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gene exp capn2 rn00567422 m1  (Thermo Fisher)
87
Thermo Fisher gene exp capn2 rn00567422 m1
A) Representative Western blot of CAPN1, <t>CAPN2,</t> CAPNS1, CAPN10, CAST, and αII-spectrin in liver samples from male Wistar rats treated with 20% sucrose (S), 50 ppm of sodium arsenite (A) or both (A + S) through drinking water for 8 weeks. Coomassie brilliant blue (CBB) staining was used as a loading control. B) Quantification of the protein abundance of the members of the calpain system. C) Quantification of the intact αII-spectrin (240 kDa), the fragment generated by calpain activity (140 kDa) and the ratio of the abundance of the fragment/ intact αII-spectrin. The optical density of the bands was normalized to the optical density of the entire CBB lane. Data are presented as fold change relative to the mean value of the control animals. The bars denote the mean ± SD of at least 5 animals per condition. Each animal is represented by dots. Analysis by two-way ANOVA with Tukey’s post-hoc test. * denotes statistically significant differences in the post-hoc test with p < 0.05.
Gene Exp Capn2 Rn00567422 M1, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 87/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/gene exp capn2 rn00567422 m1/product/Thermo Fisher
Average 87 stars, based on 1 article reviews
gene exp capn2 rn00567422 m1 - by Bioz Stars, 2026-05
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gene exp capn2 mm00486669 m1  (Thermo Fisher)
85
Thermo Fisher gene exp capn2 mm00486669 m1
A) Representative Western blot of CAPN1, <t>CAPN2,</t> CAPNS1, CAPN10, CAST, and αII-spectrin in liver samples from male Wistar rats treated with 20% sucrose (S), 50 ppm of sodium arsenite (A) or both (A + S) through drinking water for 8 weeks. Coomassie brilliant blue (CBB) staining was used as a loading control. B) Quantification of the protein abundance of the members of the calpain system. C) Quantification of the intact αII-spectrin (240 kDa), the fragment generated by calpain activity (140 kDa) and the ratio of the abundance of the fragment/ intact αII-spectrin. The optical density of the bands was normalized to the optical density of the entire CBB lane. Data are presented as fold change relative to the mean value of the control animals. The bars denote the mean ± SD of at least 5 animals per condition. Each animal is represented by dots. Analysis by two-way ANOVA with Tukey’s post-hoc test. * denotes statistically significant differences in the post-hoc test with p < 0.05.
Gene Exp Capn2 Mm00486669 M1, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 85/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/gene exp capn2 mm00486669 m1/product/Thermo Fisher
Average 85 stars, based on 1 article reviews
gene exp capn2 mm00486669 m1 - by Bioz Stars, 2026-05
85/100 stars
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rabbit anti capn2 monoclonal antibody santa cruz biotechnology sc  (Santa Cruz Biotechnology)
93
Santa Cruz Biotechnology rabbit anti capn2 monoclonal antibody santa cruz biotechnology sc
A) Representative Western blot of CAPN1, <t>CAPN2,</t> CAPNS1, CAPN10, CAST, and αII-spectrin in liver samples from male Wistar rats treated with 20% sucrose (S), 50 ppm of sodium arsenite (A) or both (A + S) through drinking water for 8 weeks. Coomassie brilliant blue (CBB) staining was used as a loading control. B) Quantification of the protein abundance of the members of the calpain system. C) Quantification of the intact αII-spectrin (240 kDa), the fragment generated by calpain activity (140 kDa) and the ratio of the abundance of the fragment/ intact αII-spectrin. The optical density of the bands was normalized to the optical density of the entire CBB lane. Data are presented as fold change relative to the mean value of the control animals. The bars denote the mean ± SD of at least 5 animals per condition. Each animal is represented by dots. Analysis by two-way ANOVA with Tukey’s post-hoc test. * denotes statistically significant differences in the post-hoc test with p < 0.05.
Rabbit Anti Capn2 Monoclonal Antibody Santa Cruz Biotechnology Sc, supplied by Santa Cruz Biotechnology, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/rabbit anti capn2 monoclonal antibody santa cruz biotechnology sc/product/Santa Cruz Biotechnology
Average 93 stars, based on 1 article reviews
rabbit anti capn2 monoclonal antibody santa cruz biotechnology sc - by Bioz Stars, 2026-05
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proteolysis regulators cast capn2 487  (Tajima Shoji Co Ltd)
86
Tajima Shoji Co Ltd proteolysis regulators cast capn2 487
A) Representative Western blot of CAPN1, <t>CAPN2,</t> CAPNS1, CAPN10, CAST, and αII-spectrin in liver samples from male Wistar rats treated with 20% sucrose (S), 50 ppm of sodium arsenite (A) or both (A + S) through drinking water for 8 weeks. Coomassie brilliant blue (CBB) staining was used as a loading control. B) Quantification of the protein abundance of the members of the calpain system. C) Quantification of the intact αII-spectrin (240 kDa), the fragment generated by calpain activity (140 kDa) and the ratio of the abundance of the fragment/ intact αII-spectrin. The optical density of the bands was normalized to the optical density of the entire CBB lane. Data are presented as fold change relative to the mean value of the control animals. The bars denote the mean ± SD of at least 5 animals per condition. Each animal is represented by dots. Analysis by two-way ANOVA with Tukey’s post-hoc test. * denotes statistically significant differences in the post-hoc test with p < 0.05.
Proteolysis Regulators Cast Capn2 487, supplied by Tajima Shoji Co Ltd, 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/proteolysis regulators cast capn2 487/product/Tajima Shoji Co Ltd
Average 86 stars, based on 1 article reviews
proteolysis regulators cast capn2 487 - by Bioz Stars, 2026-05
86/100 stars
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proteolysis regulators cast capn2  (Tajima Shoji Co Ltd)
86
Tajima Shoji Co Ltd proteolysis regulators cast capn2
A) Representative Western blot of CAPN1, <t>CAPN2,</t> CAPNS1, CAPN10, CAST, and αII-spectrin in liver samples from male Wistar rats treated with 20% sucrose (S), 50 ppm of sodium arsenite (A) or both (A + S) through drinking water for 8 weeks. Coomassie brilliant blue (CBB) staining was used as a loading control. B) Quantification of the protein abundance of the members of the calpain system. C) Quantification of the intact αII-spectrin (240 kDa), the fragment generated by calpain activity (140 kDa) and the ratio of the abundance of the fragment/ intact αII-spectrin. The optical density of the bands was normalized to the optical density of the entire CBB lane. Data are presented as fold change relative to the mean value of the control animals. The bars denote the mean ± SD of at least 5 animals per condition. Each animal is represented by dots. Analysis by two-way ANOVA with Tukey’s post-hoc test. * denotes statistically significant differences in the post-hoc test with p < 0.05.
Proteolysis Regulators Cast Capn2, supplied by Tajima Shoji Co Ltd, 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/proteolysis regulators cast capn2/product/Tajima Shoji Co Ltd
Average 86 stars, based on 1 article reviews
proteolysis regulators cast capn2 - by Bioz Stars, 2026-05
86/100 stars
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capn2  (Cell Signaling Technology Inc)
86
Cell Signaling Technology Inc capn2
A) Representative Western blot of CAPN1, <t>CAPN2,</t> CAPNS1, CAPN10, CAST, and αII-spectrin in liver samples from male Wistar rats treated with 20% sucrose (S), 50 ppm of sodium arsenite (A) or both (A + S) through drinking water for 8 weeks. Coomassie brilliant blue (CBB) staining was used as a loading control. B) Quantification of the protein abundance of the members of the calpain system. C) Quantification of the intact αII-spectrin (240 kDa), the fragment generated by calpain activity (140 kDa) and the ratio of the abundance of the fragment/ intact αII-spectrin. The optical density of the bands was normalized to the optical density of the entire CBB lane. Data are presented as fold change relative to the mean value of the control animals. The bars denote the mean ± SD of at least 5 animals per condition. Each animal is represented by dots. Analysis by two-way ANOVA with Tukey’s post-hoc test. * denotes statistically significant differences in the post-hoc test with p < 0.05.
Capn2, supplied by Cell Signaling Technology Inc, 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/capn2/product/Cell Signaling Technology Inc
Average 86 stars, based on 1 article reviews
capn2 - by Bioz Stars, 2026-05
86/100 stars
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Image Search Results


A) Representative Western blot of CAPN1, CAPN2, CAPNS1, CAPN10, CAST, and αII-spectrin in liver samples from male Wistar rats treated with 20% sucrose (S), 50 ppm of sodium arsenite (A) or both (A + S) through drinking water for 8 weeks. Coomassie brilliant blue (CBB) staining was used as a loading control. B) Quantification of the protein abundance of the members of the calpain system. C) Quantification of the intact αII-spectrin (240 kDa), the fragment generated by calpain activity (140 kDa) and the ratio of the abundance of the fragment/ intact αII-spectrin. The optical density of the bands was normalized to the optical density of the entire CBB lane. Data are presented as fold change relative to the mean value of the control animals. The bars denote the mean ± SD of at least 5 animals per condition. Each animal is represented by dots. Analysis by two-way ANOVA with Tukey’s post-hoc test. * denotes statistically significant differences in the post-hoc test with p < 0.05.

Journal: PLOS One

Article Title: Sucrose but not arsenic induce hepatic steatosis which correlates with calpain-1 inhibition

doi: 10.1371/journal.pone.0339586

Figure Lengend Snippet: A) Representative Western blot of CAPN1, CAPN2, CAPNS1, CAPN10, CAST, and αII-spectrin in liver samples from male Wistar rats treated with 20% sucrose (S), 50 ppm of sodium arsenite (A) or both (A + S) through drinking water for 8 weeks. Coomassie brilliant blue (CBB) staining was used as a loading control. B) Quantification of the protein abundance of the members of the calpain system. C) Quantification of the intact αII-spectrin (240 kDa), the fragment generated by calpain activity (140 kDa) and the ratio of the abundance of the fragment/ intact αII-spectrin. The optical density of the bands was normalized to the optical density of the entire CBB lane. Data are presented as fold change relative to the mean value of the control animals. The bars denote the mean ± SD of at least 5 animals per condition. Each animal is represented by dots. Analysis by two-way ANOVA with Tukey’s post-hoc test. * denotes statistically significant differences in the post-hoc test with p < 0.05.

Article Snippet: Taqman probes (Applied Biosystems) against the mRNA of CAPN1 (Rn01479699_m1), CAPN2 (Rn00567422_m1), CAPNS1 (Rn01498486_g1), CAPN10 (Rn00581535_m1), and CAST (Rn00583952_m1) were used to evaluate the expression levels by quantitative real-time PCR, using 15 ng of cDNA.

Techniques: Western Blot, Staining, Control, Quantitative Proteomics, Generated, Activity Assay

The mRNA expression of A) CAPN1 mRNA. B) CAPN2 mRNA. C) CAST mRNA. D) CAPN10 mRNA. E) CAPNS1 were quantitated by real-time PCR and normalized to the expression levels of glucuronidase B (GUSB). Data are reported as fold change relative to control animals. The bars denote the mean ± SD of at least 4 animals per condition; each point represents an independent animal. Analysis by two-way ANOVA with Tukey’s post-hoc test.

Journal: PLOS One

Article Title: Sucrose but not arsenic induce hepatic steatosis which correlates with calpain-1 inhibition

doi: 10.1371/journal.pone.0339586

Figure Lengend Snippet: The mRNA expression of A) CAPN1 mRNA. B) CAPN2 mRNA. C) CAST mRNA. D) CAPN10 mRNA. E) CAPNS1 were quantitated by real-time PCR and normalized to the expression levels of glucuronidase B (GUSB). Data are reported as fold change relative to control animals. The bars denote the mean ± SD of at least 4 animals per condition; each point represents an independent animal. Analysis by two-way ANOVA with Tukey’s post-hoc test.

Article Snippet: Taqman probes (Applied Biosystems) against the mRNA of CAPN1 (Rn01479699_m1), CAPN2 (Rn00567422_m1), CAPNS1 (Rn01498486_g1), CAPN10 (Rn00581535_m1), and CAST (Rn00583952_m1) were used to evaluate the expression levels by quantitative real-time PCR, using 15 ng of cDNA.

Techniques: Expressing, Real-time Polymerase Chain Reaction, Control