3 ma Search Results


sp 3d  (Nippon Instruments Corporation)
94
Nippon Instruments Corporation sp 3d
Sp 3d, supplied by Nippon Instruments Corporation, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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3 ma  (TargetMol)
99
TargetMol 3 ma
3 Ma, supplied by TargetMol, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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s0266 5g 3 methyladenine 3 ma mce  (MedChemExpress)
97
MedChemExpress s0266 5g 3 methyladenine 3 ma mce
S0266 5g 3 Methyladenine 3 Ma Mce, supplied by MedChemExpress, 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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Average 97 stars, based on 1 article reviews
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autophagy inhibitor  (Santa Cruz Biotechnology)
93
Santa Cruz Biotechnology autophagy inhibitor
Autophagy Inhibitor, supplied by Santa Cruz Biotechnology, 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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methandienone  (Cerilliant Corporation)
90
Cerilliant Corporation methandienone
Immunofluorescence for neurofilament to demonstrate neurite outgrowth in PC12 cells differentiated in NGF in tissue culture, either control treated ( left panel ), treated with 75 μM <t>methandienone</t> ( center panel ) or treated with 75 μM of 17-α-methyltestosterone ( right panel ) (A). Quantification of neurite outgrowth in the three conditions shown in (A) , as determined by cells exhibiting neurites equal to or greater than the length of one cell body, as a percentage of the total number of cells counted ( Y-axis ). Experiments were repeated at least three times and data expressed as mean ± SD ( ** P ≤ 0.01). These AAS demonstrate toxic effects on formed neurite networks in differentiated PC12 (B). Average of the sums of neurite length for identified neurite bearing cells in 10 high-power fields ( Y-axis ). Experiments were repeated at least three times and data expressed as mean ± SD ( ** P ≤ 0.01) (C) .
Methandienone, supplied by Cerilliant Corporation, 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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ma 3 solo mercury analyzer  (Nippon Instruments Corporation)
94
Nippon Instruments Corporation ma 3 solo mercury analyzer
Immunofluorescence for neurofilament to demonstrate neurite outgrowth in PC12 cells differentiated in NGF in tissue culture, either control treated ( left panel ), treated with 75 μM <t>methandienone</t> ( center panel ) or treated with 75 μM of 17-α-methyltestosterone ( right panel ) (A). Quantification of neurite outgrowth in the three conditions shown in (A) , as determined by cells exhibiting neurites equal to or greater than the length of one cell body, as a percentage of the total number of cells counted ( Y-axis ). Experiments were repeated at least three times and data expressed as mean ± SD ( ** P ≤ 0.01). These AAS demonstrate toxic effects on formed neurite networks in differentiated PC12 (B). Average of the sums of neurite length for identified neurite bearing cells in 10 high-power fields ( Y-axis ). Experiments were repeated at least three times and data expressed as mean ± SD ( ** P ≤ 0.01) (C) .
Ma 3 Solo Mercury Analyzer, supplied by Nippon Instruments Corporation, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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statistics package combistats 5 0  (European Directorate for the Quality of Medicines and HealthCare)
88
European Directorate for the Quality of Medicines and HealthCare statistics package combistats 5 0
Immunofluorescence for neurofilament to demonstrate neurite outgrowth in PC12 cells differentiated in NGF in tissue culture, either control treated ( left panel ), treated with 75 μM <t>methandienone</t> ( center panel ) or treated with 75 μM of 17-α-methyltestosterone ( right panel ) (A). Quantification of neurite outgrowth in the three conditions shown in (A) , as determined by cells exhibiting neurites equal to or greater than the length of one cell body, as a percentage of the total number of cells counted ( Y-axis ). Experiments were repeated at least three times and data expressed as mean ± SD ( ** P ≤ 0.01). These AAS demonstrate toxic effects on formed neurite networks in differentiated PC12 (B). Average of the sums of neurite length for identified neurite bearing cells in 10 high-power fields ( Y-axis ). Experiments were repeated at least three times and data expressed as mean ± SD ( ** P ≤ 0.01) (C) .
Statistics Package Combistats 5 0, supplied by European Directorate for the Quality of Medicines and HealthCare, used in various techniques. Bioz Stars score: 88/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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midpliocene 4.6–3.2 ma  (Marlow Industries)
90
Marlow Industries midpliocene 4.6–3.2 ma
Immunofluorescence for neurofilament to demonstrate neurite outgrowth in PC12 cells differentiated in NGF in tissue culture, either control treated ( left panel ), treated with 75 μM <t>methandienone</t> ( center panel ) or treated with 75 μM of 17-α-methyltestosterone ( right panel ) (A). Quantification of neurite outgrowth in the three conditions shown in (A) , as determined by cells exhibiting neurites equal to or greater than the length of one cell body, as a percentage of the total number of cells counted ( Y-axis ). Experiments were repeated at least three times and data expressed as mean ± SD ( ** P ≤ 0.01). These AAS demonstrate toxic effects on formed neurite networks in differentiated PC12 (B). Average of the sums of neurite length for identified neurite bearing cells in 10 high-power fields ( Y-axis ). Experiments were repeated at least three times and data expressed as mean ± SD ( ** P ≤ 0.01) (C) .
Midpliocene 4.6–3.2 Ma, supplied by Marlow Industries, 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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midpliocene 4.6–3.2 ma - by Bioz Stars, 2026-03
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mel norell ma 2021 high-density 3-d coordinate data of avian and non-avian dinosaur endocasts  (NORELL)
90
NORELL mel norell ma 2021 high-density 3-d coordinate data of avian and non-avian dinosaur endocasts
Immunofluorescence for neurofilament to demonstrate neurite outgrowth in PC12 cells differentiated in NGF in tissue culture, either control treated ( left panel ), treated with 75 μM <t>methandienone</t> ( center panel ) or treated with 75 μM of 17-α-methyltestosterone ( right panel ) (A). Quantification of neurite outgrowth in the three conditions shown in (A) , as determined by cells exhibiting neurites equal to or greater than the length of one cell body, as a percentage of the total number of cells counted ( Y-axis ). Experiments were repeated at least three times and data expressed as mean ± SD ( ** P ≤ 0.01). These AAS demonstrate toxic effects on formed neurite networks in differentiated PC12 (B). Average of the sums of neurite length for identified neurite bearing cells in 10 high-power fields ( Y-axis ). Experiments were repeated at least three times and data expressed as mean ± SD ( ** P ≤ 0.01) (C) .
Mel Norell Ma 2021 High Density 3 D Coordinate Data Of Avian And Non Avian Dinosaur Endocasts, supplied by NORELL, 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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3-methyladenine (3-ma)  (Beijing Solarbio Science)
90
Beijing Solarbio Science 3-methyladenine (3-ma)
Immunofluorescence for neurofilament to demonstrate neurite outgrowth in PC12 cells differentiated in NGF in tissue culture, either control treated ( left panel ), treated with 75 μM <t>methandienone</t> ( center panel ) or treated with 75 μM of 17-α-methyltestosterone ( right panel ) (A). Quantification of neurite outgrowth in the three conditions shown in (A) , as determined by cells exhibiting neurites equal to or greater than the length of one cell body, as a percentage of the total number of cells counted ( Y-axis ). Experiments were repeated at least three times and data expressed as mean ± SD ( ** P ≤ 0.01). These AAS demonstrate toxic effects on formed neurite networks in differentiated PC12 (B). Average of the sums of neurite length for identified neurite bearing cells in 10 high-power fields ( Y-axis ). Experiments were repeated at least three times and data expressed as mean ± SD ( ** P ≤ 0.01) (C) .
3 Methyladenine (3 Ma), supplied by Beijing Solarbio Science, 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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3-ma (molecular structure is shown in )  (AbMole Bioscience)
90
AbMole Bioscience 3-ma (molecular structure is shown in )
Immunofluorescence for neurofilament to demonstrate neurite outgrowth in PC12 cells differentiated in NGF in tissue culture, either control treated ( left panel ), treated with 75 μM <t>methandienone</t> ( center panel ) or treated with 75 μM of 17-α-methyltestosterone ( right panel ) (A). Quantification of neurite outgrowth in the three conditions shown in (A) , as determined by cells exhibiting neurites equal to or greater than the length of one cell body, as a percentage of the total number of cells counted ( Y-axis ). Experiments were repeated at least three times and data expressed as mean ± SD ( ** P ≤ 0.01). These AAS demonstrate toxic effects on formed neurite networks in differentiated PC12 (B). Average of the sums of neurite length for identified neurite bearing cells in 10 high-power fields ( Y-axis ). Experiments were repeated at least three times and data expressed as mean ± SD ( ** P ≤ 0.01) (C) .
3 Ma (Molecular Structure Is Shown In ), supplied by AbMole Bioscience, 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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3-ma 189490  (Merck KGaA)
90
Merck KGaA 3-ma 189490
Immunofluorescence for neurofilament to demonstrate neurite outgrowth in PC12 cells differentiated in NGF in tissue culture, either control treated ( left panel ), treated with 75 μM <t>methandienone</t> ( center panel ) or treated with 75 μM of 17-α-methyltestosterone ( right panel ) (A). Quantification of neurite outgrowth in the three conditions shown in (A) , as determined by cells exhibiting neurites equal to or greater than the length of one cell body, as a percentage of the total number of cells counted ( Y-axis ). Experiments were repeated at least three times and data expressed as mean ± SD ( ** P ≤ 0.01). These AAS demonstrate toxic effects on formed neurite networks in differentiated PC12 (B). Average of the sums of neurite length for identified neurite bearing cells in 10 high-power fields ( Y-axis ). Experiments were repeated at least three times and data expressed as mean ± SD ( ** P ≤ 0.01) (C) .
3 Ma 189490, 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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Image Search Results


Immunofluorescence for neurofilament to demonstrate neurite outgrowth in PC12 cells differentiated in NGF in tissue culture, either control treated ( left panel ), treated with 75 μM methandienone ( center panel ) or treated with 75 μM of 17-α-methyltestosterone ( right panel ) (A). Quantification of neurite outgrowth in the three conditions shown in (A) , as determined by cells exhibiting neurites equal to or greater than the length of one cell body, as a percentage of the total number of cells counted ( Y-axis ). Experiments were repeated at least three times and data expressed as mean ± SD ( ** P ≤ 0.01). These AAS demonstrate toxic effects on formed neurite networks in differentiated PC12 (B). Average of the sums of neurite length for identified neurite bearing cells in 10 high-power fields ( Y-axis ). Experiments were repeated at least three times and data expressed as mean ± SD ( ** P ≤ 0.01) (C) .

Journal: Frontiers in Cellular Neuroscience

Article Title: Supraphysiological doses of performance enhancing anabolic-androgenic steroids exert direct toxic effects on neuron-like cells

doi: 10.3389/fncel.2013.00069

Figure Lengend Snippet: Immunofluorescence for neurofilament to demonstrate neurite outgrowth in PC12 cells differentiated in NGF in tissue culture, either control treated ( left panel ), treated with 75 μM methandienone ( center panel ) or treated with 75 μM of 17-α-methyltestosterone ( right panel ) (A). Quantification of neurite outgrowth in the three conditions shown in (A) , as determined by cells exhibiting neurites equal to or greater than the length of one cell body, as a percentage of the total number of cells counted ( Y-axis ). Experiments were repeated at least three times and data expressed as mean ± SD ( ** P ≤ 0.01). These AAS demonstrate toxic effects on formed neurite networks in differentiated PC12 (B). Average of the sums of neurite length for identified neurite bearing cells in 10 high-power fields ( Y-axis ). Experiments were repeated at least three times and data expressed as mean ± SD ( ** P ≤ 0.01) (C) .

Article Snippet: 1 × 10 5 PC12 cells per square centimeter growing on poly-D-lysine coated cover slips were differentiated for 5 days in 200 ng/ml of NGF (Promega), followed by treatment with 75 μM of methandienone or 17-α-methyltestosterone (Cerilliant) or equal amounts of DME (as the carrier control).

Techniques: Immunofluorescence

PC12 cells were control treated ( left panel ) or treated with 75 μM methandienone ( center panel ) or 75 μM 17-α-methyltestosterone ( right panel ) for 48 h and a vitality assay was performed. Green cells are vital; cells in early cell death are yellow; orange indicates late cell death (A). Vitality status expressed as percentage of total live cells counted in 10 high power fields ( Y-axis ) reveals that methandienone and 17-α-methyltestosterone induce cell death in PC12. Experiments were repeated at least three times and data expressed as mean ± SD ( * P ≤ 0.05) (B) .

Journal: Frontiers in Cellular Neuroscience

Article Title: Supraphysiological doses of performance enhancing anabolic-androgenic steroids exert direct toxic effects on neuron-like cells

doi: 10.3389/fncel.2013.00069

Figure Lengend Snippet: PC12 cells were control treated ( left panel ) or treated with 75 μM methandienone ( center panel ) or 75 μM 17-α-methyltestosterone ( right panel ) for 48 h and a vitality assay was performed. Green cells are vital; cells in early cell death are yellow; orange indicates late cell death (A). Vitality status expressed as percentage of total live cells counted in 10 high power fields ( Y-axis ) reveals that methandienone and 17-α-methyltestosterone induce cell death in PC12. Experiments were repeated at least three times and data expressed as mean ± SD ( * P ≤ 0.05) (B) .

Article Snippet: 1 × 10 5 PC12 cells per square centimeter growing on poly-D-lysine coated cover slips were differentiated for 5 days in 200 ng/ml of NGF (Promega), followed by treatment with 75 μM of methandienone or 17-α-methyltestosterone (Cerilliant) or equal amounts of DME (as the carrier control).

Techniques:

Immunoblots demonstrate decreasing levels of phospho-ERK ( top panel ) in PC12 treated for 48 h with 75 μM androsterone, nandrolone, methandienone, and 17-α-methyltestosterone, compared to control treated cells (A) . Immunoblots for caspase 3 ( top panel ), PARP ( second panel ), and Hsp90 ( third panel ) in PC12, control treated or treated 48 h with 75 μM androsterone, nandrolone, methandienone, and 17-α-methyltestosterone demonstrate increasing levels of the activated fragment of caspase 3 and cleavage of PARP and Hsp90, indications of apoptosis and cell death (B) . PC12 were control treated or treated for 48 h with 50 or 75 μM methandienone ( left column ) or 17-α-methyltestosterone ( right column ). Increasing concentrations of these AAS resulted in appearance of the activated fragment of caspase 3 and cleavage of PARP and Hsp90 in a dose-dependent manner (C) . GAPDH was used as the loading control for all blots ( bottom panels ).

Journal: Frontiers in Cellular Neuroscience

Article Title: Supraphysiological doses of performance enhancing anabolic-androgenic steroids exert direct toxic effects on neuron-like cells

doi: 10.3389/fncel.2013.00069

Figure Lengend Snippet: Immunoblots demonstrate decreasing levels of phospho-ERK ( top panel ) in PC12 treated for 48 h with 75 μM androsterone, nandrolone, methandienone, and 17-α-methyltestosterone, compared to control treated cells (A) . Immunoblots for caspase 3 ( top panel ), PARP ( second panel ), and Hsp90 ( third panel ) in PC12, control treated or treated 48 h with 75 μM androsterone, nandrolone, methandienone, and 17-α-methyltestosterone demonstrate increasing levels of the activated fragment of caspase 3 and cleavage of PARP and Hsp90, indications of apoptosis and cell death (B) . PC12 were control treated or treated for 48 h with 50 or 75 μM methandienone ( left column ) or 17-α-methyltestosterone ( right column ). Increasing concentrations of these AAS resulted in appearance of the activated fragment of caspase 3 and cleavage of PARP and Hsp90 in a dose-dependent manner (C) . GAPDH was used as the loading control for all blots ( bottom panels ).

Article Snippet: 1 × 10 5 PC12 cells per square centimeter growing on poly-D-lysine coated cover slips were differentiated for 5 days in 200 ng/ml of NGF (Promega), followed by treatment with 75 μM of methandienone or 17-α-methyltestosterone (Cerilliant) or equal amounts of DME (as the carrier control).

Techniques: Western Blot

Immunoblots for caspase 3 ( top panel ), PARP ( second panel ) (A) and Hsp90 (B) in PC12, control treated or treated for 48 h with 75 μ M methandienone and 17-α-methyltestosterone alone or with 10 μM hydroxyflutamide. Indicators of apoptosis are decreased in the presence of hydroxyflutamide. GAPDH was used as the loading control for all blots ( bottom panels ).

Journal: Frontiers in Cellular Neuroscience

Article Title: Supraphysiological doses of performance enhancing anabolic-androgenic steroids exert direct toxic effects on neuron-like cells

doi: 10.3389/fncel.2013.00069

Figure Lengend Snippet: Immunoblots for caspase 3 ( top panel ), PARP ( second panel ) (A) and Hsp90 (B) in PC12, control treated or treated for 48 h with 75 μ M methandienone and 17-α-methyltestosterone alone or with 10 μM hydroxyflutamide. Indicators of apoptosis are decreased in the presence of hydroxyflutamide. GAPDH was used as the loading control for all blots ( bottom panels ).

Article Snippet: 1 × 10 5 PC12 cells per square centimeter growing on poly-D-lysine coated cover slips were differentiated for 5 days in 200 ng/ml of NGF (Promega), followed by treatment with 75 μM of methandienone or 17-α-methyltestosterone (Cerilliant) or equal amounts of DME (as the carrier control).

Techniques: Western Blot