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Cyagen Biosciences rag2
Rag2, supplied by Cyagen Biosciences, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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066ATZ reduces tumor growth rate in a xenograft model of NSCLC (A) The growth curves of H1975∗ xenograft tumor in <t>R2G2</t> mice. Data are presented as mean ± SEM ( n = 5). 066ATZ (100 mg/kg) or vehicle was IP injected 5 times a week after the tumors reached ∼150 mm 3 . One animal died in the treatment group on day 39 for an unknown cause when the tumor reached a size of ∼550 mm 3 . All other mice were sacrificed when the tumors reached ∼1,000 mm 3 . On day 24, the average tumor volume was significantly smaller in the treatment group ( p < 0.01). p values were calculated using Student’s t test (two-tailed unpaired t test) with Welch’s correction in GraphPad Prism 10.0 (GraphPad Software, San Diego, CA). (B) The growth curves of H1975∗ xenograft tumor in R2G2 mice after DOX-induced PIP4K2A/2B knockdown. Data are presented as mean ± SEM ( n = 5). When the tumors reached ∼150 mm 3 , DOX was administered to the mice continuously through drinking water (1 mg/mL). Tumor tissues were harvested at the end of the experiment, homogenized, and analyzed by WB (shown below the growth curves). (C) In vitro , neither 066ATZ (20 μM) nor DOX (0.2 μg/mL) affected the growth rate of cultured H1975∗ cells. Data are presented as mean ± SEM ( n = 6). The cell numbers were measured by CellTiter-Glo.
Female Rag2 Il2rg Double Knockout R2g2 Mice, supplied by Inotiv, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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066ATZ reduces tumor growth rate in a xenograft model of NSCLC (A) The growth curves of H1975∗ xenograft tumor in <t>R2G2</t> mice. Data are presented as mean ± SEM ( n = 5). 066ATZ (100 mg/kg) or vehicle was IP injected 5 times a week after the tumors reached ∼150 mm 3 . One animal died in the treatment group on day 39 for an unknown cause when the tumor reached a size of ∼550 mm 3 . All other mice were sacrificed when the tumors reached ∼1,000 mm 3 . On day 24, the average tumor volume was significantly smaller in the treatment group ( p < 0.01). p values were calculated using Student’s t test (two-tailed unpaired t test) with Welch’s correction in GraphPad Prism 10.0 (GraphPad Software, San Diego, CA). (B) The growth curves of H1975∗ xenograft tumor in R2G2 mice after DOX-induced PIP4K2A/2B knockdown. Data are presented as mean ± SEM ( n = 5). When the tumors reached ∼150 mm 3 , DOX was administered to the mice continuously through drinking water (1 mg/mL). Tumor tissues were harvested at the end of the experiment, homogenized, and analyzed by WB (shown below the growth curves). (C) In vitro , neither 066ATZ (20 μM) nor DOX (0.2 μg/mL) affected the growth rate of cultured H1975∗ cells. Data are presented as mean ± SEM ( n = 6). The cell numbers were measured by CellTiter-Glo.
Rag2 Deficient γ Chain, 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
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066ATZ reduces tumor growth rate in a xenograft model of NSCLC (A) The growth curves of H1975∗ xenograft tumor in <t>R2G2</t> mice. Data are presented as mean ± SEM ( n = 5). 066ATZ (100 mg/kg) or vehicle was IP injected 5 times a week after the tumors reached ∼150 mm 3 . One animal died in the treatment group on day 39 for an unknown cause when the tumor reached a size of ∼550 mm 3 . All other mice were sacrificed when the tumors reached ∼1,000 mm 3 . On day 24, the average tumor volume was significantly smaller in the treatment group ( p < 0.01). p values were calculated using Student’s t test (two-tailed unpaired t test) with Welch’s correction in GraphPad Prism 10.0 (GraphPad Software, San Diego, CA). (B) The growth curves of H1975∗ xenograft tumor in R2G2 mice after DOX-induced PIP4K2A/2B knockdown. Data are presented as mean ± SEM ( n = 5). When the tumors reached ∼150 mm 3 , DOX was administered to the mice continuously through drinking water (1 mg/mL). Tumor tissues were harvested at the end of the experiment, homogenized, and analyzed by WB (shown below the growth curves). (C) In vitro , neither 066ATZ (20 μM) nor DOX (0.2 μg/mL) affected the growth rate of cultured H1975∗ cells. Data are presented as mean ± SEM ( n = 6). The cell numbers were measured by CellTiter-Glo.
Female Recipient Rag2, supplied by Janvier Labs, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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066ATZ reduces tumor growth rate in a xenograft model of NSCLC (A) The growth curves of H1975∗ xenograft tumor in <t>R2G2</t> mice. Data are presented as mean ± SEM ( n = 5). 066ATZ (100 mg/kg) or vehicle was IP injected 5 times a week after the tumors reached ∼150 mm 3 . One animal died in the treatment group on day 39 for an unknown cause when the tumor reached a size of ∼550 mm 3 . All other mice were sacrificed when the tumors reached ∼1,000 mm 3 . On day 24, the average tumor volume was significantly smaller in the treatment group ( p < 0.01). p values were calculated using Student’s t test (two-tailed unpaired t test) with Welch’s correction in GraphPad Prism 10.0 (GraphPad Software, San Diego, CA). (B) The growth curves of H1975∗ xenograft tumor in R2G2 mice after DOX-induced PIP4K2A/2B knockdown. Data are presented as mean ± SEM ( n = 5). When the tumors reached ∼150 mm 3 , DOX was administered to the mice continuously through drinking water (1 mg/mL). Tumor tissues were harvested at the end of the experiment, homogenized, and analyzed by WB (shown below the growth curves). (C) In vitro , neither 066ATZ (20 μM) nor DOX (0.2 μg/mL) affected the growth rate of cultured H1975∗ cells. Data are presented as mean ± SEM ( n = 6). The cell numbers were measured by CellTiter-Glo.
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066ATZ reduces tumor growth rate in a xenograft model of NSCLC (A) The growth curves of H1975∗ xenograft tumor in <t>R2G2</t> mice. Data are presented as mean ± SEM ( n = 5). 066ATZ (100 mg/kg) or vehicle was IP injected 5 times a week after the tumors reached ∼150 mm 3 . One animal died in the treatment group on day 39 for an unknown cause when the tumor reached a size of ∼550 mm 3 . All other mice were sacrificed when the tumors reached ∼1,000 mm 3 . On day 24, the average tumor volume was significantly smaller in the treatment group ( p < 0.01). p values were calculated using Student’s t test (two-tailed unpaired t test) with Welch’s correction in GraphPad Prism 10.0 (GraphPad Software, San Diego, CA). (B) The growth curves of H1975∗ xenograft tumor in R2G2 mice after DOX-induced PIP4K2A/2B knockdown. Data are presented as mean ± SEM ( n = 5). When the tumors reached ∼150 mm 3 , DOX was administered to the mice continuously through drinking water (1 mg/mL). Tumor tissues were harvested at the end of the experiment, homogenized, and analyzed by WB (shown below the growth curves). (C) In vitro , neither 066ATZ (20 μM) nor DOX (0.2 μg/mL) affected the growth rate of cultured H1975∗ cells. Data are presented as mean ± SEM ( n = 6). The cell numbers were measured by CellTiter-Glo.
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066ATZ reduces tumor growth rate in a xenograft model of NSCLC (A) The growth curves of H1975∗ xenograft tumor in <t>R2G2</t> mice. Data are presented as mean ± SEM ( n = 5). 066ATZ (100 mg/kg) or vehicle was IP injected 5 times a week after the tumors reached ∼150 mm 3 . One animal died in the treatment group on day 39 for an unknown cause when the tumor reached a size of ∼550 mm 3 . All other mice were sacrificed when the tumors reached ∼1,000 mm 3 . On day 24, the average tumor volume was significantly smaller in the treatment group ( p < 0.01). p values were calculated using Student’s t test (two-tailed unpaired t test) with Welch’s correction in GraphPad Prism 10.0 (GraphPad Software, San Diego, CA). (B) The growth curves of H1975∗ xenograft tumor in R2G2 mice after DOX-induced PIP4K2A/2B knockdown. Data are presented as mean ± SEM ( n = 5). When the tumors reached ∼150 mm 3 , DOX was administered to the mice continuously through drinking water (1 mg/mL). Tumor tissues were harvested at the end of the experiment, homogenized, and analyzed by WB (shown below the growth curves). (C) In vitro , neither 066ATZ (20 μM) nor DOX (0.2 μg/mL) affected the growth rate of cultured H1975∗ cells. Data are presented as mean ± SEM ( n = 6). The cell numbers were measured by CellTiter-Glo.
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Taconic Biosciences common γchain
066ATZ reduces tumor growth rate in a xenograft model of NSCLC (A) The growth curves of H1975∗ xenograft tumor in <t>R2G2</t> mice. Data are presented as mean ± SEM ( n = 5). 066ATZ (100 mg/kg) or vehicle was IP injected 5 times a week after the tumors reached ∼150 mm 3 . One animal died in the treatment group on day 39 for an unknown cause when the tumor reached a size of ∼550 mm 3 . All other mice were sacrificed when the tumors reached ∼1,000 mm 3 . On day 24, the average tumor volume was significantly smaller in the treatment group ( p < 0.01). p values were calculated using Student’s t test (two-tailed unpaired t test) with Welch’s correction in GraphPad Prism 10.0 (GraphPad Software, San Diego, CA). (B) The growth curves of H1975∗ xenograft tumor in R2G2 mice after DOX-induced PIP4K2A/2B knockdown. Data are presented as mean ± SEM ( n = 5). When the tumors reached ∼150 mm 3 , DOX was administered to the mice continuously through drinking water (1 mg/mL). Tumor tissues were harvested at the end of the experiment, homogenized, and analyzed by WB (shown below the growth curves). (C) In vitro , neither 066ATZ (20 μM) nor DOX (0.2 μg/mL) affected the growth rate of cultured H1975∗ cells. Data are presented as mean ± SEM ( n = 6). The cell numbers were measured by CellTiter-Glo.
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Taconic Biosciences rag2
066ATZ reduces tumor growth rate in a xenograft model of NSCLC (A) The growth curves of H1975∗ xenograft tumor in <t>R2G2</t> mice. Data are presented as mean ± SEM ( n = 5). 066ATZ (100 mg/kg) or vehicle was IP injected 5 times a week after the tumors reached ∼150 mm 3 . One animal died in the treatment group on day 39 for an unknown cause when the tumor reached a size of ∼550 mm 3 . All other mice were sacrificed when the tumors reached ∼1,000 mm 3 . On day 24, the average tumor volume was significantly smaller in the treatment group ( p < 0.01). p values were calculated using Student’s t test (two-tailed unpaired t test) with Welch’s correction in GraphPad Prism 10.0 (GraphPad Software, San Diego, CA). (B) The growth curves of H1975∗ xenograft tumor in R2G2 mice after DOX-induced PIP4K2A/2B knockdown. Data are presented as mean ± SEM ( n = 5). When the tumors reached ∼150 mm 3 , DOX was administered to the mice continuously through drinking water (1 mg/mL). Tumor tissues were harvested at the end of the experiment, homogenized, and analyzed by WB (shown below the growth curves). (C) In vitro , neither 066ATZ (20 μM) nor DOX (0.2 μg/mL) affected the growth rate of cultured H1975∗ cells. Data are presented as mean ± SEM ( n = 6). The cell numbers were measured by CellTiter-Glo.
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Image Search Results


066ATZ reduces tumor growth rate in a xenograft model of NSCLC (A) The growth curves of H1975∗ xenograft tumor in R2G2 mice. Data are presented as mean ± SEM ( n = 5). 066ATZ (100 mg/kg) or vehicle was IP injected 5 times a week after the tumors reached ∼150 mm 3 . One animal died in the treatment group on day 39 for an unknown cause when the tumor reached a size of ∼550 mm 3 . All other mice were sacrificed when the tumors reached ∼1,000 mm 3 . On day 24, the average tumor volume was significantly smaller in the treatment group ( p < 0.01). p values were calculated using Student’s t test (two-tailed unpaired t test) with Welch’s correction in GraphPad Prism 10.0 (GraphPad Software, San Diego, CA). (B) The growth curves of H1975∗ xenograft tumor in R2G2 mice after DOX-induced PIP4K2A/2B knockdown. Data are presented as mean ± SEM ( n = 5). When the tumors reached ∼150 mm 3 , DOX was administered to the mice continuously through drinking water (1 mg/mL). Tumor tissues were harvested at the end of the experiment, homogenized, and analyzed by WB (shown below the growth curves). (C) In vitro , neither 066ATZ (20 μM) nor DOX (0.2 μg/mL) affected the growth rate of cultured H1975∗ cells. Data are presented as mean ± SEM ( n = 6). The cell numbers were measured by CellTiter-Glo.

Journal: iScience

Article Title: PIP4K2A/2B inhibitor suppresses tumor growth in a xenograft model of NSCLC

doi: 10.1016/j.isci.2026.115952

Figure Lengend Snippet: 066ATZ reduces tumor growth rate in a xenograft model of NSCLC (A) The growth curves of H1975∗ xenograft tumor in R2G2 mice. Data are presented as mean ± SEM ( n = 5). 066ATZ (100 mg/kg) or vehicle was IP injected 5 times a week after the tumors reached ∼150 mm 3 . One animal died in the treatment group on day 39 for an unknown cause when the tumor reached a size of ∼550 mm 3 . All other mice were sacrificed when the tumors reached ∼1,000 mm 3 . On day 24, the average tumor volume was significantly smaller in the treatment group ( p < 0.01). p values were calculated using Student’s t test (two-tailed unpaired t test) with Welch’s correction in GraphPad Prism 10.0 (GraphPad Software, San Diego, CA). (B) The growth curves of H1975∗ xenograft tumor in R2G2 mice after DOX-induced PIP4K2A/2B knockdown. Data are presented as mean ± SEM ( n = 5). When the tumors reached ∼150 mm 3 , DOX was administered to the mice continuously through drinking water (1 mg/mL). Tumor tissues were harvested at the end of the experiment, homogenized, and analyzed by WB (shown below the growth curves). (C) In vitro , neither 066ATZ (20 μM) nor DOX (0.2 μg/mL) affected the growth rate of cultured H1975∗ cells. Data are presented as mean ± SEM ( n = 6). The cell numbers were measured by CellTiter-Glo.

Article Snippet: Seven-week-old female Rag2/IL2RG double knockout (R2G2) mice were purchased from Envigo and housed under a 12-h light/12-h dark cycle in a temperature- and humidity-controlled facility maintained by the Yale Animal Resources Center (YARC), with ad libitum access to food and water.

Techniques: Injection, Two Tailed Test, Software, Knockdown, In Vitro, Cell Culture