apoa2 Search Results


apoa2 mab4215  (R&D Systems)
90
R&D Systems apoa2 mab4215
Fig. 7. Potentiation of apoC1 knockout on the apoE siRNA-mediated impairment of HCV production. (A) Determination of apolipopro- teins expression in apoC1-/- −13 cell line by Western blot. The levels of apoA1, <t>apoA2,</t> apoC1, apoC2, apoC3, and apoE in the cell ly- sates as well as apoE in the supernatants were determined by Western blotting and are com- pared between parental and apoC1-/- −13 cells. To determine potentiation of apoC1 knockout on the apoE siRNA-mediated im- pairment of HCV production, parental and ApoC1-/- Huh-7.5 cells were transfected with increasing concentrations (2, 10, and 50 nM) of apoE-specific siRNAs with a non-specific con- trol (NSC) siRNA as control. After 48 h p.t., cells were infected with HCV. At 24 h p.i., cell culture supernatants were collected for ex- traction of HCV vRNA, which were quantified by qRT-PCR (B). * indicates statistically sig- nificant difference (P < 0.05). Cell culture supernatants were also used for detection of apoE and re-infection of naïve Huh-7.5 cells (C). ApoE and NS5A in the HCV-infected cells were detected by Western blot using apoE monoclonal antibody WuE4 and NS5A mono- clonal antibody 9E10, respectively.
Apoa2 Mab4215, supplied by R&D Systems, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 90 stars, based on 1 article reviews
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gene exp apoa2 mm04210370 g1  (Thermo Fisher)
88
Thermo Fisher gene exp apoa2 mm04210370 g1
Fig. 7. Potentiation of apoC1 knockout on the apoE siRNA-mediated impairment of HCV production. (A) Determination of apolipopro- teins expression in apoC1-/- −13 cell line by Western blot. The levels of apoA1, <t>apoA2,</t> apoC1, apoC2, apoC3, and apoE in the cell ly- sates as well as apoE in the supernatants were determined by Western blotting and are com- pared between parental and apoC1-/- −13 cells. To determine potentiation of apoC1 knockout on the apoE siRNA-mediated im- pairment of HCV production, parental and ApoC1-/- Huh-7.5 cells were transfected with increasing concentrations (2, 10, and 50 nM) of apoE-specific siRNAs with a non-specific con- trol (NSC) siRNA as control. After 48 h p.t., cells were infected with HCV. At 24 h p.i., cell culture supernatants were collected for ex- traction of HCV vRNA, which were quantified by qRT-PCR (B). * indicates statistically sig- nificant difference (P < 0.05). Cell culture supernatants were also used for detection of apoE and re-infection of naïve Huh-7.5 cells (C). ApoE and NS5A in the HCV-infected cells were detected by Western blot using apoE monoclonal antibody WuE4 and NS5A mono- clonal antibody 9E10, respectively.
Gene Exp Apoa2 Mm04210370 G1, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 88/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 88 stars, based on 1 article reviews
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snp apoa2 c 16248625 10  (Thermo Fisher)
91
Thermo Fisher snp apoa2 c 16248625 10
Fig. 7. Potentiation of apoC1 knockout on the apoE siRNA-mediated impairment of HCV production. (A) Determination of apolipopro- teins expression in apoC1-/- −13 cell line by Western blot. The levels of apoA1, <t>apoA2,</t> apoC1, apoC2, apoC3, and apoE in the cell ly- sates as well as apoE in the supernatants were determined by Western blotting and are com- pared between parental and apoC1-/- −13 cells. To determine potentiation of apoC1 knockout on the apoE siRNA-mediated im- pairment of HCV production, parental and ApoC1-/- Huh-7.5 cells were transfected with increasing concentrations (2, 10, and 50 nM) of apoE-specific siRNAs with a non-specific con- trol (NSC) siRNA as control. After 48 h p.t., cells were infected with HCV. At 24 h p.i., cell culture supernatants were collected for ex- traction of HCV vRNA, which were quantified by qRT-PCR (B). * indicates statistically sig- nificant difference (P < 0.05). Cell culture supernatants were also used for detection of apoE and re-infection of naïve Huh-7.5 cells (C). ApoE and NS5A in the HCV-infected cells were detected by Western blot using apoE monoclonal antibody WuE4 and NS5A mono- clonal antibody 9E10, respectively.
Snp Apoa2 C 16248625 10, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 91/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 91 stars, based on 1 article reviews
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apoa2  (Cusabio)
93
Cusabio apoa2
Fig. 7. Potentiation of apoC1 knockout on the apoE siRNA-mediated impairment of HCV production. (A) Determination of apolipopro- teins expression in apoC1-/- −13 cell line by Western blot. The levels of apoA1, <t>apoA2,</t> apoC1, apoC2, apoC3, and apoE in the cell ly- sates as well as apoE in the supernatants were determined by Western blotting and are com- pared between parental and apoC1-/- −13 cells. To determine potentiation of apoC1 knockout on the apoE siRNA-mediated im- pairment of HCV production, parental and ApoC1-/- Huh-7.5 cells were transfected with increasing concentrations (2, 10, and 50 nM) of apoE-specific siRNAs with a non-specific con- trol (NSC) siRNA as control. After 48 h p.t., cells were infected with HCV. At 24 h p.i., cell culture supernatants were collected for ex- traction of HCV vRNA, which were quantified by qRT-PCR (B). * indicates statistically sig- nificant difference (P < 0.05). Cell culture supernatants were also used for detection of apoE and re-infection of naïve Huh-7.5 cells (C). ApoE and NS5A in the HCV-infected cells were detected by Western blot using apoE monoclonal antibody WuE4 and NS5A mono- clonal antibody 9E10, respectively.
Apoa2, supplied by Cusabio, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 93 stars, based on 1 article reviews
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snp apoa2 c 25746794 20  (Thermo Fisher)
85
Thermo Fisher snp apoa2 c 25746794 20
Fig. 7. Potentiation of apoC1 knockout on the apoE siRNA-mediated impairment of HCV production. (A) Determination of apolipopro- teins expression in apoC1-/- −13 cell line by Western blot. The levels of apoA1, <t>apoA2,</t> apoC1, apoC2, apoC3, and apoE in the cell ly- sates as well as apoE in the supernatants were determined by Western blotting and are com- pared between parental and apoC1-/- −13 cells. To determine potentiation of apoC1 knockout on the apoE siRNA-mediated im- pairment of HCV production, parental and ApoC1-/- Huh-7.5 cells were transfected with increasing concentrations (2, 10, and 50 nM) of apoE-specific siRNAs with a non-specific con- trol (NSC) siRNA as control. After 48 h p.t., cells were infected with HCV. At 24 h p.i., cell culture supernatants were collected for ex- traction of HCV vRNA, which were quantified by qRT-PCR (B). * indicates statistically sig- nificant difference (P < 0.05). Cell culture supernatants were also used for detection of apoE and re-infection of naïve Huh-7.5 cells (C). ApoE and NS5A in the HCV-infected cells were detected by Western blot using apoE monoclonal antibody WuE4 and NS5A mono- clonal antibody 9E10, respectively.
Snp Apoa2 C 25746794 20, 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/snp apoa2 c 25746794 20/product/Thermo Fisher
Average 85 stars, based on 1 article reviews
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gene exp apoa2 mm00442687 m1  (Thermo Fisher)
89
Thermo Fisher gene exp apoa2 mm00442687 m1
Fig. 7. Potentiation of apoC1 knockout on the apoE siRNA-mediated impairment of HCV production. (A) Determination of apolipopro- teins expression in apoC1-/- −13 cell line by Western blot. The levels of apoA1, <t>apoA2,</t> apoC1, apoC2, apoC3, and apoE in the cell ly- sates as well as apoE in the supernatants were determined by Western blotting and are com- pared between parental and apoC1-/- −13 cells. To determine potentiation of apoC1 knockout on the apoE siRNA-mediated im- pairment of HCV production, parental and ApoC1-/- Huh-7.5 cells were transfected with increasing concentrations (2, 10, and 50 nM) of apoE-specific siRNAs with a non-specific con- trol (NSC) siRNA as control. After 48 h p.t., cells were infected with HCV. At 24 h p.i., cell culture supernatants were collected for ex- traction of HCV vRNA, which were quantified by qRT-PCR (B). * indicates statistically sig- nificant difference (P < 0.05). Cell culture supernatants were also used for detection of apoE and re-infection of naïve Huh-7.5 cells (C). ApoE and NS5A in the HCV-infected cells were detected by Western blot using apoE monoclonal antibody WuE4 and NS5A mono- clonal antibody 9E10, respectively.
Gene Exp Apoa2 Mm00442687 M1, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 89/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/gene exp apoa2 mm00442687 m1/product/Thermo Fisher
Average 89 stars, based on 1 article reviews
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apoaii  (Proteintech)
92
Proteintech apoaii
Fig. 7. Potentiation of apoC1 knockout on the apoE siRNA-mediated impairment of HCV production. (A) Determination of apolipopro- teins expression in apoC1-/- −13 cell line by Western blot. The levels of apoA1, <t>apoA2,</t> apoC1, apoC2, apoC3, and apoE in the cell ly- sates as well as apoE in the supernatants were determined by Western blotting and are com- pared between parental and apoC1-/- −13 cells. To determine potentiation of apoC1 knockout on the apoE siRNA-mediated im- pairment of HCV production, parental and ApoC1-/- Huh-7.5 cells were transfected with increasing concentrations (2, 10, and 50 nM) of apoE-specific siRNAs with a non-specific con- trol (NSC) siRNA as control. After 48 h p.t., cells were infected with HCV. At 24 h p.i., cell culture supernatants were collected for ex- traction of HCV vRNA, which were quantified by qRT-PCR (B). * indicates statistically sig- nificant difference (P < 0.05). Cell culture supernatants were also used for detection of apoE and re-infection of naïve Huh-7.5 cells (C). ApoE and NS5A in the HCV-infected cells were detected by Western blot using apoE monoclonal antibody WuE4 and NS5A mono- clonal antibody 9E10, respectively.
Apoaii, supplied by Proteintech, used in various techniques. Bioz Stars score: 92/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/apoaii/product/Proteintech
Average 92 stars, based on 1 article reviews
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gene exp apoa2 rn00565403 m1  (Thermo Fisher)
88
Thermo Fisher gene exp apoa2 rn00565403 m1
Fig. 7. Potentiation of apoC1 knockout on the apoE siRNA-mediated impairment of HCV production. (A) Determination of apolipopro- teins expression in apoC1-/- −13 cell line by Western blot. The levels of apoA1, <t>apoA2,</t> apoC1, apoC2, apoC3, and apoE in the cell ly- sates as well as apoE in the supernatants were determined by Western blotting and are com- pared between parental and apoC1-/- −13 cells. To determine potentiation of apoC1 knockout on the apoE siRNA-mediated im- pairment of HCV production, parental and ApoC1-/- Huh-7.5 cells were transfected with increasing concentrations (2, 10, and 50 nM) of apoE-specific siRNAs with a non-specific con- trol (NSC) siRNA as control. After 48 h p.t., cells were infected with HCV. At 24 h p.i., cell culture supernatants were collected for ex- traction of HCV vRNA, which were quantified by qRT-PCR (B). * indicates statistically sig- nificant difference (P < 0.05). Cell culture supernatants were also used for detection of apoE and re-infection of naïve Huh-7.5 cells (C). ApoE and NS5A in the HCV-infected cells were detected by Western blot using apoE monoclonal antibody WuE4 and NS5A mono- clonal antibody 9E10, respectively.
Gene Exp Apoa2 Rn00565403 M1, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 88/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/gene exp apoa2 rn00565403 m1/product/Thermo Fisher
Average 88 stars, based on 1 article reviews
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apolipoprotein aii  (Athens Research)
94
Athens Research apolipoprotein aii
Fig. 7. Potentiation of apoC1 knockout on the apoE siRNA-mediated impairment of HCV production. (A) Determination of apolipopro- teins expression in apoC1-/- −13 cell line by Western blot. The levels of apoA1, <t>apoA2,</t> apoC1, apoC2, apoC3, and apoE in the cell ly- sates as well as apoE in the supernatants were determined by Western blotting and are com- pared between parental and apoC1-/- −13 cells. To determine potentiation of apoC1 knockout on the apoE siRNA-mediated im- pairment of HCV production, parental and ApoC1-/- Huh-7.5 cells were transfected with increasing concentrations (2, 10, and 50 nM) of apoE-specific siRNAs with a non-specific con- trol (NSC) siRNA as control. After 48 h p.t., cells were infected with HCV. At 24 h p.i., cell culture supernatants were collected for ex- traction of HCV vRNA, which were quantified by qRT-PCR (B). * indicates statistically sig- nificant difference (P < 0.05). Cell culture supernatants were also used for detection of apoE and re-infection of naïve Huh-7.5 cells (C). ApoE and NS5A in the HCV-infected cells were detected by Western blot using apoE monoclonal antibody WuE4 and NS5A mono- clonal antibody 9E10, respectively.
Apolipoprotein Aii, supplied by Athens Research, 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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snp apoa2 c 27848237 10  (Thermo Fisher)
85
Thermo Fisher snp apoa2 c 27848237 10
Fig. 7. Potentiation of apoC1 knockout on the apoE siRNA-mediated impairment of HCV production. (A) Determination of apolipopro- teins expression in apoC1-/- −13 cell line by Western blot. The levels of apoA1, <t>apoA2,</t> apoC1, apoC2, apoC3, and apoE in the cell ly- sates as well as apoE in the supernatants were determined by Western blotting and are com- pared between parental and apoC1-/- −13 cells. To determine potentiation of apoC1 knockout on the apoE siRNA-mediated im- pairment of HCV production, parental and ApoC1-/- Huh-7.5 cells were transfected with increasing concentrations (2, 10, and 50 nM) of apoE-specific siRNAs with a non-specific con- trol (NSC) siRNA as control. After 48 h p.t., cells were infected with HCV. At 24 h p.i., cell culture supernatants were collected for ex- traction of HCV vRNA, which were quantified by qRT-PCR (B). * indicates statistically sig- nificant difference (P < 0.05). Cell culture supernatants were also used for detection of apoE and re-infection of naïve Huh-7.5 cells (C). ApoE and NS5A in the HCV-infected cells were detected by Western blot using apoE monoclonal antibody WuE4 and NS5A mono- clonal antibody 9E10, respectively.
Snp Apoa2 C 27848237 10, 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
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apoa2  (St Johns Laboratory)
91
St Johns Laboratory apoa2
List of differentially regulated proteins in AG.1 treated group vs control group. Positive fold-change value denotes up-accumulation and negative fold change value denotes down-accumulation in comparison with control.
Apoa2, supplied by St Johns Laboratory, used in various techniques. Bioz Stars score: 91/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 91 stars, based on 1 article reviews
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Image Search Results


Fig. 7. Potentiation of apoC1 knockout on the apoE siRNA-mediated impairment of HCV production. (A) Determination of apolipopro- teins expression in apoC1-/- −13 cell line by Western blot. The levels of apoA1, apoA2, apoC1, apoC2, apoC3, and apoE in the cell ly- sates as well as apoE in the supernatants were determined by Western blotting and are com- pared between parental and apoC1-/- −13 cells. To determine potentiation of apoC1 knockout on the apoE siRNA-mediated im- pairment of HCV production, parental and ApoC1-/- Huh-7.5 cells were transfected with increasing concentrations (2, 10, and 50 nM) of apoE-specific siRNAs with a non-specific con- trol (NSC) siRNA as control. After 48 h p.t., cells were infected with HCV. At 24 h p.i., cell culture supernatants were collected for ex- traction of HCV vRNA, which were quantified by qRT-PCR (B). * indicates statistically sig- nificant difference (P < 0.05). Cell culture supernatants were also used for detection of apoE and re-infection of naïve Huh-7.5 cells (C). ApoE and NS5A in the HCV-infected cells were detected by Western blot using apoE monoclonal antibody WuE4 and NS5A mono- clonal antibody 9E10, respectively.

Journal: Virology

Article Title: Characterization of apolipoprotein C1 in hepatitis C virus infection and morphogenesis.

doi: 10.1016/j.virol.2018.08.004

Figure Lengend Snippet: Fig. 7. Potentiation of apoC1 knockout on the apoE siRNA-mediated impairment of HCV production. (A) Determination of apolipopro- teins expression in apoC1-/- −13 cell line by Western blot. The levels of apoA1, apoA2, apoC1, apoC2, apoC3, and apoE in the cell ly- sates as well as apoE in the supernatants were determined by Western blotting and are com- pared between parental and apoC1-/- −13 cells. To determine potentiation of apoC1 knockout on the apoE siRNA-mediated im- pairment of HCV production, parental and ApoC1-/- Huh-7.5 cells were transfected with increasing concentrations (2, 10, and 50 nM) of apoE-specific siRNAs with a non-specific con- trol (NSC) siRNA as control. After 48 h p.t., cells were infected with HCV. At 24 h p.i., cell culture supernatants were collected for ex- traction of HCV vRNA, which were quantified by qRT-PCR (B). * indicates statistically sig- nificant difference (P < 0.05). Cell culture supernatants were also used for detection of apoE and re-infection of naïve Huh-7.5 cells (C). ApoE and NS5A in the HCV-infected cells were detected by Western blot using apoE monoclonal antibody WuE4 and NS5A mono- clonal antibody 9E10, respectively.

Article Snippet: ApoA2 (MAB4215) and ApoC2 (AF4497) antibodies were purchased from R&D Systems.

Techniques: Knock-Out, Expressing, Western Blot, Transfection, Control, Infection, Cell Culture, Quantitative RT-PCR

List of differentially regulated proteins in AG.1 treated group vs control group. Positive fold-change value denotes up-accumulation and negative fold change value denotes down-accumulation in comparison with control.

Journal: Frontiers in Pharmacology

Article Title: Treatment With Medicinal Mushroom Extract Mixture Inhibits Translation and Reprograms Metabolism in Advanced Colorectal Cancer Animal Model as Evidenced by Tandem Mass Tags Proteomics Analysis

doi: 10.3389/fphar.2020.01202

Figure Lengend Snippet: List of differentially regulated proteins in AG.1 treated group vs control group. Positive fold-change value denotes up-accumulation and negative fold change value denotes down-accumulation in comparison with control.

Article Snippet: The PVDF membranes (BioRad, USA) were incubated with primary antibodies raised against Rps3 (1:500; rabbit pAb; St John’s Laboratory,UK) and Apoa2 (1:500; rabbit pAb; St John’s Laboratory,UK) at 4°C overnight.

Techniques: Binding Assay

List of differentially regulated proteins in AG.1 and 5-FU treated group vs control group. Positive fold-change value denotes up-accumulation and negative fold change value denotes down-accumulation in comparison with control.

Journal: Frontiers in Pharmacology

Article Title: Treatment With Medicinal Mushroom Extract Mixture Inhibits Translation and Reprograms Metabolism in Advanced Colorectal Cancer Animal Model as Evidenced by Tandem Mass Tags Proteomics Analysis

doi: 10.3389/fphar.2020.01202

Figure Lengend Snippet: List of differentially regulated proteins in AG.1 and 5-FU treated group vs control group. Positive fold-change value denotes up-accumulation and negative fold change value denotes down-accumulation in comparison with control.

Article Snippet: The PVDF membranes (BioRad, USA) were incubated with primary antibodies raised against Rps3 (1:500; rabbit pAb; St John’s Laboratory,UK) and Apoa2 (1:500; rabbit pAb; St John’s Laboratory,UK) at 4°C overnight.

Techniques: Binding Assay, Activity Assay, Chemotaxis Assay, Transduction, RNA Binding Assay, Migration, Conjugation Assay

List of differentially regulated proteins in 5-FU treated group vs control group. Positive fold-change value denotes up-accumulation and negative fold change value denotes down-accumulation in comparison with control.

Journal: Frontiers in Pharmacology

Article Title: Treatment With Medicinal Mushroom Extract Mixture Inhibits Translation and Reprograms Metabolism in Advanced Colorectal Cancer Animal Model as Evidenced by Tandem Mass Tags Proteomics Analysis

doi: 10.3389/fphar.2020.01202

Figure Lengend Snippet: List of differentially regulated proteins in 5-FU treated group vs control group. Positive fold-change value denotes up-accumulation and negative fold change value denotes down-accumulation in comparison with control.

Article Snippet: The PVDF membranes (BioRad, USA) were incubated with primary antibodies raised against Rps3 (1:500; rabbit pAb; St John’s Laboratory,UK) and Apoa2 (1:500; rabbit pAb; St John’s Laboratory,UK) at 4°C overnight.

Techniques: Transduction, Chemotaxis Assay

Representative Western blot and summary representation of relative expression of Rps3 and Apoa2 in tumor tissues obtained from control and three treated groups of animals (each group included tumors obtained from three different animals). Results are presented as relative expression values ± SEM between chemiluminescent signals obtained in three replicate experiments. Statistically significant changes (ANOVA, p < 0.05) are marked with an asterisk. C, control group of animals; G1, AG.1; G2, AG.1 and 5-FU; G3, 5-FU.

Journal: Frontiers in Pharmacology

Article Title: Treatment With Medicinal Mushroom Extract Mixture Inhibits Translation and Reprograms Metabolism in Advanced Colorectal Cancer Animal Model as Evidenced by Tandem Mass Tags Proteomics Analysis

doi: 10.3389/fphar.2020.01202

Figure Lengend Snippet: Representative Western blot and summary representation of relative expression of Rps3 and Apoa2 in tumor tissues obtained from control and three treated groups of animals (each group included tumors obtained from three different animals). Results are presented as relative expression values ± SEM between chemiluminescent signals obtained in three replicate experiments. Statistically significant changes (ANOVA, p < 0.05) are marked with an asterisk. C, control group of animals; G1, AG.1; G2, AG.1 and 5-FU; G3, 5-FU.

Article Snippet: The PVDF membranes (BioRad, USA) were incubated with primary antibodies raised against Rps3 (1:500; rabbit pAb; St John’s Laboratory,UK) and Apoa2 (1:500; rabbit pAb; St John’s Laboratory,UK) at 4°C overnight.

Techniques: Western Blot, Expressing