A promoterless mCherry reporter gene, two T2A sequence and inducible cre recombinase fusion gene (cre/ERT2) were inserted into the exon 8 in-frame upstream of the endogenous Plin2 stop codon by homologous recombination using a targeting vector encoding 6 kb 50 and 3.6 kb 30 homologous sequences. Two T2A peptide sequences separate Plin2 and mCherry and CreERT2 from each other. The targeting vector also contained a diptheria toxin A cassette for negative and a FRT-flanked PGK-neomycin cassette downstream of the mCherry-CreERT2 cassette for positive selection. Chimeric males were backcrossed onto C57BL/6J background to achieve germline transmission and bred with a mouse expressing Flp to remove the FRT-PGK-neomycin selection cassette. (J:229959, J:250476)

Basic Information

Allele
Strain of Origin
Allele Type
Mutation
Inheritance
Related Gene
Related Disease
Reference
(C57BL/6 x 129S4/SvJae)F1
Targeted
Insertion
--
1
--
2

Phenotypes

Legend:
hm: homozygous
ht: heterozygous
cn: conditional genotype
cx: complex: > 1 genome feature
tg: involves transgenes
ot: other: hemizygous, indeterminate,...
(F): Female
(M): Male
phenotype observed
N: normal phenotype
(#): related diseases count
Phenotypes:
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Phenotypes

References Literature

Title
PMID
Journal
Year
IF
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