The largest database of trusted experimental protocols

Balb c slc

Manufactured by Japan SLC
Sourced in Japan

BALB/c SLC is a mouse strain primarily used in laboratory research. It is a common inbred mouse model characterized by its susceptibility to certain diseases and immune responses. The BALB/c SLC strain is widely utilized for a variety of applications in the scientific community.

Automatically generated - may contain errors

2 protocols using balb c slc

1

Cerulein-induced Pancreatitis Murine Model

Check if the same lab product or an alternative is used in the 5 most similar protocols
The experimental protocols used in this study were approved by the Institutional Animal Care and Use Committee of Azabu University (Approval No.: 1610108-1). Male 8-week-old BALB/c mice (BALB/c SLC: JAPAN SLC INC,
Shizuoka, Japan) were kept in polycarbonate cages (CL-0106-1; 310 × 360 × 175 mm; CLEA Japan, Tokyo, Japan) with wood shavings, in a room equipped with a barrier system at the Research Institute of Biosciences, Azabu
University. We used BALB/c mice since this strain is reported to show relatively high susceptibility to cerulein [42 (link)]. The room was air-conditioned at a temperature of 22 ± 1°C and
a humidity of 55 ± 5%, and was lit for 12 hr each day from 06:00 to 18:00. The animals were acclimated to the facility for 1 week before the experiment. Mice were fed a commercial rodent pellet (mouse and rat chow; MC-2,
CLEA Japan, Tokyo, Japan) and had access ad libitum to sterilized drinking water provided in a water bottle. All animals were examined and judged healthy before the study, and were fasted overnight
before the experiment.
+ Open protocol
+ Expand
2

Tumor Model Generation and Phototherapy

Check if the same lab product or an alternative is used in the 5 most similar protocols
All animal experimental procedures were approved by the Institutional Animal Care and Use Committee of JAIST and AIST. Female BALB/cSlc (4 weeks old; average weight, 16 g) and BALB/cSlc-nu/nu mice (4 weeks old; average weight, 18 g) were purchased from Japan SLC (Hamamatsu, Japan) and were housed in specific pathogen-free facilities with a 12-h light/12-h dark cycle and free access to food and water.
To generate tumour models, nude mice were subcutaneously inoculated in the flanks with equivalent number of cells (5 × 105 cells for HT-29; 1 × 106 cells for A549 and Colon-26) suspended in 100-μl aliquots of culture medium/Matrigel (Corning) mixture (v:v = 1:1). For in vivo tumour phototherapy experiments, mice were bilaterally implanted with either control or TRPV2 overexpressing derivative cells into flanks. For in vivo biodistribution analyses, both cell types were injected into opposite flanks of the same mouse. For in vivo drug and phototherapy combination experiments, only TRPV2-transfected A549 cells were injected into the right flank of mice. Tumour sizes were monitored using vernier calipers and tumour volumes were calculated as V = L × W2/2, where L and W denote lengths and widths of tumours, respectively. Tumour models were randomly divided and used in experiments when tumour volumes reached about 100 mm3.
+ 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!