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tasso m 20 dbs  (Tasso Inc)


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    Tasso Inc tasso m 20 dbs
    Validation of RM‐EPO detection from TASSO DBS. A. Selectivity, sensitivity (Limit of detection) and reproducibility of detection are shown. PCR was performed using Taqman EPO assay on DNA extracted from DBS <t>TASSO</t> <t>M‐20</t> loaded with 10 different blood samples spiked at 0–1500–2500–5000 c/mL RM‐EPO. Cq values are indicated. Examples of size of amplified products are shown for bloods spiked at 5000 c/mL. Reproducibility experiments were performed after DNA extraction from the second and third spot of the TASSO device. B. CP performed on the fourth spot of TASSO M‐20 (“B analysis”). PCR was performed using NMI CP on DNA extracted from the fourth spot (last spot) of DBS TASSO M‐20 loaded with blood samples spiked at 5000 c/mL RM‐EPO. Cq values are indicated. Examples of size of amplified products are shown.
    Tasso M 20 Dbs, supplied by Tasso Inc, used in various techniques. Bioz Stars score: 99/100, based on 12 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/tasso+m+20+dbs/Tasso%2B/pmc12861599-5-22-22
    Average 99 stars, based on 12 article reviews
    tasso m 20 dbs - by Bioz Stars, 2026-09
    99/100 stars

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    1) Product Images from "Improvement of EPO Transgene Detection From Polymeric Dried Blood Spots for Antidoping Application"

    Article Title: Improvement of EPO Transgene Detection From Polymeric Dried Blood Spots for Antidoping Application

    Journal: Drug Testing and Analysis

    doi: 10.1002/dta.70008

    Validation of RM‐EPO detection from TASSO DBS. A. Selectivity, sensitivity (Limit of detection) and reproducibility of detection are shown. PCR was performed using Taqman EPO assay on DNA extracted from DBS TASSO M‐20 loaded with 10 different blood samples spiked at 0–1500–2500–5000 c/mL RM‐EPO. Cq values are indicated. Examples of size of amplified products are shown for bloods spiked at 5000 c/mL. Reproducibility experiments were performed after DNA extraction from the second and third spot of the TASSO device. B. CP performed on the fourth spot of TASSO M‐20 (“B analysis”). PCR was performed using NMI CP on DNA extracted from the fourth spot (last spot) of DBS TASSO M‐20 loaded with blood samples spiked at 5000 c/mL RM‐EPO. Cq values are indicated. Examples of size of amplified products are shown.
    Figure Legend Snippet: Validation of RM‐EPO detection from TASSO DBS. A. Selectivity, sensitivity (Limit of detection) and reproducibility of detection are shown. PCR was performed using Taqman EPO assay on DNA extracted from DBS TASSO M‐20 loaded with 10 different blood samples spiked at 0–1500–2500–5000 c/mL RM‐EPO. Cq values are indicated. Examples of size of amplified products are shown for bloods spiked at 5000 c/mL. Reproducibility experiments were performed after DNA extraction from the second and third spot of the TASSO device. B. CP performed on the fourth spot of TASSO M‐20 (“B analysis”). PCR was performed using NMI CP on DNA extracted from the fourth spot (last spot) of DBS TASSO M‐20 loaded with blood samples spiked at 5000 c/mL RM‐EPO. Cq values are indicated. Examples of size of amplified products are shown.

    Techniques Used: Biomarker Discovery, Amplification, DNA Extraction

    Related Articles

    Biomarker Discovery:

    Article Title: Improvement of EPO Transgene Detection From Polymeric Dried Blood Spots for Antidoping Application
    Article Snippet: Three DBS devices were evaluated: polymeric Tasso‐M20 (TASSO Inc.) and Mitra (Neoteryx), and cellulosic Protein Saver 903 (Whatman). .. The best results were achieved with polymeric DBS, and a full validation was performed for the detection of the EPO transgene using Tasso M‐20 DBS; 1500 copies/mL were detected in 50% of cases and robust detection was obtained at 5000 copies/mL (100 copies transgene in 20‐μL DBS) with the four spots of the Tasso device tested over several weeks. ..



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    tasso m 20 dbs  (Tasso Inc)
    99
    Tasso Inc tasso m 20 dbs
    Validation of RM‐EPO detection from TASSO DBS. A. Selectivity, sensitivity (Limit of detection) and reproducibility of detection are shown. PCR was performed using Taqman EPO assay on DNA extracted from DBS <t>TASSO</t> <t>M‐20</t> loaded with 10 different blood samples spiked at 0–1500–2500–5000 c/mL RM‐EPO. Cq values are indicated. Examples of size of amplified products are shown for bloods spiked at 5000 c/mL. Reproducibility experiments were performed after DNA extraction from the second and third spot of the TASSO device. B. CP performed on the fourth spot of TASSO M‐20 (“B analysis”). PCR was performed using NMI CP on DNA extracted from the fourth spot (last spot) of DBS TASSO M‐20 loaded with blood samples spiked at 5000 c/mL RM‐EPO. Cq values are indicated. Examples of size of amplified products are shown.
    Tasso M 20 Dbs, supplied by Tasso Inc, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/tasso+m+20+dbs/Tasso%2B/pmc12861599-5-22-22
    Average 99 stars, based on 1 article reviews
    tasso m 20 dbs - by Bioz Stars, 2026-09
    99/100 stars
    		  Buy from Supplier

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    Validation of RM‐EPO detection from TASSO DBS. A. Selectivity, sensitivity (Limit of detection) and reproducibility of detection are shown. PCR was performed using Taqman EPO assay on DNA extracted from DBS TASSO M‐20 loaded with 10 different blood samples spiked at 0–1500–2500–5000 c/mL RM‐EPO. Cq values are indicated. Examples of size of amplified products are shown for bloods spiked at 5000 c/mL. Reproducibility experiments were performed after DNA extraction from the second and third spot of the TASSO device. B. CP performed on the fourth spot of TASSO M‐20 (“B analysis”). PCR was performed using NMI CP on DNA extracted from the fourth spot (last spot) of DBS TASSO M‐20 loaded with blood samples spiked at 5000 c/mL RM‐EPO. Cq values are indicated. Examples of size of amplified products are shown.

    Journal: Drug Testing and Analysis

    Article Title: Improvement of EPO Transgene Detection From Polymeric Dried Blood Spots for Antidoping Application

    doi: 10.1002/dta.70008

    Figure Lengend Snippet: Validation of RM‐EPO detection from TASSO DBS. A. Selectivity, sensitivity (Limit of detection) and reproducibility of detection are shown. PCR was performed using Taqman EPO assay on DNA extracted from DBS TASSO M‐20 loaded with 10 different blood samples spiked at 0–1500–2500–5000 c/mL RM‐EPO. Cq values are indicated. Examples of size of amplified products are shown for bloods spiked at 5000 c/mL. Reproducibility experiments were performed after DNA extraction from the second and third spot of the TASSO device. B. CP performed on the fourth spot of TASSO M‐20 (“B analysis”). PCR was performed using NMI CP on DNA extracted from the fourth spot (last spot) of DBS TASSO M‐20 loaded with blood samples spiked at 5000 c/mL RM‐EPO. Cq values are indicated. Examples of size of amplified products are shown.

    Article Snippet: The best results were achieved with polymeric DBS, and a full validation was performed for the detection of the EPO transgene using Tasso M‐20 DBS; 1500 copies/mL were detected in 50% of cases and robust detection was obtained at 5000 copies/mL (100 copies transgene in 20‐μL DBS) with the four spots of the Tasso device tested over several weeks.

    Techniques: Biomarker Discovery, Amplification, DNA Extraction