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circrna expression  (Proteintech)


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    Proteintech circrna expression
    Fig. 2 Differential expression of <t>circRNA</t> in Jurkat cells after coculture with ionomycin (1 µg/mL) for 1 h. (A) The expression profiles of circRNA in Jurkat cells after coculture with ionomycin (1 µg/mL) for 1 h were evaluated using next-generation sequencing. Each scatter point in the figure represents the mean read count of circRNA in three replicates of the treatment. (B) Validation of potential candidates of Ca2+ influx-regulated circRNAs in Jurkat cells. The relative expression level of circRNA was defined as (39 - Ct) after adjusted with the internal control (GAPDH; Glyceraldehyde-3-Phosphate Dehydro genase). Data was presented as mean ± SD. (ns, not significant; *P < 0.05; **P < 0.01; ***P < 0.001)
    Circrna Expression, supplied by Proteintech, used in various techniques. Bioz Stars score: 96/100, based on 678 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/circrna+expression/pm39473004-50-33-60?v=Proteintech
    Average 96 stars, based on 678 article reviews
    circrna expression - by Bioz Stars, 2026-07
    96/100 stars

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    1) Product Images from "Circ-CAMTA1 regulated by Ca 2+ influx inhibited pyruvate carboxylase activity and modulate T cell function in patients with systemic lupus erythematosus."

    Article Title: Circ-CAMTA1 regulated by Ca 2+ influx inhibited pyruvate carboxylase activity and modulate T cell function in patients with systemic lupus erythematosus.

    Journal: Arthritis research & therapy

    doi: 10.1186/s13075-024-03422-6

    Fig. 2 Differential expression of circRNA in Jurkat cells after coculture with ionomycin (1 µg/mL) for 1 h. (A) The expression profiles of circRNA in Jurkat cells after coculture with ionomycin (1 µg/mL) for 1 h were evaluated using next-generation sequencing. Each scatter point in the figure represents the mean read count of circRNA in three replicates of the treatment. (B) Validation of potential candidates of Ca2+ influx-regulated circRNAs in Jurkat cells. The relative expression level of circRNA was defined as (39 - Ct) after adjusted with the internal control (GAPDH; Glyceraldehyde-3-Phosphate Dehydro genase). Data was presented as mean ± SD. (ns, not significant; *P < 0.05; **P < 0.01; ***P < 0.001)
    Figure Legend Snippet: Fig. 2 Differential expression of circRNA in Jurkat cells after coculture with ionomycin (1 µg/mL) for 1 h. (A) The expression profiles of circRNA in Jurkat cells after coculture with ionomycin (1 µg/mL) for 1 h were evaluated using next-generation sequencing. Each scatter point in the figure represents the mean read count of circRNA in three replicates of the treatment. (B) Validation of potential candidates of Ca2+ influx-regulated circRNAs in Jurkat cells. The relative expression level of circRNA was defined as (39 - Ct) after adjusted with the internal control (GAPDH; Glyceraldehyde-3-Phosphate Dehydro genase). Data was presented as mean ± SD. (ns, not significant; *P < 0.05; **P < 0.01; ***P < 0.001)

    Techniques Used: Quantitative Proteomics, Expressing, Next-Generation Sequencing, Biomarker Discovery, Control



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    Fig. 2 Differential expression of <t>circRNA</t> in Jurkat cells after coculture with ionomycin (1 µg/mL) for 1 h. (A) The expression profiles of circRNA in Jurkat cells after coculture with ionomycin (1 µg/mL) for 1 h were evaluated using next-generation sequencing. Each scatter point in the figure represents the mean read count of circRNA in three replicates of the treatment. (B) Validation of potential candidates of Ca2+ influx-regulated circRNAs in Jurkat cells. The relative expression level of circRNA was defined as (39 - Ct) after adjusted with the internal control (GAPDH; Glyceraldehyde-3-Phosphate Dehydro genase). Data was presented as mean ± SD. (ns, not significant; *P < 0.05; **P < 0.01; ***P < 0.001)
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    Fig. 2 Differential expression of <t>circRNA</t> in Jurkat cells after coculture with ionomycin (1 µg/mL) for 1 h. (A) The expression profiles of circRNA in Jurkat cells after coculture with ionomycin (1 µg/mL) for 1 h were evaluated using next-generation sequencing. Each scatter point in the figure represents the mean read count of circRNA in three replicates of the treatment. (B) Validation of potential candidates of Ca2+ influx-regulated circRNAs in Jurkat cells. The relative expression level of circRNA was defined as (39 - Ct) after adjusted with the internal control (GAPDH; Glyceraldehyde-3-Phosphate Dehydro genase). Data was presented as mean ± SD. (ns, not significant; *P < 0.05; **P < 0.01; ***P < 0.001)
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    Fig. 2 Differential expression of <t>circRNA</t> in Jurkat cells after coculture with ionomycin (1 µg/mL) for 1 h. (A) The expression profiles of circRNA in Jurkat cells after coculture with ionomycin (1 µg/mL) for 1 h were evaluated using next-generation sequencing. Each scatter point in the figure represents the mean read count of circRNA in three replicates of the treatment. (B) Validation of potential candidates of Ca2+ influx-regulated circRNAs in Jurkat cells. The relative expression level of circRNA was defined as (39 - Ct) after adjusted with the internal control (GAPDH; Glyceraldehyde-3-Phosphate Dehydro genase). Data was presented as mean ± SD. (ns, not significant; *P < 0.05; **P < 0.01; ***P < 0.001)
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    Image Search Results


    Fig. 2 Differential expression of circRNA in Jurkat cells after coculture with ionomycin (1 µg/mL) for 1 h. (A) The expression profiles of circRNA in Jurkat cells after coculture with ionomycin (1 µg/mL) for 1 h were evaluated using next-generation sequencing. Each scatter point in the figure represents the mean read count of circRNA in three replicates of the treatment. (B) Validation of potential candidates of Ca2+ influx-regulated circRNAs in Jurkat cells. The relative expression level of circRNA was defined as (39 - Ct) after adjusted with the internal control (GAPDH; Glyceraldehyde-3-Phosphate Dehydro genase). Data was presented as mean ± SD. (ns, not significant; *P < 0.05; **P < 0.01; ***P < 0.001)

    Journal: Arthritis research & therapy

    Article Title: Circ-CAMTA1 regulated by Ca 2+ influx inhibited pyruvate carboxylase activity and modulate T cell function in patients with systemic lupus erythematosus.

    doi: 10.1186/s13075-024-03422-6

    Figure Lengend Snippet: Fig. 2 Differential expression of circRNA in Jurkat cells after coculture with ionomycin (1 µg/mL) for 1 h. (A) The expression profiles of circRNA in Jurkat cells after coculture with ionomycin (1 µg/mL) for 1 h were evaluated using next-generation sequencing. Each scatter point in the figure represents the mean read count of circRNA in three replicates of the treatment. (B) Validation of potential candidates of Ca2+ influx-regulated circRNAs in Jurkat cells. The relative expression level of circRNA was defined as (39 - Ct) after adjusted with the internal control (GAPDH; Glyceraldehyde-3-Phosphate Dehydro genase). Data was presented as mean ± SD. (ns, not significant; *P < 0.05; **P < 0.01; ***P < 0.001)

    Article Snippet: To analyzed circRNA expression levels in Jurkat cells after stimulation, cells were treated with phorbol 12-myristate 13-acetate (PMA; 20 ng/mL; Sigma-Aldrich) and ionomycin (500 ng/mL; Sigma-Aldrich, ) for 24 h. For analysis of circRNA expression in response to interferon-alpha (IFN-α), Jurkat cells were treated with 1000 IU/mL recombinant human IFN-α for 72 h. The IFN-alpha we used was purchased from Proteintech (Rosemont, IL, USA) and was produced in HEK293.

    Techniques: Quantitative Proteomics, Expressing, Next-Generation Sequencing, Biomarker Discovery, Control