hIL23A/hTL1A(3)

品系全名

C57BL/6JSmo-Tnfsf15tm1(hTNFSF15)Il23atm3(hIL23A)Smoc

目录号

NM-XA-241237

品系状态

活体

导出PDF

基因信息

基因名
Il23a

品系描述

通过hIL23A(NM-HU-18030)与hTL1A(3)(NM-HU-233157)小鼠交配获得。

验证数据

40dfdb56-453c-48e3-bbca-65d6431f7c2a.png

Fig.1 In Vivo Efficacy of Risankizumab and Duvakitug combo in TBNS-induced acute colitis in Humanized hIL23A/hTL1A(3) Mouse Model

(A) Body weight change and (B) DAI score in the TBNS-induced acute colitis model of hIL23A/hTL1A(3) mice. In this study, all hIL23A/hTL1A(3) mice were randomly divided into experimental and control cohorts groups on Day -1. The acute colitis model was established in hIL23A/hTL1A(3) mice by a single intrarectal injection of 1.5% TNBS on Day 0. Body weight and DAI score were recorded daily. (n=4-5 males per group, 9-10 weeks old, Mean ± SEM, one-way ANOVA followed by Dunnett's multiple comparison test, *P<0.05, **P<0.01, ***P<0.0001)

f15257c8-253f-4b5a-b507-b77ae7a29f5b.png

Fig.2 In Vivo Efficacy of Risankizumab and Duvakitug combo in TBNS-induced acute colitis in hIL23A/hTL1A(3) Mouse Model.

(A) Colon length. (B) Colon weight. (C)Colon index. On Day 5, all mice were sacrificed, and the isolated colons were subjected to weight, length and photograph. The results demonstrated that, compared with the control group, combo treatment groups exhibited a significant amelioration of TBNS-induced acute colitis in hIL23A/hTL1A(3) mice. (n=4-5 males per group, 9-10 weeks old, Mean ± SEM, one-way ANOVA followed by Dunnett's multiple comparison test, *P<0.05, **P<0.01, ***P<0.001, ****P<0.0001)

0fe740bf-2fb7-4eb4-bfa7-895acaac9201.png

Fig.3 In Vivo Efficacy of Risankizumab and Duvakitug combo in TBNS-induced acute colitis in hIL23A/hTL1A(3) Mouse Model.

Colon photo.  On Day 5, all mice were sacrificed, and the isolated colons were subjected to weight and photograph. The results demonstrated that, compared with the control group, treatment groups exhibited a significant amelioration of TBNS-induced acute colitis in hTL1A mice. (n=4-5 males per group, 9-10 weeks old)


你也可能感兴趣

Tamoxifen诱导Cre-ERT2小鼠 使用指南

Cre-ERT2在无Tamoxifen诱导的情况下,在细胞质内处于无活性状态;当Tamoxifen诱导后,Tamoxifen的代谢产物4-OHT(雌激素类似物)与ERT结合,可使Cre-ERT2进核发挥Cre重组酶活性。

查看

【小鼠大学问】基因工程小鼠的命名规则

常见的基因工程小鼠可以分为两种命名方式,包括基因定点修饰的小鼠命名,比如:敲除、敲入、点突变等等,和随机转基因的小鼠命名。

查看

Cre-lox系统介绍及使用汇总

你一定听说过Cre-lox重组系统,无论你是否直接进行过基因操作。由于Cre-lox系统具有操作简单、重组率高的优点,如今已经成为体内外遗传操作的强有力工具。利用Cre-lox系统,可以在特定细胞、组织或整个生物体,甚至在特定时间点敲除或表达某个基因,实现对特定基因的时空特异性操作,这对基因功能的研究和人类疾病动物模型的建立都具有深刻影响。

查看