Review




Structured Review

Jackson Laboratory wt fvb nj stock 001800 mice
In vivo characterization of the full-length CP040 promoter packaged in the AAVDJ capsid (A) 1 × 10 13 vg/kg of AAVDJ-CP040 -eGFP or vehicle (1x PBS) was injected into the temporal vein of <t>wild-type</t> <t>FVB/NJ</t> neonatal mice (postnatal day 1–2). Necropsies were performed on the mice at six weeks of age, and tissue samples were analyzed for vg content and eGFP transcript levels. (B) Graph presenting vg copy numbers in different organs—cortex, cerebellum, kidneys, spleen, quadriceps, spinal cord, liver and heart. (C) Graph showing the fold change in e GFP transcript levels demonstrating promoter strength in the same organs as in (B). Data represent mean ± SEM, N = 10 mice, ∗∗ p < 0.01, ∗∗∗ p < 0.001, ∗∗∗∗ p < 0.0001, ns, not significant by one-way ANOVA. (D) Representative IF images showing eGFP expression along with neuronal (NeuN), astrocyte (GFAP), and oligodendrocyte (olig2) markers. Scale bar = 100 uM (E) Cells found to be double-positive for eGFP and one of the other markers (NeuN, GFAP, and olig2) were quantified from the IF images captured. Data presented as mean ± SEM, N = 3 mice, ∗∗∗∗ p < 0.0001 by one-way ANOVA.
Wt Fvb Nj Stock 001800 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/wt+fvb+nj+stock+001800+mice/pmc13148911-204-1-9?v=Jackson+Laboratory
Average 86 stars, based on 1 article reviews
wt fvb nj stock 001800 mice - by Bioz Stars, 2026-07
86/100 stars

Images

1) Product Images from "Design and initial characterization of a novel mini-promoter for gene therapies targeting the central nervous system"

Article Title: Design and initial characterization of a novel mini-promoter for gene therapies targeting the central nervous system

Journal: Molecular Therapy Advances

doi: 10.1016/j.omta.2026.201681

In vivo characterization of the full-length CP040 promoter packaged in the AAVDJ capsid (A) 1 × 10 13 vg/kg of AAVDJ-CP040 -eGFP or vehicle (1x PBS) was injected into the temporal vein of wild-type FVB/NJ neonatal mice (postnatal day 1–2). Necropsies were performed on the mice at six weeks of age, and tissue samples were analyzed for vg content and eGFP transcript levels. (B) Graph presenting vg copy numbers in different organs—cortex, cerebellum, kidneys, spleen, quadriceps, spinal cord, liver and heart. (C) Graph showing the fold change in e GFP transcript levels demonstrating promoter strength in the same organs as in (B). Data represent mean ± SEM, N = 10 mice, ∗∗ p < 0.01, ∗∗∗ p < 0.001, ∗∗∗∗ p < 0.0001, ns, not significant by one-way ANOVA. (D) Representative IF images showing eGFP expression along with neuronal (NeuN), astrocyte (GFAP), and oligodendrocyte (olig2) markers. Scale bar = 100 uM (E) Cells found to be double-positive for eGFP and one of the other markers (NeuN, GFAP, and olig2) were quantified from the IF images captured. Data presented as mean ± SEM, N = 3 mice, ∗∗∗∗ p < 0.0001 by one-way ANOVA.
Figure Legend Snippet: In vivo characterization of the full-length CP040 promoter packaged in the AAVDJ capsid (A) 1 × 10 13 vg/kg of AAVDJ-CP040 -eGFP or vehicle (1x PBS) was injected into the temporal vein of wild-type FVB/NJ neonatal mice (postnatal day 1–2). Necropsies were performed on the mice at six weeks of age, and tissue samples were analyzed for vg content and eGFP transcript levels. (B) Graph presenting vg copy numbers in different organs—cortex, cerebellum, kidneys, spleen, quadriceps, spinal cord, liver and heart. (C) Graph showing the fold change in e GFP transcript levels demonstrating promoter strength in the same organs as in (B). Data represent mean ± SEM, N = 10 mice, ∗∗ p < 0.01, ∗∗∗ p < 0.001, ∗∗∗∗ p < 0.0001, ns, not significant by one-way ANOVA. (D) Representative IF images showing eGFP expression along with neuronal (NeuN), astrocyte (GFAP), and oligodendrocyte (olig2) markers. Scale bar = 100 uM (E) Cells found to be double-positive for eGFP and one of the other markers (NeuN, GFAP, and olig2) were quantified from the IF images captured. Data presented as mean ± SEM, N = 3 mice, ∗∗∗∗ p < 0.0001 by one-way ANOVA.

Techniques Used: In Vivo, Injection, Expressing

Schematic of the overall experiment design for promoter comparison study (A) Viral vectors used in the study. (B) Six-week-old wild-type FVB/NJ mice (C) were injected with AAVDJ-CBA-eGFP, AAVDJ-EF1α-eGFP, AAVDJ-hSYN-eGFP, AAVDJ-CP040-eGFP, or vehicle (1x PBS) through the ICV or IT route. (D and E) Mice were euthanized 9 weeks after AAV injection, and tissue analysis done for viral vg and eGFP transcript and protein analysis for promoter comparison.
Figure Legend Snippet: Schematic of the overall experiment design for promoter comparison study (A) Viral vectors used in the study. (B) Six-week-old wild-type FVB/NJ mice (C) were injected with AAVDJ-CBA-eGFP, AAVDJ-EF1α-eGFP, AAVDJ-hSYN-eGFP, AAVDJ-CP040-eGFP, or vehicle (1x PBS) through the ICV or IT route. (D and E) Mice were euthanized 9 weeks after AAV injection, and tissue analysis done for viral vg and eGFP transcript and protein analysis for promoter comparison.

Techniques Used: Comparison, Injection



Similar Products

86
Jackson Laboratory wt fvb nj stock 001800 mice
In vivo characterization of the full-length CP040 promoter packaged in the AAVDJ capsid (A) 1 × 10 13 vg/kg of AAVDJ-CP040 -eGFP or vehicle (1x PBS) was injected into the temporal vein of <t>wild-type</t> <t>FVB/NJ</t> neonatal mice (postnatal day 1–2). Necropsies were performed on the mice at six weeks of age, and tissue samples were analyzed for vg content and eGFP transcript levels. (B) Graph presenting vg copy numbers in different organs—cortex, cerebellum, kidneys, spleen, quadriceps, spinal cord, liver and heart. (C) Graph showing the fold change in e GFP transcript levels demonstrating promoter strength in the same organs as in (B). Data represent mean ± SEM, N = 10 mice, ∗∗ p < 0.01, ∗∗∗ p < 0.001, ∗∗∗∗ p < 0.0001, ns, not significant by one-way ANOVA. (D) Representative IF images showing eGFP expression along with neuronal (NeuN), astrocyte (GFAP), and oligodendrocyte (olig2) markers. Scale bar = 100 uM (E) Cells found to be double-positive for eGFP and one of the other markers (NeuN, GFAP, and olig2) were quantified from the IF images captured. Data presented as mean ± SEM, N = 3 mice, ∗∗∗∗ p < 0.0001 by one-way ANOVA.
Wt Fvb Nj Stock 001800 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/wt+fvb+nj+stock+001800+mice/pmc13148911-204-1-9?v=Jackson+Laboratory
Average 86 stars, based on 1 article reviews
wt fvb nj stock 001800 mice - by Bioz Stars, 2026-07
86/100 stars
  Buy from Supplier

90
Jackson Laboratory fvb wt mice fvb/nj jax stock number: 001800

Fvb Wt Mice Fvb/Nj Jax Stock Number: 001800, 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/wt+fvb+nj+stock+001800+mice/pmc09986820-323-17-22?v=Jackson+Laboratory
Average 90 stars, based on 1 article reviews
fvb wt mice fvb/nj jax stock number: 001800 - by Bioz Stars, 2026-07
90/100 stars
  Buy from Supplier

Image Search Results


In vivo characterization of the full-length CP040 promoter packaged in the AAVDJ capsid (A) 1 × 10 13 vg/kg of AAVDJ-CP040 -eGFP or vehicle (1x PBS) was injected into the temporal vein of wild-type FVB/NJ neonatal mice (postnatal day 1–2). Necropsies were performed on the mice at six weeks of age, and tissue samples were analyzed for vg content and eGFP transcript levels. (B) Graph presenting vg copy numbers in different organs—cortex, cerebellum, kidneys, spleen, quadriceps, spinal cord, liver and heart. (C) Graph showing the fold change in e GFP transcript levels demonstrating promoter strength in the same organs as in (B). Data represent mean ± SEM, N = 10 mice, ∗∗ p < 0.01, ∗∗∗ p < 0.001, ∗∗∗∗ p < 0.0001, ns, not significant by one-way ANOVA. (D) Representative IF images showing eGFP expression along with neuronal (NeuN), astrocyte (GFAP), and oligodendrocyte (olig2) markers. Scale bar = 100 uM (E) Cells found to be double-positive for eGFP and one of the other markers (NeuN, GFAP, and olig2) were quantified from the IF images captured. Data presented as mean ± SEM, N = 3 mice, ∗∗∗∗ p < 0.0001 by one-way ANOVA.

Journal: Molecular Therapy Advances

Article Title: Design and initial characterization of a novel mini-promoter for gene therapies targeting the central nervous system

doi: 10.1016/j.omta.2026.201681

Figure Lengend Snippet: In vivo characterization of the full-length CP040 promoter packaged in the AAVDJ capsid (A) 1 × 10 13 vg/kg of AAVDJ-CP040 -eGFP or vehicle (1x PBS) was injected into the temporal vein of wild-type FVB/NJ neonatal mice (postnatal day 1–2). Necropsies were performed on the mice at six weeks of age, and tissue samples were analyzed for vg content and eGFP transcript levels. (B) Graph presenting vg copy numbers in different organs—cortex, cerebellum, kidneys, spleen, quadriceps, spinal cord, liver and heart. (C) Graph showing the fold change in e GFP transcript levels demonstrating promoter strength in the same organs as in (B). Data represent mean ± SEM, N = 10 mice, ∗∗ p < 0.01, ∗∗∗ p < 0.001, ∗∗∗∗ p < 0.0001, ns, not significant by one-way ANOVA. (D) Representative IF images showing eGFP expression along with neuronal (NeuN), astrocyte (GFAP), and oligodendrocyte (olig2) markers. Scale bar = 100 uM (E) Cells found to be double-positive for eGFP and one of the other markers (NeuN, GFAP, and olig2) were quantified from the IF images captured. Data presented as mean ± SEM, N = 3 mice, ∗∗∗∗ p < 0.0001 by one-way ANOVA.

Article Snippet: Five-week-old WT FVB/NJ (stock# 001800) mice were ordered from Jackson Laboratory.

Techniques: In Vivo, Injection, Expressing

Schematic of the overall experiment design for promoter comparison study (A) Viral vectors used in the study. (B) Six-week-old wild-type FVB/NJ mice (C) were injected with AAVDJ-CBA-eGFP, AAVDJ-EF1α-eGFP, AAVDJ-hSYN-eGFP, AAVDJ-CP040-eGFP, or vehicle (1x PBS) through the ICV or IT route. (D and E) Mice were euthanized 9 weeks after AAV injection, and tissue analysis done for viral vg and eGFP transcript and protein analysis for promoter comparison.

Journal: Molecular Therapy Advances

Article Title: Design and initial characterization of a novel mini-promoter for gene therapies targeting the central nervous system

doi: 10.1016/j.omta.2026.201681

Figure Lengend Snippet: Schematic of the overall experiment design for promoter comparison study (A) Viral vectors used in the study. (B) Six-week-old wild-type FVB/NJ mice (C) were injected with AAVDJ-CBA-eGFP, AAVDJ-EF1α-eGFP, AAVDJ-hSYN-eGFP, AAVDJ-CP040-eGFP, or vehicle (1x PBS) through the ICV or IT route. (D and E) Mice were euthanized 9 weeks after AAV injection, and tissue analysis done for viral vg and eGFP transcript and protein analysis for promoter comparison.

Article Snippet: Five-week-old WT FVB/NJ (stock# 001800) mice were ordered from Jackson Laboratory.

Techniques: Comparison, Injection

Journal: EMBO Reports

Article Title: T cell‐dependent bispecific antibodies alter organ‐specific endothelial cell–T cell interaction

doi: 10.15252/embr.202255532

Figure Lengend Snippet:

Article Snippet: A 1‐cm incision was made in the skin just rostral to the third mammary fat pad on FVB WT mice obtained from Jackson Laboratory (FVB/NJ JAX stock number: 001800).

Techniques: Recombinant, Purification, Blocking Assay, Produced, RNAscope, Sequencing, Negative Control, Protease Inhibitor, Software, Multiplex Assay, Cell Isolation, Enzyme-linked Immunosorbent Assay, Library Quantification, BIA-KA, Gene Expression