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Mabtech Inc elispot plate reader mabtech astortm
Elispot Plate Reader Mabtech Astortm, supplied by Mabtech 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/result/elispot plate reader mabtech astortm/product/Mabtech Inc
Average 90 stars, based on 1 article reviews
elispot plate reader mabtech astortm - by Bioz Stars, 2026-04
90/100 stars

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AID Diagnostika elispot plate reader
HIP CAR T cells do not induce an allogeneic immune response in NZB/W lupus mice (A) One million WT or HIP CAR T cells were intravenously injected into fully allogeneic NZB/W lupus mice and the host immune response was quantified after 6 days. CD8 T cells were recovered from the spleen of these mice, NK cells and macrophages were taken from C57BL/6 mice, and IgM and IgG donor CAR T cell-specific antibodies (DSA) were quantified. (B) <t>Interferon-γ</t> <t>(IFN-γ)</t> <t>ELISpot</t> assays were performed with CD8 lymphocytes isolated from the NZB/W recipients and the injected WT or HIP CAR T cells as stimulators. Spot frequencies were automatically enumerated (5 animals per group, all single animals are shown, mean ± SD, Mann-Whitney test). (C) Impedance cytotoxicity assays with WT and or HIP CAR T cells as targets and isolated CD8 lymphocytes from the lupus mice as effector cells (5 animals per group, mean ± SD per time point). The cell index is normalized at time point zero hours and a drop of the curve indicates target cell killing, while a stable signal indicates target cell survival. Fluctuations in the first few hours reflect cell culture perturbations from the addition of the effector cells. (D) IgM and IgG DSAs were quantified by flow cytometry (5 animals per group, all single animals are shown, mean ± SD, Mann-Whitney test). The background of this assay is shown in a dashed line. (E and F) Impedance cytotoxicity assays with WT or HIP CAR T cells or MHC class I and II-deficient double knockout (DKO) cells as targets and C57BL/6 NK cells (E) or macrophages (Mac; F) as effector cells (5 animals per group, mean ± SD per time point).
Elispot Plate Reader, supplied by AID Diagnostika, 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/result/elispot plate reader/product/AID Diagnostika
Average 90 stars, based on 1 article reviews
elispot plate reader - by Bioz Stars, 2026-04
90/100 stars
  Buy from Supplier

90
Cellular Technology Ltd elispot plate reader
HIP CAR T cells do not induce an allogeneic immune response in NZB/W lupus mice (A) One million WT or HIP CAR T cells were intravenously injected into fully allogeneic NZB/W lupus mice and the host immune response was quantified after 6 days. CD8 T cells were recovered from the spleen of these mice, NK cells and macrophages were taken from C57BL/6 mice, and IgM and IgG donor CAR T cell-specific antibodies (DSA) were quantified. (B) <t>Interferon-γ</t> <t>(IFN-γ)</t> <t>ELISpot</t> assays were performed with CD8 lymphocytes isolated from the NZB/W recipients and the injected WT or HIP CAR T cells as stimulators. Spot frequencies were automatically enumerated (5 animals per group, all single animals are shown, mean ± SD, Mann-Whitney test). (C) Impedance cytotoxicity assays with WT and or HIP CAR T cells as targets and isolated CD8 lymphocytes from the lupus mice as effector cells (5 animals per group, mean ± SD per time point). The cell index is normalized at time point zero hours and a drop of the curve indicates target cell killing, while a stable signal indicates target cell survival. Fluctuations in the first few hours reflect cell culture perturbations from the addition of the effector cells. (D) IgM and IgG DSAs were quantified by flow cytometry (5 animals per group, all single animals are shown, mean ± SD, Mann-Whitney test). The background of this assay is shown in a dashed line. (E and F) Impedance cytotoxicity assays with WT or HIP CAR T cells or MHC class I and II-deficient double knockout (DKO) cells as targets and C57BL/6 NK cells (E) or macrophages (Mac; F) as effector cells (5 animals per group, mean ± SD per time point).
Elispot Plate Reader, supplied by Cellular Technology Ltd, 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/result/elispot plate reader/product/Cellular Technology Ltd
Average 90 stars, based on 1 article reviews
elispot plate reader - by Bioz Stars, 2026-04
90/100 stars
  Buy from Supplier

90
Mabtech Inc elispot plate reader mabtech astortm
HIP CAR T cells do not induce an allogeneic immune response in NZB/W lupus mice (A) One million WT or HIP CAR T cells were intravenously injected into fully allogeneic NZB/W lupus mice and the host immune response was quantified after 6 days. CD8 T cells were recovered from the spleen of these mice, NK cells and macrophages were taken from C57BL/6 mice, and IgM and IgG donor CAR T cell-specific antibodies (DSA) were quantified. (B) <t>Interferon-γ</t> <t>(IFN-γ)</t> <t>ELISpot</t> assays were performed with CD8 lymphocytes isolated from the NZB/W recipients and the injected WT or HIP CAR T cells as stimulators. Spot frequencies were automatically enumerated (5 animals per group, all single animals are shown, mean ± SD, Mann-Whitney test). (C) Impedance cytotoxicity assays with WT and or HIP CAR T cells as targets and isolated CD8 lymphocytes from the lupus mice as effector cells (5 animals per group, mean ± SD per time point). The cell index is normalized at time point zero hours and a drop of the curve indicates target cell killing, while a stable signal indicates target cell survival. Fluctuations in the first few hours reflect cell culture perturbations from the addition of the effector cells. (D) IgM and IgG DSAs were quantified by flow cytometry (5 animals per group, all single animals are shown, mean ± SD, Mann-Whitney test). The background of this assay is shown in a dashed line. (E and F) Impedance cytotoxicity assays with WT or HIP CAR T cells or MHC class I and II-deficient double knockout (DKO) cells as targets and C57BL/6 NK cells (E) or macrophages (Mac; F) as effector cells (5 animals per group, mean ± SD per time point).
Elispot Plate Reader Mabtech Astortm, supplied by Mabtech 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/result/elispot plate reader mabtech astortm/product/Mabtech Inc
Average 90 stars, based on 1 article reviews
elispot plate reader mabtech astortm - by Bioz Stars, 2026-04
90/100 stars
  Buy from Supplier

90
Cellular Technology Ltd automated elispot plate reader
HIP CAR T cells do not induce an allogeneic immune response in NZB/W lupus mice (A) One million WT or HIP CAR T cells were intravenously injected into fully allogeneic NZB/W lupus mice and the host immune response was quantified after 6 days. CD8 T cells were recovered from the spleen of these mice, NK cells and macrophages were taken from C57BL/6 mice, and IgM and IgG donor CAR T cell-specific antibodies (DSA) were quantified. (B) <t>Interferon-γ</t> <t>(IFN-γ)</t> <t>ELISpot</t> assays were performed with CD8 lymphocytes isolated from the NZB/W recipients and the injected WT or HIP CAR T cells as stimulators. Spot frequencies were automatically enumerated (5 animals per group, all single animals are shown, mean ± SD, Mann-Whitney test). (C) Impedance cytotoxicity assays with WT and or HIP CAR T cells as targets and isolated CD8 lymphocytes from the lupus mice as effector cells (5 animals per group, mean ± SD per time point). The cell index is normalized at time point zero hours and a drop of the curve indicates target cell killing, while a stable signal indicates target cell survival. Fluctuations in the first few hours reflect cell culture perturbations from the addition of the effector cells. (D) IgM and IgG DSAs were quantified by flow cytometry (5 animals per group, all single animals are shown, mean ± SD, Mann-Whitney test). The background of this assay is shown in a dashed line. (E and F) Impedance cytotoxicity assays with WT or HIP CAR T cells or MHC class I and II-deficient double knockout (DKO) cells as targets and C57BL/6 NK cells (E) or macrophages (Mac; F) as effector cells (5 animals per group, mean ± SD per time point).
Automated Elispot Plate Reader, supplied by Cellular Technology Ltd, 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/result/automated elispot plate reader/product/Cellular Technology Ltd
Average 90 stars, based on 1 article reviews
automated elispot plate reader - by Bioz Stars, 2026-04
90/100 stars
  Buy from Supplier

90
AID Diagnostika elispot plate reader ispot spectrum system
HIP CAR T cells do not induce an allogeneic immune response in NZB/W lupus mice (A) One million WT or HIP CAR T cells were intravenously injected into fully allogeneic NZB/W lupus mice and the host immune response was quantified after 6 days. CD8 T cells were recovered from the spleen of these mice, NK cells and macrophages were taken from C57BL/6 mice, and IgM and IgG donor CAR T cell-specific antibodies (DSA) were quantified. (B) <t>Interferon-γ</t> <t>(IFN-γ)</t> <t>ELISpot</t> assays were performed with CD8 lymphocytes isolated from the NZB/W recipients and the injected WT or HIP CAR T cells as stimulators. Spot frequencies were automatically enumerated (5 animals per group, all single animals are shown, mean ± SD, Mann-Whitney test). (C) Impedance cytotoxicity assays with WT and or HIP CAR T cells as targets and isolated CD8 lymphocytes from the lupus mice as effector cells (5 animals per group, mean ± SD per time point). The cell index is normalized at time point zero hours and a drop of the curve indicates target cell killing, while a stable signal indicates target cell survival. Fluctuations in the first few hours reflect cell culture perturbations from the addition of the effector cells. (D) IgM and IgG DSAs were quantified by flow cytometry (5 animals per group, all single animals are shown, mean ± SD, Mann-Whitney test). The background of this assay is shown in a dashed line. (E and F) Impedance cytotoxicity assays with WT or HIP CAR T cells or MHC class I and II-deficient double knockout (DKO) cells as targets and C57BL/6 NK cells (E) or macrophages (Mac; F) as effector cells (5 animals per group, mean ± SD per time point).
Elispot Plate Reader Ispot Spectrum System, supplied by AID Diagnostika, 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/result/elispot plate reader ispot spectrum system/product/AID Diagnostika
Average 90 stars, based on 1 article reviews
elispot plate reader ispot spectrum system - by Bioz Stars, 2026-04
90/100 stars
  Buy from Supplier

90
AID Diagnostika elispot plate reader aid elispot reader-ispot
HIP CAR T cells do not induce an allogeneic immune response in NZB/W lupus mice (A) One million WT or HIP CAR T cells were intravenously injected into fully allogeneic NZB/W lupus mice and the host immune response was quantified after 6 days. CD8 T cells were recovered from the spleen of these mice, NK cells and macrophages were taken from C57BL/6 mice, and IgM and IgG donor CAR T cell-specific antibodies (DSA) were quantified. (B) <t>Interferon-γ</t> <t>(IFN-γ)</t> <t>ELISpot</t> assays were performed with CD8 lymphocytes isolated from the NZB/W recipients and the injected WT or HIP CAR T cells as stimulators. Spot frequencies were automatically enumerated (5 animals per group, all single animals are shown, mean ± SD, Mann-Whitney test). (C) Impedance cytotoxicity assays with WT and or HIP CAR T cells as targets and isolated CD8 lymphocytes from the lupus mice as effector cells (5 animals per group, mean ± SD per time point). The cell index is normalized at time point zero hours and a drop of the curve indicates target cell killing, while a stable signal indicates target cell survival. Fluctuations in the first few hours reflect cell culture perturbations from the addition of the effector cells. (D) IgM and IgG DSAs were quantified by flow cytometry (5 animals per group, all single animals are shown, mean ± SD, Mann-Whitney test). The background of this assay is shown in a dashed line. (E and F) Impedance cytotoxicity assays with WT or HIP CAR T cells or MHC class I and II-deficient double knockout (DKO) cells as targets and C57BL/6 NK cells (E) or macrophages (Mac; F) as effector cells (5 animals per group, mean ± SD per time point).
Elispot Plate Reader Aid Elispot Reader Ispot, supplied by AID Diagnostika, 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/result/elispot plate reader aid elispot reader-ispot/product/AID Diagnostika
Average 90 stars, based on 1 article reviews
elispot plate reader aid elispot reader-ispot - by Bioz Stars, 2026-04
90/100 stars
  Buy from Supplier

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HIP CAR T cells do not induce an allogeneic immune response in NZB/W lupus mice (A) One million WT or HIP CAR T cells were intravenously injected into fully allogeneic NZB/W lupus mice and the host immune response was quantified after 6 days. CD8 T cells were recovered from the spleen of these mice, NK cells and macrophages were taken from C57BL/6 mice, and IgM and IgG donor CAR T cell-specific antibodies (DSA) were quantified. (B) Interferon-γ (IFN-γ) ELISpot assays were performed with CD8 lymphocytes isolated from the NZB/W recipients and the injected WT or HIP CAR T cells as stimulators. Spot frequencies were automatically enumerated (5 animals per group, all single animals are shown, mean ± SD, Mann-Whitney test). (C) Impedance cytotoxicity assays with WT and or HIP CAR T cells as targets and isolated CD8 lymphocytes from the lupus mice as effector cells (5 animals per group, mean ± SD per time point). The cell index is normalized at time point zero hours and a drop of the curve indicates target cell killing, while a stable signal indicates target cell survival. Fluctuations in the first few hours reflect cell culture perturbations from the addition of the effector cells. (D) IgM and IgG DSAs were quantified by flow cytometry (5 animals per group, all single animals are shown, mean ± SD, Mann-Whitney test). The background of this assay is shown in a dashed line. (E and F) Impedance cytotoxicity assays with WT or HIP CAR T cells or MHC class I and II-deficient double knockout (DKO) cells as targets and C57BL/6 NK cells (E) or macrophages (Mac; F) as effector cells (5 animals per group, mean ± SD per time point).

Journal: iScience

Article Title: Hypoimmune CD19 CAR T cells treat allogeneic mice with features of spontaneous systemic lupus erythematosus

doi: 10.1016/j.isci.2025.112806

Figure Lengend Snippet: HIP CAR T cells do not induce an allogeneic immune response in NZB/W lupus mice (A) One million WT or HIP CAR T cells were intravenously injected into fully allogeneic NZB/W lupus mice and the host immune response was quantified after 6 days. CD8 T cells were recovered from the spleen of these mice, NK cells and macrophages were taken from C57BL/6 mice, and IgM and IgG donor CAR T cell-specific antibodies (DSA) were quantified. (B) Interferon-γ (IFN-γ) ELISpot assays were performed with CD8 lymphocytes isolated from the NZB/W recipients and the injected WT or HIP CAR T cells as stimulators. Spot frequencies were automatically enumerated (5 animals per group, all single animals are shown, mean ± SD, Mann-Whitney test). (C) Impedance cytotoxicity assays with WT and or HIP CAR T cells as targets and isolated CD8 lymphocytes from the lupus mice as effector cells (5 animals per group, mean ± SD per time point). The cell index is normalized at time point zero hours and a drop of the curve indicates target cell killing, while a stable signal indicates target cell survival. Fluctuations in the first few hours reflect cell culture perturbations from the addition of the effector cells. (D) IgM and IgG DSAs were quantified by flow cytometry (5 animals per group, all single animals are shown, mean ± SD, Mann-Whitney test). The background of this assay is shown in a dashed line. (E and F) Impedance cytotoxicity assays with WT or HIP CAR T cells or MHC class I and II-deficient double knockout (DKO) cells as targets and C57BL/6 NK cells (E) or macrophages (Mac; F) as effector cells (5 animals per group, mean ± SD per time point).

Article Snippet: One hundred thousand stimulator cells were incubated with one million recipient responder splenocytes for 24 h and IFN-γ spot frequencies were enumerated using an Elispot plate reader (AID Diagnostika GmbH, Strassburg, Germany).

Techniques: Injection, Enzyme-linked Immunospot, Isolation, MANN-WHITNEY, Cell Culture, Flow Cytometry, Double Knockout