The largest database of trusted experimental protocols

R26r lacz mice

Manufactured by Jackson ImmunoResearch
Sourced in United States

The R26R-lacZ mice are a genetically modified mouse strain that expresses the lacZ reporter gene under the control of the ubiquitously expressed ROSA26 promoter. The lacZ gene encodes the bacterial enzyme β-galactosidase, which can be detected through histochemical staining. This mouse line allows for the visualization and lineage tracing of cells and their descendants in vivo.

Automatically generated - may contain errors

5 protocols using r26r lacz mice

1

Conditional Knockout Mouse Models

Check if the same lab product or an alternative is used in the 5 most similar protocols
C57BL/6J mice at 6–8 weeks of age were purchased from Japan Clea (Tokyo, Japan). Lgr5- EGFP- ires- CreERT2 mice (Stock No. 008875) and R26R-lacZ mice (Stock No. 003309) were purchased from The Jackson Laboratory (Bar Harbor, Maine, USA). Dll1-floxed mice (Hozumi et al., 2004 (link)) and Dll4-floxed mice (Hozumi et al., 2008 (link)) have been previously described. To generate Lgr5- EGFP- ires- CreERT2/ Dll1fl/fl mice or Lgr5- EGFP- ires- CreERT2/ Dll4fl/fl mice, each floxed mice were crossed with Lgr5- EGFP- ires- CreERT2 mice. Mice carrying the R26R-LacZ allele served as control (Lgr5- EGFP- ires- CreERT2/ R26R-LacZ). Those mice were housed in the animal facility of Tokyo Medical and Dental University. All animal experiments were approved by the Institutional Animal Care and Use Committee of Tokyo Medical and Dental University (Approval Number 0140053A).
+ Open protocol
+ Expand
2

Lineage Tracing of Lgr6+ Cells

Check if the same lab product or an alternative is used in the 5 most similar protocols
Lgr6-EGFP-Ires-CreERT2 (a kind gift of Prof. Hans Clevers) and Cre reporter R26R-LacZ mice (Jackson Laboratories, Bar Harbor, USA) were crossed to incorporate the LacZ reporter under the control of the Rosa (R26R) promoter for lineage tracing upon administering tamoxifen [6 (link)]. These Lgr6-EGFP-Ires-CreERT2/R26R-LacZ mice were also backcrossed into a hairless background using Crl:SKH1-HR hairless albino mice (Charles River, Sulzfeld, Germany).
Both male and female mice entered the experiments at 6-10 weeks of age (for each time point in the hyperplasia and ablation experiments n= 4). They were kept individually in Macrolon type 1 cages at 25 ± 2°C and about 50% humidity in a 12 hours light-12 hours dark cycle during experiments. The room in which the mice were kept and experiments were performed was illuminated by fluorescent tubes that did not emit any UV radiation. Standard chow and tap water were available ad libitum. As legally required, all mouse experiments were performed with the approval of the Leiden University Medical Centers's ethics committee (approval number DEC 10229).
+ Open protocol
+ Expand
3

Tbx18 expression during heart development

Check if the same lab product or an alternative is used in the 5 most similar protocols
Animals experiments were performed under protocols approved by the animal research committee of Chongqing Medical University. All animal experiments were carried out in accordance with relevant guidelines and regulations of the animal research committee of Chongqing Medical University. Our laboratory has bred Tbx18:Cre knock-in mice (Evans laboratory) and the Cre-lineage reporter R26REYFP and R26RLacz mice (Jackson Laboratory). These three mouse lines were maintained on a C57BL/6 background. To generate Tbx18:Cre/R26REYFP/LacZ double heterozygous mice, we crossed the Tbx18:Cre knock-in mice with the R26REYFP mice or R26RLacZ mice separately and then screened out these double heterozygous mice by the PCR method, according to the reported literature39 (link)40 (link). Using these mice, we were able to visualize the expression of endogenous Tbx18 during embryonic heart development9 (link).
+ Open protocol
+ Expand
4

Genetic Modulation of Duchenne Muscular Dystrophy

Check if the same lab product or an alternative is used in the 5 most similar protocols
Pax7-CreERtm males (85 (link)) (herein referred to as Pax7CreER) were crossed to R26RYFP/YFP females (The Jackson Laboratory, no. 006148) to obtain Pax7CreER/WT; R26RYFP/WT males. These breeders were crossed with mdx5Cv/5Cv or WT female (both in the C57BL6 background, The Jackson Laboratory) to obtain the male experimental animals. TMX (Sigma) was dissolved at 50 mg/ml in 92.5% corn oil/7.5% ethanol, and 5 mg was administrated intraperitoneally to 5-week-old experimental mice twice a week for 2 weeks. For specific experiments, R26RLacZ mice were used (The Jackson Laboratory, no. 003474). BAT-GAL mice (The Jackson Laboratory, no. 005317) are engineered with copies of the Wnt-inducible TCF/LEF–responsive element driving the expression of β-Gal. Geno-typing was performed with primers listed in table S2.
In chronic studies, mdx5Cv mice were injected with 300 ng of anti-TGFβ (1D11) or anti-Shigella toxin (control) antibodies on alternate days for 6 months (36 (link)). Purified antibodies were provided by Genzyme (37 (link)). Losartan was administrated for 7 months (0.6 g/liter in drinking water) (35 (link)). Treatments were started at 5 weeks of age. Experiments were done in accordance with protocols approved by the Institutional Animal Care and Use Committee at the Veterinary Medical Unit at the VA Palo Alto Health Care System.
+ Open protocol
+ Expand
5

Genetically Modified Mouse Models for Gastric Cancer

Check if the same lab product or an alternative is used in the 5 most similar protocols
The animal protocol was reviewed and approved by the Columbia University Medical Center Institutional Animal Care and Use Committee (IACUC), and all mice were bred under specific pathogen free (SPF) conditions. INS-GAS mice27 (link) and hGAS mice23 (link) were backcrossed to C57BL6 background. Lgr5-GFP-IRES-CreER knockin mice28 (link) (Lgr5-GFP mice) were provided by Dr Hans Clevers, and mated with hGAS mice and B6.129S4-Gt(ROSA)26Sortm1Sor5/J, referred to as R26rLacZ mice (Jackson Laboratories). CCK2R−/− mice were purchased from Jackson Laboratories. CCK2R-GFP BAC transgenic mice were purchased from MMRRC (GENSAT project29 (link)). For generation of CCK2R-BAC-CreERT mice, BAC recombination was carried out as described at http://web.ncifcrf.gov/research/brb/recombineeringInformation.aspx using the CreTM-FrtNeoFrt cassette as described previously.30 (link) For lineage tracing experiments, mice were administered 1–6 mg tamoxifen in 200 μL corn oil containing 5–30 mg/mL tamoxifen by oral gavage. The CCK2R antagonist YF476 was a kind gift of Dr Keiji Miyata and Dr Hidenobu Yuki (Astellas Pharma, Tokyo, Japan). The drug was dissolved in PEG 300 at the concentration of 12 mg/mL and intraperitoneally injected twice per week at the dose of 40 mg/kg.31 (link)
+ 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!