rabbit polyclonal anti cdk1  (Proteintech)

 
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    Proteintech rabbit polyclonal anti cdk1
    Rabbit Polyclonal Anti Cdk1, supplied by Proteintech, 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 polyclonal anti cdk1/product/Proteintech
    Average 86 stars, based on 1 article reviews
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    rabbit polyclonal anti phospho cdk1  (Thermo Fisher)


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    Bioz Manufacturer Symbol Thermo Fisher manufactures this product  
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    Thermo Fisher rabbit polyclonal anti phospho cdk1
    Rabbit Polyclonal Anti Phospho Cdk1, supplied by Thermo Fisher, 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 polyclonal anti phospho cdk1/product/Thermo Fisher
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    rabbit polyclonal anti cdk1  (Millipore)

     
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    Millipore rabbit polyclonal anti cdk1
    KEY RESOURCES TABLE
    Rabbit Polyclonal Anti Cdk1, supplied by Millipore, 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 polyclonal anti cdk1/product/Millipore
    Average 86 stars, based on 1 article reviews
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    rabbit polyclonal anti cdk1 - by Bioz Stars, 2024-09
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    1) Product Images from "Elevating PLK1 overcomes BETi resistance in prostate cancer via triggering BRD4 phosphorylation-dependent degradation in mitosis"

    Article Title: Elevating PLK1 overcomes BETi resistance in prostate cancer via triggering BRD4 phosphorylation-dependent degradation in mitosis

    Journal: Cell reports

    doi: 10.1016/j.celrep.2024.114431

    KEY RESOURCES TABLE
    Figure Legend Snippet: KEY RESOURCES TABLE

    Techniques Used: Virus, Plasmid Preparation, Recombinant, Magnetic Beads, Mutagenesis, Proximity Ligation Assay, Reverse Transcription, SYBR Green Assay, Software

    rabbit polyclonal anti cdk1  (Proteintech)

     
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    Proteintech rabbit polyclonal anti cdk1
    Changes in formation of nuclear foci and protein solubility under cellular senescence. ( A) Top panel: Congo red staining images showing amyloids during cellular senescence induced by treatment with etoposide, decitabine, or H 2 O 2 . Scale bar: 20 μm. Middle panel: Bright-field images showing nucleoli. Bottom panel: Quantification of Congo red fluorescence intensity along the dashed line in the top panels. (B) Immunofluorescence <t>with</t> <t>anti-CDK1</t> antibody in U2OS GFP-NPM1 cells during etoposide-induced cellular senescence. Scale bar: 20 μm. (C) Immunofluorescence with anti-VHL (left) and anti-DDX39B (right) antibodies in U2OS GFP-NPM1 cells during etoposide-induced cellular senescence. Scale bar: 20 μm. (D) Quantification of nuclear foci by the number and size of three biological replicates. (Upper left panel) The number of VHL foci per cell. (upper right panel) Size of VHL foci (vehicle n = 103, etoposide n = 48). Lower left panel: number of DDX39B foci per cell. Lower right panel: size of DDX39B foci (vehicle, n = 45; etoposide, n = 39). Error bars indicate SD. * P < 0.05, **** P < 0.0001 (unpaired t -test). (E) Quantification of foci localization during etoposide-induced cellular senescence based on the percentage of nuclear foci per total foci in a cell. The total number of foci was counted with a minimum of 200 per group. ( F and G) Western blot images detecting changes in protein solubility dependent on recovery in heat shock (HS)-exposed U2OS cells (F) and U2OS cells with cellular senescence induced by etoposide (G) . ( H and I) Quantification of the changes in the solubility of VHL and FIB under HS (H) and cellular senescence induced by etoposide treatment (I) . Each dot represents biological replicates. Error bars indicate SEM. * P < 0.05, ** P < 0.01, ns, non-significant (ordinary one-way ANOV(A) followed by correction for multiple comparison by controlling the FDR). Immunofluorescence images against an anti-TDP43 antibody (J) and quantification of colocalization between TDP-43 and NPM1 by Pearson's colocalization coefficient (K) . U2OS cells expressing GFP-NPM1 were treated with sodium arsenite or etoposide. U2OS cells expressing GFP-NPM1 recovered after one and three days of treatment with sodium arsenite and etoposide, respectively. D, day s (sodium arsenite: n = 13; sodium arsenite and recovery: n = 15; etoposide: n = 18; etoposide and washout: n = 20). (For interpretation of the references to color in this figure legend, the reader is referred to the Web version of this article.)
    Rabbit Polyclonal Anti Cdk1, supplied by Proteintech, 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 polyclonal anti cdk1/product/Proteintech
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    1) Product Images from "Reduced dynamicity and increased high-order protein assemblies in dense fibrillar component of the nucleolus under cellular senescence"

    Article Title: Reduced dynamicity and increased high-order protein assemblies in dense fibrillar component of the nucleolus under cellular senescence

    Journal: Redox Biology

    doi: 10.1016/j.redox.2024.103279

    Changes in formation of nuclear foci and protein solubility under cellular senescence. ( A) Top panel: Congo red staining images showing amyloids during cellular senescence induced by treatment with etoposide, decitabine, or H 2 O 2 . Scale bar: 20 μm. Middle panel: Bright-field images showing nucleoli. Bottom panel: Quantification of Congo red fluorescence intensity along the dashed line in the top panels. (B) Immunofluorescence with anti-CDK1 antibody in U2OS GFP-NPM1 cells during etoposide-induced cellular senescence. Scale bar: 20 μm. (C) Immunofluorescence with anti-VHL (left) and anti-DDX39B (right) antibodies in U2OS GFP-NPM1 cells during etoposide-induced cellular senescence. Scale bar: 20 μm. (D) Quantification of nuclear foci by the number and size of three biological replicates. (Upper left panel) The number of VHL foci per cell. (upper right panel) Size of VHL foci (vehicle n = 103, etoposide n = 48). Lower left panel: number of DDX39B foci per cell. Lower right panel: size of DDX39B foci (vehicle, n = 45; etoposide, n = 39). Error bars indicate SD. * P < 0.05, **** P < 0.0001 (unpaired t -test). (E) Quantification of foci localization during etoposide-induced cellular senescence based on the percentage of nuclear foci per total foci in a cell. The total number of foci was counted with a minimum of 200 per group. ( F and G) Western blot images detecting changes in protein solubility dependent on recovery in heat shock (HS)-exposed U2OS cells (F) and U2OS cells with cellular senescence induced by etoposide (G) . ( H and I) Quantification of the changes in the solubility of VHL and FIB under HS (H) and cellular senescence induced by etoposide treatment (I) . Each dot represents biological replicates. Error bars indicate SEM. * P < 0.05, ** P < 0.01, ns, non-significant (ordinary one-way ANOV(A) followed by correction for multiple comparison by controlling the FDR). Immunofluorescence images against an anti-TDP43 antibody (J) and quantification of colocalization between TDP-43 and NPM1 by Pearson's colocalization coefficient (K) . U2OS cells expressing GFP-NPM1 were treated with sodium arsenite or etoposide. U2OS cells expressing GFP-NPM1 recovered after one and three days of treatment with sodium arsenite and etoposide, respectively. D, day s (sodium arsenite: n = 13; sodium arsenite and recovery: n = 15; etoposide: n = 18; etoposide and washout: n = 20). (For interpretation of the references to color in this figure legend, the reader is referred to the Web version of this article.)
    Figure Legend Snippet: Changes in formation of nuclear foci and protein solubility under cellular senescence. ( A) Top panel: Congo red staining images showing amyloids during cellular senescence induced by treatment with etoposide, decitabine, or H 2 O 2 . Scale bar: 20 μm. Middle panel: Bright-field images showing nucleoli. Bottom panel: Quantification of Congo red fluorescence intensity along the dashed line in the top panels. (B) Immunofluorescence with anti-CDK1 antibody in U2OS GFP-NPM1 cells during etoposide-induced cellular senescence. Scale bar: 20 μm. (C) Immunofluorescence with anti-VHL (left) and anti-DDX39B (right) antibodies in U2OS GFP-NPM1 cells during etoposide-induced cellular senescence. Scale bar: 20 μm. (D) Quantification of nuclear foci by the number and size of three biological replicates. (Upper left panel) The number of VHL foci per cell. (upper right panel) Size of VHL foci (vehicle n = 103, etoposide n = 48). Lower left panel: number of DDX39B foci per cell. Lower right panel: size of DDX39B foci (vehicle, n = 45; etoposide, n = 39). Error bars indicate SD. * P < 0.05, **** P < 0.0001 (unpaired t -test). (E) Quantification of foci localization during etoposide-induced cellular senescence based on the percentage of nuclear foci per total foci in a cell. The total number of foci was counted with a minimum of 200 per group. ( F and G) Western blot images detecting changes in protein solubility dependent on recovery in heat shock (HS)-exposed U2OS cells (F) and U2OS cells with cellular senescence induced by etoposide (G) . ( H and I) Quantification of the changes in the solubility of VHL and FIB under HS (H) and cellular senescence induced by etoposide treatment (I) . Each dot represents biological replicates. Error bars indicate SEM. * P < 0.05, ** P < 0.01, ns, non-significant (ordinary one-way ANOV(A) followed by correction for multiple comparison by controlling the FDR). Immunofluorescence images against an anti-TDP43 antibody (J) and quantification of colocalization between TDP-43 and NPM1 by Pearson's colocalization coefficient (K) . U2OS cells expressing GFP-NPM1 were treated with sodium arsenite or etoposide. U2OS cells expressing GFP-NPM1 recovered after one and three days of treatment with sodium arsenite and etoposide, respectively. D, day s (sodium arsenite: n = 13; sodium arsenite and recovery: n = 15; etoposide: n = 18; etoposide and washout: n = 20). (For interpretation of the references to color in this figure legend, the reader is referred to the Web version of this article.)

    Techniques Used: Solubility, Staining, Fluorescence, Immunofluorescence, Western Blot, Comparison, Expressing

    rabbit anti cdk1 polyclonal antibody  (ABclonal Biotechnology)

     
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    ABclonal Biotechnology rabbit anti cdk1 polyclonal antibody
    Abnormal expression of 6 key genes in HBV-related HCC. A. 6 key genes were more highly expressed in liver cancer tissues compared with those in the normal tissues in GEPIA database. The red and gray boxes represent cancer and normal tissues, respectively. B. The stage of (a) AURKA, (b) BIRC5, (c) CCNB1, (d) <t>CDK1,</t> (e) CDKN3 and (f) TYMS using UALCAN database. C. The immunohistochemical images of (a) AURKA, (b) BIRC5, (c) CCNB1, (d) CDK1, (e) TYMS in liver and HCC tissues using the HPA database
    Rabbit Anti Cdk1 Polyclonal Antibody, supplied by ABclonal Biotechnology, 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 cdk1 polyclonal antibody/product/ABclonal Biotechnology
    Average 86 stars, based on 1 article reviews
    Price from $9.99 to $1999.99
    rabbit anti cdk1 polyclonal antibody - by Bioz Stars, 2024-09
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    1) Product Images from "A systematic study on the treatment of hepatitis B-related hepatocellular carcinoma with drugs based on bioinformatics and key target reverse network pharmacology and experimental verification"

    Article Title: A systematic study on the treatment of hepatitis B-related hepatocellular carcinoma with drugs based on bioinformatics and key target reverse network pharmacology and experimental verification

    Journal: Infectious Agents and Cancer

    doi: 10.1186/s13027-023-00520-z

    Abnormal expression of 6 key genes in HBV-related HCC. A. 6 key genes were more highly expressed in liver cancer tissues compared with those in the normal tissues in GEPIA database. The red and gray boxes represent cancer and normal tissues, respectively. B. The stage of (a) AURKA, (b) BIRC5, (c) CCNB1, (d) CDK1, (e) CDKN3 and (f) TYMS using UALCAN database. C. The immunohistochemical images of (a) AURKA, (b) BIRC5, (c) CCNB1, (d) CDK1, (e) TYMS in liver and HCC tissues using the HPA database
    Figure Legend Snippet: Abnormal expression of 6 key genes in HBV-related HCC. A. 6 key genes were more highly expressed in liver cancer tissues compared with those in the normal tissues in GEPIA database. The red and gray boxes represent cancer and normal tissues, respectively. B. The stage of (a) AURKA, (b) BIRC5, (c) CCNB1, (d) CDK1, (e) CDKN3 and (f) TYMS using UALCAN database. C. The immunohistochemical images of (a) AURKA, (b) BIRC5, (c) CCNB1, (d) CDK1, (e) TYMS in liver and HCC tissues using the HPA database

    Techniques Used: Expressing, Immunohistochemical staining

    Survival analysis of 6 key genes (A) AURKA, (B) BIRC5, (C) CCNB1, (D) CDK1, (E) CDKN3 and (F) TYMS
    Figure Legend Snippet: Survival analysis of 6 key genes (A) AURKA, (B) BIRC5, (C) CCNB1, (D) CDK1, (E) CDKN3 and (F) TYMS

    Techniques Used:

    The drug-gene interaction network of chemotherapeutic drugs and 6 key genes, (A) AURKA, (B) BIRC5, (C) CCNB1, (D) CDK1, (E) CDKN3 and (F) TYMS, was constructed using CTD database
    Figure Legend Snippet: The drug-gene interaction network of chemotherapeutic drugs and 6 key genes, (A) AURKA, (B) BIRC5, (C) CCNB1, (D) CDK1, (E) CDKN3 and (F) TYMS, was constructed using CTD database

    Techniques Used: Construct

    In the Herb database, the components corresponding to key targets
    Figure Legend Snippet: In the Herb database, the components corresponding to key targets

    Techniques Used:

    Molecular docking binding energy results (kcal/mol)
    Figure Legend Snippet: Molecular docking binding energy results (kcal/mol)

    Techniques Used: Binding Assay

    Effects of quercetin, celastrol and cantharidin on the expression of CDK1 and CCNB1. A. Effects of quercetin, celastrol and cantharidin on the expression of CDK1 and CCNB1 in HepG2215 cells. B. Effects of quercetin, celastrol and cantharidin on the expression of CDK1 and CCNB1 in Hep3B cells
    Figure Legend Snippet: Effects of quercetin, celastrol and cantharidin on the expression of CDK1 and CCNB1. A. Effects of quercetin, celastrol and cantharidin on the expression of CDK1 and CCNB1 in HepG2215 cells. B. Effects of quercetin, celastrol and cantharidin on the expression of CDK1 and CCNB1 in Hep3B cells

    Techniques Used: Expressing

    rabbit anti cdk1 polyclonal antibody  (ABclonal Biotechnology)

     
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    ABclonal Biotechnology rabbit anti cdk1 polyclonal antibody
    Rabbit Anti Cdk1 Polyclonal Antibody, supplied by ABclonal Biotechnology, 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 cdk1 polyclonal antibody/product/ABclonal Biotechnology
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    rabbit anti cdk1 polyclonal antibody  (ABclonal Biotechnology)

     
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    ABclonal Biotechnology rabbit anti cdk1 polyclonal antibody
    Oligonucleotide primers used in the present study.
    Rabbit Anti Cdk1 Polyclonal Antibody, supplied by ABclonal Biotechnology, 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 cdk1 polyclonal antibody/product/ABclonal Biotechnology
    Average 86 stars, based on 1 article reviews
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    rabbit anti cdk1 polyclonal antibody - by Bioz Stars, 2024-09
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    1) Product Images from "AURKA, TOP2A and MELK are the key genes identified by WGCNA for the pathogenesis of lung adenocarcinoma"

    Article Title: AURKA, TOP2A and MELK are the key genes identified by WGCNA for the pathogenesis of lung adenocarcinoma

    Journal: Oncology Letters

    doi: 10.3892/ol.2023.13824

    Oligonucleotide primers used in the present study.
    Figure Legend Snippet: Oligonucleotide primers used in the present study.

    Techniques Used: Sequencing

    In total, 59 control samples and 504 cancer samples were derived from TCGA database for verification. From the 10 genes selected from the two modules, a total of 20 genes were verified. A total of 19 of these changes were verified, and the other one (CXCR4) was excluded. (A) The expression of AURKA, BUB1, CCNB1, CDC45, CDK1, MELK, NUSAP1, PBK, TOP2A and TTK genes in normal lung tissues and lung adenocarcinoma tissues, where red indicates normal lung tissues and green indicates lung adenocarcinoma tissues. (B) The expression of BDKRB2, CCL19, CX3CR1, CXCL13, CXCL9, CXCR4, CXCR5, GNAI1, GNG11 and NMUR1 genes in normal lung tissues and lung adenocarcinoma tissues, with red indicating normal lung tissues and green indicating lung adenocarcinoma tissues. t-test of normal lung tissue and lung adenocarcinoma tissue. *P<0.05, **P<0.01 and ****P<0.0001.
    Figure Legend Snippet: In total, 59 control samples and 504 cancer samples were derived from TCGA database for verification. From the 10 genes selected from the two modules, a total of 20 genes were verified. A total of 19 of these changes were verified, and the other one (CXCR4) was excluded. (A) The expression of AURKA, BUB1, CCNB1, CDC45, CDK1, MELK, NUSAP1, PBK, TOP2A and TTK genes in normal lung tissues and lung adenocarcinoma tissues, where red indicates normal lung tissues and green indicates lung adenocarcinoma tissues. (B) The expression of BDKRB2, CCL19, CX3CR1, CXCL13, CXCL9, CXCR4, CXCR5, GNAI1, GNG11 and NMUR1 genes in normal lung tissues and lung adenocarcinoma tissues, with red indicating normal lung tissues and green indicating lung adenocarcinoma tissues. t-test of normal lung tissue and lung adenocarcinoma tissue. *P<0.05, **P<0.01 and ****P<0.0001.

    Techniques Used: Derivative Assay, Expressing

    ROC curve analysis of 20 genes. AUCs >0.9 were included in the subsequent analysis. A total of 13 genes ( AURKA, CDC45, TTK, TOP2A, CCNB1, NUSAP1, MELK, PBK, BUB1, CDK1, CXCL13, GNG11 and NMUR1 ) were included, and seven genes were excluded. (A) ROC curve analysis was performed for the AURKA, CDC45, TTK, TOP2A and CCNB1 genes sequentially. (B) ROC curve analysis was performed for the NUSAP1, MELK, PBK, BPKPB2 and BUB1 genes sequentially. (C) ROC curve analysis was performed for the CDK1, CCL19, CXCR5, CXCL13 and CXCL9 genes sequentially. (D) ROC curve analysis was performed for the CXCR4, GNG11, GNAL1 and NMUR1, CX3CR1 genes sequentially. ROC, receiver operating characteristic; AUC, area under the curve.
    Figure Legend Snippet: ROC curve analysis of 20 genes. AUCs >0.9 were included in the subsequent analysis. A total of 13 genes ( AURKA, CDC45, TTK, TOP2A, CCNB1, NUSAP1, MELK, PBK, BUB1, CDK1, CXCL13, GNG11 and NMUR1 ) were included, and seven genes were excluded. (A) ROC curve analysis was performed for the AURKA, CDC45, TTK, TOP2A and CCNB1 genes sequentially. (B) ROC curve analysis was performed for the NUSAP1, MELK, PBK, BPKPB2 and BUB1 genes sequentially. (C) ROC curve analysis was performed for the CDK1, CCL19, CXCR5, CXCL13 and CXCL9 genes sequentially. (D) ROC curve analysis was performed for the CXCR4, GNG11, GNAL1 and NMUR1, CX3CR1 genes sequentially. ROC, receiver operating characteristic; AUC, area under the curve.

    Techniques Used:

    Survival analysis was performed and survival curves were obtained using GEPIA database. According to the P-values, there were eight genes with P<0.05 ( AURKA, TOP2A, CCNB1, NUSAP1, MELK, PBK, BUB1 and CDK1). (A-H) The survival curves of CDK1, BUB1, CCNB1, TOP2A, PBK, NUSAP1, AURKA and MELK genes in TCGA database are presented in order. TCGA, The Cancer Genome Atlas.
    Figure Legend Snippet: Survival analysis was performed and survival curves were obtained using GEPIA database. According to the P-values, there were eight genes with P<0.05 ( AURKA, TOP2A, CCNB1, NUSAP1, MELK, PBK, BUB1 and CDK1). (A-H) The survival curves of CDK1, BUB1, CCNB1, TOP2A, PBK, NUSAP1, AURKA and MELK genes in TCGA database are presented in order. TCGA, The Cancer Genome Atlas.

    Techniques Used:

    mRNA expression of eight genes screened using WGCNA in clinical tissue samples. Clinical samples are divided into lung adenocarcinoma adjacent tissues and lung adenocarcinoma tissue samples. (A-H) In each graph, the left bar represents the lung adenocarcinoma adjacent tissues, and the right bar the lung adenocarcinoma tissues. The mRNA expression levels of AURKA, BUB1, CCNB1, CDK1, MELK, NUSAP1 and TOP2A genes in lung adenocarcinoma were higher than those in paired adjacent normal tissues. WGCNA, weighted gene co-expression network analysis.
    Figure Legend Snippet: mRNA expression of eight genes screened using WGCNA in clinical tissue samples. Clinical samples are divided into lung adenocarcinoma adjacent tissues and lung adenocarcinoma tissue samples. (A-H) In each graph, the left bar represents the lung adenocarcinoma adjacent tissues, and the right bar the lung adenocarcinoma tissues. The mRNA expression levels of AURKA, BUB1, CCNB1, CDK1, MELK, NUSAP1 and TOP2A genes in lung adenocarcinoma were higher than those in paired adjacent normal tissues. WGCNA, weighted gene co-expression network analysis.

    Techniques Used: Expressing

    Protein expression of seven genes screened using WGCNA in clinical tissue samples. (A) Representative western blots of AURKA, BUB1, CCNB1, CDK1, MELK, NUSAP1 and TOP2A protein expression in adjacent lung adenocarcinoma tissues and lung adenocarcinoma tissue samples. (B) The quantitative analysis of the data in panel A, in which the protein levels of AURKA, TOP2A and MELK in lung adenocarcinoma tissues were higher than those in matched adjacent lung adenocarcinoma tissues. WGCNA, weighted gene co-expression network analysis.
    Figure Legend Snippet: Protein expression of seven genes screened using WGCNA in clinical tissue samples. (A) Representative western blots of AURKA, BUB1, CCNB1, CDK1, MELK, NUSAP1 and TOP2A protein expression in adjacent lung adenocarcinoma tissues and lung adenocarcinoma tissue samples. (B) The quantitative analysis of the data in panel A, in which the protein levels of AURKA, TOP2A and MELK in lung adenocarcinoma tissues were higher than those in matched adjacent lung adenocarcinoma tissues. WGCNA, weighted gene co-expression network analysis.

    Techniques Used: Expressing, Western Blot

    rabbit polyclonal anti cdk1 p34  (Santa Cruz Biotechnology)

     
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    Santa Cruz Biotechnology rabbit polyclonal anti cdk1 p34
    Rabbit Polyclonal Anti Cdk1 P34, supplied by Santa Cruz Biotechnology, 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 polyclonal anti cdk1 p34/product/Santa Cruz Biotechnology
    Average 86 stars, based on 1 article reviews
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    polyclonal anti rabbit cdc2 p34  (Santa Cruz Biotechnology)

     
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    Santa Cruz Biotechnology polyclonal anti rabbit cdc2 p34
    Polyclonal Anti Rabbit Cdc2 P34, supplied by Santa Cruz Biotechnology, 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/polyclonal anti rabbit cdc2 p34/product/Santa Cruz Biotechnology
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    rabbit polyclonal anti phospho cdk1 thr161  (Beyotime)

     
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    Beyotime rabbit polyclonal anti phospho cdk1 thr161
    Rabbit Polyclonal Anti Phospho Cdk1 Thr161, supplied by Beyotime, 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 polyclonal anti phospho cdk1 thr161/product/Beyotime
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    • rabbit polyclonal anti cdk1  (Proteintech)
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    Proteintech rabbit polyclonal anti cdk1
    Rabbit Polyclonal Anti Cdk1, supplied by Proteintech, 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 polyclonal anti cdk1/product/Proteintech
    Average 86 stars, based on 1 article reviews
    Price from $9.99 to $1999.99
    rabbit polyclonal anti cdk1 - by Bioz Stars, 2024-09
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    rabbit polyclonal anti phospho cdk1  (Thermo Fisher)
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    Thermo Fisher rabbit polyclonal anti phospho cdk1
    Rabbit Polyclonal Anti Phospho Cdk1, supplied by Thermo Fisher, 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 polyclonal anti phospho cdk1/product/Thermo Fisher
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    rabbit polyclonal anti cdk1  (Millipore)
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    Millipore rabbit polyclonal anti cdk1
    KEY RESOURCES TABLE
    Rabbit Polyclonal Anti Cdk1, supplied by Millipore, 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 polyclonal anti cdk1/product/Millipore
    Average 86 stars, based on 1 article reviews
    Price from $9.99 to $1999.99
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    rabbit anti cdk1 polyclonal antibody  (ABclonal Biotechnology)
    86
    ABclonal Biotechnology rabbit anti cdk1 polyclonal antibody
    Abnormal expression of 6 key genes in HBV-related HCC. A. 6 key genes were more highly expressed in liver cancer tissues compared with those in the normal tissues in GEPIA database. The red and gray boxes represent cancer and normal tissues, respectively. B. The stage of (a) AURKA, (b) BIRC5, (c) CCNB1, (d) <t>CDK1,</t> (e) CDKN3 and (f) TYMS using UALCAN database. C. The immunohistochemical images of (a) AURKA, (b) BIRC5, (c) CCNB1, (d) CDK1, (e) TYMS in liver and HCC tissues using the HPA database
    Rabbit Anti Cdk1 Polyclonal Antibody, supplied by ABclonal Biotechnology, 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 cdk1 polyclonal antibody/product/ABclonal Biotechnology
    Average 86 stars, based on 1 article reviews
    Price from $9.99 to $1999.99
    rabbit anti cdk1 polyclonal antibody - by Bioz Stars, 2024-09
    86/100 stars
    		  Buy from Supplier
    rabbit polyclonal anti cdk1 p34  (Santa Cruz Biotechnology)
    86
    Santa Cruz Biotechnology rabbit polyclonal anti cdk1 p34
    Abnormal expression of 6 key genes in HBV-related HCC. A. 6 key genes were more highly expressed in liver cancer tissues compared with those in the normal tissues in GEPIA database. The red and gray boxes represent cancer and normal tissues, respectively. B. The stage of (a) AURKA, (b) BIRC5, (c) CCNB1, (d) <t>CDK1,</t> (e) CDKN3 and (f) TYMS using UALCAN database. C. The immunohistochemical images of (a) AURKA, (b) BIRC5, (c) CCNB1, (d) CDK1, (e) TYMS in liver and HCC tissues using the HPA database
    Rabbit Polyclonal Anti Cdk1 P34, supplied by Santa Cruz Biotechnology, 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 polyclonal anti cdk1 p34/product/Santa Cruz Biotechnology
    Average 86 stars, based on 1 article reviews
    Price from $9.99 to $1999.99
    rabbit polyclonal anti cdk1 p34 - by Bioz Stars, 2024-09
    86/100 stars
    		  Buy from Supplier
    polyclonal anti rabbit cdc2 p34  (Santa Cruz Biotechnology)
    86
    Santa Cruz Biotechnology polyclonal anti rabbit cdc2 p34
    Abnormal expression of 6 key genes in HBV-related HCC. A. 6 key genes were more highly expressed in liver cancer tissues compared with those in the normal tissues in GEPIA database. The red and gray boxes represent cancer and normal tissues, respectively. B. The stage of (a) AURKA, (b) BIRC5, (c) CCNB1, (d) <t>CDK1,</t> (e) CDKN3 and (f) TYMS using UALCAN database. C. The immunohistochemical images of (a) AURKA, (b) BIRC5, (c) CCNB1, (d) CDK1, (e) TYMS in liver and HCC tissues using the HPA database
    Polyclonal Anti Rabbit Cdc2 P34, supplied by Santa Cruz Biotechnology, 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/polyclonal anti rabbit cdc2 p34/product/Santa Cruz Biotechnology
    Average 86 stars, based on 1 article reviews
    Price from $9.99 to $1999.99
    polyclonal anti rabbit cdc2 p34 - by Bioz Stars, 2024-09
    86/100 stars
    		  Buy from Supplier
    rabbit polyclonal anti phospho cdk1 thr161  (Beyotime)
    86
    Beyotime rabbit polyclonal anti phospho cdk1 thr161
    Abnormal expression of 6 key genes in HBV-related HCC. A. 6 key genes were more highly expressed in liver cancer tissues compared with those in the normal tissues in GEPIA database. The red and gray boxes represent cancer and normal tissues, respectively. B. The stage of (a) AURKA, (b) BIRC5, (c) CCNB1, (d) <t>CDK1,</t> (e) CDKN3 and (f) TYMS using UALCAN database. C. The immunohistochemical images of (a) AURKA, (b) BIRC5, (c) CCNB1, (d) CDK1, (e) TYMS in liver and HCC tissues using the HPA database
    Rabbit Polyclonal Anti Phospho Cdk1 Thr161, supplied by Beyotime, 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 polyclonal anti phospho cdk1 thr161/product/Beyotime
    Average 86 stars, based on 1 article reviews
    Price from $9.99 to $1999.99
    rabbit polyclonal anti phospho cdk1 thr161 - by Bioz Stars, 2024-09
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    Image Search Results


    KEY RESOURCES TABLE

    Journal: Cell reports

    Article Title: Elevating PLK1 overcomes BETi resistance in prostate cancer via triggering BRD4 phosphorylation-dependent degradation in mitosis

    doi: 10.1016/j.celrep.2024.114431

    Figure Lengend Snippet: KEY RESOURCES TABLE

    Article Snippet: Rabbit polyclonal anti-CDK1 , Millipore , Cat# 06–923; RRID:AB_310302.

    Techniques: Virus, Plasmid Preparation, Recombinant, Magnetic Beads, Mutagenesis, Proximity Ligation Assay, Reverse Transcription, SYBR Green Assay, Software

    Abnormal expression of 6 key genes in HBV-related HCC. A. 6 key genes were more highly expressed in liver cancer tissues compared with those in the normal tissues in GEPIA database. The red and gray boxes represent cancer and normal tissues, respectively. B. The stage of (a) AURKA, (b) BIRC5, (c) CCNB1, (d) CDK1, (e) CDKN3 and (f) TYMS using UALCAN database. C. The immunohistochemical images of (a) AURKA, (b) BIRC5, (c) CCNB1, (d) CDK1, (e) TYMS in liver and HCC tissues using the HPA database

    Journal: Infectious Agents and Cancer

    Article Title: A systematic study on the treatment of hepatitis B-related hepatocellular carcinoma with drugs based on bioinformatics and key target reverse network pharmacology and experimental verification

    doi: 10.1186/s13027-023-00520-z

    Figure Lengend Snippet: Abnormal expression of 6 key genes in HBV-related HCC. A. 6 key genes were more highly expressed in liver cancer tissues compared with those in the normal tissues in GEPIA database. The red and gray boxes represent cancer and normal tissues, respectively. B. The stage of (a) AURKA, (b) BIRC5, (c) CCNB1, (d) CDK1, (e) CDKN3 and (f) TYMS using UALCAN database. C. The immunohistochemical images of (a) AURKA, (b) BIRC5, (c) CCNB1, (d) CDK1, (e) TYMS in liver and HCC tissues using the HPA database

    Article Snippet: The primary antibodies were rabbit anti-CDK1 polyclonal antibody (Cat. # CY5061, Abways, diluted to 1:2000), anti-CCNB1 polyclonal antibody (Cat. # CY5378, Abways, diluted to 1:2000), and β-actin antibody (Cat. # AC026, abclonal, diluted to 1:50,000).

    Techniques: Expressing, Immunohistochemical staining

    Survival analysis of 6 key genes (A) AURKA, (B) BIRC5, (C) CCNB1, (D) CDK1, (E) CDKN3 and (F) TYMS

    Journal: Infectious Agents and Cancer

    Article Title: A systematic study on the treatment of hepatitis B-related hepatocellular carcinoma with drugs based on bioinformatics and key target reverse network pharmacology and experimental verification

    doi: 10.1186/s13027-023-00520-z

    Figure Lengend Snippet: Survival analysis of 6 key genes (A) AURKA, (B) BIRC5, (C) CCNB1, (D) CDK1, (E) CDKN3 and (F) TYMS

    Article Snippet: The primary antibodies were rabbit anti-CDK1 polyclonal antibody (Cat. # CY5061, Abways, diluted to 1:2000), anti-CCNB1 polyclonal antibody (Cat. # CY5378, Abways, diluted to 1:2000), and β-actin antibody (Cat. # AC026, abclonal, diluted to 1:50,000).

    Techniques:

    The drug-gene interaction network of chemotherapeutic drugs and 6 key genes, (A) AURKA, (B) BIRC5, (C) CCNB1, (D) CDK1, (E) CDKN3 and (F) TYMS, was constructed using CTD database

    Journal: Infectious Agents and Cancer

    Article Title: A systematic study on the treatment of hepatitis B-related hepatocellular carcinoma with drugs based on bioinformatics and key target reverse network pharmacology and experimental verification

    doi: 10.1186/s13027-023-00520-z

    Figure Lengend Snippet: The drug-gene interaction network of chemotherapeutic drugs and 6 key genes, (A) AURKA, (B) BIRC5, (C) CCNB1, (D) CDK1, (E) CDKN3 and (F) TYMS, was constructed using CTD database

    Article Snippet: The primary antibodies were rabbit anti-CDK1 polyclonal antibody (Cat. # CY5061, Abways, diluted to 1:2000), anti-CCNB1 polyclonal antibody (Cat. # CY5378, Abways, diluted to 1:2000), and β-actin antibody (Cat. # AC026, abclonal, diluted to 1:50,000).

    Techniques: Construct

    In the Herb database, the components corresponding to key targets

    Journal: Infectious Agents and Cancer

    Article Title: A systematic study on the treatment of hepatitis B-related hepatocellular carcinoma with drugs based on bioinformatics and key target reverse network pharmacology and experimental verification

    doi: 10.1186/s13027-023-00520-z

    Figure Lengend Snippet: In the Herb database, the components corresponding to key targets

    Article Snippet: The primary antibodies were rabbit anti-CDK1 polyclonal antibody (Cat. # CY5061, Abways, diluted to 1:2000), anti-CCNB1 polyclonal antibody (Cat. # CY5378, Abways, diluted to 1:2000), and β-actin antibody (Cat. # AC026, abclonal, diluted to 1:50,000).

    Techniques:

    Molecular docking binding energy results (kcal/mol)

    Journal: Infectious Agents and Cancer

    Article Title: A systematic study on the treatment of hepatitis B-related hepatocellular carcinoma with drugs based on bioinformatics and key target reverse network pharmacology and experimental verification

    doi: 10.1186/s13027-023-00520-z

    Figure Lengend Snippet: Molecular docking binding energy results (kcal/mol)

    Article Snippet: The primary antibodies were rabbit anti-CDK1 polyclonal antibody (Cat. # CY5061, Abways, diluted to 1:2000), anti-CCNB1 polyclonal antibody (Cat. # CY5378, Abways, diluted to 1:2000), and β-actin antibody (Cat. # AC026, abclonal, diluted to 1:50,000).

    Techniques: Binding Assay

    Effects of quercetin, celastrol and cantharidin on the expression of CDK1 and CCNB1. A. Effects of quercetin, celastrol and cantharidin on the expression of CDK1 and CCNB1 in HepG2215 cells. B. Effects of quercetin, celastrol and cantharidin on the expression of CDK1 and CCNB1 in Hep3B cells

    Journal: Infectious Agents and Cancer

    Article Title: A systematic study on the treatment of hepatitis B-related hepatocellular carcinoma with drugs based on bioinformatics and key target reverse network pharmacology and experimental verification

    doi: 10.1186/s13027-023-00520-z

    Figure Lengend Snippet: Effects of quercetin, celastrol and cantharidin on the expression of CDK1 and CCNB1. A. Effects of quercetin, celastrol and cantharidin on the expression of CDK1 and CCNB1 in HepG2215 cells. B. Effects of quercetin, celastrol and cantharidin on the expression of CDK1 and CCNB1 in Hep3B cells

    Article Snippet: The primary antibodies were rabbit anti-CDK1 polyclonal antibody (Cat. # CY5061, Abways, diluted to 1:2000), anti-CCNB1 polyclonal antibody (Cat. # CY5378, Abways, diluted to 1:2000), and β-actin antibody (Cat. # AC026, abclonal, diluted to 1:50,000).

    Techniques: Expressing