Description
abm | Cytochrome c Stable Knockout Mouse Fibroblast Cell Line | T6305
Mice harboring a heterozygous somatic cyt c KO allele (cyt cs+/−) with mice harboring a homozygous testis cyt c KO allele (cyt ct−/−) were crossed. We used homozygous cyt ct−/− females for the crosses. Embryonic lethal phenotype was rescued by introducing a ubiquitously expressed somatic cyt c transgene flanked by loxP sites. Crosses of one of the transgenic animals with the cyt cyt−/−cyt cs+/− animals gave rise to F1 mice that when backcrossed produced mice with the cyt ct−/−cyt cs−/− cyt cflox/o genotype, demonstrating that the transgene was able to rescue the embryonic lethal phenotype of the cyt cs KO. Lung fibroblasts (LF) from these animals were cultured and the transgenic cyt c cDNA deleted ex vivo by an adenovirus preparation expressing the Cre recombinase. clones by serial dilution and screened them for the presence of Cyt c via immunocytochemistry or western blot, in which the resultant clone had no detectable Cyt c to generate the Cytochrome c Stable Knockout Mouse Fibroblast Cell Line.
Biosafety:
II
Organism:
Mouse (M. musculus)
Source Organ:
Lung
Growth Properties:
Adherent
Morphology:
Fibroblast
Clones:
N/A
Passage Number:
N/A
Population Doner:
24 hours
Seeding Density:
N/A
Markers:
G418 and hygromycin-resistant
Applications:
For Research Use Only
Doner Gender:
N/A
Donor Ethnicity:
N/A
Knockdown Method:
N/A
Induction:
N/A
Overexpression:
N/A
Freeze Thaw:
N/A
Propagation:
The base medium for this cell line is Prigrow III medium available at abm
Preservation:
1. Freeze Medium: Complete growth medium with 20% FBS and 10% DMSO.
2. Storage Temperature: Liquid nitrogen vapour phase.
Quality Control:
1) Western blot; 2) IHC
Tumorgenicn:
N/A
Shipping Conditions:
Dry Ice
Storage Contidions:
-180°C