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trap assay trapeze  (Oncor Inc)

 
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    Structured Review

    Oncor Inc trap assay trapeze
    Trap Assay Trapeze, supplied by Oncor Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/trap+assay+trapeze/trap+assay/us08709995-2972-1-4
    Average 90 stars, based on 1 article reviews
    trap assay trapeze - by Bioz Stars, 2026-10
    90/100 stars

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    Related Articles

    TRAP Assay:

    Article Title: Method for eliciting an immune response to human telomerase reverse transcriptase
    Article Snippet: A TRAP assay (TRAPeze, Oncor, Inc, Gaithersburg, Md.) demonstrated that telomerase activity was generated in the sense construct transfected cells.

    Activity Assay:

    Article Title: Method for eliciting an immune response to human telomerase reverse transcriptase
    Article Snippet: A TRAP assay (TRAPeze, Oncor, Inc, Gaithersburg, Md.) demonstrated that telomerase activity was generated in the sense construct transfected cells.

    Generated:

    Article Title: Method for eliciting an immune response to human telomerase reverse transcriptase
    Article Snippet: A TRAP assay (TRAPeze, Oncor, Inc, Gaithersburg, Md.) demonstrated that telomerase activity was generated in the sense construct transfected cells.

    Construct:

    Article Title: Method for eliciting an immune response to human telomerase reverse transcriptase
    Article Snippet: A TRAP assay (TRAPeze, Oncor, Inc, Gaithersburg, Md.) demonstrated that telomerase activity was generated in the sense construct transfected cells.

    Transfection:

    Article Title: Method for eliciting an immune response to human telomerase reverse transcriptase
    Article Snippet: A TRAP assay (TRAPeze, Oncor, Inc, Gaithersburg, Md.) demonstrated that telomerase activity was generated in the sense construct transfected cells.



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    A . Percentage of leukemic blasts, telomerase expression (WB and lane quantification normalized on β-actin) and enzymatic activity levels in THP1 cell line, PBMCs from AML patients and age-matched HDs (representative cases out of 10 AML patients and 4 HDs are shown). B . AML leukemic cells were recognized in vitro by engineered hTERT 865-873 -specific T-cells upon 24-hour co-culture, as assayed both by hIFN-γ release assay (upper panel) and flow cytometry cytotoxicity assay (lower panel). Data are mean ± SD of three independent experiments: hTERT 865-873 pulsed HLA-A2 + HD PBMCs ( n = 3; CTRL+); hHCV 1406-1415 -pulsed HLA-A2 + HD PBMCs ( n = 3; CTRL-); HLA-A2 + HD PBMCs ( n = 4); HLA-A2 + PBMCs from AML patients ( n = 10); THP1 cell line ( n = 3). Statistical analysis was performed with ANOVA test.

    Journal: Oncotarget

    Article Title: Effective control of acute myeloid leukaemia and acute lymphoblastic leukaemia progression by telomerase specific adoptive T-cell therapy

    doi: 10.18632/oncotarget.18115

    Figure Lengend Snippet: A . Percentage of leukemic blasts, telomerase expression (WB and lane quantification normalized on β-actin) and enzymatic activity levels in THP1 cell line, PBMCs from AML patients and age-matched HDs (representative cases out of 10 AML patients and 4 HDs are shown). B . AML leukemic cells were recognized in vitro by engineered hTERT 865-873 -specific T-cells upon 24-hour co-culture, as assayed both by hIFN-γ release assay (upper panel) and flow cytometry cytotoxicity assay (lower panel). Data are mean ± SD of three independent experiments: hTERT 865-873 pulsed HLA-A2 + HD PBMCs ( n = 3; CTRL+); hHCV 1406-1415 -pulsed HLA-A2 + HD PBMCs ( n = 3; CTRL-); HLA-A2 + HD PBMCs ( n = 4); HLA-A2 + PBMCs from AML patients ( n = 10); THP1 cell line ( n = 3). Statistical analysis was performed with ANOVA test.

    Article Snippet: Telomerase activity was measured using TRAP assay (TRAPeze ® XL telomerase detection kit; Millipore), following manufacturer's instructions.

    Techniques: Expressing, Activity Assay, In Vitro, Co-Culture Assay, Release Assay, Flow Cytometry, Cytotoxicity Assay

    A . Percentage of leukemic blasts, telomerase expression (WB and lane quantification normalized on β-actin) and enzymatic activity levels in ALL-CM cell line, B-cells isolated from PBMCs of B-ALL patients and age-matched HDs (shown some representative cases out of 10 B-ALL patients and 5 HDs). B . Leukemic cells isolated from B-ALL patients were recognized in vitro by engineered hTERT 865-873 -specific T-cells upon 24-hour co-culture, as assayed both by hIFN-γ release assay (upper panel) and flow cytometry cytotoxicity assay (lower panel). Data are mean ± SD of three independent experiments: hTERT 865-873 pulsed HLA-A2 + HD B-cells ( n = 3; CTRL+); hHCV 1406-1415 -pulsed HLA-A2 + HD B-cells ( n = 3; CTRL-); HLA-A2 + HD B-cells ( n = 5); HLA-A2 + B-cells from B-ALL patients ( n = 10); ALL-CM cell line ( n = 3). Statistical analysis was performed with ANOVA test.

    Journal: Oncotarget

    Article Title: Effective control of acute myeloid leukaemia and acute lymphoblastic leukaemia progression by telomerase specific adoptive T-cell therapy

    doi: 10.18632/oncotarget.18115

    Figure Lengend Snippet: A . Percentage of leukemic blasts, telomerase expression (WB and lane quantification normalized on β-actin) and enzymatic activity levels in ALL-CM cell line, B-cells isolated from PBMCs of B-ALL patients and age-matched HDs (shown some representative cases out of 10 B-ALL patients and 5 HDs). B . Leukemic cells isolated from B-ALL patients were recognized in vitro by engineered hTERT 865-873 -specific T-cells upon 24-hour co-culture, as assayed both by hIFN-γ release assay (upper panel) and flow cytometry cytotoxicity assay (lower panel). Data are mean ± SD of three independent experiments: hTERT 865-873 pulsed HLA-A2 + HD B-cells ( n = 3; CTRL+); hHCV 1406-1415 -pulsed HLA-A2 + HD B-cells ( n = 3; CTRL-); HLA-A2 + HD B-cells ( n = 5); HLA-A2 + B-cells from B-ALL patients ( n = 10); ALL-CM cell line ( n = 3). Statistical analysis was performed with ANOVA test.

    Article Snippet: Telomerase activity was measured using TRAP assay (TRAPeze ® XL telomerase detection kit; Millipore), following manufacturer's instructions.

    Techniques: Expressing, Activity Assay, Isolation, In Vitro, Co-Culture Assay, Release Assay, Flow Cytometry, Cytotoxicity Assay