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Jackson Laboratory epithelial cell targeted cdx2 cre
Epithelial Cell Targeted Cdx2 Cre, supplied by Jackson Laboratory, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/cdx2-cre/pm42248857-323-21-24?v=Jackson+Laboratory
Average 86 stars, based on 1 article reviews
epithelial cell targeted cdx2 cre - by Bioz Stars, 2026-07
86/100 stars

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Jackson Laboratory epithelial cell targeted cdx2 cre
Epithelial Cell Targeted Cdx2 Cre, supplied by Jackson Laboratory, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/cdx2-cre/pm42248857-323-21-24?v=Jackson+Laboratory
Average 86 stars, based on 1 article reviews
epithelial cell targeted cdx2 cre - by Bioz Stars, 2026-07
86/100 stars
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Jackson Laboratory cdx2 cre transgenic mice
Cdx2 Cre Transgenic Mice, supplied by Jackson Laboratory, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/cdx2-cre/bio_rxiv__64898__2026__05__15__725523-218-0-35?v=Jackson+Laboratory
Average 86 stars, based on 1 article reviews
cdx2 cre transgenic mice - by Bioz Stars, 2026-07
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Jackson Laboratory cdx2 cre 101erf j mice designated as cdx2 cre 009350
Generation of the <t>Cdx2</t> cre/+ ;Pax3 fl/fl mouse model. (A) Genetic cross used to generate mice with spina bifida (SB). Cdx2 cre drives Pax3 knockout in the body only (light-green highlight), whereas the head remains wild type. See <xref ref-type=Table 1 for offspring genotypes. (B,C) Cdx2 cre driving mTmG reporter expression in the body at embryonic day (E)10.5 (B; blue) and E15.5 (C; green). Magenta in B indicates a region of no Cdx2 cre -mediated recombination. Dashed line in C indicates outline of the fetus. See also Fig. S1 . (D,E) Representative images of E15.5 control ( Cdx2 +/+ ;Pax3 fl/fl ; D) and mutant ( Cdx2 cre/+ ;Pax3 fl/fl ; E) fetuses. White arrowheads indicate the location of the open SB lesion (in E). See also Fig. S2 . (F) Phenotypic developmental timeline of Cdx2 cre/+ ;Pax3 fl/fl embryos and fetuses, with dashed lines indicating the extent of open SB lesions. Scale bars: 1.0 mm. " width="250" height="auto" />
Cdx2 Cre 101erf J Mice Designated As Cdx2 Cre 009350, supplied by Jackson Laboratory, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/cdx2-cre/pm40818741-234-1-24?v=Jackson+Laboratory
Average 86 stars, based on 1 article reviews
cdx2 cre 101erf j mice designated as cdx2 cre 009350 - by Bioz Stars, 2026-07
86/100 stars
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Jackson Laboratory mouse: cdx2 cre
(A) The gracile nucleus (Gr, green) receives sensory inputs from lower body DRG afferents (cyan) and spinal projections (magenta). Retrograde virus injections into the VPL (right) labeled Gr VPL-projecting neurons (PNs). (B) Injection of cholera toxin β subunit (CTb, cyan) into the hindpaw glabrous skin labeled hindlimb afferents targeting the Gr (white dashed circle). Scale bar, 200 μm. (C) Advillin Cre ;Rosa26 LSL-Synaptophysin-GFP mice labeled synaptic terminals of primary afferents (cyan) in the Gr core (solid white line) and shell (dashed white line). Scale bar, 100 μm. (D) <t>Cdx2</t> Cre ;Lbx1 FlpO ;Rosa26 LSL-FSF-Synaptophysin-GFP mice labeled terminals of spinal projections (magenta) in the Gr core (solid white line) and shell (dashed white line). Scale bar, 100 μm. (E) In situ hybridization of excitatory (vGluT2, blue) and inhibitory (vGAT, red; GlyT2, green) neurons in the Gr core (solid white line) and shell (dashed white line). Scale bar, 100 μm. (F and G) Quantification of excitatory and inhibitory neuronal markers in the Gr core (F) and shell (G). (H) Strategy to label VPL-PNs (green) or inhibitory neurons (red). Inset: representative injection of AAV-retro GFP into the VPL. Scale bar, 1,000 μm. (I and J) Representative images of Gr VPL-PNs (I) (green), inhibitory neurons (J) (red), and NeuN + immunostaining of neurons (blue). Scale bar, 100 μm. (K and L) Quantification of VPL-PNs and inhibitory neurons in the Gr core (K) and shell (L) normalized to total NeuN.
Mouse: Cdx2 Cre, supplied by Jackson Laboratory, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/cdx2-cre/pmc12093272-31-0-4?v=Jackson+Laboratory
Average 90 stars, based on 1 article reviews
mouse: cdx2 cre - by Bioz Stars, 2026-07
90/100 stars
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Jackson Laboratory cdx2 cre-ert2 transgene
(A) The gracile nucleus (Gr, green) receives sensory inputs from lower body DRG afferents (cyan) and spinal projections (magenta). Retrograde virus injections into the VPL (right) labeled Gr VPL-projecting neurons (PNs). (B) Injection of cholera toxin β subunit (CTb, cyan) into the hindpaw glabrous skin labeled hindlimb afferents targeting the Gr (white dashed circle). Scale bar, 200 μm. (C) Advillin Cre ;Rosa26 LSL-Synaptophysin-GFP mice labeled synaptic terminals of primary afferents (cyan) in the Gr core (solid white line) and shell (dashed white line). Scale bar, 100 μm. (D) <t>Cdx2</t> Cre ;Lbx1 FlpO ;Rosa26 LSL-FSF-Synaptophysin-GFP mice labeled terminals of spinal projections (magenta) in the Gr core (solid white line) and shell (dashed white line). Scale bar, 100 μm. (E) In situ hybridization of excitatory (vGluT2, blue) and inhibitory (vGAT, red; GlyT2, green) neurons in the Gr core (solid white line) and shell (dashed white line). Scale bar, 100 μm. (F and G) Quantification of excitatory and inhibitory neuronal markers in the Gr core (F) and shell (G). (H) Strategy to label VPL-PNs (green) or inhibitory neurons (red). Inset: representative injection of AAV-retro GFP into the VPL. Scale bar, 1,000 μm. (I and J) Representative images of Gr VPL-PNs (I) (green), inhibitory neurons (J) (red), and NeuN + immunostaining of neurons (blue). Scale bar, 100 μm. (K and L) Quantification of VPL-PNs and inhibitory neurons in the Gr core (K) and shell (L) normalized to total NeuN.
Cdx2 Cre Ert2 Transgene, supplied by Jackson Laboratory, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/cdx2-cre/pmc12001959-365-10-13?v=Jackson+Laboratory
Average 90 stars, based on 1 article reviews
cdx2 cre-ert2 transgene - by Bioz Stars, 2026-07
90/100 stars
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Jackson Laboratory cdx2-cre
(A) The gracile nucleus (Gr, green) receives sensory inputs from lower body DRG afferents (cyan) and spinal projections (magenta). Retrograde virus injections into the VPL (right) labeled Gr VPL-projecting neurons (PNs). (B) Injection of cholera toxin β subunit (CTb, cyan) into the hindpaw glabrous skin labeled hindlimb afferents targeting the Gr (white dashed circle). Scale bar, 200 μm. (C) Advillin Cre ;Rosa26 LSL-Synaptophysin-GFP mice labeled synaptic terminals of primary afferents (cyan) in the Gr core (solid white line) and shell (dashed white line). Scale bar, 100 μm. (D) <t>Cdx2</t> Cre ;Lbx1 FlpO ;Rosa26 LSL-FSF-Synaptophysin-GFP mice labeled terminals of spinal projections (magenta) in the Gr core (solid white line) and shell (dashed white line). Scale bar, 100 μm. (E) In situ hybridization of excitatory (vGluT2, blue) and inhibitory (vGAT, red; GlyT2, green) neurons in the Gr core (solid white line) and shell (dashed white line). Scale bar, 100 μm. (F and G) Quantification of excitatory and inhibitory neuronal markers in the Gr core (F) and shell (G). (H) Strategy to label VPL-PNs (green) or inhibitory neurons (red). Inset: representative injection of AAV-retro GFP into the VPL. Scale bar, 1,000 μm. (I and J) Representative images of Gr VPL-PNs (I) (green), inhibitory neurons (J) (red), and NeuN + immunostaining of neurons (blue). Scale bar, 100 μm. (K and L) Quantification of VPL-PNs and inhibitory neurons in the Gr core (K) and shell (L) normalized to total NeuN.
Cdx2 Cre, supplied by Jackson Laboratory, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/cdx2-cre/pm40044853-1035-43-14?v=Jackson+Laboratory
Average 90 stars, based on 1 article reviews
cdx2-cre - by Bioz Stars, 2026-07
90/100 stars
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Image Search Results


Generation of the Cdx2 cre/+ ;Pax3 fl/fl mouse model. (A) Genetic cross used to generate mice with spina bifida (SB). Cdx2 cre drives Pax3 knockout in the body only (light-green highlight), whereas the head remains wild type. See <xref ref-type=Table 1 for offspring genotypes. (B,C) Cdx2 cre driving mTmG reporter expression in the body at embryonic day (E)10.5 (B; blue) and E15.5 (C; green). Magenta in B indicates a region of no Cdx2 cre -mediated recombination. Dashed line in C indicates outline of the fetus. See also Fig. S1 . (D,E) Representative images of E15.5 control ( Cdx2 +/+ ;Pax3 fl/fl ; D) and mutant ( Cdx2 cre/+ ;Pax3 fl/fl ; E) fetuses. White arrowheads indicate the location of the open SB lesion (in E). See also Fig. S2 . (F) Phenotypic developmental timeline of Cdx2 cre/+ ;Pax3 fl/fl embryos and fetuses, with dashed lines indicating the extent of open SB lesions. Scale bars: 1.0 mm. " width="100%" height="100%">

Journal: Disease Models & Mechanisms

Article Title: Chiari II brain malformation is secondary to open spina bifida

doi: 10.1242/dmm.052528

Figure Lengend Snippet: Generation of the Cdx2 cre/+ ;Pax3 fl/fl mouse model. (A) Genetic cross used to generate mice with spina bifida (SB). Cdx2 cre drives Pax3 knockout in the body only (light-green highlight), whereas the head remains wild type. See Table 1 for offspring genotypes. (B,C) Cdx2 cre driving mTmG reporter expression in the body at embryonic day (E)10.5 (B; blue) and E15.5 (C; green). Magenta in B indicates a region of no Cdx2 cre -mediated recombination. Dashed line in C indicates outline of the fetus. See also Fig. S1 . (D,E) Representative images of E15.5 control ( Cdx2 +/+ ;Pax3 fl/fl ; D) and mutant ( Cdx2 cre/+ ;Pax3 fl/fl ; E) fetuses. White arrowheads indicate the location of the open SB lesion (in E). See also Fig. S2 . (F) Phenotypic developmental timeline of Cdx2 cre/+ ;Pax3 fl/fl embryos and fetuses, with dashed lines indicating the extent of open SB lesions. Scale bars: 1.0 mm.

Article Snippet: Cdx2 cre/+ male mice ( ) were obtained from The Jackson Laboratory [JAX; strain 009350 : B6.Cg-Tg(CDX2-cre)101Erf/J] and maintained by breeding with C57BL/6J females.

Techniques: Knock-Out, Expressing, Control, Mutagenesis

PAX3 expression in E10.5 control and Cdx2 cre/+ ;Pax3 fl/fl embryos. Sagittal cryosections of control ( n =3) and SB ( n =3) embryos, immunostained for PAX3 (yellow) and nuclear stained with DAPI (magenta). (A,B) Head sections: PAX3 expression is present in the neural tube (hindbrain, outlined by dashed lines) in both control (A) and SB (B) embryos (yellow arrowheads). (C,D) Lower body: PAX3 expression is present in the dorsal neural tube and dermomyotomes of the control spinal region (yellow arrowheads in C), but is not detectable in the SB embryo (D), consistent with knockout of Pax3 in the lower body. Bracket in D indicates spina bifida region. Scale bar: 0.5 mm.

Journal: Disease Models & Mechanisms

Article Title: Chiari II brain malformation is secondary to open spina bifida

doi: 10.1242/dmm.052528

Figure Lengend Snippet: PAX3 expression in E10.5 control and Cdx2 cre/+ ;Pax3 fl/fl embryos. Sagittal cryosections of control ( n =3) and SB ( n =3) embryos, immunostained for PAX3 (yellow) and nuclear stained with DAPI (magenta). (A,B) Head sections: PAX3 expression is present in the neural tube (hindbrain, outlined by dashed lines) in both control (A) and SB (B) embryos (yellow arrowheads). (C,D) Lower body: PAX3 expression is present in the dorsal neural tube and dermomyotomes of the control spinal region (yellow arrowheads in C), but is not detectable in the SB embryo (D), consistent with knockout of Pax3 in the lower body. Bracket in D indicates spina bifida region. Scale bar: 0.5 mm.

Article Snippet: Cdx2 cre/+ male mice ( ) were obtained from The Jackson Laboratory [JAX; strain 009350 : B6.Cg-Tg(CDX2-cre)101Erf/J] and maintained by breeding with C57BL/6J females.

Techniques: Expressing, Control, Staining, Knock-Out

(A) The gracile nucleus (Gr, green) receives sensory inputs from lower body DRG afferents (cyan) and spinal projections (magenta). Retrograde virus injections into the VPL (right) labeled Gr VPL-projecting neurons (PNs). (B) Injection of cholera toxin β subunit (CTb, cyan) into the hindpaw glabrous skin labeled hindlimb afferents targeting the Gr (white dashed circle). Scale bar, 200 μm. (C) Advillin Cre ;Rosa26 LSL-Synaptophysin-GFP mice labeled synaptic terminals of primary afferents (cyan) in the Gr core (solid white line) and shell (dashed white line). Scale bar, 100 μm. (D) Cdx2 Cre ;Lbx1 FlpO ;Rosa26 LSL-FSF-Synaptophysin-GFP mice labeled terminals of spinal projections (magenta) in the Gr core (solid white line) and shell (dashed white line). Scale bar, 100 μm. (E) In situ hybridization of excitatory (vGluT2, blue) and inhibitory (vGAT, red; GlyT2, green) neurons in the Gr core (solid white line) and shell (dashed white line). Scale bar, 100 μm. (F and G) Quantification of excitatory and inhibitory neuronal markers in the Gr core (F) and shell (G). (H) Strategy to label VPL-PNs (green) or inhibitory neurons (red). Inset: representative injection of AAV-retro GFP into the VPL. Scale bar, 1,000 μm. (I and J) Representative images of Gr VPL-PNs (I) (green), inhibitory neurons (J) (red), and NeuN + immunostaining of neurons (blue). Scale bar, 100 μm. (K and L) Quantification of VPL-PNs and inhibitory neurons in the Gr core (K) and shell (L) normalized to total NeuN.

Journal: Cell reports

Article Title: The dorsal column nuclei scale mechanical sensitivity in naive and neuropathic pain states

doi: 10.1016/j.celrep.2025.115556

Figure Lengend Snippet: (A) The gracile nucleus (Gr, green) receives sensory inputs from lower body DRG afferents (cyan) and spinal projections (magenta). Retrograde virus injections into the VPL (right) labeled Gr VPL-projecting neurons (PNs). (B) Injection of cholera toxin β subunit (CTb, cyan) into the hindpaw glabrous skin labeled hindlimb afferents targeting the Gr (white dashed circle). Scale bar, 200 μm. (C) Advillin Cre ;Rosa26 LSL-Synaptophysin-GFP mice labeled synaptic terminals of primary afferents (cyan) in the Gr core (solid white line) and shell (dashed white line). Scale bar, 100 μm. (D) Cdx2 Cre ;Lbx1 FlpO ;Rosa26 LSL-FSF-Synaptophysin-GFP mice labeled terminals of spinal projections (magenta) in the Gr core (solid white line) and shell (dashed white line). Scale bar, 100 μm. (E) In situ hybridization of excitatory (vGluT2, blue) and inhibitory (vGAT, red; GlyT2, green) neurons in the Gr core (solid white line) and shell (dashed white line). Scale bar, 100 μm. (F and G) Quantification of excitatory and inhibitory neuronal markers in the Gr core (F) and shell (G). (H) Strategy to label VPL-PNs (green) or inhibitory neurons (red). Inset: representative injection of AAV-retro GFP into the VPL. Scale bar, 1,000 μm. (I and J) Representative images of Gr VPL-PNs (I) (green), inhibitory neurons (J) (red), and NeuN + immunostaining of neurons (blue). Scale bar, 100 μm. (K and L) Quantification of VPL-PNs and inhibitory neurons in the Gr core (K) and shell (L) normalized to total NeuN.

Article Snippet: Mouse: Cdx2 Cre , Jackson Laboratories , Jax#009350.

Techniques: Virus, Labeling, Injection, In Situ Hybridization, Immunostaining