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Sall1-Ncre:Cx3cr1-CCre (No. M7-2131)

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Overview

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These Sall1ncre:Cx3cr1ccre (CX/Sall1) mice use a binary transgenic cre approach to dissect functions of central nervous system (CNS) macrophage subpopulations.

This dual-recombinase strain enables microglia-specific Cre activity by reconstituting functional Cre recombinase from two complementary fragments. The Sall1<sup>ncre</sup> allele expresses the N-terminal fragment of Cre (NCre, 40 aa) under the Sall1 promoter, which marks microglia and selected mesenchymal and CNS cells. The Cx3cr1<sup>ccre</sup> allele expresses the C-terminal Cre fragment (CCre, 283 aa) under the macrophage-lineage Cx3cr1 promoter. Each fragment alone is inactive but contains leucine-zipper domains that mediate dimerization.

Co-expression of NCre and CCre in parenchymal microglia restores full Cre recombinase activity, enabling selective deletion of floxed alleles in microglia while preserving endogenous gene expression via 2A self-cleaving peptides. Double homozygotes are viable and fertile, and recombination occurs specifically in microglial cells of the CNS.

Prof Steffen Jung

Steffen Jung

Faculty of Biology
Immunology and Regenerative Biology
All projects (2)
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Dr. Nitzan Rimon

Business Development Associate

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