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Biozol Diagnostica Vertrieb GmbH mouse srebp 1c
Adaption of gene expression of key players of lipid homeostasis in steatotic PHHs. PHHs were treated with 1 mM FFAs for 24 h and relative mRNA expression levels of gene targets were determined using RT-qPCR. Investigation of genes centrally involved in lipid catabolism (PPARα, ACSL1 and CPT1L) and anabolism <t>(SREBP-1c</t> and FASN) in PHHs compared to control. Data are shown as the mean + SD, n = 5, paired t-test, statistical analyses were conducted on ΔC T values, p ≤ 0.05 (*), p < 0.01 (**).
Mouse Srebp 1c, supplied by Biozol Diagnostica Vertrieb GmbH, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/mouse srebp 1c/product/Biozol Diagnostica Vertrieb GmbH
Average 86 stars, based on 1 article reviews
Price from $9.99 to $1999.99
mouse srebp 1c - by Bioz Stars, 2023-06
86/100 stars

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1) Product Images from "Influence of Genistein on Hepatic Lipid Metabolism in an In Vitro Model of Hepatic Steatosis"

Article Title: Influence of Genistein on Hepatic Lipid Metabolism in an In Vitro Model of Hepatic Steatosis

Journal: Molecules

doi: 10.3390/molecules26041156

Adaption of gene expression of key players of lipid homeostasis in steatotic PHHs. PHHs were treated with 1 mM FFAs for 24 h and relative mRNA expression levels of gene targets were determined using RT-qPCR. Investigation of genes centrally involved in lipid catabolism (PPARα, ACSL1 and CPT1L) and anabolism (SREBP-1c and FASN) in PHHs compared to control. Data are shown as the mean + SD, n = 5, paired t-test, statistical analyses were conducted on ΔC T values, p ≤ 0.05 (*), p < 0.01 (**).
Figure Legend Snippet: Adaption of gene expression of key players of lipid homeostasis in steatotic PHHs. PHHs were treated with 1 mM FFAs for 24 h and relative mRNA expression levels of gene targets were determined using RT-qPCR. Investigation of genes centrally involved in lipid catabolism (PPARα, ACSL1 and CPT1L) and anabolism (SREBP-1c and FASN) in PHHs compared to control. Data are shown as the mean + SD, n = 5, paired t-test, statistical analyses were conducted on ΔC T values, p ≤ 0.05 (*), p < 0.01 (**).

Techniques Used: Expressing, Quantitative RT-PCR

Activation of key signaling pathways in lipid homeostasis in steatotic hepatocytes. PHHs were treated with 1 mM FFAs for 24 h and protein levels of PPARα and SREBP-1c were investigated. Western blot analyses were performed after protein extraction from different subcellular fractions of FFA-treated PHHs and control. Densitometric measurements of ( A ) cytosolic PPARα normalized to the expression levels of α-tubulin, nucleic PPARα normalized to p84, ( B ) ER membrane-bound SREBP-1c normalized to Na + /K + -ATPase and nucleic SREBP-1c normalized to p84 expression. Data are shown as the mean + SD, n = 5, paired t-test, p ≤ 0.05 (*). ( C ) Representative Western blot images show the specific bands of PPARα, α-tubulin, p84, SREBP-1c, and Na + /K + -ATPase in control and steatotic PHHs.
Figure Legend Snippet: Activation of key signaling pathways in lipid homeostasis in steatotic hepatocytes. PHHs were treated with 1 mM FFAs for 24 h and protein levels of PPARα and SREBP-1c were investigated. Western blot analyses were performed after protein extraction from different subcellular fractions of FFA-treated PHHs and control. Densitometric measurements of ( A ) cytosolic PPARα normalized to the expression levels of α-tubulin, nucleic PPARα normalized to p84, ( B ) ER membrane-bound SREBP-1c normalized to Na + /K + -ATPase and nucleic SREBP-1c normalized to p84 expression. Data are shown as the mean + SD, n = 5, paired t-test, p ≤ 0.05 (*). ( C ) Representative Western blot images show the specific bands of PPARα, α-tubulin, p84, SREBP-1c, and Na + /K + -ATPase in control and steatotic PHHs.

Techniques Used: Activation Assay, Western Blot, Protein Extraction, Expressing

Transcriptional and translational response of genistein-treated steatotic PHHs on ( A ) PPARα and ( B ) SREBP-1c, two central regulators of hepatic lipid homeostasis. PHHs were treated with 1 mM FFAs for 24 h, followed by 24 h of additive treatment with genistein (0, 1, 5, 10, 50, and 100 µM). ( Ai ) PPARα mRNA levels were determined by RT-qPCR; ( Aii ) cytosolic and; ( Aiii ) nucleic PPARα protein levels were assessed by Western blot (α-tubulin and p84 served as the respective reference proteins). ( Bi ) Relative mRNA expression levels of SREBP-1c as measured by RT-qPCR; ( Bii ) densitometric measurements of ER membrane-bound SREBP-1c normalized to Na + /K + -ATPase and ( Biii ) nucleic SREBP-1c normalized to p84 expression. Data are shown as the mean + SD, n = 5 for RT-qPCR data, n = 4 for Western blot measurements, two-way ANOVA with Tukey or Sidak post hoc test. p ≤ 0.05 (*), p < 0.01 (**). Selected comparisons are shown; for details on the statistical evaluation, see . ( C ) Representative Western blot images show the specific bands of PPARα, α-tubulin, p84, SREBP-1c, and Na + /K + -ATPase in control and steatotic PHHs after genistein treatment.
Figure Legend Snippet: Transcriptional and translational response of genistein-treated steatotic PHHs on ( A ) PPARα and ( B ) SREBP-1c, two central regulators of hepatic lipid homeostasis. PHHs were treated with 1 mM FFAs for 24 h, followed by 24 h of additive treatment with genistein (0, 1, 5, 10, 50, and 100 µM). ( Ai ) PPARα mRNA levels were determined by RT-qPCR; ( Aii ) cytosolic and; ( Aiii ) nucleic PPARα protein levels were assessed by Western blot (α-tubulin and p84 served as the respective reference proteins). ( Bi ) Relative mRNA expression levels of SREBP-1c as measured by RT-qPCR; ( Bii ) densitometric measurements of ER membrane-bound SREBP-1c normalized to Na + /K + -ATPase and ( Biii ) nucleic SREBP-1c normalized to p84 expression. Data are shown as the mean + SD, n = 5 for RT-qPCR data, n = 4 for Western blot measurements, two-way ANOVA with Tukey or Sidak post hoc test. p ≤ 0.05 (*), p < 0.01 (**). Selected comparisons are shown; for details on the statistical evaluation, see . ( C ) Representative Western blot images show the specific bands of PPARα, α-tubulin, p84, SREBP-1c, and Na + /K + -ATPase in control and steatotic PHHs after genistein treatment.

Techniques Used: Quantitative RT-PCR, Western Blot, Expressing

TaqMan ® gene expression assays (Applied Biosystems, Foster City, CA, USA) applied for qPCR.
Figure Legend Snippet: TaqMan ® gene expression assays (Applied Biosystems, Foster City, CA, USA) applied for qPCR.

Techniques Used: Expressing, Binding Assay

Antibodies for Western blotting.
Figure Legend Snippet: Antibodies for Western blotting.

Techniques Used: Western Blot, Incubation

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    Biozol Diagnostica Vertrieb GmbH mouse srebp 1c
    Adaption of gene expression of key players of lipid homeostasis in steatotic PHHs. PHHs were treated with 1 mM FFAs for 24 h and relative mRNA expression levels of gene targets were determined using RT-qPCR. Investigation of genes centrally involved in lipid catabolism (PPARα, ACSL1 and CPT1L) and anabolism <t>(SREBP-1c</t> and FASN) in PHHs compared to control. Data are shown as the mean + SD, n = 5, paired t-test, statistical analyses were conducted on ΔC T values, p ≤ 0.05 (*), p < 0.01 (**).
    Mouse Srebp 1c, supplied by Biozol Diagnostica Vertrieb GmbH, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/mouse srebp 1c/product/Biozol Diagnostica Vertrieb GmbH
    Average 86 stars, based on 1 article reviews
    Price from $9.99 to $1999.99
    mouse srebp 1c - by Bioz Stars, 2023-06
    86/100 stars
      Buy from Supplier

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    Adaption of gene expression of key players of lipid homeostasis in steatotic PHHs. PHHs were treated with 1 mM FFAs for 24 h and relative mRNA expression levels of gene targets were determined using RT-qPCR. Investigation of genes centrally involved in lipid catabolism (PPARα, ACSL1 and CPT1L) and anabolism (SREBP-1c and FASN) in PHHs compared to control. Data are shown as the mean + SD, n = 5, paired t-test, statistical analyses were conducted on ΔC T values, p ≤ 0.05 (*), p < 0.01 (**).

    Journal: Molecules

    Article Title: Influence of Genistein on Hepatic Lipid Metabolism in an In Vitro Model of Hepatic Steatosis

    doi: 10.3390/molecules26041156

    Figure Lengend Snippet: Adaption of gene expression of key players of lipid homeostasis in steatotic PHHs. PHHs were treated with 1 mM FFAs for 24 h and relative mRNA expression levels of gene targets were determined using RT-qPCR. Investigation of genes centrally involved in lipid catabolism (PPARα, ACSL1 and CPT1L) and anabolism (SREBP-1c and FASN) in PHHs compared to control. Data are shown as the mean + SD, n = 5, paired t-test, statistical analyses were conducted on ΔC T values, p ≤ 0.05 (*), p < 0.01 (**).

    Article Snippet: Mouse SREBP-1c (Biozol, Eching, Germany) , 1:200 , 2 h.

    Techniques: Expressing, Quantitative RT-PCR

    Activation of key signaling pathways in lipid homeostasis in steatotic hepatocytes. PHHs were treated with 1 mM FFAs for 24 h and protein levels of PPARα and SREBP-1c were investigated. Western blot analyses were performed after protein extraction from different subcellular fractions of FFA-treated PHHs and control. Densitometric measurements of ( A ) cytosolic PPARα normalized to the expression levels of α-tubulin, nucleic PPARα normalized to p84, ( B ) ER membrane-bound SREBP-1c normalized to Na + /K + -ATPase and nucleic SREBP-1c normalized to p84 expression. Data are shown as the mean + SD, n = 5, paired t-test, p ≤ 0.05 (*). ( C ) Representative Western blot images show the specific bands of PPARα, α-tubulin, p84, SREBP-1c, and Na + /K + -ATPase in control and steatotic PHHs.

    Journal: Molecules

    Article Title: Influence of Genistein on Hepatic Lipid Metabolism in an In Vitro Model of Hepatic Steatosis

    doi: 10.3390/molecules26041156

    Figure Lengend Snippet: Activation of key signaling pathways in lipid homeostasis in steatotic hepatocytes. PHHs were treated with 1 mM FFAs for 24 h and protein levels of PPARα and SREBP-1c were investigated. Western blot analyses were performed after protein extraction from different subcellular fractions of FFA-treated PHHs and control. Densitometric measurements of ( A ) cytosolic PPARα normalized to the expression levels of α-tubulin, nucleic PPARα normalized to p84, ( B ) ER membrane-bound SREBP-1c normalized to Na + /K + -ATPase and nucleic SREBP-1c normalized to p84 expression. Data are shown as the mean + SD, n = 5, paired t-test, p ≤ 0.05 (*). ( C ) Representative Western blot images show the specific bands of PPARα, α-tubulin, p84, SREBP-1c, and Na + /K + -ATPase in control and steatotic PHHs.

    Article Snippet: Mouse SREBP-1c (Biozol, Eching, Germany) , 1:200 , 2 h.

    Techniques: Activation Assay, Western Blot, Protein Extraction, Expressing

    Transcriptional and translational response of genistein-treated steatotic PHHs on ( A ) PPARα and ( B ) SREBP-1c, two central regulators of hepatic lipid homeostasis. PHHs were treated with 1 mM FFAs for 24 h, followed by 24 h of additive treatment with genistein (0, 1, 5, 10, 50, and 100 µM). ( Ai ) PPARα mRNA levels were determined by RT-qPCR; ( Aii ) cytosolic and; ( Aiii ) nucleic PPARα protein levels were assessed by Western blot (α-tubulin and p84 served as the respective reference proteins). ( Bi ) Relative mRNA expression levels of SREBP-1c as measured by RT-qPCR; ( Bii ) densitometric measurements of ER membrane-bound SREBP-1c normalized to Na + /K + -ATPase and ( Biii ) nucleic SREBP-1c normalized to p84 expression. Data are shown as the mean + SD, n = 5 for RT-qPCR data, n = 4 for Western blot measurements, two-way ANOVA with Tukey or Sidak post hoc test. p ≤ 0.05 (*), p < 0.01 (**). Selected comparisons are shown; for details on the statistical evaluation, see . ( C ) Representative Western blot images show the specific bands of PPARα, α-tubulin, p84, SREBP-1c, and Na + /K + -ATPase in control and steatotic PHHs after genistein treatment.

    Journal: Molecules

    Article Title: Influence of Genistein on Hepatic Lipid Metabolism in an In Vitro Model of Hepatic Steatosis

    doi: 10.3390/molecules26041156

    Figure Lengend Snippet: Transcriptional and translational response of genistein-treated steatotic PHHs on ( A ) PPARα and ( B ) SREBP-1c, two central regulators of hepatic lipid homeostasis. PHHs were treated with 1 mM FFAs for 24 h, followed by 24 h of additive treatment with genistein (0, 1, 5, 10, 50, and 100 µM). ( Ai ) PPARα mRNA levels were determined by RT-qPCR; ( Aii ) cytosolic and; ( Aiii ) nucleic PPARα protein levels were assessed by Western blot (α-tubulin and p84 served as the respective reference proteins). ( Bi ) Relative mRNA expression levels of SREBP-1c as measured by RT-qPCR; ( Bii ) densitometric measurements of ER membrane-bound SREBP-1c normalized to Na + /K + -ATPase and ( Biii ) nucleic SREBP-1c normalized to p84 expression. Data are shown as the mean + SD, n = 5 for RT-qPCR data, n = 4 for Western blot measurements, two-way ANOVA with Tukey or Sidak post hoc test. p ≤ 0.05 (*), p < 0.01 (**). Selected comparisons are shown; for details on the statistical evaluation, see . ( C ) Representative Western blot images show the specific bands of PPARα, α-tubulin, p84, SREBP-1c, and Na + /K + -ATPase in control and steatotic PHHs after genistein treatment.

    Article Snippet: Mouse SREBP-1c (Biozol, Eching, Germany) , 1:200 , 2 h.

    Techniques: Quantitative RT-PCR, Western Blot, Expressing

    TaqMan ® gene expression assays (Applied Biosystems, Foster City, CA, USA) applied for qPCR.

    Journal: Molecules

    Article Title: Influence of Genistein on Hepatic Lipid Metabolism in an In Vitro Model of Hepatic Steatosis

    doi: 10.3390/molecules26041156

    Figure Lengend Snippet: TaqMan ® gene expression assays (Applied Biosystems, Foster City, CA, USA) applied for qPCR.

    Article Snippet: Mouse SREBP-1c (Biozol, Eching, Germany) , 1:200 , 2 h.

    Techniques: Expressing, Binding Assay

    Antibodies for Western blotting.

    Journal: Molecules

    Article Title: Influence of Genistein on Hepatic Lipid Metabolism in an In Vitro Model of Hepatic Steatosis

    doi: 10.3390/molecules26041156

    Figure Lengend Snippet: Antibodies for Western blotting.

    Article Snippet: Mouse SREBP-1c (Biozol, Eching, Germany) , 1:200 , 2 h.

    Techniques: Western Blot, Incubation