The largest database of trusted experimental protocols

Tgfbr2fl fl mice

Manufactured by Jackson ImmunoResearch
Sourced in United States

The Tgfbr2fl/fl mice are genetically modified mice with a floxed Tgfbr2 gene. The Tgfbr2 gene encodes the transforming growth factor-beta receptor type II, which plays a critical role in various cellular processes. This mouse model allows for the conditional deletion of the Tgfbr2 gene in specific cell types or tissues, enabling researchers to study the functional consequences of Tgfbr2 deficiency.

Automatically generated - may contain errors

3 protocols using tgfbr2fl fl mice

1

Genetic Manipulation of Murine Immune Cells

Check if the same lab product or an alternative is used in the 5 most similar protocols
All mouse strains were bred and housed in specific pathogen-free conditions in accordance with the Institutional Animal Care and Use Guidelines of the University of California, San Diego (UCSD) at a temperature between 18 °C and 23 °C with 40–60% humidity. Male and female mice were both used in the present study. All mice used were on a C57BL/6J background. P14, Tgfbr2fl/fl mice (stock no. 012603, Jackson Laboratory), R26Cre-ERT2 (stock no. 008463, Jackson Laboratory), Thy1.1 and CD45.1 congenic mice were bred in house. Prdm1fl/fl (stock no. 008100, Jackson Laboratory) and Gzmb-cre (stock no. 003734, Jackson Laboratory) spleens were a gift from the laboratory of S. Kaech. To delete floxed alleles using Cre-ERT2, we administered 1 mg of tamoxifen (Cayman Chemical Company) emulsified in 100 μl of sunflower seed oil (Sigma-Aldrich) via daily intraperitoneal injections on days 14–18 of infection. All animal studies were approved by the Institutional Animal Care and Use Committees of UCSD and performed in accordance with UC guidelines.
+ Open protocol
+ Expand
2

Granulosa Cell-Specific Tgfbr2 Knockout Mice

Check if the same lab product or an alternative is used in the 5 most similar protocols
WT C57/BL6 female mice and ICR (CD1) female mice were purchased from the Laboratory Animal Center of the Institute of Genetics and Developmental Biology (Beijing, China). Tgfbr2fl/fl mice (stock number 012603) were purchased from The Jackson Laboratory (Bar Harbor, ME, USA). Mice with granulosa cell-specific knockout of Tgfbr2 (Tgfbr2gc−/−) were generated by crossing Tgfbr2fl/fl mice with previously reported Fshr-Cre mice51 (link),52 (link). Female mice (21–23 days old) were injected with 5 IU of eCG 48 h before use to stimulate follicle development. In some experiments, the female mice were treated with 5 IU eCG followed by 5 IU hCG to stimulate ovulation. All animal procedures were approved by the Institutional Animal Care and Use Committee of China Agricultural University and maintained according to the Guide for the Care and Use of Laboratory Animals (Institute for Learning and Animal Research at China Agricultural University). The reagents used in this study, unless otherwise stated, were purchased from Sigma-Aldrich (St. Louis, MO, USA).
+ Open protocol
+ Expand
3

Conditional Transgenic Mouse Models

Check if the same lab product or an alternative is used in the 5 most similar protocols
DptIresCreERT2 mice10 (link) and Lrrc15DTRGFP mice were designed, generated and bred at Genentech. Tgfbr2fl/fl mice (012603) were obtained from the Jackson Laboratory. Age- and sex-matched mice (6–12 weeks old) were used for all studies. Mice were maintained under specific pathogen-free conditions using the guidelines of the US National Institutes of Health. The sample sizes for each study are described in the figure legends. All experiments were performed under protocols approved by the Institutional Animal Care and Use Committee at Genentech.
+ Open protocol
+ Expand

About PubCompare

Our mission is to provide scientists with the largest repository of trustworthy protocols and intelligent analytical tools, thereby offering them extensive information to design robust protocols aimed at minimizing the risk of failures.

We believe that the most crucial aspect is to grant scientists access to a wide range of reliable sources and new useful tools that surpass human capabilities.

However, we trust in allowing scientists to determine how to construct their own protocols based on this information, as they are the experts in their field.

Ready to get started?

Sign up for free.
Registration takes 20 seconds.
Available from any computer
No download required

Sign up now

Revolutionizing how scientists
search and build protocols!