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hil 15 nsg mice  (Jackson Laboratory)

 
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    Jackson Laboratory hil 15 nsg mice
    | In vivo assessment of hypoimmunogenic iT cells <t>using</t> <t>an</t> <t>hIL-15-NSG</t> mouse. A , Experimental timeline. Human NK cells (donor #4) were mixed with parental or dKO iT cells at a 1:1 ratio, or with medium alone (control), and co-injected intraperitoneally into hIL-15-NSG mice. B , Bioluminescence imaging was performed at 2, 3, 4, and 7 days post-injection using IVIS. W/O = without; W/ = with. C , Quantification of total bioluminescence at the indicated time points. Relative survival ratios were calculated as the bioluminescence signal of iT cells co-injected with NK cells divided by the signal from iT cells injected without NK cells. P values were determined using a two-tailed, unpaired t -test. Data are mean ± s.d. (n = 4 per group).
    Hil 15 Nsg Mice, supplied by Jackson Laboratory, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/hil+15+nsg+mice/pmc12828601-36-0-8?v=Jackson+Laboratory
    Average 86 stars, based on 1 article reviews
    hil 15 nsg mice - by Bioz Stars, 2026-07
    86/100 stars

    Images

    1) Product Images from "Immune synapse molecules knockout in induced pluripotent stem cells enables broad NK cell resistance in T cell progeny"

    Article Title: Immune synapse molecules knockout in induced pluripotent stem cells enables broad NK cell resistance in T cell progeny

    Journal: Regenerative Therapy

    doi: 10.1016/j.reth.2026.101060

    | In vivo assessment of hypoimmunogenic iT cells using an hIL-15-NSG mouse. A , Experimental timeline. Human NK cells (donor #4) were mixed with parental or dKO iT cells at a 1:1 ratio, or with medium alone (control), and co-injected intraperitoneally into hIL-15-NSG mice. B , Bioluminescence imaging was performed at 2, 3, 4, and 7 days post-injection using IVIS. W/O = without; W/ = with. C , Quantification of total bioluminescence at the indicated time points. Relative survival ratios were calculated as the bioluminescence signal of iT cells co-injected with NK cells divided by the signal from iT cells injected without NK cells. P values were determined using a two-tailed, unpaired t -test. Data are mean ± s.d. (n = 4 per group).
    Figure Legend Snippet: | In vivo assessment of hypoimmunogenic iT cells using an hIL-15-NSG mouse. A , Experimental timeline. Human NK cells (donor #4) were mixed with parental or dKO iT cells at a 1:1 ratio, or with medium alone (control), and co-injected intraperitoneally into hIL-15-NSG mice. B , Bioluminescence imaging was performed at 2, 3, 4, and 7 days post-injection using IVIS. W/O = without; W/ = with. C , Quantification of total bioluminescence at the indicated time points. Relative survival ratios were calculated as the bioluminescence signal of iT cells co-injected with NK cells divided by the signal from iT cells injected without NK cells. P values were determined using a two-tailed, unpaired t -test. Data are mean ± s.d. (n = 4 per group).

    Techniques Used: In Vivo, Control, Injection, Imaging, Two Tailed Test



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    | In vivo assessment of hypoimmunogenic iT cells <t>using</t> <t>an</t> <t>hIL-15-NSG</t> mouse. A , Experimental timeline. Human NK cells (donor #4) were mixed with parental or dKO iT cells at a 1:1 ratio, or with medium alone (control), and co-injected intraperitoneally into hIL-15-NSG mice. B , Bioluminescence imaging was performed at 2, 3, 4, and 7 days post-injection using IVIS. W/O = without; W/ = with. C , Quantification of total bioluminescence at the indicated time points. Relative survival ratios were calculated as the bioluminescence signal of iT cells co-injected with NK cells divided by the signal from iT cells injected without NK cells. P values were determined using a two-tailed, unpaired t -test. Data are mean ± s.d. (n = 4 per group).
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    | In vivo assessment of hypoimmunogenic iT cells <t>using</t> <t>an</t> <t>hIL-15-NSG</t> mouse. A , Experimental timeline. Human NK cells (donor #4) were mixed with parental or dKO iT cells at a 1:1 ratio, or with medium alone (control), and co-injected intraperitoneally into hIL-15-NSG mice. B , Bioluminescence imaging was performed at 2, 3, 4, and 7 days post-injection using IVIS. W/O = without; W/ = with. C , Quantification of total bioluminescence at the indicated time points. Relative survival ratios were calculated as the bioluminescence signal of iT cells co-injected with NK cells divided by the signal from iT cells injected without NK cells. P values were determined using a two-tailed, unpaired t -test. Data are mean ± s.d. (n = 4 per group).
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    | In vivo assessment of hypoimmunogenic iT cells <t>using</t> <t>an</t> <t>hIL-15-NSG</t> mouse. A , Experimental timeline. Human NK cells (donor #4) were mixed with parental or dKO iT cells at a 1:1 ratio, or with medium alone (control), and co-injected intraperitoneally into hIL-15-NSG mice. B , Bioluminescence imaging was performed at 2, 3, 4, and 7 days post-injection using IVIS. W/O = without; W/ = with. C , Quantification of total bioluminescence at the indicated time points. Relative survival ratios were calculated as the bioluminescence signal of iT cells co-injected with NK cells divided by the signal from iT cells injected without NK cells. P values were determined using a two-tailed, unpaired t -test. Data are mean ± s.d. (n = 4 per group).
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    | In vivo assessment of hypoimmunogenic iT cells <t>using</t> <t>an</t> <t>hIL-15-NSG</t> mouse. A , Experimental timeline. Human NK cells (donor #4) were mixed with parental or dKO iT cells at a 1:1 ratio, or with medium alone (control), and co-injected intraperitoneally into hIL-15-NSG mice. B , Bioluminescence imaging was performed at 2, 3, 4, and 7 days post-injection using IVIS. W/O = without; W/ = with. C , Quantification of total bioluminescence at the indicated time points. Relative survival ratios were calculated as the bioluminescence signal of iT cells co-injected with NK cells divided by the signal from iT cells injected without NK cells. P values were determined using a two-tailed, unpaired t -test. Data are mean ± s.d. (n = 4 per group).
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    Image Search Results


    | In vivo assessment of hypoimmunogenic iT cells using an hIL-15-NSG mouse. A , Experimental timeline. Human NK cells (donor #4) were mixed with parental or dKO iT cells at a 1:1 ratio, or with medium alone (control), and co-injected intraperitoneally into hIL-15-NSG mice. B , Bioluminescence imaging was performed at 2, 3, 4, and 7 days post-injection using IVIS. W/O = without; W/ = with. C , Quantification of total bioluminescence at the indicated time points. Relative survival ratios were calculated as the bioluminescence signal of iT cells co-injected with NK cells divided by the signal from iT cells injected without NK cells. P values were determined using a two-tailed, unpaired t -test. Data are mean ± s.d. (n = 4 per group).

    Journal: Regenerative Therapy

    Article Title: Immune synapse molecules knockout in induced pluripotent stem cells enables broad NK cell resistance in T cell progeny

    doi: 10.1016/j.reth.2026.101060

    Figure Lengend Snippet: | In vivo assessment of hypoimmunogenic iT cells using an hIL-15-NSG mouse. A , Experimental timeline. Human NK cells (donor #4) were mixed with parental or dKO iT cells at a 1:1 ratio, or with medium alone (control), and co-injected intraperitoneally into hIL-15-NSG mice. B , Bioluminescence imaging was performed at 2, 3, 4, and 7 days post-injection using IVIS. W/O = without; W/ = with. C , Quantification of total bioluminescence at the indicated time points. Relative survival ratios were calculated as the bioluminescence signal of iT cells co-injected with NK cells divided by the signal from iT cells injected without NK cells. P values were determined using a two-tailed, unpaired t -test. Data are mean ± s.d. (n = 4 per group).

    Article Snippet: hIL-15-NSG mice (NOD.Cg-Prkdc^scid Il2rg^tm1Wjl Tg(IL15)1Sz/SzJ) were obtained from The Jackson Laboratory.

    Techniques: In Vivo, Control, Injection, Imaging, Two Tailed Test