Structured Review

ABclonal Biotechnology rabbit monoclonal anti cyclin d1 ccnd1
MORC3 plays negative roles in cancer cell proliferation. (A) CAL 27 cells were transfected with anti-MORC3 or non-specific (NS) siRNA, and cell numbers were counted on Day 2 and Day 4. (B, C) The expression levels of CDH1, KRT14, JUN, <t>CCND1,</t> CCND2, CCN1, and IL6 in CAL 27 cells with or without MORC3 knockdown were analyzed by qRT-PCR. *, p < 0.05.
Rabbit Monoclonal Anti Cyclin D1 Ccnd1, 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 monoclonal anti cyclin d1 ccnd1/product/ABclonal Biotechnology
Average 86 stars, based on 1 article reviews
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1) Product Images from "Genome-wide analysis reveals the MORC3-mediated repression of PD-L1 expression in head and neck cancer"

Article Title: Genome-wide analysis reveals the MORC3-mediated repression of PD-L1 expression in head and neck cancer

Journal: Frontiers in Cell and Developmental Biology

doi: 10.3389/fcell.2024.1410130

MORC3 plays negative roles in cancer cell proliferation. (A) CAL 27 cells were transfected with anti-MORC3 or non-specific (NS) siRNA, and cell numbers were counted on Day 2 and Day 4. (B, C) The expression levels of CDH1, KRT14, JUN, CCND1, CCND2, CCN1, and IL6 in CAL 27 cells with or without MORC3 knockdown were analyzed by qRT-PCR. *, p < 0.05.
Figure Legend Snippet: MORC3 plays negative roles in cancer cell proliferation. (A) CAL 27 cells were transfected with anti-MORC3 or non-specific (NS) siRNA, and cell numbers were counted on Day 2 and Day 4. (B, C) The expression levels of CDH1, KRT14, JUN, CCND1, CCND2, CCN1, and IL6 in CAL 27 cells with or without MORC3 knockdown were analyzed by qRT-PCR. *, p < 0.05.

Techniques Used: Transfection, Expressing, Knockdown, Quantitative RT-PCR

cyclin d1 ccnd1  (Bioss)


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    Bioss cyclin d1 ccnd1
    The primer sequence of the target genes
    Cyclin D1 Ccnd1, supplied by Bioss, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Images

    1) Product Images from "The miR-15b-5p/miR-379-3p-FOXO axis regulates cell cycle and apoptosis in scleral remodeling during experimental myopia"

    Article Title: The miR-15b-5p/miR-379-3p-FOXO axis regulates cell cycle and apoptosis in scleral remodeling during experimental myopia

    Journal: Journal of Translational Medicine

    doi: 10.1186/s12967-024-05523-x

    The primer sequence of the target genes
    Figure Legend Snippet: The primer sequence of the target genes

    Techniques Used: Sequencing

    List of Western blotting primary antibody
    Figure Legend Snippet: List of Western blotting primary antibody

    Techniques Used: Western Blot

    List of Immunofluorescence staining primary antibody
    Figure Legend Snippet: List of Immunofluorescence staining primary antibody

    Techniques Used: Immunofluorescence, Staining

    Scleral cell cycle measurement and apoptotic analysis. A , B Measurement of CDK2 and CCND1 expression at the mRNA level in the sclera of the guinea pigs in NC and LIM groups (n = 4–6). C CDK2 and CCND1 immunoblots. D , E Measurement of CDK2 and CCND1 expression at protein level by Western blot in the sclera of the guinea pigs in NC and LIM groups (n = 6). F Measurement of CDK2 and CCND1 expression at protein level by immunofluorescence in the sclera of the guinea pigs in NC and LIM groups. (Western Blot cropped) (n = 6)
    Figure Legend Snippet: Scleral cell cycle measurement and apoptotic analysis. A , B Measurement of CDK2 and CCND1 expression at the mRNA level in the sclera of the guinea pigs in NC and LIM groups (n = 4–6). C CDK2 and CCND1 immunoblots. D , E Measurement of CDK2 and CCND1 expression at protein level by Western blot in the sclera of the guinea pigs in NC and LIM groups (n = 6). F Measurement of CDK2 and CCND1 expression at protein level by immunofluorescence in the sclera of the guinea pigs in NC and LIM groups. (Western Blot cropped) (n = 6)

    Techniques Used: Expressing, Western Blot, Immunofluorescence

    cyclin d1 ccnd1  (Danaher Inc)


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    Danaher Inc cyclin d1 ccnd1
    (A) Validation of the differentially expressed genes by q-PCR with eight replicates. (B and C) Western blot analysis of the expression of proteins related to cell proliferation. (D and E) Cell immunofluorescence detection of the protein levels of c-Jun and <t>CCND1.</t> Three biological replicates were performed for Western blot assay. The p values of the comparison between control group and Halo-rhEGF group are all less than 0.05. Scale bar: 200 μm.
    Cyclin D1 Ccnd1, supplied by Danaher Inc, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Images

    1) Product Images from "Production of recombinant human epidermal growth factor fused with HaloTag protein and characterisation of its biological functions"

    Article Title: Production of recombinant human epidermal growth factor fused with HaloTag protein and characterisation of its biological functions

    Journal: PeerJ

    doi: 10.7717/peerj.17806

    (A) Validation of the differentially expressed genes by q-PCR with eight replicates. (B and C) Western blot analysis of the expression of proteins related to cell proliferation. (D and E) Cell immunofluorescence detection of the protein levels of c-Jun and CCND1. Three biological replicates were performed for Western blot assay. The p values of the comparison between control group and Halo-rhEGF group are all less than 0.05. Scale bar: 200 μm.
    Figure Legend Snippet: (A) Validation of the differentially expressed genes by q-PCR with eight replicates. (B and C) Western blot analysis of the expression of proteins related to cell proliferation. (D and E) Cell immunofluorescence detection of the protein levels of c-Jun and CCND1. Three biological replicates were performed for Western blot assay. The p values of the comparison between control group and Halo-rhEGF group are all less than 0.05. Scale bar: 200 μm.

    Techniques Used: Western Blot, Expressing, Immunofluorescence, Comparison, Control

    cyclin d1 ccnd1 mcl marker  (Agilent technologies)


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    Agilent technologies cyclin d1 ccnd1 mcl marker
    Cyclin D1 Ccnd1 Mcl Marker, supplied by Agilent technologies, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    cyclin d1 ccnd1 mcl marker  (Agilent technologies)


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    Agilent technologies cyclin d1 ccnd1 mcl marker
    Cyclin D1 Ccnd1 Mcl Marker, supplied by Agilent technologies, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    anti cyclin d1 ccnd1  (Cell Signaling Technology Inc)


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    Cell Signaling Technology Inc anti cyclin d1 ccnd1
    Anti Cyclin D1 Ccnd1, 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
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    anti cyclin d1 ccnd1  (Cell Signaling Technology Inc)


    Bioz Manufacturer Symbol Cell Signaling Technology Inc manufactures this product  
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    Cell Signaling Technology Inc anti cyclin d1 ccnd1
    Anti Cyclin D1 Ccnd1, 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
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    Structured Review

    Santa Cruz Biotechnology mouse anti cyclin d1 ccnd1 monoclonal antibody
    Involvement with apoptosis and cell cycle by treatment with of SE against at RA in HEPM cells Fig. 3A: Apotracker staining (green) of HEPM cells after treatment with 100 μM at RA and 0.03% SE for 48 h. The nuclei were counterstained with Hoechst 33342 (blue). Scale bar, 50 μm. Fig. 3B: Immunoblotting of HEPM cells after treatment with 100 μM at RA and 0.03% SE for 48 h. β-actin was served as an internal control. *p < 0.05 and ***p < 0.001 versus at RA. at RA: all-trans -retinoic acid HEPM: human embryonic palatal mesenchymal SE: Sasa veitchii extract <t>CCND1:</t> <t>cyclin</t> <t>D1</t>
    Mouse Anti Cyclin D1 Ccnd1 Monoclonal Antibody, 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/mouse anti cyclin d1 ccnd1 monoclonal antibody/product/Santa Cruz Biotechnology
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    1) Product Images from "Protective effect of Sasa veitchii extract against all-trans-retinoic acid-induced inhibition of proliferation of cultured human palate cells"

    Article Title: Protective effect of Sasa veitchii extract against all-trans-retinoic acid-induced inhibition of proliferation of cultured human palate cells

    Journal: Nagoya Journal of Medical Science

    doi: 10.18999/nagjms.86.2.223

    Involvement with apoptosis and cell cycle by treatment with of SE against at RA in HEPM cells Fig. 3A: Apotracker staining (green) of HEPM cells after treatment with 100 μM at RA and 0.03% SE for 48 h. The nuclei were counterstained with Hoechst 33342 (blue). Scale bar, 50 μm. Fig. 3B: Immunoblotting of HEPM cells after treatment with 100 μM at RA and 0.03% SE for 48 h. β-actin was served as an internal control. *p < 0.05 and ***p < 0.001 versus at RA. at RA: all-trans -retinoic acid HEPM: human embryonic palatal mesenchymal SE: Sasa veitchii extract CCND1: cyclin D1
    Figure Legend Snippet: Involvement with apoptosis and cell cycle by treatment with of SE against at RA in HEPM cells Fig. 3A: Apotracker staining (green) of HEPM cells after treatment with 100 μM at RA and 0.03% SE for 48 h. The nuclei were counterstained with Hoechst 33342 (blue). Scale bar, 50 μm. Fig. 3B: Immunoblotting of HEPM cells after treatment with 100 μM at RA and 0.03% SE for 48 h. β-actin was served as an internal control. *p < 0.05 and ***p < 0.001 versus at RA. at RA: all-trans -retinoic acid HEPM: human embryonic palatal mesenchymal SE: Sasa veitchii extract CCND1: cyclin D1

    Techniques Used: Staining, Western Blot, Control

    Proposed mechanism of SE against at RA-induced cell proliferation inhibition ERBB2: Erb-B2 receptor tyrosine kinase 2 JADE1 : jade family PHD finger 1 CCND1: cyclin D1
    Figure Legend Snippet: Proposed mechanism of SE against at RA-induced cell proliferation inhibition ERBB2: Erb-B2 receptor tyrosine kinase 2 JADE1 : jade family PHD finger 1 CCND1: cyclin D1

    Techniques Used: Inhibition


    Structured Review

    Santa Cruz Biotechnology anti mouse cyclin d1 ccnd1
    Anti Mouse Cyclin D1 Ccnd1, 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
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    g1 s specific cyclin d1 ccnd1  (Danaher Inc)


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    Danaher Inc g1 s specific cyclin d1 ccnd1
    G1 S Specific Cyclin D1 Ccnd1, supplied by Danaher Inc, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    ABclonal Biotechnology rabbit monoclonal anti cyclin d1 ccnd1
    MORC3 plays negative roles in cancer cell proliferation. (A) CAL 27 cells were transfected with anti-MORC3 or non-specific (NS) siRNA, and cell numbers were counted on Day 2 and Day 4. (B, C) The expression levels of CDH1, KRT14, JUN, <t>CCND1,</t> CCND2, CCN1, and IL6 in CAL 27 cells with or without MORC3 knockdown were analyzed by qRT-PCR. *, p < 0.05.
    Rabbit Monoclonal Anti Cyclin D1 Ccnd1, 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
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    The primer sequence of the target genes
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    (A) Validation of the differentially expressed genes by q-PCR with eight replicates. (B and C) Western blot analysis of the expression of proteins related to cell proliferation. (D and E) Cell immunofluorescence detection of the protein levels of c-Jun and <t>CCND1.</t> Three biological replicates were performed for Western blot assay. The p values of the comparison between control group and Halo-rhEGF group are all less than 0.05. Scale bar: 200 μm.
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    Agilent technologies cyclin d1 ccnd1 mcl marker
    (A) Validation of the differentially expressed genes by q-PCR with eight replicates. (B and C) Western blot analysis of the expression of proteins related to cell proliferation. (D and E) Cell immunofluorescence detection of the protein levels of c-Jun and <t>CCND1.</t> Three biological replicates were performed for Western blot assay. The p values of the comparison between control group and Halo-rhEGF group are all less than 0.05. Scale bar: 200 μm.
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    (A) Validation of the differentially expressed genes by q-PCR with eight replicates. (B and C) Western blot analysis of the expression of proteins related to cell proliferation. (D and E) Cell immunofluorescence detection of the protein levels of c-Jun and <t>CCND1.</t> Three biological replicates were performed for Western blot assay. The p values of the comparison between control group and Halo-rhEGF group are all less than 0.05. Scale bar: 200 μm.
    Anti Cyclin D1 Ccnd1, 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
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    Involvement with apoptosis and cell cycle by treatment with of SE against at RA in HEPM cells Fig. 3A: Apotracker staining (green) of HEPM cells after treatment with 100 μM at RA and 0.03% SE for 48 h. The nuclei were counterstained with Hoechst 33342 (blue). Scale bar, 50 μm. Fig. 3B: Immunoblotting of HEPM cells after treatment with 100 μM at RA and 0.03% SE for 48 h. β-actin was served as an internal control. *p < 0.05 and ***p < 0.001 versus at RA. at RA: all-trans -retinoic acid HEPM: human embryonic palatal mesenchymal SE: Sasa veitchii extract <t>CCND1:</t> <t>cyclin</t> <t>D1</t>
    Mouse Anti Cyclin D1 Ccnd1 Monoclonal Antibody, 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
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    Involvement with apoptosis and cell cycle by treatment with of SE against at RA in HEPM cells Fig. 3A: Apotracker staining (green) of HEPM cells after treatment with 100 μM at RA and 0.03% SE for 48 h. The nuclei were counterstained with Hoechst 33342 (blue). Scale bar, 50 μm. Fig. 3B: Immunoblotting of HEPM cells after treatment with 100 μM at RA and 0.03% SE for 48 h. β-actin was served as an internal control. *p < 0.05 and ***p < 0.001 versus at RA. at RA: all-trans -retinoic acid HEPM: human embryonic palatal mesenchymal SE: Sasa veitchii extract <t>CCND1:</t> <t>cyclin</t> <t>D1</t>
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    Danaher Inc g1 s specific cyclin d1 ccnd1
    Involvement with apoptosis and cell cycle by treatment with of SE against at RA in HEPM cells Fig. 3A: Apotracker staining (green) of HEPM cells after treatment with 100 μM at RA and 0.03% SE for 48 h. The nuclei were counterstained with Hoechst 33342 (blue). Scale bar, 50 μm. Fig. 3B: Immunoblotting of HEPM cells after treatment with 100 μM at RA and 0.03% SE for 48 h. β-actin was served as an internal control. *p < 0.05 and ***p < 0.001 versus at RA. at RA: all-trans -retinoic acid HEPM: human embryonic palatal mesenchymal SE: Sasa veitchii extract <t>CCND1:</t> <t>cyclin</t> <t>D1</t>
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    Image Search Results


    MORC3 plays negative roles in cancer cell proliferation. (A) CAL 27 cells were transfected with anti-MORC3 or non-specific (NS) siRNA, and cell numbers were counted on Day 2 and Day 4. (B, C) The expression levels of CDH1, KRT14, JUN, CCND1, CCND2, CCN1, and IL6 in CAL 27 cells with or without MORC3 knockdown were analyzed by qRT-PCR. *, p < 0.05.

    Journal: Frontiers in Cell and Developmental Biology

    Article Title: Genome-wide analysis reveals the MORC3-mediated repression of PD-L1 expression in head and neck cancer

    doi: 10.3389/fcell.2024.1410130

    Figure Lengend Snippet: MORC3 plays negative roles in cancer cell proliferation. (A) CAL 27 cells were transfected with anti-MORC3 or non-specific (NS) siRNA, and cell numbers were counted on Day 2 and Day 4. (B, C) The expression levels of CDH1, KRT14, JUN, CCND1, CCND2, CCN1, and IL6 in CAL 27 cells with or without MORC3 knockdown were analyzed by qRT-PCR. *, p < 0.05.

    Article Snippet: The membranes were blocked with 5% skimmed milk and incubated overnight at 4°C with following antibodies: mouse monoclonal anti-MORC3 antibody (Santa Cruz Biotechnology, United States), rabbit monoclonal anti- interferon induced protein with tetratricopeptide repeats 2 (IFIT2) antibody (abcam, United States), rabbit monoclonal anti-interferon induced transmembrane protein 3 (IFITM3) antibody (Cell Signaling Technology, United States), rabbit monoclonal anti-interferon induced protein with tetratricopeptide repeats 1 (IFIT1) antibody (Cell Signaling Technology, United States), rabbit monoclonal anti-cyclin D1 (CCND1) (ABclonal, China), rabbit monoclonal anti-cyclinD2 (CCND2) (ABclonal, China), rabbit polyclonal anti-JUN (ABclonal, China), rabbit polyclonal anti-interferon regulatory factor 7 (IRF7) (Proteintech, China), rabbit polyclonal anti-PD-L1 antibody (Proteintech, China), rabbit polyclonal anti-DExD/H-Box Helicase 60 (DDX60) antibody (Proteintech, China), and mouse anti-β-actin (Abmart, China).

    Techniques: Transfection, Expressing, Knockdown, Quantitative RT-PCR

    The primer sequence of the target genes

    Journal: Journal of Translational Medicine

    Article Title: The miR-15b-5p/miR-379-3p-FOXO axis regulates cell cycle and apoptosis in scleral remodeling during experimental myopia

    doi: 10.1186/s12967-024-05523-x

    Figure Lengend Snippet: The primer sequence of the target genes

    Article Snippet: Cyclin D1 (CCND1) , 1:1000 , Bioss, China.

    Techniques: Sequencing

    List of Western blotting primary antibody

    Journal: Journal of Translational Medicine

    Article Title: The miR-15b-5p/miR-379-3p-FOXO axis regulates cell cycle and apoptosis in scleral remodeling during experimental myopia

    doi: 10.1186/s12967-024-05523-x

    Figure Lengend Snippet: List of Western blotting primary antibody

    Article Snippet: Cyclin D1 (CCND1) , 1:1000 , Bioss, China.

    Techniques: Western Blot

    List of Immunofluorescence staining primary antibody

    Journal: Journal of Translational Medicine

    Article Title: The miR-15b-5p/miR-379-3p-FOXO axis regulates cell cycle and apoptosis in scleral remodeling during experimental myopia

    doi: 10.1186/s12967-024-05523-x

    Figure Lengend Snippet: List of Immunofluorescence staining primary antibody

    Article Snippet: Cyclin D1 (CCND1) , 1:1000 , Bioss, China.

    Techniques: Immunofluorescence, Staining

    Scleral cell cycle measurement and apoptotic analysis. A , B Measurement of CDK2 and CCND1 expression at the mRNA level in the sclera of the guinea pigs in NC and LIM groups (n = 4–6). C CDK2 and CCND1 immunoblots. D , E Measurement of CDK2 and CCND1 expression at protein level by Western blot in the sclera of the guinea pigs in NC and LIM groups (n = 6). F Measurement of CDK2 and CCND1 expression at protein level by immunofluorescence in the sclera of the guinea pigs in NC and LIM groups. (Western Blot cropped) (n = 6)

    Journal: Journal of Translational Medicine

    Article Title: The miR-15b-5p/miR-379-3p-FOXO axis regulates cell cycle and apoptosis in scleral remodeling during experimental myopia

    doi: 10.1186/s12967-024-05523-x

    Figure Lengend Snippet: Scleral cell cycle measurement and apoptotic analysis. A , B Measurement of CDK2 and CCND1 expression at the mRNA level in the sclera of the guinea pigs in NC and LIM groups (n = 4–6). C CDK2 and CCND1 immunoblots. D , E Measurement of CDK2 and CCND1 expression at protein level by Western blot in the sclera of the guinea pigs in NC and LIM groups (n = 6). F Measurement of CDK2 and CCND1 expression at protein level by immunofluorescence in the sclera of the guinea pigs in NC and LIM groups. (Western Blot cropped) (n = 6)

    Article Snippet: Cyclin D1 (CCND1) , 1:1000 , Bioss, China.

    Techniques: Expressing, Western Blot, Immunofluorescence

    (A) Validation of the differentially expressed genes by q-PCR with eight replicates. (B and C) Western blot analysis of the expression of proteins related to cell proliferation. (D and E) Cell immunofluorescence detection of the protein levels of c-Jun and CCND1. Three biological replicates were performed for Western blot assay. The p values of the comparison between control group and Halo-rhEGF group are all less than 0.05. Scale bar: 200 μm.

    Journal: PeerJ

    Article Title: Production of recombinant human epidermal growth factor fused with HaloTag protein and characterisation of its biological functions

    doi: 10.7717/peerj.17806

    Figure Lengend Snippet: (A) Validation of the differentially expressed genes by q-PCR with eight replicates. (B and C) Western blot analysis of the expression of proteins related to cell proliferation. (D and E) Cell immunofluorescence detection of the protein levels of c-Jun and CCND1. Three biological replicates were performed for Western blot assay. The p values of the comparison between control group and Halo-rhEGF group are all less than 0.05. Scale bar: 200 μm.

    Article Snippet: The membrane was blocked with 5% (w/v) skimmed milk in TBST (20 mM Tris, 150 mM NaCl and 0.1% Tween in water, pH 7.5) and incubated with primary antibodies against ERK1/2, phos-ERK1/2, c-Jun, phos-c-Jun, Tubulin, Cyclin D1 (CCND1) at 4 °C for 24 h. The membranes were incubated with HRP-conjugated secondary antibodies at room temperature for 1 h and the labelled protein bands were visualized on Amersham Imager 600 (Amersham Biosciences, Piscataway, NJ, USA).

    Techniques: Western Blot, Expressing, Immunofluorescence, Comparison, Control

    Involvement with apoptosis and cell cycle by treatment with of SE against at RA in HEPM cells Fig. 3A: Apotracker staining (green) of HEPM cells after treatment with 100 μM at RA and 0.03% SE for 48 h. The nuclei were counterstained with Hoechst 33342 (blue). Scale bar, 50 μm. Fig. 3B: Immunoblotting of HEPM cells after treatment with 100 μM at RA and 0.03% SE for 48 h. β-actin was served as an internal control. *p < 0.05 and ***p < 0.001 versus at RA. at RA: all-trans -retinoic acid HEPM: human embryonic palatal mesenchymal SE: Sasa veitchii extract CCND1: cyclin D1

    Journal: Nagoya Journal of Medical Science

    Article Title: Protective effect of Sasa veitchii extract against all-trans-retinoic acid-induced inhibition of proliferation of cultured human palate cells

    doi: 10.18999/nagjms.86.2.223

    Figure Lengend Snippet: Involvement with apoptosis and cell cycle by treatment with of SE against at RA in HEPM cells Fig. 3A: Apotracker staining (green) of HEPM cells after treatment with 100 μM at RA and 0.03% SE for 48 h. The nuclei were counterstained with Hoechst 33342 (blue). Scale bar, 50 μm. Fig. 3B: Immunoblotting of HEPM cells after treatment with 100 μM at RA and 0.03% SE for 48 h. β-actin was served as an internal control. *p < 0.05 and ***p < 0.001 versus at RA. at RA: all-trans -retinoic acid HEPM: human embryonic palatal mesenchymal SE: Sasa veitchii extract CCND1: cyclin D1

    Article Snippet: Rabbit anti-cleaved caspase-3 polyclonal antibody (1:2,500 dilution; Cell Signaling Technology, Beverly, MA), mouse anti-cyclin D1 (CCND1) monoclonal antibody (1:1,000 dilution; Santa Cruz Biotechnology, Dallas, TX), mouse anti-CCNA (1:1,000 dilution; Santa Cruz Biotechnology), anti-mouse CCNB (1:1,000 dilution; Santa Cruz Biotechnology), anti-mouse CCNE (1:1,000 dilution; Santa Cruz Biotechnology), and anti-mouse β-actin monoclonal antibody (1:2,500 dilution; MBL, Aichi, Japan) were used as primary antibodies for immunoblotting.

    Techniques: Staining, Western Blot, Control

    Proposed mechanism of SE against at RA-induced cell proliferation inhibition ERBB2: Erb-B2 receptor tyrosine kinase 2 JADE1 : jade family PHD finger 1 CCND1: cyclin D1

    Journal: Nagoya Journal of Medical Science

    Article Title: Protective effect of Sasa veitchii extract against all-trans-retinoic acid-induced inhibition of proliferation of cultured human palate cells

    doi: 10.18999/nagjms.86.2.223

    Figure Lengend Snippet: Proposed mechanism of SE against at RA-induced cell proliferation inhibition ERBB2: Erb-B2 receptor tyrosine kinase 2 JADE1 : jade family PHD finger 1 CCND1: cyclin D1

    Article Snippet: Rabbit anti-cleaved caspase-3 polyclonal antibody (1:2,500 dilution; Cell Signaling Technology, Beverly, MA), mouse anti-cyclin D1 (CCND1) monoclonal antibody (1:1,000 dilution; Santa Cruz Biotechnology, Dallas, TX), mouse anti-CCNA (1:1,000 dilution; Santa Cruz Biotechnology), anti-mouse CCNB (1:1,000 dilution; Santa Cruz Biotechnology), anti-mouse CCNE (1:1,000 dilution; Santa Cruz Biotechnology), and anti-mouse β-actin monoclonal antibody (1:2,500 dilution; MBL, Aichi, Japan) were used as primary antibodies for immunoblotting.

    Techniques: Inhibition