hFGFR1/hGCGR/hGLP1R

品系全名

C57BL/6JSmo-Fgfr1tm(hFGFR1)Gcgrtm(hGCGR)Glp1rtm2(hGLP1R)Smoc

目录号

NM-XA-250626

品系状态

活体

导出PDF

品系描述

通过hFGFR1(NM-HU-230070)与hGCGR/hGLP1R(NM-HU-233747)小鼠交配获得。

验证数据

image.png

Fig.1 Detection of FGFR1 expression in hFGFR1/hGCGR/hGLP1R mice by WB. FGFR1 was detectable in heart, liver, lung, kidney and gastrocnemius muscle from both WT C57BL/6 and HO/HO/HO hFGFR1/hGCGR/hGLP1R mice , as the antibody was cross-reactive between human and mouse FGFR1. The heart, liver, lung, kidney and gastrocnemius muscle tissue lysates were collected from 10-week-old male wild-type C57BL/6 mice and 10-week-old male homozygous hFGFR1/hGCGR/hGLP1R mice, and then analyzed by western blot with anti-FGFR1 antibody. 

Abbr. HO, homozygous; WT, wild type; PC, positive control, HepG2 cells.

image.png

Fig.2 Detection of GCGR expression in hFGFR1/hGCGR/hGLP1R mice by WB. GCGR was detectable in liver and kidney from both WT C57BL/6 and HO/HO/HO hFGFR1/hGCGR/hGLP1R mice, as the antibody was cross-reactive between human and mouse GCGR. The liver and kidney tissue lysates were collected from 10-week-old male wild-type C57BL/6 mice and 10-week-old male homozygous hFGFR1/hGCGR/hGLP1R mice, and then analyzed by western blot with anti-GCGR antibody. 

Abbr. HO, homozygous; WT, wild type; PC, positive control, HepG2 cells.

image.png

Fig.3 Detection of human GLP-1R expression in hFGFR1/hGCGR/hGLP1R mice by IHC. Human GLP-1R was exclusively detectable in pancreatic islets and neurons located in the hypothalamus and medulla from HO/HO/HO hFGFR1/hGCGR/hGLP1R mice but not in WT mice. Tissues were collected from 10-week-old male WT C57BL/6 mice and 10-week-old male HO/HO/HO hFGFR1/hGCGR/hGLP1R mice, then analyzed by IHC with anti-GLP-1R antibody. Black arrows indicate positive staining (brown). Scale bar: 100 μm. Magnification, 200×.

Abbr. HO, homozygous; WT, wild type.

image.png

Fig.4 Detection of human GLP-1R expression in hFGFR1/hGCGR/hGLP1R mice by IHC. Human GLP-1R was exclusively detectable in the kidney, stomach, and the myenteric plexus of the ileum from HO/HO/HO hFGFR1/hGCGR/hGLP1R mice but not in WT mice. Tissues were collected from 10-week-old male WT C57BL/6 mice and 10-week-old male HO/HO/HO hFGFR1/hGCGR/hGLP1R mice, then analyzed by IHC with anti-GLP-1R antibody. Black arrows indicate positive staining (brown). Scale bar: 100 μm. Magnification, 200×.

Abbr. HO, homozygous; WT, wild type.

image.png

Table 1. Biochemical test of serum from HO/HO/HO hFGFR1/hGCGR/hGLP1R knockin mice without fasting. Values are expressed as mean±SD.

Abbr. HO, homozygous; WT, wild type.

image.png

Table 2. Biochemical test of serum from fasted HO/HO/HO hFGFR1/hGCGR/hGLP1R knockin mice. Values are expressed as mean±SD.

Abbr. HO, homozygous; WT, wild type.


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