pegfp c1 ataxin3 q84 Search Results


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Addgene inc hek293 cells
A Cell viability at the indicated concentrations of SC79 (0.1–100 μM), an Akt1 activator, in <t>HEK293</t> cells. Data are the mean and SEM of biological replicates ( n = 4–10). * denotes P ‐value < 0.05 (Student's t ‐test). B–E Determination of the alleviating effect of SC79 (1 or 10 μM) on cell death in human cell‐based models for AD (B), HD (C), SCA1 (D), and SCA3 (E). Data are the mean and SEM of biological replicates ( n = 3–7). * denotes P ‐value < 0.05 (Student's t ‐test). F, G SC79 was administered to 7‐month‐old AD mice for 1 month, and their memory remedy was investigated by Barnes Maze Test. For 5 days, the time to find a target hole decreased due to learning. The mice were tested on day 15 and 16 after a blank period to investigate long‐term memory. The time to find a target hole on tested days (F) and the average of latencies on days 15 and 16 (G) are shown. Data are the mean and SEM of three biological replicates. * denotes P ‐value < 0.05 (Student's t ‐test). H The dysregulated anxiety levels in AD mice were investigated using the elevated plus maze test. In (G) and (H), + and – denote the treatment and nontreatment with SC79, respectively. Bar graphs were drawn from at least three independent experiments (biological replicates) and represent mean and SEM. * denotes P ‐value < 0.05 (Student's t ‐test). Source data are available online for this figure.
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A Cell viability at the indicated concentrations of SC79 (0.1–100 μM), an Akt1 activator, in <t>HEK293</t> cells. Data are the mean and SEM of biological replicates ( n = 4–10). * denotes P ‐value < 0.05 (Student's t ‐test). B–E Determination of the alleviating effect of SC79 (1 or 10 μM) on cell death in human cell‐based models for AD (B), HD (C), SCA1 (D), and SCA3 (E). Data are the mean and SEM of biological replicates ( n = 3–7). * denotes P ‐value < 0.05 (Student's t ‐test). F, G SC79 was administered to 7‐month‐old AD mice for 1 month, and their memory remedy was investigated by Barnes Maze Test. For 5 days, the time to find a target hole decreased due to learning. The mice were tested on day 15 and 16 after a blank period to investigate long‐term memory. The time to find a target hole on tested days (F) and the average of latencies on days 15 and 16 (G) are shown. Data are the mean and SEM of three biological replicates. * denotes P ‐value < 0.05 (Student's t ‐test). H The dysregulated anxiety levels in AD mice were investigated using the elevated plus maze test. In (G) and (H), + and – denote the treatment and nontreatment with SC79, respectively. Bar graphs were drawn from at least three independent experiments (biological replicates) and represent mean and SEM. * denotes P ‐value < 0.05 (Student's t ‐test). Source data are available online for this figure.
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Addgene inc pegfp c1 ataxin 3 q84
A Cell viability at the indicated concentrations of SC79 (0.1–100 μM), an Akt1 activator, in <t>HEK293</t> cells. Data are the mean and SEM of biological replicates ( n = 4–10). * denotes P ‐value < 0.05 (Student's t ‐test). B–E Determination of the alleviating effect of SC79 (1 or 10 μM) on cell death in human cell‐based models for AD (B), HD (C), SCA1 (D), and SCA3 (E). Data are the mean and SEM of biological replicates ( n = 3–7). * denotes P ‐value < 0.05 (Student's t ‐test). F, G SC79 was administered to 7‐month‐old AD mice for 1 month, and their memory remedy was investigated by Barnes Maze Test. For 5 days, the time to find a target hole decreased due to learning. The mice were tested on day 15 and 16 after a blank period to investigate long‐term memory. The time to find a target hole on tested days (F) and the average of latencies on days 15 and 16 (G) are shown. Data are the mean and SEM of three biological replicates. * denotes P ‐value < 0.05 (Student's t ‐test). H The dysregulated anxiety levels in AD mice were investigated using the elevated plus maze test. In (G) and (H), + and – denote the treatment and nontreatment with SC79, respectively. Bar graphs were drawn from at least three independent experiments (biological replicates) and represent mean and SEM. * denotes P ‐value < 0.05 (Student's t ‐test). Source data are available online for this figure.
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A Cell viability at the indicated concentrations of SC79 (0.1–100 μM), an Akt1 activator, in HEK293 cells. Data are the mean and SEM of biological replicates ( n = 4–10). * denotes P ‐value < 0.05 (Student's t ‐test). B–E Determination of the alleviating effect of SC79 (1 or 10 μM) on cell death in human cell‐based models for AD (B), HD (C), SCA1 (D), and SCA3 (E). Data are the mean and SEM of biological replicates ( n = 3–7). * denotes P ‐value < 0.05 (Student's t ‐test). F, G SC79 was administered to 7‐month‐old AD mice for 1 month, and their memory remedy was investigated by Barnes Maze Test. For 5 days, the time to find a target hole decreased due to learning. The mice were tested on day 15 and 16 after a blank period to investigate long‐term memory. The time to find a target hole on tested days (F) and the average of latencies on days 15 and 16 (G) are shown. Data are the mean and SEM of three biological replicates. * denotes P ‐value < 0.05 (Student's t ‐test). H The dysregulated anxiety levels in AD mice were investigated using the elevated plus maze test. In (G) and (H), + and – denote the treatment and nontreatment with SC79, respectively. Bar graphs were drawn from at least three independent experiments (biological replicates) and represent mean and SEM. * denotes P ‐value < 0.05 (Student's t ‐test). Source data are available online for this figure.

Journal: Molecular Systems Biology

Article Title: A multi‐layered network model identifies Akt1 as a common modulator of neurodegeneration

doi: 10.15252/msb.202311801

Figure Lengend Snippet: A Cell viability at the indicated concentrations of SC79 (0.1–100 μM), an Akt1 activator, in HEK293 cells. Data are the mean and SEM of biological replicates ( n = 4–10). * denotes P ‐value < 0.05 (Student's t ‐test). B–E Determination of the alleviating effect of SC79 (1 or 10 μM) on cell death in human cell‐based models for AD (B), HD (C), SCA1 (D), and SCA3 (E). Data are the mean and SEM of biological replicates ( n = 3–7). * denotes P ‐value < 0.05 (Student's t ‐test). F, G SC79 was administered to 7‐month‐old AD mice for 1 month, and their memory remedy was investigated by Barnes Maze Test. For 5 days, the time to find a target hole decreased due to learning. The mice were tested on day 15 and 16 after a blank period to investigate long‐term memory. The time to find a target hole on tested days (F) and the average of latencies on days 15 and 16 (G) are shown. Data are the mean and SEM of three biological replicates. * denotes P ‐value < 0.05 (Student's t ‐test). H The dysregulated anxiety levels in AD mice were investigated using the elevated plus maze test. In (G) and (H), + and – denote the treatment and nontreatment with SC79, respectively. Bar graphs were drawn from at least three independent experiments (biological replicates) and represent mean and SEM. * denotes P ‐value < 0.05 (Student's t ‐test). Source data are available online for this figure.

Article Snippet: HEK293 cells having 70–80% cell density were transiently transfected with pEGFP‐C1‐Aβ 1‐42 , pEGFP‐Htt‐exon1‐Q74 (Addgene #40262), pEGFP‐Ataxin1‐52Q (Addgene #32492), or pEGFP‐C1‐Ataxin3‐Q84 (Addgene #22123) DNA using Lipofectamine 2000 (Invitrogen, CA, USA) following the manufacturer's instructions.

Techniques:

Journal: Molecular Systems Biology

Article Title: A multi‐layered network model identifies Akt1 as a common modulator of neurodegeneration

doi: 10.15252/msb.202311801

Figure Lengend Snippet:

Article Snippet: HEK293 cells having 70–80% cell density were transiently transfected with pEGFP‐C1‐Aβ 1‐42 , pEGFP‐Htt‐exon1‐Q74 (Addgene #40262), pEGFP‐Ataxin1‐52Q (Addgene #32492), or pEGFP‐C1‐Ataxin3‐Q84 (Addgene #22123) DNA using Lipofectamine 2000 (Invitrogen, CA, USA) following the manufacturer's instructions.

Techniques: Over Expression, Plasmid Preparation, Construct