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Shanghai Model Organisms Center apoe knockout
Apoe Knockout, supplied by Shanghai Model Organisms Center, 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/apoe+knockout/mice/pmc12860263-292-0-15
Average 86 stars, based on 1 article reviews
apoe knockout - by Bioz Stars, 2026-10
86/100 stars

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Article Title: Apolipoprotein E knockout attenuates vascular graft fibrosis by reducing profibrotic macrophage formation through low-density lipoprotein receptor related protein 1
Article Snippet: Apoe-knockout (KO, Apoe −/− ) SD rats (SD-Apoe em1Smoc , NR-KO-190003) were purchased from the Shanghai Model Organisms Center.



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Jackson Laboratory homozygous apoe knockout apoe mice
The mouse was anesthetized using CO2 in an induction chamber until the absence of pedal reflex was confirmed. Dissection was performed under aseptic conditions. Upper panel shows (A, B, C, D, E, F) (from left to right), the mouse was positioned supine on a dissection board and secured with colored tab through the limbs. An incision was made through the abdominal skin using sterile scissors, starting from the lower abdomen and extending to the thoracic cavity. The skin was gently retracted laterally to expose the abdominal wall muscles. Lower panel shows (G, H, I, J, K, L) (from left to right), an incision was made below the xiphoid process (subxiphoid incision) and then cuts through the diaphragm muscle to access the thoracic cavity of <t>Apoe-/-.</t> The diaphragm was carefully incised to access the thoracic cavity, revealing the organs including heart and lungs Dissection of the internal thoracic cavity to expose LIMA. (B) To visualize and isolate LIMA and RIMA, the inner wall of thoracic cavity was carefully dissected, and image was taken with high resolution camera to show LIMA and RIMA. (C) Both LIMA (black arrow) and RIMA (white arrow) run along the inner surface of the anterior chest wall, and both are running parallel to the sternum (yellow star), along the posterior surface of the thoracic wall behind the sternal ends of the costal cartilages. (D) Notably, LIMA is not adherent to the thoracic wall immediately upon branching from the subclavian artery, allowing for easier removal of surrounding fascia and connective tissue through this natural plane of separation. (E) The internal thoracic wall of Apoe-/- mouse post-dissection and prior to perfusion showing LIMA and RIMA originate from subclavian arteries that are branching off the aortic arch. (F) Following dissection and removal of the heart to expose the aortic arch and its three major arteries coming form the aorta shows that LIMA and RIMA originate form left subclavian artery and right subclavian artery, respectively. (G) Closer examination reveals that LIMA (right black arrow) and RIMA (left black arrow) branches off from the inferior aspect of the left subclavian artery (right yellow arrow) and the right subclavian artery (left yellow arrow) and then both are descending along the anterior chest wall. (H) Pulling out LIMA confirms anatomical attachment to subclavian artery.
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<t>ApoE,</t> apolipoprotein E; KO, knockout; DMSO, dimethyl sulfoxide; NF-κB, nuclear factor kappa-light-chain-enhancer of activated B cells; ICAM-1, intercellular adhesion molecule-1. * Indicates p <0.05 Student’s t -test. Scale bar indicates 50 µm.
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The mouse was anesthetized using CO2 in an induction chamber until the absence of pedal reflex was confirmed. Dissection was performed under aseptic conditions. Upper panel shows (A, B, C, D, E, F) (from left to right), the mouse was positioned supine on a dissection board and secured with colored tab through the limbs. An incision was made through the abdominal skin using sterile scissors, starting from the lower abdomen and extending to the thoracic cavity. The skin was gently retracted laterally to expose the abdominal wall muscles. Lower panel shows (G, H, I, J, K, L) (from left to right), an incision was made below the xiphoid process (subxiphoid incision) and then cuts through the diaphragm muscle to access the thoracic cavity of Apoe-/-. The diaphragm was carefully incised to access the thoracic cavity, revealing the organs including heart and lungs Dissection of the internal thoracic cavity to expose LIMA. (B) To visualize and isolate LIMA and RIMA, the inner wall of thoracic cavity was carefully dissected, and image was taken with high resolution camera to show LIMA and RIMA. (C) Both LIMA (black arrow) and RIMA (white arrow) run along the inner surface of the anterior chest wall, and both are running parallel to the sternum (yellow star), along the posterior surface of the thoracic wall behind the sternal ends of the costal cartilages. (D) Notably, LIMA is not adherent to the thoracic wall immediately upon branching from the subclavian artery, allowing for easier removal of surrounding fascia and connective tissue through this natural plane of separation. (E) The internal thoracic wall of Apoe-/- mouse post-dissection and prior to perfusion showing LIMA and RIMA originate from subclavian arteries that are branching off the aortic arch. (F) Following dissection and removal of the heart to expose the aortic arch and its three major arteries coming form the aorta shows that LIMA and RIMA originate form left subclavian artery and right subclavian artery, respectively. (G) Closer examination reveals that LIMA (right black arrow) and RIMA (left black arrow) branches off from the inferior aspect of the left subclavian artery (right yellow arrow) and the right subclavian artery (left yellow arrow) and then both are descending along the anterior chest wall. (H) Pulling out LIMA confirms anatomical attachment to subclavian artery.

Journal: bioRxiv

Article Title: Microsurgical Isolation and Molecular Characterization of the Mouse Left Internal Mammary Artery: Insights into Natural Resistance to Atherosclerosis

doi: 10.64898/2026.01.08.698440

Figure Lengend Snippet: The mouse was anesthetized using CO2 in an induction chamber until the absence of pedal reflex was confirmed. Dissection was performed under aseptic conditions. Upper panel shows (A, B, C, D, E, F) (from left to right), the mouse was positioned supine on a dissection board and secured with colored tab through the limbs. An incision was made through the abdominal skin using sterile scissors, starting from the lower abdomen and extending to the thoracic cavity. The skin was gently retracted laterally to expose the abdominal wall muscles. Lower panel shows (G, H, I, J, K, L) (from left to right), an incision was made below the xiphoid process (subxiphoid incision) and then cuts through the diaphragm muscle to access the thoracic cavity of Apoe-/-. The diaphragm was carefully incised to access the thoracic cavity, revealing the organs including heart and lungs Dissection of the internal thoracic cavity to expose LIMA. (B) To visualize and isolate LIMA and RIMA, the inner wall of thoracic cavity was carefully dissected, and image was taken with high resolution camera to show LIMA and RIMA. (C) Both LIMA (black arrow) and RIMA (white arrow) run along the inner surface of the anterior chest wall, and both are running parallel to the sternum (yellow star), along the posterior surface of the thoracic wall behind the sternal ends of the costal cartilages. (D) Notably, LIMA is not adherent to the thoracic wall immediately upon branching from the subclavian artery, allowing for easier removal of surrounding fascia and connective tissue through this natural plane of separation. (E) The internal thoracic wall of Apoe-/- mouse post-dissection and prior to perfusion showing LIMA and RIMA originate from subclavian arteries that are branching off the aortic arch. (F) Following dissection and removal of the heart to expose the aortic arch and its three major arteries coming form the aorta shows that LIMA and RIMA originate form left subclavian artery and right subclavian artery, respectively. (G) Closer examination reveals that LIMA (right black arrow) and RIMA (left black arrow) branches off from the inferior aspect of the left subclavian artery (right yellow arrow) and the right subclavian artery (left yellow arrow) and then both are descending along the anterior chest wall. (H) Pulling out LIMA confirms anatomical attachment to subclavian artery.

Article Snippet: Homozygous Apoe-knockout (Apoe-/-) mice were bought from Jackson lab.

Techniques: Dissection, Sterility, Muscles

(A) Isolated RIMA and LIMA before fat removal. (B) LIMA and RIMA after the removal of perivascular adipose tissue. (C) Aorta from apoe-/- mouse showing plaque build ups in the arch and branched arteries Characterization of LIMA. (D) Analysis of 4 LIMA and 4 aorta samples based on normalized expression values of 1541 genes. Hierarchical clustering shows the Pearson rank correlation between all samples. (E) Principal component analysis (PCA) plot showing the distribution of LIMA and aorta sample groups. (F) Heatmap showing z-scores for arterial gene modules across aorta (blue) and LIMA (red) samples. (G) Comparison of the read counts of arterial genes in aorta and LIMA of mice.

Journal: bioRxiv

Article Title: Microsurgical Isolation and Molecular Characterization of the Mouse Left Internal Mammary Artery: Insights into Natural Resistance to Atherosclerosis

doi: 10.64898/2026.01.08.698440

Figure Lengend Snippet: (A) Isolated RIMA and LIMA before fat removal. (B) LIMA and RIMA after the removal of perivascular adipose tissue. (C) Aorta from apoe-/- mouse showing plaque build ups in the arch and branched arteries Characterization of LIMA. (D) Analysis of 4 LIMA and 4 aorta samples based on normalized expression values of 1541 genes. Hierarchical clustering shows the Pearson rank correlation between all samples. (E) Principal component analysis (PCA) plot showing the distribution of LIMA and aorta sample groups. (F) Heatmap showing z-scores for arterial gene modules across aorta (blue) and LIMA (red) samples. (G) Comparison of the read counts of arterial genes in aorta and LIMA of mice.

Article Snippet: Homozygous Apoe-knockout (Apoe-/-) mice were bought from Jackson lab.

Techniques: Isolation, Expressing, Comparison

ApoE, apolipoprotein E; KO, knockout; DMSO, dimethyl sulfoxide; NF-κB, nuclear factor kappa-light-chain-enhancer of activated B cells; ICAM-1, intercellular adhesion molecule-1. * Indicates p <0.05 Student’s t -test. Scale bar indicates 50 µm.

Journal: Journal of Lipid and Atherosclerosis

Article Title: Tigloylgomisin P Inhibits Endothelial Inflammation by Regulating the NF-κB and Smad1/5/9 Pathways

doi: 10.12997/jla.2026.15.1.173

Figure Lengend Snippet: ApoE, apolipoprotein E; KO, knockout; DMSO, dimethyl sulfoxide; NF-κB, nuclear factor kappa-light-chain-enhancer of activated B cells; ICAM-1, intercellular adhesion molecule-1. * Indicates p <0.05 Student’s t -test. Scale bar indicates 50 µm.

Article Snippet: Eight-week-old male apolipoprotein E (ApoE) knockout mice (The Jackson Laboratory), maintained on normal chow, were intraperitoneally injected with tigloylgomisin P at 5 mg/kg, dissolved in DMSO/corn oil (total injection volume 200 μL, consisting of 12.1 μL of the compound in DMSO and 187.9 μL of the corn oil).

Techniques: Knock-Out