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Proteintech hsp60
HSP90AA1 plays a pivotal role in the heat stress response of liver cancer cells. (a) WB analysis was employed to assess alterations in the expression levels of HSP110, HSP90AA1, HSP70, and <t>HSP60</t> in liver cancer cells following exposure to heat stress. (b) To evaluate transfection efficiency, WB analysis was performed to assess the effects of HSP110 or HSP90AA1 silence in HepG2 and Huh7 cells. (c) MTT assay was used to evaluate changes in cell viability of HepG2 and Huh7 cells after heat stress treatment with or without the silencing of HSP90 and HSP110, respectively. (d) Flow cytometry was used to analyze changes in the apoptosis rate of HepG2 and Huh7 cells after heat stress treatment with or without the silencing of HSP90 and HSP110, respectively. All experiments were performed with at least three replicates. Statistical significance was denoted as * P < 0.05 and ** P < 0.01.
Hsp60, supplied by Proteintech, used in various techniques. Bioz Stars score: 96/100, based on 229 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/hsp60/product/Proteintech
Average 96 stars, based on 229 article reviews
hsp60 - by Bioz Stars, 2026-02
96/100 stars

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1) Product Images from "Heat stress-induced heat shock protein 90 alpha family class A member 1 upregulation stabilizes yes-associated protein through ubiquitination inhibition to boost hepatic cancer radiofrequency hyperthermia resistance"

Article Title: Heat stress-induced heat shock protein 90 alpha family class A member 1 upregulation stabilizes yes-associated protein through ubiquitination inhibition to boost hepatic cancer radiofrequency hyperthermia resistance

Journal: Cell Stress & Chaperones

doi: 10.1016/j.cstres.2025.100140

HSP90AA1 plays a pivotal role in the heat stress response of liver cancer cells. (a) WB analysis was employed to assess alterations in the expression levels of HSP110, HSP90AA1, HSP70, and HSP60 in liver cancer cells following exposure to heat stress. (b) To evaluate transfection efficiency, WB analysis was performed to assess the effects of HSP110 or HSP90AA1 silence in HepG2 and Huh7 cells. (c) MTT assay was used to evaluate changes in cell viability of HepG2 and Huh7 cells after heat stress treatment with or without the silencing of HSP90 and HSP110, respectively. (d) Flow cytometry was used to analyze changes in the apoptosis rate of HepG2 and Huh7 cells after heat stress treatment with or without the silencing of HSP90 and HSP110, respectively. All experiments were performed with at least three replicates. Statistical significance was denoted as * P < 0.05 and ** P < 0.01.
Figure Legend Snippet: HSP90AA1 plays a pivotal role in the heat stress response of liver cancer cells. (a) WB analysis was employed to assess alterations in the expression levels of HSP110, HSP90AA1, HSP70, and HSP60 in liver cancer cells following exposure to heat stress. (b) To evaluate transfection efficiency, WB analysis was performed to assess the effects of HSP110 or HSP90AA1 silence in HepG2 and Huh7 cells. (c) MTT assay was used to evaluate changes in cell viability of HepG2 and Huh7 cells after heat stress treatment with or without the silencing of HSP90 and HSP110, respectively. (d) Flow cytometry was used to analyze changes in the apoptosis rate of HepG2 and Huh7 cells after heat stress treatment with or without the silencing of HSP90 and HSP110, respectively. All experiments were performed with at least three replicates. Statistical significance was denoted as * P < 0.05 and ** P < 0.01.

Techniques Used: Expressing, Transfection, MTT Assay, Flow Cytometry



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HSP90AA1 plays a pivotal role in the heat stress response of liver cancer cells. (a) WB analysis was employed to assess alterations in the expression levels of HSP110, HSP90AA1, HSP70, and <t>HSP60</t> in liver cancer cells following exposure to heat stress. (b) To evaluate transfection efficiency, WB analysis was performed to assess the effects of HSP110 or HSP90AA1 silence in HepG2 and Huh7 cells. (c) MTT assay was used to evaluate changes in cell viability of HepG2 and Huh7 cells after heat stress treatment with or without the silencing of HSP90 and HSP110, respectively. (d) Flow cytometry was used to analyze changes in the apoptosis rate of HepG2 and Huh7 cells after heat stress treatment with or without the silencing of HSP90 and HSP110, respectively. All experiments were performed with at least three replicates. Statistical significance was denoted as * P < 0.05 and ** P < 0.01.
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HSP90AA1 plays a pivotal role in the heat stress response of liver cancer cells. (a) WB analysis was employed to assess alterations in the expression levels of HSP110, HSP90AA1, HSP70, and <t>HSP60</t> in liver cancer cells following exposure to heat stress. (b) To evaluate transfection efficiency, WB analysis was performed to assess the effects of HSP110 or HSP90AA1 silence in HepG2 and Huh7 cells. (c) MTT assay was used to evaluate changes in cell viability of HepG2 and Huh7 cells after heat stress treatment with or without the silencing of HSP90 and HSP110, respectively. (d) Flow cytometry was used to analyze changes in the apoptosis rate of HepG2 and Huh7 cells after heat stress treatment with or without the silencing of HSP90 and HSP110, respectively. All experiments were performed with at least three replicates. Statistical significance was denoted as * P < 0.05 and ** P < 0.01.
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HSP90AA1 plays a pivotal role in the heat stress response of liver cancer cells. (a) WB analysis was employed to assess alterations in the expression levels of HSP110, HSP90AA1, HSP70, and <t>HSP60</t> in liver cancer cells following exposure to heat stress. (b) To evaluate transfection efficiency, WB analysis was performed to assess the effects of HSP110 or HSP90AA1 silence in HepG2 and Huh7 cells. (c) MTT assay was used to evaluate changes in cell viability of HepG2 and Huh7 cells after heat stress treatment with or without the silencing of HSP90 and HSP110, respectively. (d) Flow cytometry was used to analyze changes in the apoptosis rate of HepG2 and Huh7 cells after heat stress treatment with or without the silencing of HSP90 and HSP110, respectively. All experiments were performed with at least three replicates. Statistical significance was denoted as * P < 0.05 and ** P < 0.01.
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HSP90AA1 plays a pivotal role in the heat stress response of liver cancer cells. (a) WB analysis was employed to assess alterations in the expression levels of HSP110, HSP90AA1, HSP70, and <t>HSP60</t> in liver cancer cells following exposure to heat stress. (b) To evaluate transfection efficiency, WB analysis was performed to assess the effects of HSP110 or HSP90AA1 silence in HepG2 and Huh7 cells. (c) MTT assay was used to evaluate changes in cell viability of HepG2 and Huh7 cells after heat stress treatment with or without the silencing of HSP90 and HSP110, respectively. (d) Flow cytometry was used to analyze changes in the apoptosis rate of HepG2 and Huh7 cells after heat stress treatment with or without the silencing of HSP90 and HSP110, respectively. All experiments were performed with at least three replicates. Statistical significance was denoted as * P < 0.05 and ** P < 0.01.
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HSP90AA1 plays a pivotal role in the heat stress response of liver cancer cells. (a) WB analysis was employed to assess alterations in the expression levels of HSP110, HSP90AA1, HSP70, and <t>HSP60</t> in liver cancer cells following exposure to heat stress. (b) To evaluate transfection efficiency, WB analysis was performed to assess the effects of HSP110 or HSP90AA1 silence in HepG2 and Huh7 cells. (c) MTT assay was used to evaluate changes in cell viability of HepG2 and Huh7 cells after heat stress treatment with or without the silencing of HSP90 and HSP110, respectively. (d) Flow cytometry was used to analyze changes in the apoptosis rate of HepG2 and Huh7 cells after heat stress treatment with or without the silencing of HSP90 and HSP110, respectively. All experiments were performed with at least three replicates. Statistical significance was denoted as * P < 0.05 and ** P < 0.01.
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Image Search Results


HSP90AA1 plays a pivotal role in the heat stress response of liver cancer cells. (a) WB analysis was employed to assess alterations in the expression levels of HSP110, HSP90AA1, HSP70, and HSP60 in liver cancer cells following exposure to heat stress. (b) To evaluate transfection efficiency, WB analysis was performed to assess the effects of HSP110 or HSP90AA1 silence in HepG2 and Huh7 cells. (c) MTT assay was used to evaluate changes in cell viability of HepG2 and Huh7 cells after heat stress treatment with or without the silencing of HSP90 and HSP110, respectively. (d) Flow cytometry was used to analyze changes in the apoptosis rate of HepG2 and Huh7 cells after heat stress treatment with or without the silencing of HSP90 and HSP110, respectively. All experiments were performed with at least three replicates. Statistical significance was denoted as * P < 0.05 and ** P < 0.01.

Journal: Cell Stress & Chaperones

Article Title: Heat stress-induced heat shock protein 90 alpha family class A member 1 upregulation stabilizes yes-associated protein through ubiquitination inhibition to boost hepatic cancer radiofrequency hyperthermia resistance

doi: 10.1016/j.cstres.2025.100140

Figure Lengend Snippet: HSP90AA1 plays a pivotal role in the heat stress response of liver cancer cells. (a) WB analysis was employed to assess alterations in the expression levels of HSP110, HSP90AA1, HSP70, and HSP60 in liver cancer cells following exposure to heat stress. (b) To evaluate transfection efficiency, WB analysis was performed to assess the effects of HSP110 or HSP90AA1 silence in HepG2 and Huh7 cells. (c) MTT assay was used to evaluate changes in cell viability of HepG2 and Huh7 cells after heat stress treatment with or without the silencing of HSP90 and HSP110, respectively. (d) Flow cytometry was used to analyze changes in the apoptosis rate of HepG2 and Huh7 cells after heat stress treatment with or without the silencing of HSP90 and HSP110, respectively. All experiments were performed with at least three replicates. Statistical significance was denoted as * P < 0.05 and ** P < 0.01.

Article Snippet: HSP60 , Proteintech , 15282-1-AP , 1:2000.

Techniques: Expressing, Transfection, MTT Assay, Flow Cytometry