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cells ecs differentiation  (Lonza)


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    Lonza cells ecs differentiation
    According to treatment outline, the CPCs expressed CM, EC, SMC specific proteins. (A) CM progenitors expressed α-sarcomeric actinin, cTnI, MLC2v, cTnT and Cx43, scale bar = 50 μm. (B) Under TEM, these cells were rich in endoplasmic reticulum (ER) studded with ribosomes, developing myofilaments (mf), mitochondria (arrowhead) and glycogen particles. Nuclear chromatin material (N) was uniformly distributed in the nucleoplasm. <t>(C)</t> <t>Endothelial</t> progenitors expressed VE-cadherin and CD31, scale bar = 200 μm. LDL uptake by these cells was observed (D) and these also formed tube like structures (E). (F) Smooth muscle progenitors expressed a-SMA and calponin, scale bar = 200 μm. (G) FACS analysis revealed 95.2 ± 2.1% CMS, 90.3 ± 2.5% <t>ECs</t> and 92.3 ± 1.8% SMCs in basal differentiation medium.
    Cells Ecs Differentiation, supplied by Lonza, used in various techniques. Bioz Stars score: 97/100, based on 339 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/cells ecs differentiation/product/Lonza
    Average 97 stars, based on 339 article reviews
    cells ecs differentiation - by Bioz Stars, 2026-03
    97/100 stars

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    1) Product Images from "Cardiac Progenitors Induced from Human Induced Pluripotent Stem Cells with Cardiogenic Small Molecule Effectively Regenerate Infarcted Hearts and Attenuate Fibrosis"

    Article Title: Cardiac Progenitors Induced from Human Induced Pluripotent Stem Cells with Cardiogenic Small Molecule Effectively Regenerate Infarcted Hearts and Attenuate Fibrosis

    Journal: Shock (Augusta, Ga.)

    doi: 10.1097/SHK.0000000000001133

    According to treatment outline, the CPCs expressed CM, EC, SMC specific proteins. (A) CM progenitors expressed α-sarcomeric actinin, cTnI, MLC2v, cTnT and Cx43, scale bar = 50 μm. (B) Under TEM, these cells were rich in endoplasmic reticulum (ER) studded with ribosomes, developing myofilaments (mf), mitochondria (arrowhead) and glycogen particles. Nuclear chromatin material (N) was uniformly distributed in the nucleoplasm. (C) Endothelial progenitors expressed VE-cadherin and CD31, scale bar = 200 μm. LDL uptake by these cells was observed (D) and these also formed tube like structures (E). (F) Smooth muscle progenitors expressed a-SMA and calponin, scale bar = 200 μm. (G) FACS analysis revealed 95.2 ± 2.1% CMS, 90.3 ± 2.5% ECs and 92.3 ± 1.8% SMCs in basal differentiation medium.
    Figure Legend Snippet: According to treatment outline, the CPCs expressed CM, EC, SMC specific proteins. (A) CM progenitors expressed α-sarcomeric actinin, cTnI, MLC2v, cTnT and Cx43, scale bar = 50 μm. (B) Under TEM, these cells were rich in endoplasmic reticulum (ER) studded with ribosomes, developing myofilaments (mf), mitochondria (arrowhead) and glycogen particles. Nuclear chromatin material (N) was uniformly distributed in the nucleoplasm. (C) Endothelial progenitors expressed VE-cadherin and CD31, scale bar = 200 μm. LDL uptake by these cells was observed (D) and these also formed tube like structures (E). (F) Smooth muscle progenitors expressed a-SMA and calponin, scale bar = 200 μm. (G) FACS analysis revealed 95.2 ± 2.1% CMS, 90.3 ± 2.5% ECs and 92.3 ± 1.8% SMCs in basal differentiation medium.

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    Image Search Results


    According to treatment outline, the CPCs expressed CM, EC, SMC specific proteins. (A) CM progenitors expressed α-sarcomeric actinin, cTnI, MLC2v, cTnT and Cx43, scale bar = 50 μm. (B) Under TEM, these cells were rich in endoplasmic reticulum (ER) studded with ribosomes, developing myofilaments (mf), mitochondria (arrowhead) and glycogen particles. Nuclear chromatin material (N) was uniformly distributed in the nucleoplasm. (C) Endothelial progenitors expressed VE-cadherin and CD31, scale bar = 200 μm. LDL uptake by these cells was observed (D) and these also formed tube like structures (E). (F) Smooth muscle progenitors expressed a-SMA and calponin, scale bar = 200 μm. (G) FACS analysis revealed 95.2 ± 2.1% CMS, 90.3 ± 2.5% ECs and 92.3 ± 1.8% SMCs in basal differentiation medium.

    Journal: Shock (Augusta, Ga.)

    Article Title: Cardiac Progenitors Induced from Human Induced Pluripotent Stem Cells with Cardiogenic Small Molecule Effectively Regenerate Infarcted Hearts and Attenuate Fibrosis

    doi: 10.1097/SHK.0000000000001133

    Figure Lengend Snippet: According to treatment outline, the CPCs expressed CM, EC, SMC specific proteins. (A) CM progenitors expressed α-sarcomeric actinin, cTnI, MLC2v, cTnT and Cx43, scale bar = 50 μm. (B) Under TEM, these cells were rich in endoplasmic reticulum (ER) studded with ribosomes, developing myofilaments (mf), mitochondria (arrowhead) and glycogen particles. Nuclear chromatin material (N) was uniformly distributed in the nucleoplasm. (C) Endothelial progenitors expressed VE-cadherin and CD31, scale bar = 200 μm. LDL uptake by these cells was observed (D) and these also formed tube like structures (E). (F) Smooth muscle progenitors expressed a-SMA and calponin, scale bar = 200 μm. (G) FACS analysis revealed 95.2 ± 2.1% CMS, 90.3 ± 2.5% ECs and 92.3 ± 1.8% SMCs in basal differentiation medium.

    Article Snippet: For endothelial cells (ECs) differentiation, culture medium was switched to EGM-2V medium (Lonza) for another 10days.

    Techniques: