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Il 2, supplied by MedChemExpress, used in various techniques. Bioz Stars score: 95/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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(A) Schematic representation of B cell lymphopoiesis and markers that define stages of B cell development. (B, C) Representative contour plots (B) and frequency (C) of bone marrow B220 + CD19 - CD43 + CD93 + cells in C57BL/6 mice with IC injection of PBS or E0771 cells at day 17. (D, E) Representative contour plots (D) and frequency (E) of bone marrow B220 + CD19 + CD43 + CD93 + IgM - pro-B/large pre-B cells in mice described in (B). (F-I) Representative contour plots (F) and frequency of bone marrow B220 + CD19 + CD43 - IgM - IgD - small pre-B cells (G), B220 + CD19 + CD43 - IgM + IgD - immature B cells (H), and B220 + CD19 + CD43 - IgM + IgD + mature B cells (I) in mice described in (B). (J-O) Absolute numbers of B220 + CD19 + B cells (J) and frequency of bone marrow B cell subsets (K-O) in C57BL/6 mice with IC injection of PBS or E0771 cells at day 7. (P, Q) Representative pictures (P) of colony formation unit (CFU) assay of pre-B cells and quantification of CFUs (Q) from bone marrow of mice described in (B). (R) Frequency of bone marrow B cell subsets from bone marrow of mice described in (B) cultured <t>with</t> <t>IL-7</t> for 3 days, relative to day 0. Statistical analysis was performed using unpaired two-tailed Student’s t test (C, E, G-O, Q, R). Data are represented as means ± SEM. Each dot represents a mouse in (C, E, G-O, Q, R). ∗p ≤ 0.05, ∗∗p ≤ 0.01, ∗∗∗p ≤ 0.001, ∗∗∗∗p ≤ 0.0001.
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(A) Schematic representation of B cell lymphopoiesis and markers that define stages of B cell development. (B, C) Representative contour plots (B) and frequency (C) of bone marrow B220 + CD19 - CD43 + CD93 + cells in C57BL/6 mice with IC injection of PBS or E0771 cells at day 17. (D, E) Representative contour plots (D) and frequency (E) of bone marrow B220 + CD19 + CD43 + CD93 + IgM - pro-B/large pre-B cells in mice described in (B). (F-I) Representative contour plots (F) and frequency of bone marrow B220 + CD19 + CD43 - IgM - IgD - small pre-B cells (G), B220 + CD19 + CD43 - IgM + IgD - immature B cells (H), and B220 + CD19 + CD43 - IgM + IgD + mature B cells (I) in mice described in (B). (J-O) Absolute numbers of B220 + CD19 + B cells (J) and frequency of bone marrow B cell subsets (K-O) in C57BL/6 mice with IC injection of PBS or E0771 cells at day 7. (P, Q) Representative pictures (P) of colony formation unit (CFU) assay of pre-B cells and quantification of CFUs (Q) from bone marrow of mice described in (B). (R) Frequency of bone marrow B cell subsets from bone marrow of mice described in (B) cultured <t>with</t> <t>IL-7</t> for 3 days, relative to day 0. Statistical analysis was performed using unpaired two-tailed Student’s t test (C, E, G-O, Q, R). Data are represented as means ± SEM. Each dot represents a mouse in (C, E, G-O, Q, R). ∗p ≤ 0.05, ∗∗p ≤ 0.01, ∗∗∗p ≤ 0.001, ∗∗∗∗p ≤ 0.0001.
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Mabtech Inc elispot plus mouse il 2 hrp
Cellular immune responses elicited by H5 Texas Mut mRNA-LNP (SM102) in mice (A–C) The number of splenocytes secreting IFN-γ (a), TNF-α (b), <t>and</t> <t>IL-2</t> (c) was detected by ELISpot. (D–F) The percentage of CD4 + T cells secreting IFN-γ (D), TNF-α (E), and IL-2 (F) was quantified by flow cytometry. (G–I) The percentage of CD8 + T cells secreting IFN-γ (G), TNF-α (H), and IL-2 (I) was quantified by flow cytometry. (J) IgG1 and IgG2a subclass Abs against Texas HA were determined, and the ratio of IgG2a/IgG1 was calculated. Data are presented as the mean ± SD, and n = 8 biological replicates for each group (A–J). p values are analyzed with t test (ns p > 0.05, ∗ p < 0.05, ∗∗∗ p < 0.001) (A–J).
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R&D Systems mouse anti hil2
Cellular immune responses elicited by H5 Texas Mut mRNA-LNP (SM102) in mice (A–C) The number of splenocytes secreting IFN-γ (a), TNF-α (b), <t>and</t> <t>IL-2</t> (c) was detected by ELISpot. (D–F) The percentage of CD4 + T cells secreting IFN-γ (D), TNF-α (E), and IL-2 (F) was quantified by flow cytometry. (G–I) The percentage of CD8 + T cells secreting IFN-γ (G), TNF-α (H), and IL-2 (I) was quantified by flow cytometry. (J) IgG1 and IgG2a subclass Abs against Texas HA were determined, and the ratio of IgG2a/IgG1 was calculated. Data are presented as the mean ± SD, and n = 8 biological replicates for each group (A–J). p values are analyzed with t test (ns p > 0.05, ∗ p < 0.05, ∗∗∗ p < 0.001) (A–J).
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Cellular immune responses elicited by H5 Texas Mut mRNA-LNP (SM102) in mice (A–C) The number of splenocytes secreting IFN-γ (a), TNF-α (b), <t>and</t> <t>IL-2</t> (c) was detected by ELISpot. (D–F) The percentage of CD4 + T cells secreting IFN-γ (D), TNF-α (E), and IL-2 (F) was quantified by flow cytometry. (G–I) The percentage of CD8 + T cells secreting IFN-γ (G), TNF-α (H), and IL-2 (I) was quantified by flow cytometry. (J) IgG1 and IgG2a subclass Abs against Texas HA were determined, and the ratio of IgG2a/IgG1 was calculated. Data are presented as the mean ± SD, and n = 8 biological replicates for each group (A–J). p values are analyzed with t test (ns p > 0.05, ∗ p < 0.05, ∗∗∗ p < 0.001) (A–J).
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Image Search Results


(A) Schematic representation of B cell lymphopoiesis and markers that define stages of B cell development. (B, C) Representative contour plots (B) and frequency (C) of bone marrow B220 + CD19 - CD43 + CD93 + cells in C57BL/6 mice with IC injection of PBS or E0771 cells at day 17. (D, E) Representative contour plots (D) and frequency (E) of bone marrow B220 + CD19 + CD43 + CD93 + IgM - pro-B/large pre-B cells in mice described in (B). (F-I) Representative contour plots (F) and frequency of bone marrow B220 + CD19 + CD43 - IgM - IgD - small pre-B cells (G), B220 + CD19 + CD43 - IgM + IgD - immature B cells (H), and B220 + CD19 + CD43 - IgM + IgD + mature B cells (I) in mice described in (B). (J-O) Absolute numbers of B220 + CD19 + B cells (J) and frequency of bone marrow B cell subsets (K-O) in C57BL/6 mice with IC injection of PBS or E0771 cells at day 7. (P, Q) Representative pictures (P) of colony formation unit (CFU) assay of pre-B cells and quantification of CFUs (Q) from bone marrow of mice described in (B). (R) Frequency of bone marrow B cell subsets from bone marrow of mice described in (B) cultured with IL-7 for 3 days, relative to day 0. Statistical analysis was performed using unpaired two-tailed Student’s t test (C, E, G-O, Q, R). Data are represented as means ± SEM. Each dot represents a mouse in (C, E, G-O, Q, R). ∗p ≤ 0.05, ∗∗p ≤ 0.01, ∗∗∗p ≤ 0.001, ∗∗∗∗p ≤ 0.0001.

Journal: bioRxiv

Article Title: Bone marrow B cell collapse promotes bone metastasis in breast cancer

doi: 10.64898/2026.04.21.720007

Figure Lengend Snippet: (A) Schematic representation of B cell lymphopoiesis and markers that define stages of B cell development. (B, C) Representative contour plots (B) and frequency (C) of bone marrow B220 + CD19 - CD43 + CD93 + cells in C57BL/6 mice with IC injection of PBS or E0771 cells at day 17. (D, E) Representative contour plots (D) and frequency (E) of bone marrow B220 + CD19 + CD43 + CD93 + IgM - pro-B/large pre-B cells in mice described in (B). (F-I) Representative contour plots (F) and frequency of bone marrow B220 + CD19 + CD43 - IgM - IgD - small pre-B cells (G), B220 + CD19 + CD43 - IgM + IgD - immature B cells (H), and B220 + CD19 + CD43 - IgM + IgD + mature B cells (I) in mice described in (B). (J-O) Absolute numbers of B220 + CD19 + B cells (J) and frequency of bone marrow B cell subsets (K-O) in C57BL/6 mice with IC injection of PBS or E0771 cells at day 7. (P, Q) Representative pictures (P) of colony formation unit (CFU) assay of pre-B cells and quantification of CFUs (Q) from bone marrow of mice described in (B). (R) Frequency of bone marrow B cell subsets from bone marrow of mice described in (B) cultured with IL-7 for 3 days, relative to day 0. Statistical analysis was performed using unpaired two-tailed Student’s t test (C, E, G-O, Q, R). Data are represented as means ± SEM. Each dot represents a mouse in (C, E, G-O, Q, R). ∗p ≤ 0.05, ∗∗p ≤ 0.01, ∗∗∗p ≤ 0.001, ∗∗∗∗p ≤ 0.0001.

Article Snippet: 7.5 x 10 5 cells/ml were cultured in IMDM media containing Glutamax (Gibco, 31980030) supplemented with 10% FBS, 1 × P/S and 5μM 2-Mercaptoethanol, and 10 ng/ml of recombinant mouse IL-7 (Invitrogen, RP-8664) in a humidified incubator at 37 °C and 5% CO 2 .

Techniques: Injection, Colony-forming Unit Assay, Cell Culture, Two Tailed Test

Cellular immune responses elicited by H5 Texas Mut mRNA-LNP (SM102) in mice (A–C) The number of splenocytes secreting IFN-γ (a), TNF-α (b), and IL-2 (c) was detected by ELISpot. (D–F) The percentage of CD4 + T cells secreting IFN-γ (D), TNF-α (E), and IL-2 (F) was quantified by flow cytometry. (G–I) The percentage of CD8 + T cells secreting IFN-γ (G), TNF-α (H), and IL-2 (I) was quantified by flow cytometry. (J) IgG1 and IgG2a subclass Abs against Texas HA were determined, and the ratio of IgG2a/IgG1 was calculated. Data are presented as the mean ± SD, and n = 8 biological replicates for each group (A–J). p values are analyzed with t test (ns p > 0.05, ∗ p < 0.05, ∗∗∗ p < 0.001) (A–J).

Journal: Cell Reports Medicine

Article Title: Preclinical evaluation of an mRNA vaccine developed from the first human isolate of bovine H5N1

doi: 10.1016/j.xcrm.2026.102702

Figure Lengend Snippet: Cellular immune responses elicited by H5 Texas Mut mRNA-LNP (SM102) in mice (A–C) The number of splenocytes secreting IFN-γ (a), TNF-α (b), and IL-2 (c) was detected by ELISpot. (D–F) The percentage of CD4 + T cells secreting IFN-γ (D), TNF-α (E), and IL-2 (F) was quantified by flow cytometry. (G–I) The percentage of CD8 + T cells secreting IFN-γ (G), TNF-α (H), and IL-2 (I) was quantified by flow cytometry. (J) IgG1 and IgG2a subclass Abs against Texas HA were determined, and the ratio of IgG2a/IgG1 was calculated. Data are presented as the mean ± SD, and n = 8 biological replicates for each group (A–J). p values are analyzed with t test (ns p > 0.05, ∗ p < 0.05, ∗∗∗ p < 0.001) (A–J).

Article Snippet: ELISpot Plus: Mouse IL-2 (HRP) , MabTech , 3441-4HPW-2.

Techniques: Enzyme-linked Immunospot, Flow Cytometry