rabbit anti cdk2 Search Results


90
Boster Bio rabbit anti cdk2
Rabbit Anti Cdk2, supplied by Boster Bio, 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 cdk2/product/Boster Bio
Average 90 stars, based on 1 article reviews
rabbit anti cdk2 - by Bioz Stars, 2026-06
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Bio-Rad anti rabbit cdk2
Fig. 2. Effect of E. milii on mRNA expression of specific gene of cell cycle regulators. (A) qRT-PCR was performed to assess the mRNA levels of cells regulators genes. HepG2 cells were cultured in the presence or absence of 11.2 mM E. milii water extract for 24 h. The GAPDH was used as internal positive control. The data for E. milii-treated samples were presented as the mean ± SEM of triplicate determination and compared with the control group. *p < 0.05; **p < 0.01. (B) Effect of E. milii on expression of cell cycle regulators. The cells were treated with or without E. milii for indicated time. The expression of <t>CDK2,</t> E2F1 and cyclin E were determined with western blot analysis.
Anti Rabbit Cdk2, supplied by Bio-Rad, 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/anti rabbit cdk2/product/Bio-Rad
Average 90 stars, based on 1 article reviews
anti rabbit cdk2 - by Bioz Stars, 2026-06
90/100 stars
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90
BioGenes GmbH rabbit anti-cdk2
Fig. 2. Effect of E. milii on mRNA expression of specific gene of cell cycle regulators. (A) qRT-PCR was performed to assess the mRNA levels of cells regulators genes. HepG2 cells were cultured in the presence or absence of 11.2 mM E. milii water extract for 24 h. The GAPDH was used as internal positive control. The data for E. milii-treated samples were presented as the mean ± SEM of triplicate determination and compared with the control group. *p < 0.05; **p < 0.01. (B) Effect of E. milii on expression of cell cycle regulators. The cells were treated with or without E. milii for indicated time. The expression of <t>CDK2,</t> E2F1 and cyclin E were determined with western blot analysis.
Rabbit Anti Cdk2, supplied by BioGenes GmbH, 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-cdk2/product/BioGenes GmbH
Average 90 stars, based on 1 article reviews
rabbit anti-cdk2 - by Bioz Stars, 2026-06
90/100 stars
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86
Cell Signaling Technology Inc rabbit anti cdk2 e8j9t
Fig. 2. Effect of E. milii on mRNA expression of specific gene of cell cycle regulators. (A) qRT-PCR was performed to assess the mRNA levels of cells regulators genes. HepG2 cells were cultured in the presence or absence of 11.2 mM E. milii water extract for 24 h. The GAPDH was used as internal positive control. The data for E. milii-treated samples were presented as the mean ± SEM of triplicate determination and compared with the control group. *p < 0.05; **p < 0.01. (B) Effect of E. milii on expression of cell cycle regulators. The cells were treated with or without E. milii for indicated time. The expression of <t>CDK2,</t> E2F1 and cyclin E were determined with western blot analysis.
Rabbit Anti Cdk2 E8j9t, 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/rabbit anti cdk2 e8j9t/product/Cell Signaling Technology Inc
Average 86 stars, based on 1 article reviews
rabbit anti cdk2 e8j9t - by Bioz Stars, 2026-06
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Cell Signaling Technology Inc cat 9101 rrid ab 331646 cdk2 78b2 rabbit mab cell signaling
Fig. 2. Effect of E. milii on mRNA expression of specific gene of cell cycle regulators. (A) qRT-PCR was performed to assess the mRNA levels of cells regulators genes. HepG2 cells were cultured in the presence or absence of 11.2 mM E. milii water extract for 24 h. The GAPDH was used as internal positive control. The data for E. milii-treated samples were presented as the mean ± SEM of triplicate determination and compared with the control group. *p < 0.05; **p < 0.01. (B) Effect of E. milii on expression of cell cycle regulators. The cells were treated with or without E. milii for indicated time. The expression of <t>CDK2,</t> E2F1 and cyclin E were determined with western blot analysis.
Cat 9101 Rrid Ab 331646 Cdk2 78b2 Rabbit Mab Cell Signaling, 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/cat 9101 rrid ab 331646 cdk2 78b2 rabbit mab cell signaling/product/Cell Signaling Technology Inc
Average 86 stars, based on 1 article reviews
cat 9101 rrid ab 331646 cdk2 78b2 rabbit mab cell signaling - by Bioz Stars, 2026-06
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Rabbit anti-Human CDK2 Polyclonal Antibody
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Rabbit anti-Human CDK2 Polyclonal Antibody
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Rabbit Anti-Human CDK2 (C-term) Antibody, 400 µl
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Boster Bio Anti-Phospho-CDK2 (Y15) Rabbit Monoclonal Antibody catalog # MP00166. Tested in WB, IHC, IP applications. This antibody reacts with Human, Mouse, Rat.
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Rabbit Anti Human CDK2 Monoclonal Clone GBB-3 from Innovative Research is a monoclonal antibody in a Liquid format, buffered in phosphate buffered saline, pH 7.4, 150mM NaCl, 0.02% sodium azide and 50% glycerol, 0.4-0.5mg/ml BSA.
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Image Search Results


Fig. 2. Effect of E. milii on mRNA expression of specific gene of cell cycle regulators. (A) qRT-PCR was performed to assess the mRNA levels of cells regulators genes. HepG2 cells were cultured in the presence or absence of 11.2 mM E. milii water extract for 24 h. The GAPDH was used as internal positive control. The data for E. milii-treated samples were presented as the mean ± SEM of triplicate determination and compared with the control group. *p < 0.05; **p < 0.01. (B) Effect of E. milii on expression of cell cycle regulators. The cells were treated with or without E. milii for indicated time. The expression of CDK2, E2F1 and cyclin E were determined with western blot analysis.

Journal: Saudi journal of biological sciences

Article Title: Phytochemical profiling, antioxidant and antiproliferation potential of Euphorbia milii var.: Experimental analysis and in-silico validation.

doi: 10.1016/j.sjbs.2020.08.003

Figure Lengend Snippet: Fig. 2. Effect of E. milii on mRNA expression of specific gene of cell cycle regulators. (A) qRT-PCR was performed to assess the mRNA levels of cells regulators genes. HepG2 cells were cultured in the presence or absence of 11.2 mM E. milii water extract for 24 h. The GAPDH was used as internal positive control. The data for E. milii-treated samples were presented as the mean ± SEM of triplicate determination and compared with the control group. *p < 0.05; **p < 0.01. (B) Effect of E. milii on expression of cell cycle regulators. The cells were treated with or without E. milii for indicated time. The expression of CDK2, E2F1 and cyclin E were determined with western blot analysis.

Article Snippet: The nitrocellulose membranes were put into the blocking solution (5% fat free milk) for 1 h, then incubated the monoclonal anti-rabbit CDK2, cyclin E, E2F1 and anti-b-actin with shaking over night at 4 C. The horseradish peroxidase (HRP)conjugated secondary antibody given for at least 1 h, then chemiluminescence was detected using a chemiluminescence imaging system (Bio-Rad, Hercules, CA).

Techniques: Expressing, Quantitative RT-PCR, Cell Culture, Positive Control, Control, Western Blot

Fig. 4. Obtained binding modes of ligands in the binding domain of CDK2 (magenta) and Thymidlate synthase (skyblue). (A) Binding mode of compound BAN in CDK2 ATP binding site. (B) Compound CBT bonded to CDK2. (C) Docking complex of CDK2-MBT. Binding mode of selected compounds in the active site of Thymidlate synthase (TS): (D) BAN-TS, (E) CBT-TS, (F) MBT-TS and (G) compound 5-FU (standard) bonded to TS.

Journal: Saudi journal of biological sciences

Article Title: Phytochemical profiling, antioxidant and antiproliferation potential of Euphorbia milii var.: Experimental analysis and in-silico validation.

doi: 10.1016/j.sjbs.2020.08.003

Figure Lengend Snippet: Fig. 4. Obtained binding modes of ligands in the binding domain of CDK2 (magenta) and Thymidlate synthase (skyblue). (A) Binding mode of compound BAN in CDK2 ATP binding site. (B) Compound CBT bonded to CDK2. (C) Docking complex of CDK2-MBT. Binding mode of selected compounds in the active site of Thymidlate synthase (TS): (D) BAN-TS, (E) CBT-TS, (F) MBT-TS and (G) compound 5-FU (standard) bonded to TS.

Article Snippet: The nitrocellulose membranes were put into the blocking solution (5% fat free milk) for 1 h, then incubated the monoclonal anti-rabbit CDK2, cyclin E, E2F1 and anti-b-actin with shaking over night at 4 C. The horseradish peroxidase (HRP)conjugated secondary antibody given for at least 1 h, then chemiluminescence was detected using a chemiluminescence imaging system (Bio-Rad, Hercules, CA).

Techniques: Binding Assay

Fig. 5. RMSDs of Ca atoms of the protein, backbone atoms of binding pocket (within 6.5 Å), and the heavy atoms in the ligand for: (A) CDK2-BAN, (B) CDK2-CBT, (C) TS-CBT and (D) TS-5-FU. Comparison between binding free energy terms of: (E) CDK2 bonded to BAN and CBT; (F) TS bonded to CBT and 5-FU.

Journal: Saudi journal of biological sciences

Article Title: Phytochemical profiling, antioxidant and antiproliferation potential of Euphorbia milii var.: Experimental analysis and in-silico validation.

doi: 10.1016/j.sjbs.2020.08.003

Figure Lengend Snippet: Fig. 5. RMSDs of Ca atoms of the protein, backbone atoms of binding pocket (within 6.5 Å), and the heavy atoms in the ligand for: (A) CDK2-BAN, (B) CDK2-CBT, (C) TS-CBT and (D) TS-5-FU. Comparison between binding free energy terms of: (E) CDK2 bonded to BAN and CBT; (F) TS bonded to CBT and 5-FU.

Article Snippet: The nitrocellulose membranes were put into the blocking solution (5% fat free milk) for 1 h, then incubated the monoclonal anti-rabbit CDK2, cyclin E, E2F1 and anti-b-actin with shaking over night at 4 C. The horseradish peroxidase (HRP)conjugated secondary antibody given for at least 1 h, then chemiluminescence was detected using a chemiluminescence imaging system (Bio-Rad, Hercules, CA).

Techniques: Binding Assay, Comparison