bic  (Alomone Labs)


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    Structured Review

    Alomone Labs bic
    Fxr1 protein expression is decreased during homeostatic synaptic upscaling Western blot analysis of Fxr1 during (A), <t>TTX</t> (48 h treatment) induced upscaling ( n = 6 in each condition) and (B), <t>BIC</t> (48 h treatment) induced downscaling ( n = 8 in each condition) of primary postnatal cortical cultures. Student's t ‐test * P
    Bic, supplied by Alomone Labs, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/bic/product/Alomone Labs
    Average 94 stars, based on 1 article reviews
    Price from $9.99 to $1999.99
    bic - by Bioz Stars, 2021-12
    94/100 stars

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    1) Product Images from "Fxr1 regulates sleep and synaptic homeostasis"

    Article Title: Fxr1 regulates sleep and synaptic homeostasis

    Journal: The EMBO Journal

    doi: 10.15252/embj.2019103864

    Fxr1 protein expression is decreased during homeostatic synaptic upscaling Western blot analysis of Fxr1 during (A), TTX (48 h treatment) induced upscaling ( n = 6 in each condition) and (B), BIC (48 h treatment) induced downscaling ( n = 8 in each condition) of primary postnatal cortical cultures. Student's t ‐test * P
    Figure Legend Snippet: Fxr1 protein expression is decreased during homeostatic synaptic upscaling Western blot analysis of Fxr1 during (A), TTX (48 h treatment) induced upscaling ( n = 6 in each condition) and (B), BIC (48 h treatment) induced downscaling ( n = 8 in each condition) of primary postnatal cortical cultures. Student's t ‐test * P

    Techniques Used: Expressing, Western Blot

    Expression of GluA2 during synaptic scaling Quantification of the % of infection by (A) AAV1 Syn GFP ( n = 3) or (B) AAV1 Syn GFP‐Fxr1 ( n = 3). Surface expression of GluA2 during upscaling (Veh n = 28, TTX n = 29). Expression of total GluA2 during upscaling (Veh n = 7, TTX n = 6). Surface expression of GluA2 during downscaling (Veh n = 18, BIC n = 18). Expression of total GluA2 during downscaling (Veh n = 4, BIC n = 4). Data information: Error bars are SEM.
    Figure Legend Snippet: Expression of GluA2 during synaptic scaling Quantification of the % of infection by (A) AAV1 Syn GFP ( n = 3) or (B) AAV1 Syn GFP‐Fxr1 ( n = 3). Surface expression of GluA2 during upscaling (Veh n = 28, TTX n = 29). Expression of total GluA2 during upscaling (Veh n = 7, TTX n = 6). Surface expression of GluA2 during downscaling (Veh n = 18, BIC n = 18). Expression of total GluA2 during downscaling (Veh n = 4, BIC n = 4). Data information: Error bars are SEM.

    Techniques Used: Expressing, Infection

    2) Product Images from "Fxr1 regulates sleep and synaptic homeostasis"

    Article Title: Fxr1 regulates sleep and synaptic homeostasis

    Journal: bioRxiv

    doi: 10.1101/709345

    Fxr1 protein expression is decreased during homeostatic synaptic upscaling. Western blot analysis of Fxr1 during a , TTX induced upscaling (n=6 in each condition) and b , BIC induced downscaling (n=4 in each condition) of primary postnatal cortical cultures. Student’s T-test *p
    Figure Legend Snippet: Fxr1 protein expression is decreased during homeostatic synaptic upscaling. Western blot analysis of Fxr1 during a , TTX induced upscaling (n=6 in each condition) and b , BIC induced downscaling (n=4 in each condition) of primary postnatal cortical cultures. Student’s T-test *p

    Techniques Used: Expressing, Western Blot

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    Alomone Labs bic
    Fxr1 protein expression is decreased during homeostatic synaptic upscaling Western blot analysis of Fxr1 during (A), <t>TTX</t> (48 h treatment) induced upscaling ( n = 6 in each condition) and (B), <t>BIC</t> (48 h treatment) induced downscaling ( n = 8 in each condition) of primary postnatal cortical cultures. Student's t ‐test * P
    Bic, supplied by Alomone Labs, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/bic/product/Alomone Labs
    Average 94 stars, based on 1 article reviews
    Price from $9.99 to $1999.99
    bic - by Bioz Stars, 2021-12
    94/100 stars
      Buy from Supplier

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    Alomone Labs forskolin
    CREB phosphorylation mediates AKT2-regulated induction of PEPCK. ( A ) CREB phosphorylation induced by PTEN loss is regulated by AKT2. Liver lysates from mice with different genotypes were analysis for p-CREB. PM, Pten deleted; DM, Pten and Akt2 deleted; AM, Akt2 deleted. Two biological replicas are included for each genotype group. Protein levels of p-AKT, PTEN and p-GSK3 are analyzed and showed up-regulation of AKT and GSK-3 with PTEN loss and inhibition when AKT2 is lost. Phosphorylation of CREB is only observed when PTEN is lost. AKT2 loss together with PTEN blocked this phosphorylation in the DM livers. ( B ) Akt2 +/+ and Akt2 − / − cell were treated with <t>forskolin</t> (100 μM) for 24 h to induce cAMP and CREB phosphorylation or vehicle as controls. Phosphorylation of CREB is detected and showed to be lower when AKT2 is lost. When forskolin is added to induce cAMP, protein expression of p-CREB is evaluated in both Akt2 +/+ and Akt2 − / − cells even though its levels remains lower in the Akt2 − / − cells. Vinculin is probed as loading control. ( C ) Introduction of CREB-133A and wtCREB to Akt2 +/+ and Akt2 −/− hepatocytes. Expression of PEPCK is analyzed using quantitative PCR analysis. Left panel, CREB-S133A is introduced to Akt2 +/+ cells. Middle panel, wtCREB is introduced to Akt2 −/− cells; Right panel, wtCREB is introduced to Akt2 +/+ cells. n = 3. Data presented as mean ± SEM. * P ≤ 0.05. Different from vector transfected cells of the same genotype. Experiments repeated at least three times.
    Forskolin, supplied by Alomone Labs, 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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    Average 94 stars, based on 1 article reviews
    Price from $9.99 to $1999.99
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    Fxr1 protein expression is decreased during homeostatic synaptic upscaling Western blot analysis of Fxr1 during (A), TTX (48 h treatment) induced upscaling ( n = 6 in each condition) and (B), BIC (48 h treatment) induced downscaling ( n = 8 in each condition) of primary postnatal cortical cultures. Student's t ‐test * P

    Journal: The EMBO Journal

    Article Title: Fxr1 regulates sleep and synaptic homeostasis

    doi: 10.15252/embj.2019103864

    Figure Lengend Snippet: Fxr1 protein expression is decreased during homeostatic synaptic upscaling Western blot analysis of Fxr1 during (A), TTX (48 h treatment) induced upscaling ( n = 6 in each condition) and (B), BIC (48 h treatment) induced downscaling ( n = 8 in each condition) of primary postnatal cortical cultures. Student's t ‐test * P

    Article Snippet: To induce upscaling or downscaling, cells were incubated in the presence of 1 μM TTX or 50 μM BIC (Alomone Labs, Jerusalem, Israel) or vehicle, respectively, from DIV12 to DIV14.

    Techniques: Expressing, Western Blot

    Expression of GluA2 during synaptic scaling Quantification of the % of infection by (A) AAV1 Syn GFP ( n = 3) or (B) AAV1 Syn GFP‐Fxr1 ( n = 3). Surface expression of GluA2 during upscaling (Veh n = 28, TTX n = 29). Expression of total GluA2 during upscaling (Veh n = 7, TTX n = 6). Surface expression of GluA2 during downscaling (Veh n = 18, BIC n = 18). Expression of total GluA2 during downscaling (Veh n = 4, BIC n = 4). Data information: Error bars are SEM.

    Journal: The EMBO Journal

    Article Title: Fxr1 regulates sleep and synaptic homeostasis

    doi: 10.15252/embj.2019103864

    Figure Lengend Snippet: Expression of GluA2 during synaptic scaling Quantification of the % of infection by (A) AAV1 Syn GFP ( n = 3) or (B) AAV1 Syn GFP‐Fxr1 ( n = 3). Surface expression of GluA2 during upscaling (Veh n = 28, TTX n = 29). Expression of total GluA2 during upscaling (Veh n = 7, TTX n = 6). Surface expression of GluA2 during downscaling (Veh n = 18, BIC n = 18). Expression of total GluA2 during downscaling (Veh n = 4, BIC n = 4). Data information: Error bars are SEM.

    Article Snippet: To induce upscaling or downscaling, cells were incubated in the presence of 1 μM TTX or 50 μM BIC (Alomone Labs, Jerusalem, Israel) or vehicle, respectively, from DIV12 to DIV14.

    Techniques: Expressing, Infection

    CREB phosphorylation mediates AKT2-regulated induction of PEPCK. ( A ) CREB phosphorylation induced by PTEN loss is regulated by AKT2. Liver lysates from mice with different genotypes were analysis for p-CREB. PM, Pten deleted; DM, Pten and Akt2 deleted; AM, Akt2 deleted. Two biological replicas are included for each genotype group. Protein levels of p-AKT, PTEN and p-GSK3 are analyzed and showed up-regulation of AKT and GSK-3 with PTEN loss and inhibition when AKT2 is lost. Phosphorylation of CREB is only observed when PTEN is lost. AKT2 loss together with PTEN blocked this phosphorylation in the DM livers. ( B ) Akt2 +/+ and Akt2 − / − cell were treated with forskolin (100 μM) for 24 h to induce cAMP and CREB phosphorylation or vehicle as controls. Phosphorylation of CREB is detected and showed to be lower when AKT2 is lost. When forskolin is added to induce cAMP, protein expression of p-CREB is evaluated in both Akt2 +/+ and Akt2 − / − cells even though its levels remains lower in the Akt2 − / − cells. Vinculin is probed as loading control. ( C ) Introduction of CREB-133A and wtCREB to Akt2 +/+ and Akt2 −/− hepatocytes. Expression of PEPCK is analyzed using quantitative PCR analysis. Left panel, CREB-S133A is introduced to Akt2 +/+ cells. Middle panel, wtCREB is introduced to Akt2 −/− cells; Right panel, wtCREB is introduced to Akt2 +/+ cells. n = 3. Data presented as mean ± SEM. * P ≤ 0.05. Different from vector transfected cells of the same genotype. Experiments repeated at least three times.

    Journal: The Biochemical journal

    Article Title: Regulation of basal expression of hepatic PEPCK and G6Pase by AKT2

    doi: 10.1042/BCJ20190570

    Figure Lengend Snippet: CREB phosphorylation mediates AKT2-regulated induction of PEPCK. ( A ) CREB phosphorylation induced by PTEN loss is regulated by AKT2. Liver lysates from mice with different genotypes were analysis for p-CREB. PM, Pten deleted; DM, Pten and Akt2 deleted; AM, Akt2 deleted. Two biological replicas are included for each genotype group. Protein levels of p-AKT, PTEN and p-GSK3 are analyzed and showed up-regulation of AKT and GSK-3 with PTEN loss and inhibition when AKT2 is lost. Phosphorylation of CREB is only observed when PTEN is lost. AKT2 loss together with PTEN blocked this phosphorylation in the DM livers. ( B ) Akt2 +/+ and Akt2 − / − cell were treated with forskolin (100 μM) for 24 h to induce cAMP and CREB phosphorylation or vehicle as controls. Phosphorylation of CREB is detected and showed to be lower when AKT2 is lost. When forskolin is added to induce cAMP, protein expression of p-CREB is evaluated in both Akt2 +/+ and Akt2 − / − cells even though its levels remains lower in the Akt2 − / − cells. Vinculin is probed as loading control. ( C ) Introduction of CREB-133A and wtCREB to Akt2 +/+ and Akt2 −/− hepatocytes. Expression of PEPCK is analyzed using quantitative PCR analysis. Left panel, CREB-S133A is introduced to Akt2 +/+ cells. Middle panel, wtCREB is introduced to Akt2 −/− cells; Right panel, wtCREB is introduced to Akt2 +/+ cells. n = 3. Data presented as mean ± SEM. * P ≤ 0.05. Different from vector transfected cells of the same genotype. Experiments repeated at least three times.

    Article Snippet: The medium was replaced with fresh medium with 100 μM Forskolin (Alomone Labs Cat# F-500) or vehicle and incubated for 24 h before harvesting.

    Techniques: Mouse Assay, Inhibition, Expressing, Real-time Polymerase Chain Reaction, Plasmid Preparation, Transfection