adv5 peptivator Search Results


peptivator sars cov 2 prot m miltenyi biotec  (Miltenyi Biotec)
94
Miltenyi Biotec peptivator sars cov 2 prot m miltenyi biotec
Peptivator Sars Cov 2 Prot M Miltenyi Biotec, supplied by Miltenyi Biotec, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/peptivator sars cov 2 prot m miltenyi biotec/product/Miltenyi Biotec
Average 94 stars, based on 1 article reviews
peptivator sars cov 2 prot m miltenyi biotec - by Bioz Stars, 2026-03
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adv5 penton  (Miltenyi Biotec)
94
Miltenyi Biotec adv5 penton
Impact of a single continuous and interval exercise on antigen-specific T-cell responses. Peripheral blood samples of healthy donors (n = 12) were analysed at different time points before and after a single 30 min continuous (CONT) or interval (HIT) exercise (before, directly after, 1 h after and 24 h after exercise). Isolated PBMCs were stimulated overnight with a CMV-, b EBV- and c AdV-specific peptide pools (CMV pp65, CMV IE1, EBV EBNA1, EBV Consensus, <t>AdV5</t> Hexon and AdV5 <t>Penton)</t> and frequencies of functional-active virus-specific T cells were determined by IFN-γ EliSpot assay. Negative and positive controls were carried out by using either medium without stimuli or 1 μg/ml staphylococcal enterotoxins B (SEB). Results are indicated as the number of spots per 2.5 × 10 5 cells/well (spw) and spots per 1000 CD3 + T cells, respectively after substracting the number of spw of the respective negative control. Positive controls showed a positive result for all analysed samples detected as TNTC (too numerous to count, TNTC ≥ 1000 spw). Results are displayed as mean ± SD. Asterisks indicate statistically significant differences between levels of induced cytokine responses (*p < 0.05)
Adv5 Penton, supplied by Miltenyi Biotec, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/adv5 penton/product/Miltenyi Biotec
Average 94 stars, based on 1 article reviews
adv5 penton - by Bioz Stars, 2026-03
94/100 stars
  Buy from Supplier
adv5  (Miltenyi Biotec)
93
Miltenyi Biotec adv5
Impact of a single continuous and interval exercise on antigen-specific T-cell responses. Peripheral blood samples of healthy donors (n = 12) were analysed at different time points before and after a single 30 min continuous (CONT) or interval (HIT) exercise (before, directly after, 1 h after and 24 h after exercise). Isolated PBMCs were stimulated overnight with a CMV-, b EBV- and c AdV-specific peptide pools (CMV pp65, CMV IE1, EBV EBNA1, EBV Consensus, <t>AdV5</t> Hexon and AdV5 <t>Penton)</t> and frequencies of functional-active virus-specific T cells were determined by IFN-γ EliSpot assay. Negative and positive controls were carried out by using either medium without stimuli or 1 μg/ml staphylococcal enterotoxins B (SEB). Results are indicated as the number of spots per 2.5 × 10 5 cells/well (spw) and spots per 1000 CD3 + T cells, respectively after substracting the number of spw of the respective negative control. Positive controls showed a positive result for all analysed samples detected as TNTC (too numerous to count, TNTC ≥ 1000 spw). Results are displayed as mean ± SD. Asterisks indicate statistically significant differences between levels of induced cytokine responses (*p < 0.05)
Adv5, supplied by Miltenyi Biotec, 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/adv5/product/Miltenyi Biotec
Average 93 stars, based on 1 article reviews
adv5 - by Bioz Stars, 2026-03
93/100 stars
  Buy from Supplier

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Impact of a single continuous and interval exercise on antigen-specific T-cell responses. Peripheral blood samples of healthy donors (n = 12) were analysed at different time points before and after a single 30 min continuous (CONT) or interval (HIT) exercise (before, directly after, 1 h after and 24 h after exercise). Isolated PBMCs were stimulated overnight with a CMV-, b EBV- and c AdV-specific peptide pools (CMV pp65, CMV IE1, EBV EBNA1, EBV Consensus, AdV5 Hexon and AdV5 Penton) and frequencies of functional-active virus-specific T cells were determined by IFN-γ EliSpot assay. Negative and positive controls were carried out by using either medium without stimuli or 1 μg/ml staphylococcal enterotoxins B (SEB). Results are indicated as the number of spots per 2.5 × 10 5 cells/well (spw) and spots per 1000 CD3 + T cells, respectively after substracting the number of spw of the respective negative control. Positive controls showed a positive result for all analysed samples detected as TNTC (too numerous to count, TNTC ≥ 1000 spw). Results are displayed as mean ± SD. Asterisks indicate statistically significant differences between levels of induced cytokine responses (*p < 0.05)

Journal: Journal of Translational Medicine

Article Title: High-intensity interval training in allogeneic adoptive T-cell immunotherapy – a big HIT?

doi: 10.1186/s12967-020-02301-3

Figure Lengend Snippet: Impact of a single continuous and interval exercise on antigen-specific T-cell responses. Peripheral blood samples of healthy donors (n = 12) were analysed at different time points before and after a single 30 min continuous (CONT) or interval (HIT) exercise (before, directly after, 1 h after and 24 h after exercise). Isolated PBMCs were stimulated overnight with a CMV-, b EBV- and c AdV-specific peptide pools (CMV pp65, CMV IE1, EBV EBNA1, EBV Consensus, AdV5 Hexon and AdV5 Penton) and frequencies of functional-active virus-specific T cells were determined by IFN-γ EliSpot assay. Negative and positive controls were carried out by using either medium without stimuli or 1 μg/ml staphylococcal enterotoxins B (SEB). Results are indicated as the number of spots per 2.5 × 10 5 cells/well (spw) and spots per 1000 CD3 + T cells, respectively after substracting the number of spw of the respective negative control. Positive controls showed a positive result for all analysed samples detected as TNTC (too numerous to count, TNTC ≥ 1000 spw). Results are displayed as mean ± SD. Asterisks indicate statistically significant differences between levels of induced cytokine responses (*p < 0.05)

Article Snippet: For stimulation CMV-derived peptide pools CMV pp65 and CMV IE-1, EBV-derived peptide pools EBV EBNA1 and EBV Consensus and AdV-derived peptide pools AdV5 Hexon and AdV5 Penton were used at a final concentration of 1 μg of each peptide/ml peptide pool (Miltenyi Biotec, Bergisch Gladbach, Germany).

Techniques: Isolation, Functional Assay, Virus, Enzyme-linked Immunospot, Negative Control

Effects. of a single continuous and interval exercise on the activation capacity of functional IFN-γ + antigen-specific T cells. Peripheral blood samples of healthy donors (n = 6) were analysed before, 1 h after and 24 h after a single 30 min interval (HIT) using IFN-γ Cytokine Secretion Assay (CSA). Isolated PBMCs were stimulated overnight with a CMV-, b EBV- and c AdV-specific peptide pools (CMV pp65, CMV IE1, EBV EBNA1, EBV Consensus, AdV5 Hexon and AdV5 Penton). Negative control was carried out by using unstimulated PBMCs. The relevant cell fractions before and after enrichment were used for a detailed flow cytometric analysis of IFN-γ + T-cell subsets. Results are shown as fold changes of the frequency of CD3 + /IFN-γ + , CD8 + /IFN-γ + and CD4 + /IFN-γ + cells after subtracting those of the respective negative control. CMV and AdV results are displayed as mean ± SD

Journal: Journal of Translational Medicine

Article Title: High-intensity interval training in allogeneic adoptive T-cell immunotherapy – a big HIT?

doi: 10.1186/s12967-020-02301-3

Figure Lengend Snippet: Effects. of a single continuous and interval exercise on the activation capacity of functional IFN-γ + antigen-specific T cells. Peripheral blood samples of healthy donors (n = 6) were analysed before, 1 h after and 24 h after a single 30 min interval (HIT) using IFN-γ Cytokine Secretion Assay (CSA). Isolated PBMCs were stimulated overnight with a CMV-, b EBV- and c AdV-specific peptide pools (CMV pp65, CMV IE1, EBV EBNA1, EBV Consensus, AdV5 Hexon and AdV5 Penton). Negative control was carried out by using unstimulated PBMCs. The relevant cell fractions before and after enrichment were used for a detailed flow cytometric analysis of IFN-γ + T-cell subsets. Results are shown as fold changes of the frequency of CD3 + /IFN-γ + , CD8 + /IFN-γ + and CD4 + /IFN-γ + cells after subtracting those of the respective negative control. CMV and AdV results are displayed as mean ± SD

Article Snippet: For stimulation CMV-derived peptide pools CMV pp65 and CMV IE-1, EBV-derived peptide pools EBV EBNA1 and EBV Consensus and AdV-derived peptide pools AdV5 Hexon and AdV5 Penton were used at a final concentration of 1 μg of each peptide/ml peptide pool (Miltenyi Biotec, Bergisch Gladbach, Germany).

Techniques: Activation Assay, Functional Assay, Isolation, Negative Control