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chondrocyte differentiation medium cdmtm  (Lonza)


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    Lonza chondrocyte differentiation medium cdmtm
    Chondrocyte Differentiation Medium Cdmtm, supplied by Lonza, 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/result/chondrocyte differentiation medium cdmtm/product/Lonza
    Average 90 stars, based on 1 article reviews
    chondrocyte differentiation medium cdmtm - by Bioz Stars, 2026-03
    90/100 stars

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    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.
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    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: