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Adaptive Biotechnologies Corp tcrvb sequencing
Tcrvb Sequencing, supplied by Adaptive Biotechnologies Corp, 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/tcrvb+sequencing/high+throughput+tcr+dna+sequencing+immunoseq/pmc10208956-518-1-19
Average 90 stars, based on 1 article reviews
tcrvb sequencing - by Bioz Stars, 2026-09
90/100 stars

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Article Title: Microbial peptides activate tumour-infiltrating lymphocytes in glioblastoma
Article Snippet: .. The TCRVB sequencing results reported in this paper are available and can be accessed via the immuneACCESS database of Adaptive Biotechnologies ( https://clients.adaptivebiotech.com/pub/naghavian-2023-n ). .. The MS immunopeptidomic raw data have been deposited to the ProteomeXchange Consortium via the PRIDE partner repository with the dataset identifier PXD036811 .



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PTCy eradicates the most xenoreactive clones NSG mice were injected with 2 × 10 7 hPBMC and treated (n = 10) or not (n = 10) with PTCy (100 mg/kg) on day three. Mice were sacrificed on day 21 for harvesting CD4 + and CD8 + T cells from the spleen and lungs. DNA was extracted and <t>TCRVB</t> <t>sequencing</t> analysis was performed. (A) Productive clonality (higher clonality indicates a less diverse repertoire) of CD4 + and CD8 + T cells between the donor (before infusion to mice) and spleen/lungs from control mice. (B) Productive clonality of CD4 + and CD8 + T cells from the spleen and lung between control and PTCy-treated mice. (C) Heatmap of clonotypes overlap between samples calculated by Morista index for CD4 + T cells (left panel) and CD8 + T cells (right panel). (D) Proportion of CD4 + and CD8 + clonotypes upregulated (Up, = xenoreactive clonotypes) and clonotypes downregulated (Down, = bystanders) in control found in PTCy-treated mice. (E) Proportion of CD4 + and CD8 + clonotypes upregulated in spleen/lungs from control vs donor or from treated vs donor. (F) Frequency of CD4 + and CD8 + xenoreactive clonotypes from the spleen/lungs shared between control and PTCy-treated mice. Data show median values with min to max for boxplot. (∗p ≤ 0.05, ∗∗p < 0.01, ∗∗∗p < 0.001, ∗∗∗∗p < 0.0001). See also <xref ref-type=Figure S6 . " width="250" height="auto" />
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PTCy eradicates the most xenoreactive clones NSG mice were injected with 2 × 10 7 hPBMC and treated (n = 10) or not (n = 10) with PTCy (100 mg/kg) on day three. Mice were sacrificed on day 21 for harvesting CD4 + and CD8 + T cells from the spleen and lungs. DNA was extracted and <t>TCRVB</t> <t>sequencing</t> analysis was performed. (A) Productive clonality (higher clonality indicates a less diverse repertoire) of CD4 + and CD8 + T cells between the donor (before infusion to mice) and spleen/lungs from control mice. (B) Productive clonality of CD4 + and CD8 + T cells from the spleen and lung between control and PTCy-treated mice. (C) Heatmap of clonotypes overlap between samples calculated by Morista index for CD4 + T cells (left panel) and CD8 + T cells (right panel). (D) Proportion of CD4 + and CD8 + clonotypes upregulated (Up, = xenoreactive clonotypes) and clonotypes downregulated (Down, = bystanders) in control found in PTCy-treated mice. (E) Proportion of CD4 + and CD8 + clonotypes upregulated in spleen/lungs from control vs donor or from treated vs donor. (F) Frequency of CD4 + and CD8 + xenoreactive clonotypes from the spleen/lungs shared between control and PTCy-treated mice. Data show median values with min to max for boxplot. (∗p ≤ 0.05, ∗∗p < 0.01, ∗∗∗p < 0.001, ∗∗∗∗p < 0.0001). See also <xref ref-type=Figure S6 . " width="250" height="auto" />
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PTCy eradicates the most xenoreactive clones NSG mice were injected with 2 × 10 7 hPBMC and treated (n = 10) or not (n = 10) with PTCy (100 mg/kg) on day three. Mice were sacrificed on day 21 for harvesting CD4 + and CD8 + T cells from the spleen and lungs. DNA was extracted and <t>TCRVB</t> <t>sequencing</t> analysis was performed. (A) Productive clonality (higher clonality indicates a less diverse repertoire) of CD4 + and CD8 + T cells between the donor (before infusion to mice) and spleen/lungs from control mice. (B) Productive clonality of CD4 + and CD8 + T cells from the spleen and lung between control and PTCy-treated mice. (C) Heatmap of clonotypes overlap between samples calculated by Morista index for CD4 + T cells (left panel) and CD8 + T cells (right panel). (D) Proportion of CD4 + and CD8 + clonotypes upregulated (Up, = xenoreactive clonotypes) and clonotypes downregulated (Down, = bystanders) in control found in PTCy-treated mice. (E) Proportion of CD4 + and CD8 + clonotypes upregulated in spleen/lungs from control vs donor or from treated vs donor. (F) Frequency of CD4 + and CD8 + xenoreactive clonotypes from the spleen/lungs shared between control and PTCy-treated mice. Data show median values with min to max for boxplot. (∗p ≤ 0.05, ∗∗p < 0.01, ∗∗∗p < 0.001, ∗∗∗∗p < 0.0001). See also <xref ref-type=Figure S6 . " width="250" height="auto" />
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PTCy eradicates the most xenoreactive clones NSG mice were injected with 2 × 10 7 hPBMC and treated (n = 10) or not (n = 10) with PTCy (100 mg/kg) on day three. Mice were sacrificed on day 21 for harvesting CD4 + and CD8 + T cells from the spleen and lungs. DNA was extracted and <t>TCRVB</t> <t>sequencing</t> analysis was performed. (A) Productive clonality (higher clonality indicates a less diverse repertoire) of CD4 + and CD8 + T cells between the donor (before infusion to mice) and spleen/lungs from control mice. (B) Productive clonality of CD4 + and CD8 + T cells from the spleen and lung between control and PTCy-treated mice. (C) Heatmap of clonotypes overlap between samples calculated by Morista index for CD4 + T cells (left panel) and CD8 + T cells (right panel). (D) Proportion of CD4 + and CD8 + clonotypes upregulated (Up, = xenoreactive clonotypes) and clonotypes downregulated (Down, = bystanders) in control found in PTCy-treated mice. (E) Proportion of CD4 + and CD8 + clonotypes upregulated in spleen/lungs from control vs donor or from treated vs donor. (F) Frequency of CD4 + and CD8 + xenoreactive clonotypes from the spleen/lungs shared between control and PTCy-treated mice. Data show median values with min to max for boxplot. (∗p ≤ 0.05, ∗∗p < 0.01, ∗∗∗p < 0.001, ∗∗∗∗p < 0.0001). See also <xref ref-type=Figure S6 . " width="250" height="auto" />
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PTCy eradicates the most xenoreactive clones NSG mice were injected with 2 × 10 7 hPBMC and treated (n = 10) or not (n = 10) with PTCy (100 mg/kg) on day three. Mice were sacrificed on day 21 for harvesting CD4 + and CD8 + T cells from the spleen and lungs. DNA was extracted and TCRVB sequencing analysis was performed. (A) Productive clonality (higher clonality indicates a less diverse repertoire) of CD4 + and CD8 + T cells between the donor (before infusion to mice) and spleen/lungs from control mice. (B) Productive clonality of CD4 + and CD8 + T cells from the spleen and lung between control and PTCy-treated mice. (C) Heatmap of clonotypes overlap between samples calculated by Morista index for CD4 + T cells (left panel) and CD8 + T cells (right panel). (D) Proportion of CD4 + and CD8 + clonotypes upregulated (Up, = xenoreactive clonotypes) and clonotypes downregulated (Down, = bystanders) in control found in PTCy-treated mice. (E) Proportion of CD4 + and CD8 + clonotypes upregulated in spleen/lungs from control vs donor or from treated vs donor. (F) Frequency of CD4 + and CD8 + xenoreactive clonotypes from the spleen/lungs shared between control and PTCy-treated mice. Data show median values with min to max for boxplot. (∗p ≤ 0.05, ∗∗p < 0.01, ∗∗∗p < 0.001, ∗∗∗∗p < 0.0001). See also <xref ref-type=Figure S6 . " width="100%" height="100%">

Journal: iScience

Article Title: Post-transplant cyclophosphamide prevents xenogeneic graft-versus-host disease while depleting proliferating regulatory T cells

doi: 10.1016/j.isci.2023.106085

Figure Lengend Snippet: PTCy eradicates the most xenoreactive clones NSG mice were injected with 2 × 10 7 hPBMC and treated (n = 10) or not (n = 10) with PTCy (100 mg/kg) on day three. Mice were sacrificed on day 21 for harvesting CD4 + and CD8 + T cells from the spleen and lungs. DNA was extracted and TCRVB sequencing analysis was performed. (A) Productive clonality (higher clonality indicates a less diverse repertoire) of CD4 + and CD8 + T cells between the donor (before infusion to mice) and spleen/lungs from control mice. (B) Productive clonality of CD4 + and CD8 + T cells from the spleen and lung between control and PTCy-treated mice. (C) Heatmap of clonotypes overlap between samples calculated by Morista index for CD4 + T cells (left panel) and CD8 + T cells (right panel). (D) Proportion of CD4 + and CD8 + clonotypes upregulated (Up, = xenoreactive clonotypes) and clonotypes downregulated (Down, = bystanders) in control found in PTCy-treated mice. (E) Proportion of CD4 + and CD8 + clonotypes upregulated in spleen/lungs from control vs donor or from treated vs donor. (F) Frequency of CD4 + and CD8 + xenoreactive clonotypes from the spleen/lungs shared between control and PTCy-treated mice. Data show median values with min to max for boxplot. (∗p ≤ 0.05, ∗∗p < 0.01, ∗∗∗p < 0.001, ∗∗∗∗p < 0.0001). See also Figure S6 .

Article Snippet: One hundred fifty μg from each sample were used for T-cell receptor Vβ (TCRVB) deep sequencing performed by Adaptive Biotechnologies (Seattle, Washington, WA, USA).

Techniques: Clone Assay, Injection, Sequencing, Control

Journal: iScience

Article Title: Post-transplant cyclophosphamide prevents xenogeneic graft-versus-host disease while depleting proliferating regulatory T cells

doi: 10.1016/j.isci.2023.106085

Figure Lengend Snippet:

Article Snippet: One hundred fifty μg from each sample were used for T-cell receptor Vβ (TCRVB) deep sequencing performed by Adaptive Biotechnologies (Seattle, Washington, WA, USA).

Techniques: Staining, Recombinant, Activation Assay, Red Blood Cell Lysis, Cell Isolation, Selection, Flow Cytometry, Luminex, Cell Stimulation, Sequencing, Isolation, Transduction, Luciferase, Expressing, Software, Imaging