 activation downstream of ACE2 activity, with 20E (BIO101), a non-peptidic Mas receptor (Mas1) activator developed by Biophytis ( ).

Techniques: Radioactivity, Concentration Assay

Comparison of the temporal ( A ) and cumulative ( B ) urinary and fecal elimination of radioactivity after the oral application of [5,7,9- 3 H]20E to 6–7 week-old male Wistar rats. After oral application of [ 3 H]20E, elimination of radioactively labelled 20E and its metabolites is completed within 48 h. The amount of radioactivity recovered from the feces is by far the major route of excretion, since the amount in the urine corresponds to only 1.40% of the total radioactivity recovered. (Reproduced, with permission, from ).

Journal: Biomedicines

Article Title: 20-Hydroxyecdysone, from Plant Extracts to Clinical Use: Therapeutic Potential for the Treatment of Neuromuscular, Cardio-Metabolic and Respiratory Diseases

doi: 10.3390/biomedicines9050492

Figure Lengend Snippet: Comparison of the temporal ( A ) and cumulative ( B ) urinary and fecal elimination of radioactivity after the oral application of [5,7,9- 3 H]20E to 6–7 week-old male Wistar rats. After oral application of [ 3 H]20E, elimination of radioactively labelled 20E and its metabolites is completed within 48 h. The amount of radioactivity recovered from the feces is by far the major route of excretion, since the amount in the urine corresponds to only 1.40% of the total radioactivity recovered. (Reproduced, with permission, from ).

Article Snippet: It is proposed that RAS balance could be restored in COVID-19 patients through Mas1 activation downstream of ACE2 activity, with 20E (BIO101), a non-peptidic Mas receptor (Mas1) activator developed by Biophytis ( ).

Techniques: Comparison, Radioactivity

Kinetic parameters of  BIO101  (=97% pure  20E)  after a single oral administration ( n = 6, fasted). Values in parentheses indicate the SEM (C max , AUC) or the range (t max ).

Journal: Biomedicines

Article Title: 20-Hydroxyecdysone, from Plant Extracts to Clinical Use: Therapeutic Potential for the Treatment of Neuromuscular, Cardio-Metabolic and Respiratory Diseases

doi: 10.3390/biomedicines9050492

Figure Lengend Snippet: Kinetic parameters of BIO101 (=97% pure 20E) after a single oral administration ( n = 6, fasted). Values in parentheses indicate the SEM (C max , AUC) or the range (t max ).

Article Snippet: It is proposed that RAS balance could be restored in COVID-19 patients through Mas1 activation downstream of ACE2 activity, with 20E (BIO101), a non-peptidic Mas receptor (Mas1) activator developed by Biophytis ( ).

Techniques:

Pharmacokinetics of 20E in young and elderly humans given a single dose of 1400 mg. 20E was quantified by HPLC-MS [ , ].

Journal: Biomedicines

Article Title: 20-Hydroxyecdysone, from Plant Extracts to Clinical Use: Therapeutic Potential for the Treatment of Neuromuscular, Cardio-Metabolic and Respiratory Diseases

doi: 10.3390/biomedicines9050492

Figure Lengend Snippet: Pharmacokinetics of 20E in young and elderly humans given a single dose of 1400 mg. 20E was quantified by HPLC-MS [ , ].

Article Snippet: It is proposed that RAS balance could be restored in COVID-19 patients through Mas1 activation downstream of ACE2 activity, with 20E (BIO101), a non-peptidic Mas receptor (Mas1) activator developed by Biophytis ( ).

Techniques: Drug discovery

The principal routes of metabolism of 20E in rodents and humans (modified from Kumpun et al., 2011). The circles and arrows in red highlight the changes associated with 14-dehydroxylation, while the boxes and arrows in blue highlight the changes associated with side-chain cleavage.

Journal: Biomedicines

Article Title: 20-Hydroxyecdysone, from Plant Extracts to Clinical Use: Therapeutic Potential for the Treatment of Neuromuscular, Cardio-Metabolic and Respiratory Diseases

doi: 10.3390/biomedicines9050492

Figure Lengend Snippet: The principal routes of metabolism of 20E in rodents and humans (modified from Kumpun et al., 2011). The circles and arrows in red highlight the changes associated with 14-dehydroxylation, while the boxes and arrows in blue highlight the changes associated with side-chain cleavage.

Article Snippet: It is proposed that RAS balance could be restored in COVID-19 patients through Mas1 activation downstream of ACE2 activity, with 20E (BIO101), a non-peptidic Mas receptor (Mas1) activator developed by Biophytis ( ).

Techniques: Modification

A representative flow-diagram for the large-scale extraction and purification of 20E from roots of Cyanotis sp.

Journal: Biomedicines

Article Title: 20-Hydroxyecdysone, from Plant Extracts to Clinical Use: Therapeutic Potential for the Treatment of Neuromuscular, Cardio-Metabolic and Respiratory Diseases

doi: 10.3390/biomedicines9050492

Figure Lengend Snippet: A representative flow-diagram for the large-scale extraction and purification of 20E from roots of Cyanotis sp.

Article Snippet: It is proposed that RAS balance could be restored in COVID-19 patients through Mas1 activation downstream of ACE2 activity, with 20E (BIO101), a non-peptidic Mas receptor (Mas1) activator developed by Biophytis ( ).

Techniques: Extraction, Purification

Drugability scores for ecdysteroids.

Journal: Biomedicines

Article Title: 20-Hydroxyecdysone, from Plant Extracts to Clinical Use: Therapeutic Potential for the Treatment of Neuromuscular, Cardio-Metabolic and Respiratory Diseases

doi: 10.3390/biomedicines9050492

Figure Lengend Snippet: Drugability scores for ecdysteroids.

Article Snippet: It is proposed that RAS balance could be restored in COVID-19 patients through Mas1 activation downstream of ACE2 activity, with 20E (BIO101), a non-peptidic Mas receptor (Mas1) activator developed by Biophytis ( ).

Techniques:

Clinical studies on humans using pure  20E.

Journal: Biomedicines

Article Title: 20-Hydroxyecdysone, from Plant Extracts to Clinical Use: Therapeutic Potential for the Treatment of Neuromuscular, Cardio-Metabolic and Respiratory Diseases

doi: 10.3390/biomedicines9050492

Figure Lengend Snippet: Clinical studies on humans using pure 20E.

Article Snippet: It is proposed that RAS balance could be restored in COVID-19 patients through Mas1 activation downstream of ACE2 activity, with 20E (BIO101), a non-peptidic Mas receptor (Mas1) activator developed by Biophytis ( ).

Techniques: Activity Assay, Clinical Proteomics, Control

SARS-CoV-2 infection will result in a strong impairment of the activity of angiotensin converting enzyme 2 (ACE2), hence a lack of angiotensin-(1-7) production and a disequilibrium between the harmful and protective arms of the renin–angiotensin system (RAS). Treatment with BIO101 (20E) is expected to activate Mas receptor and the protective arm of RAS, thus preventing inflammation and lung damage.

Journal: Biomedicines

Article Title: 20-Hydroxyecdysone, from Plant Extracts to Clinical Use: Therapeutic Potential for the Treatment of Neuromuscular, Cardio-Metabolic and Respiratory Diseases

doi: 10.3390/biomedicines9050492

Figure Lengend Snippet: SARS-CoV-2 infection will result in a strong impairment of the activity of angiotensin converting enzyme 2 (ACE2), hence a lack of angiotensin-(1-7) production and a disequilibrium between the harmful and protective arms of the renin–angiotensin system (RAS). Treatment with BIO101 (20E) is expected to activate Mas receptor and the protective arm of RAS, thus preventing inflammation and lung damage.

Article Snippet: It is proposed that RAS balance could be restored in COVID-19 patients through Mas1 activation downstream of ACE2 activity, with 20E (BIO101), a non-peptidic Mas receptor (Mas1) activator developed by Biophytis ( ).

Techniques: Infection, Activity Assay