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human telomerase reverse transcriptase levels  (Cusabio)


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    Cusabio human telomerase reverse transcriptase levels
    Figure 3. GREM1 overexpression inhibited ADSC senescence. (a) SA-β-gal staining showed fewer positive cells in GREM1 over- expressing ADSCs compared to vector control. Scale bar: 100 μm. (b) A quantitative analysis of SA-β-gal positive cells. (c) The relative <t>telomerase</t> activity was measured by the telomerase ELISA kit. (d, e) Real-time RT-PCR results showed that GREM1 overexpression decreased the expressions of P16 (d) and P53 (e). The control gene was GAPDH. The statistical significance was evaluated by Student’s t-test. The error bar was indicated by SD. (n = 3). *p ≤0.05.
    Human Telomerase Reverse Transcriptase Levels, supplied by Cusabio, used in various techniques. Bioz Stars score: 93/100, based on 8 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/human telomerase reverse transcriptase levels/product/Cusabio
    Average 93 stars, based on 8 article reviews
    human telomerase reverse transcriptase levels - by Bioz Stars, 2026-02
    93/100 stars

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    1) Product Images from "GREM1 inhibits osteogenic differentiation, senescence and BMP transcription of adipose-derived stem cells."

    Article Title: GREM1 inhibits osteogenic differentiation, senescence and BMP transcription of adipose-derived stem cells.

    Journal: Connective tissue research

    doi: 10.1080/03008207.2020.1736054

    Figure 3. GREM1 overexpression inhibited ADSC senescence. (a) SA-β-gal staining showed fewer positive cells in GREM1 over- expressing ADSCs compared to vector control. Scale bar: 100 μm. (b) A quantitative analysis of SA-β-gal positive cells. (c) The relative telomerase activity was measured by the telomerase ELISA kit. (d, e) Real-time RT-PCR results showed that GREM1 overexpression decreased the expressions of P16 (d) and P53 (e). The control gene was GAPDH. The statistical significance was evaluated by Student’s t-test. The error bar was indicated by SD. (n = 3). *p ≤0.05.
    Figure Legend Snippet: Figure 3. GREM1 overexpression inhibited ADSC senescence. (a) SA-β-gal staining showed fewer positive cells in GREM1 over- expressing ADSCs compared to vector control. Scale bar: 100 μm. (b) A quantitative analysis of SA-β-gal positive cells. (c) The relative telomerase activity was measured by the telomerase ELISA kit. (d, e) Real-time RT-PCR results showed that GREM1 overexpression decreased the expressions of P16 (d) and P53 (e). The control gene was GAPDH. The statistical significance was evaluated by Student’s t-test. The error bar was indicated by SD. (n = 3). *p ≤0.05.

    Techniques Used: Over Expression, Staining, Expressing, Plasmid Preparation, Control, Activity Assay, Enzyme-linked Immunosorbent Assay, Quantitative RT-PCR

    Figure 4. GREM1 knockdown accelerated ADSC senescence. (a) SA-β-gal staining showed an increased number of positive cells in the ADSC-GREM1sh group compared to the control group. Scale bar: 100 μm. (b) The quantitative analysis of SA-β-gal positive cells. (c) Telomerase activity assay results showed that GREM1 knockdown significantly decreased ADSCs telomerase activity. (d, e) Real- time RT-PCR results showed that GREM1 knockdown upregulated the expressions of P16 (d) and P53 (e). The control gene was GAPDH. The statistical significance was evaluated by Student’s t-test. The error bar was indicated by SD. (n = 3). *p ≤0.05.
    Figure Legend Snippet: Figure 4. GREM1 knockdown accelerated ADSC senescence. (a) SA-β-gal staining showed an increased number of positive cells in the ADSC-GREM1sh group compared to the control group. Scale bar: 100 μm. (b) The quantitative analysis of SA-β-gal positive cells. (c) Telomerase activity assay results showed that GREM1 knockdown significantly decreased ADSCs telomerase activity. (d, e) Real- time RT-PCR results showed that GREM1 knockdown upregulated the expressions of P16 (d) and P53 (e). The control gene was GAPDH. The statistical significance was evaluated by Student’s t-test. The error bar was indicated by SD. (n = 3). *p ≤0.05.

    Techniques Used: Knockdown, Staining, Control, Telomerase Activity Assay, Activity Assay, Quantitative RT-PCR



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    human telomerase reverse transcriptase levels  (Cusabio)
    93
    Cusabio human telomerase reverse transcriptase levels
    Figure 3. GREM1 overexpression inhibited ADSC senescence. (a) SA-β-gal staining showed fewer positive cells in GREM1 over- expressing ADSCs compared to vector control. Scale bar: 100 μm. (b) A quantitative analysis of SA-β-gal positive cells. (c) The relative <t>telomerase</t> activity was measured by the telomerase ELISA kit. (d, e) Real-time RT-PCR results showed that GREM1 overexpression decreased the expressions of P16 (d) and P53 (e). The control gene was GAPDH. The statistical significance was evaluated by Student’s t-test. The error bar was indicated by SD. (n = 3). *p ≤0.05.
    Human Telomerase Reverse Transcriptase Levels, 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
    https://www.bioz.com/result/human telomerase reverse transcriptase levels/product/Cusabio
    Average 93 stars, based on 1 article reviews
    human telomerase reverse transcriptase levels - by Bioz Stars, 2026-02
    93/100 stars
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    Figure 3. GREM1 overexpression inhibited ADSC senescence. (a) SA-β-gal staining showed fewer positive cells in GREM1 over- expressing ADSCs compared to vector control. Scale bar: 100 μm. (b) A quantitative analysis of SA-β-gal positive cells. (c) The relative telomerase activity was measured by the telomerase ELISA kit. (d, e) Real-time RT-PCR results showed that GREM1 overexpression decreased the expressions of P16 (d) and P53 (e). The control gene was GAPDH. The statistical significance was evaluated by Student’s t-test. The error bar was indicated by SD. (n = 3). *p ≤0.05.

    Journal: Connective tissue research

    Article Title: GREM1 inhibits osteogenic differentiation, senescence and BMP transcription of adipose-derived stem cells.

    doi: 10.1080/03008207.2020.1736054

    Figure Lengend Snippet: Figure 3. GREM1 overexpression inhibited ADSC senescence. (a) SA-β-gal staining showed fewer positive cells in GREM1 over- expressing ADSCs compared to vector control. Scale bar: 100 μm. (b) A quantitative analysis of SA-β-gal positive cells. (c) The relative telomerase activity was measured by the telomerase ELISA kit. (d, e) Real-time RT-PCR results showed that GREM1 overexpression decreased the expressions of P16 (d) and P53 (e). The control gene was GAPDH. The statistical significance was evaluated by Student’s t-test. The error bar was indicated by SD. (n = 3). *p ≤0.05.

    Article Snippet: We measured the human telomerase reverse transcriptase levels in the cells by ELISA following the manufacturer’s protocol (Human Telomerase Reverse Transcriptase, TERT ELISA Kit, Cusabio, Wuhan, China).

    Techniques: Over Expression, Staining, Expressing, Plasmid Preparation, Control, Activity Assay, Enzyme-linked Immunosorbent Assay, Quantitative RT-PCR

    Figure 4. GREM1 knockdown accelerated ADSC senescence. (a) SA-β-gal staining showed an increased number of positive cells in the ADSC-GREM1sh group compared to the control group. Scale bar: 100 μm. (b) The quantitative analysis of SA-β-gal positive cells. (c) Telomerase activity assay results showed that GREM1 knockdown significantly decreased ADSCs telomerase activity. (d, e) Real- time RT-PCR results showed that GREM1 knockdown upregulated the expressions of P16 (d) and P53 (e). The control gene was GAPDH. The statistical significance was evaluated by Student’s t-test. The error bar was indicated by SD. (n = 3). *p ≤0.05.

    Journal: Connective tissue research

    Article Title: GREM1 inhibits osteogenic differentiation, senescence and BMP transcription of adipose-derived stem cells.

    doi: 10.1080/03008207.2020.1736054

    Figure Lengend Snippet: Figure 4. GREM1 knockdown accelerated ADSC senescence. (a) SA-β-gal staining showed an increased number of positive cells in the ADSC-GREM1sh group compared to the control group. Scale bar: 100 μm. (b) The quantitative analysis of SA-β-gal positive cells. (c) Telomerase activity assay results showed that GREM1 knockdown significantly decreased ADSCs telomerase activity. (d, e) Real- time RT-PCR results showed that GREM1 knockdown upregulated the expressions of P16 (d) and P53 (e). The control gene was GAPDH. The statistical significance was evaluated by Student’s t-test. The error bar was indicated by SD. (n = 3). *p ≤0.05.

    Article Snippet: We measured the human telomerase reverse transcriptase levels in the cells by ELISA following the manufacturer’s protocol (Human Telomerase Reverse Transcriptase, TERT ELISA Kit, Cusabio, Wuhan, China).

    Techniques: Knockdown, Staining, Control, Telomerase Activity Assay, Activity Assay, Quantitative RT-PCR