hCB1
品系全名
C57BL/6JSmo-Cnr1tm1(hCB1)Smoc
目录号
NM-HU-225027
品系状态
活体
基因信息
基因名
Cnr1
品系描述
验证数据

Fig1. Detection of CB1 expression in cerebellum by RT-PCR.
Wild type: only one band at 373 bp with primers F1/R1(mCb1);
Homozygous: only one band at 209 bp with primers F2/R2(hCB1);
Abbr. M, DNA marker; HO, homozygous; WT, wild type.

Fig2. Detection of human CB1 expression in Brains, liver and kidney in hCB1 knockin mice by WB.
Abbr. HO, homozygous; WT, wild type.
Note. The anti-human CB1 Antibody cross-reacted with mouse CB1 and humanized CB1.

Fig3. Detection of human CB1 expression in brain (Hippocampus) in hCB1 knockin mice by IF.
Brains were collected from wild-type mice and HO hCB1 mice, and analyzed by IF with anti-human CB1 antibody.
Abbr. HO, homozygous; WT, wild type.
Note. The anti-human CB1 Antibody cross-reacted with mouse CB1 and humanized CB1.

Fig4. Detection of human CB1 expression in CA1 in hCB1 knockin mice by IF.
Brains were collected from wild-type mice and HO hCB1 mice, and analyzed by IF with anti-human CB1 antibody.
Abbr. HO, homozygous; WT, wild type.
Note. The anti-human CB1 Antibody cross-reacted with mouse CB1 and humanized CB1.

Fig5. Detection of human CB1 expression in CA3 in hCB1 knockin mice by IF.
Brains were collected from wild-type mice and HO hCB1 mice, and analyzed by IF with anti-human CB1 antibody.
Abbr. HO, homozygous; WT, wild type.
Note. The anti-human CB1 Antibody cross-reacted with mouse CB1 and humanized CB1.

Fig6. Detection of human CB1 expression in dentate gyrus(DG) in hCB1 knockin mice by IF.
Brains were collected from wild-type mice and HO hCB1 mice, and analyzed by IF with anti-human CB1 antibody.
Abbr. HO, homozygous; WT, wild type.
Note. The anti-human CB1 Antibody cross-reacted with mouse CB1 and humanized CB1.

Fig7. Detection of human CB1 expression in cerebellum in hCB1 knockin mice by IF.
Brains were collected from wild-type mice and HO hCB1 mice, and analyzed by IF with anti-human CB1 antibody.
Abbr. HO, homozygous; WT, wild type.
Note. The anti-human CB1 Antibody cross-reacted with mouse CB1 and humanized CB1.

Fig8. Detection of human CB1 mRNA knockdown in iWAT, pgWAT and BAT by qPCR. 8-week-old, male homozygous hCB1 (HO) mice were assigned to three groups (n=4 per group). Mice in Group 1 received a single subcutaneous injection of vehicle, while mice in Group 2 and 3 were administered a single subcutaneous dose of the test drug, a small nucleic drug from a client. At 28 days post-dosing, the inguinal (iWAT) and perigonadal (pgWAT) white adipose tissue and brown adipose tissue (BAT) were harvested to quantify human CB1 mRNA levels. Data were normalized to mouse Ppia mRNA levels. Results indicated that the baseline expression of hCB1 mRNA was lower in BAT relative to WAT. Notably, high-dose administration of the test drug elicited a significant downregulation (over 50%) of human CB1 mRNA levels especially within the WAT.
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
