The largest database of trusted experimental protocols

Crl nih foxn1rnu

Manufactured by Charles River Laboratories
Sourced in United States, Germany

The Crl:NIH-Foxn1rnu is a laboratory animal model used in research. It is a strain of athymic nude mice that lack a functional thymus gland, resulting in a deficiency of T cells. This model is commonly used in areas of research involving immune system function and the study of tumor growth and development.

Automatically generated - may contain errors

22 protocols using crl nih foxn1rnu

1

CPC Therapy for Nonischemic Heart Failure in Rats

Check if the same lab product or an alternative is used in the 5 most similar protocols
All animal experiments were performed with the approval of the Institutional Animal Care and Use Committee. Male adolescent (6 week old) athymic rats (Crl:NIH-Foxn1rnu) (~150 g) were obtained from Charles River Laboratories (Wilmington, MA). Nonischemic HF was induced by pulmonary artery banding (PAB) at 7–8 weeks old as previously described.18 (link) Animals were randomized to treatment groups and 500,000 monolayer cultured CPCs (2D), or approximately 400 freshly formed (Day 0) CPC spheres (3D) totaling ~500,000 CPCs, were delivered two weeks after banding (Supplemental Figure I). To minimize potential differences between CPC donors, animals received injections containing equal parts of all child CPC populations. Cells were labeled with DiR (Thermo Fisher Scientific Life Sciences, Waltham, MA) per manufacturer’s protocol and cell retention was tracked using an IVIS Spectrum in vivo imager (Perkin Elmer, Waltham, MA). To evaluate RV function, echocardiography was performed on PAB and sham rats on the day of surgery, immediately after treatment 2 weeks later, and then every week thereafter up to 4 weeks after treatment. Data were collected and analyzed by blinded researchers. Additional details on randomization and blinding process are given in the Supplemental Methods. No animals were excluded from the analysis.
+ Open protocol
+ Expand
2

Hepatocellular Carcinoma Induction in Rats

Check if the same lab product or an alternative is used in the 5 most similar protocols
Animal experiments were approved by the local governmental committee for animal protection and welfare (Tierschutzbehörde Regierung von Oberbayern, Protocol Nr. 55.2-1-54-2532-25-2016). All procedures were carried out in accordance with applicable laws and regulations. Two animal cohorts were employed in the study. Cohort A included 17 male Wistar rats (RccHan:WIST; six to eight weeks old; Envigo; Re Schaijk, Netherlands), consisting of 13 rats in which HCCs were induced by oral administration of 0.01% diethyl-nitrosamine (DENA, SigmaAldrich) dissolved in drinking water over ten weeks, as previously described19 (link), and 4 healthy control rats. Cohort B consisted of ten male nude rats (Crl:NIH-Foxn1rnu; six to eight weeks old; Charles River, Sulzfeld, Germany) in which subcutaneous tumors were implanted in each flank. Tumor screening in cohort A rats was performed by T2-weighted (T2w) anatomical imaging on a human 3 T clinical MRI system (Philips Ingenia 3.0 T; Philips Medical, Amsterdam, Netherlands) as previously described12 (link). Tumor screening in cohort B rats was performed by caliper measurement. Tumor bearing animals were included in HPMRS(I) experiments once tumors reached ≥ 10 mm in diameter.
+ Open protocol
+ Expand
3

Healthy Nude Rat Feeding Study

Check if the same lab product or an alternative is used in the 5 most similar protocols
Healthy male nude NIH rats (Crl:NIH-Foxn1 rnu, Charles River, Germany) bread in a specific pathogen-free (SPF) animal care unit were fed sterile, irradiated food granules (V1246-703, Soest, Germany). Animal procedures were reviewed by the Animal Care and Use Committee of Pharmacy and Medicine University of Dijon or Oncodesign’s ethical committee.
+ Open protocol
+ Expand
4

Ovariectomized Female Rats for Tumor Studies

Check if the same lab product or an alternative is used in the 5 most similar protocols
Ovariectomized female athymic, inbred nude rats (Crl:NIH- Foxn1rnu), 1–2 weeks of age were purchased from Charles River Laboratories (Wilmington, MA) and were maintained in environmentally controlled rooms (25° C; 50–55% humidity) with controlled diurnal lighting schedule of 12h light:12h dark (LD12:12, 300 lux; 123 mW/Cm2; lights on 06:00 hours, and off at 18:00 hours). All rats were supplemented with estrogen pellets (0.72 mg of 17b-estradiol 60-day release form Innovative Research of America). One week prior to tumor implantation, the animals were switched to 12-hour light:12-hour dim light at night (dLAN) cycle (0.2 lux, with lighs on at 06:00 hours and off at 18:00 hours, a dLAN on at 18:00 hours and off at 06:00 hours), as previously described37 (link). All procedures employed for animal studies were approved by the Tulane University Institutional Animal Care and Use Committee.
+ Open protocol
+ Expand
5

In Vivo Angiogenic Potential of HESC-EC and HUVEC

Check if the same lab product or an alternative is used in the 5 most similar protocols
HESC-EC and HUVEC were expanded in vitro and 106 cells were injected subcutaneously into 3-month-old athymic nude rats (Crl:NIH-Foxn1rnu, Charles River) in a suspension of 50 µl Matrigel (Becton Dickinson, Massachusetts, USA), heparin (64 U/ml), recombinant murine basic FGF (80 ng/ml, R & D Systems), 70 µl Lonza-EGM2. A Matrigel suspension with no cells served as negative control. After 3 weeks, rats were sacrificed and plugs removed, photographed and stored for cryosectioning and RNA isolation. Animals used (n = 24) were RNU rats, Crl:NIH-Foxn1rnu, stain code 316. Anaesthetics ketamine (Richter Gedeon Pharmaceutical Company, Budapest, Hungary; 75 mg/kg, ip) and xylazine (Produlab Pharma, Rammsdonksveer, Netherlands; 5 mg/kg, ip) were used in surgical procedures.. Matrigel plugs with cells were lysed in TriReagent for total RNA extraction. The RNA was purified using RNeasy columns (Qiagen, Hilden, Germany), quantified, and checked for quality. 500 ng of total RNA was used for DNA generation using High Capacity cDNA Reverse Transcription Kit (Applied Biosystems, California, USA) according to manufactures instructions.
+ Open protocol
+ Expand
6

Nude Rat Experiment Protocol

Check if the same lab product or an alternative is used in the 5 most similar protocols
Ten nude male rats (Crl:NIH‐Foxn1rnu, 250–300 g; Charles River Laboratories, Inc.) were used. Animals were kept in a regular 12‐h light/dark cycle with food and water provided ad libitum. All animal experiments were conducted at Charles River's AAALAC‐accredited animal facility and were reviewed and approved by the Institutional Animal Care and Use Committee (IACUC). Procedures were conducted under veterinary supervision with appropriate anesthesia and analgesia protocols.
+ Open protocol
+ Expand
7

SCID-beige Mice and Nude Rat Maintenance

Check if the same lab product or an alternative is used in the 5 most similar protocols
All experiments were approved by the UBC Animal Care Committee. Male 8- to 10-week-old SCID-beige mice (C.B-Igh-1b/GbmsTac-Prkdcscid-LystbgN7, Taconic) and male 8- to 10-week-old nude rats (Crl:NIH-Foxn1rnu, Charles River Laboratories) were maintained on a 12-h light/dark cycle with ad libitum access to a standard irradiated diet (Teklad diet no.2918, Harlan Laboratories).
+ Open protocol
+ Expand
8

Immunodeficient Rat Xenograft Model

Check if the same lab product or an alternative is used in the 5 most similar protocols
All procedures were approved by the Institutional Animal Care and Use Committee by the University of California, San Diego (Protocol No.: S01193). All studies were performed in such a manner as to minimize group size and animal suffering. Adult Sprague‐Dawley immunodeficient rats (Crl:NIH‐Foxn1rnu; Charles River) male and female, 250‐350 g; (n = 6) were used in this study.
+ Open protocol
+ Expand
9

Pulmonary Artery Banding in Rats

Check if the same lab product or an alternative is used in the 5 most similar protocols
All animal experiments were performed with the approval of the Institutional Animal Care and Use Committee of Emory University. Adolescent athymic rats (Crl:NIH-Foxn1rnu) (∼150 g) were obtained from Charles River Laboratories (Wilmington, MA, http://www.criver.com). Rats were anesthetized with 2% isoflurane (Isoflurane USP; Piramal Healthcare, Boston, MA, http://www.piramel.com), orally intubated, and ventilated (Harvard Apparatus, Holliston, MA, http://www.harvardapparatus.com). A limited left thoracotomy was performed, the pulmonary trunk was exposed, and the pulmonary artery (PA) was dissected carefully from the aorta and partially ligated over an 18-gauge angiocatheter with a silk thread positioned under the PA. The catheter was removed rapidly to allow for antegrade flow through the band. Sham rats underwent the same procedure without banding the PA. Two weeks after banding, animals were randomized to treatment groups, and cells were delivered in a blinded manner.
+ Open protocol
+ Expand
10

Transplantation of hiPSC-EB-HLCs in Acute Liver Failure

Check if the same lab product or an alternative is used in the 5 most similar protocols
The Institutional Animal Care and Use Committee (IACUC) approved the use of animals for experimentation in this study. Through intraperitoneal injection of 950 mg kg−1 of sterile D-galactosamine dissolved in Hanks Balanced Salt Solution (Sigma-Aldrich), acute liver failure was induced in 270–350 g athymic nude rats (Crl:NIH-Foxn1rnu, Charles River Laboratories, Wilmington, MA). Then under inhalational anaesthesia, 80–100 hiPSC-EB-HLCs were injected into the spleen body through the caudal pole of the spleen. The caudal pole was ligated following injection. Experimental groups consisted of animals transplanted with the hiPSC-EB-HLCs with HAMEC and hiPSC-EB-HLCs without HAMEC. Animals receiving differentiation medium only constituted our negative control. The healthy controls consisted of animals without liver injury transplanted with hiPSC-EBs. Animals were monitored daily and received standard chow and water ad libitum. The animals’ survival was tracked as a primary end point. They were sacrificed either after 14 days or earlier if they had moribund appearance or greater than 30% body weight loss in accordance with predefined humane care criteria. All of our experiments were conducted in accordance with the approved IACUC guidelines.
+ 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!