hFCRN(2)

品系全名

C57BL/6Smoc-Fcgrttm2(hFCGRT)Smoc

目录号

NM-HU-190070

品系状态

活体

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基因信息

基因名
Fcgrt

品系描述

通过同源重组,将小鼠基因Fcgrt(FcRn)进行人源化修饰。与此相似的品系还有hFCRN(NM-HU-00109)、hFCRN(NM-HU-2000032),详细信息请咨询技术顾问。
应用领域:免疫治疗;肿瘤研究;药物筛选

验证数据

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Fig1. Validation of hFCGRT and mFCGRT expression in humanized Fcgrt mice by WB. These results showed that hFCGRT can be expressed in the liver and kidney of humanized Fcgrt homozygous and heterozygous mice,while mFCGRT can not be expressed in the humanized Fcgrt homozygous mice.

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Fig2. Detection of FCRN expression in hFCRN(2) mice by WB. The spleen, large intestine and small intestine tissue lysates were collected from 12-week-old female wild-type C57BL/6 mice and 12-week-old female homozygous hFCRN(2) mice, and then analyzed by western blot with anti-FCRN antibody. FCRN was detectable in spleen, large intestine from both WT C57BL/6 and HO hFCRN(2) mice. 

Abbr. HO, homozygous; WT, wild type.

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Fig3. Blood concentration curves of Keytruda in C57BL/6 and hFcRn KI mice. (n=3/time point/group)

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Fig4. Blood concentration curves of Cyramza(A) and Keytruda(B) in C57BL/6, hFcRn KI and Fcgrt-KO mice.(n=3/time point/group)

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Fig5. In vivo PK profiles of TAA scfv-anti HSA VHH in hALB/hFCRN mice(NM-HU-200278) (female, 10-12weeks, n=3 mice/timepoint), which were generated by crossing hFCRN(NM-HU-190070) with hALB(NM-HU-200003). (In cooperation with the third party).

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Fig6. Blood concentration curves of test articles in C57BL/6 and hFcRn/hALB dKI mice(NM-HU-200278), which were generated by crossing hFCRN(NM-HU-190070) with hALB(NM-HU-200003).(In cooperation with the third party)

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Fig7. Pharmacokinetic analysis of IBI112 in HO hFcRn mice. (A) Body weight. (B) Pharmacokinetic analysis parameters. On Day 0, WT C57BL/6 and Hom hFcRn mice were intravenously injected via the tail vein with IBI112 (hIgG1 Fc) and the YTE-modified IBI112 antibody (5 mg/kg), respectively. Blood was drawn at the indicated times, and serum was obtained for pharmacokinetic analysis (n=3 females, 8-10 weeks old). The results showed that, although a prolonged half-life of the YTE-modified IBI112 antibody in Hom hFcRn mice compared to WT C57BL/6 mice, the difference was not statistically significant due to large within-group variation. Data are shown as mean ± SEM.



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