primary antibody against chop Search Results


primary antibody against chop  (Stressgen Biotechnologies)
90
Stressgen Biotechnologies primary antibody against chop
Primary Antibody Against Chop, supplied by Stressgen Biotechnologies, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/primary antibody against chop/product/Stressgen Biotechnologies
Average 90 stars, based on 1 article reviews
primary antibody against chop - by Bioz Stars, 2026-03
90/100 stars
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primary antibodies against chop  (Bimake Inc)
90
Bimake Inc primary antibodies against chop
Effects of PA on LOX-1 and ER stress marker expression in HUVECs. (a) The protein expression level of LOX-1 was measured by Western blotting. (b) The expression of LOX-1 was quantified via densitometry using ImageJ software ( n = 3; 1-way ANOVA with Duncan's posthoc test). (c) The mRNA expression level of LOX-1 was measured via quantitative PCR ( n = 3; 1-way ANOVA with Duncan's posthoc test). (d) The protein expression levels <t>of</t> <t>Bip</t> and <t>CHOP</t> were measured by Western blotting. The expression of Bip (e) and CHOP (f) was quantified via densitometry using ImageJ software ( n = 3; 1-way ANOVA with Duncan's posthoc test). (g–i) The mRNA expression levels of ER stress-related genes ( Bip, CHOP , and XBP1s ) were measured using quantitative PCR ( n = 3; 1-way ANOVA with Duncan's posthoc test). The data are shown as means ± SD ( ∗∗∗ P < 0.001, ∗∗ P < 0.01, ∗ P < 0.05 vs. the Cont group).
Primary Antibodies Against Chop, supplied by Bimake Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/primary antibodies against chop/product/Bimake Inc
Average 90 stars, based on 1 article reviews
primary antibodies against chop - by Bioz Stars, 2026-03
90/100 stars
  Buy from Supplier
primary antibodies against chop  (Elabscience Biotechnology)
90
Elabscience Biotechnology primary antibodies against chop
Representative light microscopic screen images of liver tissue sections incubated with <t>CHOP</t> primary antibody. ( A ) (×20). Control group: In the liver tissue sections from the control group, hepatocytes with a normal structure (arrow) were observed to be CHOP-negative (CHOP positivity score: 0(0-0)). ( B ) (×20). I/R group: In the intralobular areas, primarily in Zone 1, hepatocytes showing intense CHOP positivity (spiral arrow) are observed (CHOP positivity score: 2(1-2)). ( C ) (×20). I/R+TMZ group: A decrease in hepatocytes showing CHOP positivity was observed in the perinobular areas, particularly in the intralobular regions (CHOP positivity score: 1(0-1)). ( D ) (×20). I/R+DEX group: A decrease in hepatocytes showing intense immunopositivity in the intralobular and perilobular areas was observed, with a widespread presence of CHOP-negative hepatocytes (arrow, CHOP positivity score: 0.5 (0-1)).
Primary Antibodies Against Chop, supplied by Elabscience Biotechnology, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/primary antibodies against chop/product/Elabscience Biotechnology
Average 90 stars, based on 1 article reviews
primary antibodies against chop - by Bioz Stars, 2026-03
90/100 stars
  Buy from Supplier
rabbit anti-mouse monoclonal primary antibodies against chop  (ABclonal Biotechnology)
90
ABclonal Biotechnology rabbit anti-mouse monoclonal primary antibodies against chop
Representative light microscopic screen images of liver tissue sections incubated with <t>CHOP</t> primary antibody. ( A ) (×20). Control group: In the liver tissue sections from the control group, hepatocytes with a normal structure (arrow) were observed to be CHOP-negative (CHOP positivity score: 0(0-0)). ( B ) (×20). I/R group: In the intralobular areas, primarily in Zone 1, hepatocytes showing intense CHOP positivity (spiral arrow) are observed (CHOP positivity score: 2(1-2)). ( C ) (×20). I/R+TMZ group: A decrease in hepatocytes showing CHOP positivity was observed in the perinobular areas, particularly in the intralobular regions (CHOP positivity score: 1(0-1)). ( D ) (×20). I/R+DEX group: A decrease in hepatocytes showing intense immunopositivity in the intralobular and perilobular areas was observed, with a widespread presence of CHOP-negative hepatocytes (arrow, CHOP positivity score: 0.5 (0-1)).
Rabbit Anti Mouse Monoclonal Primary Antibodies Against Chop, supplied by ABclonal Biotechnology, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/rabbit anti-mouse monoclonal primary antibodies against chop/product/ABclonal Biotechnology
Average 90 stars, based on 1 article reviews
rabbit anti-mouse monoclonal primary antibodies against chop - by Bioz Stars, 2026-03
90/100 stars
  Buy from Supplier

Image Search Results


Effects of PA on LOX-1 and ER stress marker expression in HUVECs. (a) The protein expression level of LOX-1 was measured by Western blotting. (b) The expression of LOX-1 was quantified via densitometry using ImageJ software ( n = 3; 1-way ANOVA with Duncan's posthoc test). (c) The mRNA expression level of LOX-1 was measured via quantitative PCR ( n = 3; 1-way ANOVA with Duncan's posthoc test). (d) The protein expression levels of Bip and CHOP were measured by Western blotting. The expression of Bip (e) and CHOP (f) was quantified via densitometry using ImageJ software ( n = 3; 1-way ANOVA with Duncan's posthoc test). (g–i) The mRNA expression levels of ER stress-related genes ( Bip, CHOP , and XBP1s ) were measured using quantitative PCR ( n = 3; 1-way ANOVA with Duncan's posthoc test). The data are shown as means ± SD ( ∗∗∗ P < 0.001, ∗∗ P < 0.01, ∗ P < 0.05 vs. the Cont group).

Journal: BioMed Research International

Article Title: Curcumin Alleviates Palmitic Acid-Induced LOX-1 Upregulation by Suppressing Endoplasmic Reticulum Stress in HUVECs

doi: 10.1155/2021/9983725

Figure Lengend Snippet: Effects of PA on LOX-1 and ER stress marker expression in HUVECs. (a) The protein expression level of LOX-1 was measured by Western blotting. (b) The expression of LOX-1 was quantified via densitometry using ImageJ software ( n = 3; 1-way ANOVA with Duncan's posthoc test). (c) The mRNA expression level of LOX-1 was measured via quantitative PCR ( n = 3; 1-way ANOVA with Duncan's posthoc test). (d) The protein expression levels of Bip and CHOP were measured by Western blotting. The expression of Bip (e) and CHOP (f) was quantified via densitometry using ImageJ software ( n = 3; 1-way ANOVA with Duncan's posthoc test). (g–i) The mRNA expression levels of ER stress-related genes ( Bip, CHOP , and XBP1s ) were measured using quantitative PCR ( n = 3; 1-way ANOVA with Duncan's posthoc test). The data are shown as means ± SD ( ∗∗∗ P < 0.001, ∗∗ P < 0.01, ∗ P < 0.05 vs. the Cont group).

Article Snippet: Protein extracts were separated by SDS-PAGE, transferred to a 0.22- μ m PVDF membrane, and incubated with primary antibodies against CHOP (A5462; Bimake), Bip (11587-1-AP; Proteintech, Wuhan, China), and LOX-1 (ab214427; Abcam, Cambridge, UK).

Techniques: Marker, Expressing, Western Blot, Software, Real-time Polymerase Chain Reaction

ER stress is involved in PA-induced LOX-1 upregulation. (a) The protein expression levels of Bip, CHOP, and LOX-1 were measured by Western blotting. (b) The expression levels of Bip, CHOP, and LOX-1 were quantified via densitometry using ImageJ software ( n = 3; 1-way ANOVA with Duncan's posthoc test). (c) The protein expression levels of Bip, CHOP, and LOX-1 were measured by Western blotting. The expression levels of Bip (d), CHOP (e), and LOX-1 (f) were quantified via densitometry using ImageJ software ( n = 4; 1-way ANOVA with Duncan's posthoc test). The data are shown as means ± SD ( ∗∗∗ P < 0.001, ∗∗ P < 0.01 vs. the Cont group; ## P < 0.01, # P < 0.05 vs. the PA group).

Journal: BioMed Research International

Article Title: Curcumin Alleviates Palmitic Acid-Induced LOX-1 Upregulation by Suppressing Endoplasmic Reticulum Stress in HUVECs

doi: 10.1155/2021/9983725

Figure Lengend Snippet: ER stress is involved in PA-induced LOX-1 upregulation. (a) The protein expression levels of Bip, CHOP, and LOX-1 were measured by Western blotting. (b) The expression levels of Bip, CHOP, and LOX-1 were quantified via densitometry using ImageJ software ( n = 3; 1-way ANOVA with Duncan's posthoc test). (c) The protein expression levels of Bip, CHOP, and LOX-1 were measured by Western blotting. The expression levels of Bip (d), CHOP (e), and LOX-1 (f) were quantified via densitometry using ImageJ software ( n = 4; 1-way ANOVA with Duncan's posthoc test). The data are shown as means ± SD ( ∗∗∗ P < 0.001, ∗∗ P < 0.01 vs. the Cont group; ## P < 0.01, # P < 0.05 vs. the PA group).

Article Snippet: Protein extracts were separated by SDS-PAGE, transferred to a 0.22- μ m PVDF membrane, and incubated with primary antibodies against CHOP (A5462; Bimake), Bip (11587-1-AP; Proteintech, Wuhan, China), and LOX-1 (ab214427; Abcam, Cambridge, UK).

Techniques: Expressing, Western Blot, Software

Curcumin inhibits PA-induced LOX-1 upregulation. (a) The protein expression level of LOX-1 was measured by Western blotting. (b) The expression was quantified via densitometry using ImageJ software ( n = 3; 1-way ANOVA with Duncan's posthoc test). (c) The protein expression levels of Bip, CHOP, and LOX-1 were measured by Western blotting. The expression of LOX-1 (d) was quantified via densitometry using ImageJ software ( n = 3; 1-way ANOVA with Duncan's posthoc test). (e) The mRNA expression level of LOX-1 was measured via quantitative PCR ( n = 3; 1-way ANOVA with Duncan's posthoc test). (f) Images of immunofluorescence staining of LOX-1 in HUVECs in different groups. The data are shown as means ± SD ( ∗∗∗ P < 0.001, ∗ P < 0.05 vs. the Cont group; # P < 0.05 vs. the PA group).

Journal: BioMed Research International

Article Title: Curcumin Alleviates Palmitic Acid-Induced LOX-1 Upregulation by Suppressing Endoplasmic Reticulum Stress in HUVECs

doi: 10.1155/2021/9983725

Figure Lengend Snippet: Curcumin inhibits PA-induced LOX-1 upregulation. (a) The protein expression level of LOX-1 was measured by Western blotting. (b) The expression was quantified via densitometry using ImageJ software ( n = 3; 1-way ANOVA with Duncan's posthoc test). (c) The protein expression levels of Bip, CHOP, and LOX-1 were measured by Western blotting. The expression of LOX-1 (d) was quantified via densitometry using ImageJ software ( n = 3; 1-way ANOVA with Duncan's posthoc test). (e) The mRNA expression level of LOX-1 was measured via quantitative PCR ( n = 3; 1-way ANOVA with Duncan's posthoc test). (f) Images of immunofluorescence staining of LOX-1 in HUVECs in different groups. The data are shown as means ± SD ( ∗∗∗ P < 0.001, ∗ P < 0.05 vs. the Cont group; # P < 0.05 vs. the PA group).

Article Snippet: Protein extracts were separated by SDS-PAGE, transferred to a 0.22- μ m PVDF membrane, and incubated with primary antibodies against CHOP (A5462; Bimake), Bip (11587-1-AP; Proteintech, Wuhan, China), and LOX-1 (ab214427; Abcam, Cambridge, UK).

Techniques: Expressing, Western Blot, Software, Real-time Polymerase Chain Reaction, Immunofluorescence, Staining

Curcumin ameliorates ER stress in HUVECs. (a) The protein expression levels of Bip and CHOP were measured by Western blotting. The expression of Bip (b) and CHOP (c) was quantified via densitometry using ImageJ software ( n = 3; 1-way ANOVA with Duncan's posthoc test). (d) The expression of Bip and CHOP was quantified via densitometry using ImageJ software ( n = 3; 1-way ANOVA with Duncan's posthoc test). (e–g) The mRNA expression levels of ER stress-related genes ( Bip , CHOP and XBP1s ) were measured by quantitative PCR ( n = 4; 1-way ANOVA with Duncan's posthoc test). (h) Images of immunofluorescence staining of Bip in HUVECs in different groups. (i) Cellular ultrastructure in different groups. The arrows indicate endoplasmic reticulum. The data are shown as means ± SD ( ∗∗∗ P < 0.001, ∗∗ P < 0.01 vs. the Cont group; ### P < 0.001, ## P < 0.01, # P < 0.05 vs. the PA group).

Journal: BioMed Research International

Article Title: Curcumin Alleviates Palmitic Acid-Induced LOX-1 Upregulation by Suppressing Endoplasmic Reticulum Stress in HUVECs

doi: 10.1155/2021/9983725

Figure Lengend Snippet: Curcumin ameliorates ER stress in HUVECs. (a) The protein expression levels of Bip and CHOP were measured by Western blotting. The expression of Bip (b) and CHOP (c) was quantified via densitometry using ImageJ software ( n = 3; 1-way ANOVA with Duncan's posthoc test). (d) The expression of Bip and CHOP was quantified via densitometry using ImageJ software ( n = 3; 1-way ANOVA with Duncan's posthoc test). (e–g) The mRNA expression levels of ER stress-related genes ( Bip , CHOP and XBP1s ) were measured by quantitative PCR ( n = 4; 1-way ANOVA with Duncan's posthoc test). (h) Images of immunofluorescence staining of Bip in HUVECs in different groups. (i) Cellular ultrastructure in different groups. The arrows indicate endoplasmic reticulum. The data are shown as means ± SD ( ∗∗∗ P < 0.001, ∗∗ P < 0.01 vs. the Cont group; ### P < 0.001, ## P < 0.01, # P < 0.05 vs. the PA group).

Article Snippet: Protein extracts were separated by SDS-PAGE, transferred to a 0.22- μ m PVDF membrane, and incubated with primary antibodies against CHOP (A5462; Bimake), Bip (11587-1-AP; Proteintech, Wuhan, China), and LOX-1 (ab214427; Abcam, Cambridge, UK).

Techniques: Expressing, Western Blot, Software, Real-time Polymerase Chain Reaction, Immunofluorescence, Staining

Curcumin alleviates PA-induced LOX-1 upregulation by suppressing ER stress. (a) The protein expression levels of Bip, CHOP, and LOX-1 were measured by Western blotting. (b) The expression levels of Bip, CHOP, and LOX-1 were quantified via densitometry using ImageJ software ( n = 3; 1-way ANOVA with Duncan's posthoc test). (c) The protein expression levels of Bip, CHOP, and LOX-1 were measured by Western blotting. The expression levels of Bip (d), CHOP (e), and LOX-1 (f) were quantified via densitometry using ImageJ software ( n = 3; 1-way ANOVA with Duncan's posthoc test). The data are shown as means ± SD ( ∗∗∗ P < 0.001, ∗∗ P < 0.01, ∗ P < 0.05 vs. the Cont group; # P < 0.05 vs. the PA group).

Journal: BioMed Research International

Article Title: Curcumin Alleviates Palmitic Acid-Induced LOX-1 Upregulation by Suppressing Endoplasmic Reticulum Stress in HUVECs

doi: 10.1155/2021/9983725

Figure Lengend Snippet: Curcumin alleviates PA-induced LOX-1 upregulation by suppressing ER stress. (a) The protein expression levels of Bip, CHOP, and LOX-1 were measured by Western blotting. (b) The expression levels of Bip, CHOP, and LOX-1 were quantified via densitometry using ImageJ software ( n = 3; 1-way ANOVA with Duncan's posthoc test). (c) The protein expression levels of Bip, CHOP, and LOX-1 were measured by Western blotting. The expression levels of Bip (d), CHOP (e), and LOX-1 (f) were quantified via densitometry using ImageJ software ( n = 3; 1-way ANOVA with Duncan's posthoc test). The data are shown as means ± SD ( ∗∗∗ P < 0.001, ∗∗ P < 0.01, ∗ P < 0.05 vs. the Cont group; # P < 0.05 vs. the PA group).

Article Snippet: Protein extracts were separated by SDS-PAGE, transferred to a 0.22- μ m PVDF membrane, and incubated with primary antibodies against CHOP (A5462; Bimake), Bip (11587-1-AP; Proteintech, Wuhan, China), and LOX-1 (ab214427; Abcam, Cambridge, UK).

Techniques: Expressing, Western Blot, Software

Representative light microscopic screen images of liver tissue sections incubated with CHOP primary antibody. ( A ) (×20). Control group: In the liver tissue sections from the control group, hepatocytes with a normal structure (arrow) were observed to be CHOP-negative (CHOP positivity score: 0(0-0)). ( B ) (×20). I/R group: In the intralobular areas, primarily in Zone 1, hepatocytes showing intense CHOP positivity (spiral arrow) are observed (CHOP positivity score: 2(1-2)). ( C ) (×20). I/R+TMZ group: A decrease in hepatocytes showing CHOP positivity was observed in the perinobular areas, particularly in the intralobular regions (CHOP positivity score: 1(0-1)). ( D ) (×20). I/R+DEX group: A decrease in hepatocytes showing intense immunopositivity in the intralobular and perilobular areas was observed, with a widespread presence of CHOP-negative hepatocytes (arrow, CHOP positivity score: 0.5 (0-1)).

Journal: Biomedicines

Article Title: Protective Effects of Trimetazidine and Dexmedetomidine on Liver Injury in a Mesenteric Artery Ischemia–Reperfusion Rat Model via Endoplasmic Reticulum Stress

doi: 10.3390/biomedicines12102299

Figure Lengend Snippet: Representative light microscopic screen images of liver tissue sections incubated with CHOP primary antibody. ( A ) (×20). Control group: In the liver tissue sections from the control group, hepatocytes with a normal structure (arrow) were observed to be CHOP-negative (CHOP positivity score: 0(0-0)). ( B ) (×20). I/R group: In the intralobular areas, primarily in Zone 1, hepatocytes showing intense CHOP positivity (spiral arrow) are observed (CHOP positivity score: 2(1-2)). ( C ) (×20). I/R+TMZ group: A decrease in hepatocytes showing CHOP positivity was observed in the perinobular areas, particularly in the intralobular regions (CHOP positivity score: 1(0-1)). ( D ) (×20). I/R+DEX group: A decrease in hepatocytes showing intense immunopositivity in the intralobular and perilobular areas was observed, with a widespread presence of CHOP-negative hepatocytes (arrow, CHOP positivity score: 0.5 (0-1)).

Article Snippet: The liver tissue slices were analyzed via immunohistochemistry labeling with primary antibodies against CHOP (E-AB-70087, 1/300, Elabscience, Houston, TX, USA), GPR78 (SC-13539, 1/350, Santa Cruz Biotechnology Inc. Dallas, TX, USA), 8-hydroxy-2′-deoxyguanosine (8-OHdG) (Santa Cruz, SC-66036, 1/200, Santa Cruz Biotechnology Inc., Dallas, TX, USA), cleaved caspase-3 (Abcam, ab4051, 1/100), anti-Bax ab32503, 1/200, (Abcam, Cambridge, UK), and anti-Bcl-2 (Abcam, ab32124, 1/200).

Techniques: Incubation, Control