proteintech 15571 1 ap calnexin antibody Search Results


96
Proteintech calnexin
Calnexin, supplied by Proteintech, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/proteintech+15571+1+ap+calnexin+antibody/Calnexin+Antibody/pmc09312839-67-3-4
Average 96 stars, based on 1 article reviews
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Proteintech 4060 ab 2315049 calnexin proteintech
4060 Ab 2315049 Calnexin Proteintech, supplied by Proteintech, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/proteintech+15571+1+ap+calnexin+antibody/Phospho-AKT1+(Ser473)+Antibody/pm40637352-115-27-30
Average 96 stars, based on 1 article reviews
4060 ab 2315049 calnexin proteintech - by Bioz Stars, 2026-11
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94
Boster Bio calnexin
Calnexin, supplied by Boster Bio, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/proteintech+15571+1+ap+calnexin+antibody/Anti-CANX+Antibody/pmc11059144-165-18-24
Average 94 stars, based on 1 article reviews
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96
Proteintech cd81 tsg101 cd63 an calnexin
Isolation and characterization of plasma exosomes. ( A ) Transmission electron microscopy (TEM) image of plasma exosomes. ( B ) Western blot analysis of exosome protein markers <t>(CD63,</t> <t>CD81,</t> <t>TSG101,</t> and Calnexin C). BMECs denote bovine mammary epithelial cells. ( C , D ) Nanoparticle tracking analysis (NTA) of plasma exosomes.
Cd81 Tsg101 Cd63 An Calnexin, supplied by Proteintech, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/proteintech+15571+1+ap+calnexin+antibody/CD81+Antibody/pmc12345520-111-17-22
Average 96 stars, based on 1 article reviews
cd81 tsg101 cd63 an calnexin - by Bioz Stars, 2026-11
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Cell Signaling Technology Inc calnexin
Characterization of hucMSCs, sEVs, and CFs. (a) The surface markers of hucMSCs measured by flow cytometry. (b) Morphology of hucMSCs. Scale bar: 1000 μ m (i) and 500 μ m (ii). (c) Morphology of sEVs observed by TEM. Scale bar: 200 nm. (d) Particle size distribution of sEVs measured by NTA. (e) Brownian motion image of hucMSCs. (f) Protein expression of <t>CD9,</t> <t>TSG101,</t> CD81, and <t>calnexin</t> in hucMSCs and sEVs. (g, h) The expression of α -SMA, vimentin, collagen I, periostin, and CD31 on primary CFs was measured by immunofluorescence (g) and western blotting (h). Scale bar: 50 μ m.
Calnexin, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/proteintech+15571+1+ap+calnexin+antibody/Calnexin+Antibody/pmc08824744-62-38-53
Average 96 stars, based on 1 article reviews
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Proteintech rabbit igg
Characterization of hucMSCs, sEVs, and CFs. (a) The surface markers of hucMSCs measured by flow cytometry. (b) Morphology of hucMSCs. Scale bar: 1000 μ m (i) and 500 μ m (ii). (c) Morphology of sEVs observed by TEM. Scale bar: 200 nm. (d) Particle size distribution of sEVs measured by NTA. (e) Brownian motion image of hucMSCs. (f) Protein expression of <t>CD9,</t> <t>TSG101,</t> CD81, and <t>calnexin</t> in hucMSCs and sEVs. (g, h) The expression of α -SMA, vimentin, collagen I, periostin, and CD31 on primary CFs was measured by immunofluorescence (g) and western blotting (h). Scale bar: 50 μ m.
Rabbit Igg, supplied by Proteintech, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 96 stars, based on 1 article reviews
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Santa Cruz Biotechnology anti calnexin
Characterization of hucMSCs, sEVs, and CFs. (a) The surface markers of hucMSCs measured by flow cytometry. (b) Morphology of hucMSCs. Scale bar: 1000 μ m (i) and 500 μ m (ii). (c) Morphology of sEVs observed by TEM. Scale bar: 200 nm. (d) Particle size distribution of sEVs measured by NTA. (e) Brownian motion image of hucMSCs. (f) Protein expression of <t>CD9,</t> <t>TSG101,</t> CD81, and <t>calnexin</t> in hucMSCs and sEVs. (g, h) The expression of α -SMA, vimentin, collagen I, periostin, and CD31 on primary CFs was measured by immunofluorescence (g) and western blotting (h). Scale bar: 50 μ m.
Anti Calnexin, supplied by Santa Cruz Biotechnology, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/proteintech+15571+1+ap+calnexin+antibody/Calnexin+Antibody/pmc05811557-278-23-35
Average 96 stars, based on 1 article reviews
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Image Search Results


Isolation and characterization of plasma exosomes. ( A ) Transmission electron microscopy (TEM) image of plasma exosomes. ( B ) Western blot analysis of exosome protein markers (CD63, CD81, TSG101, and Calnexin C). BMECs denote bovine mammary epithelial cells. ( C , D ) Nanoparticle tracking analysis (NTA) of plasma exosomes.

Journal: Animals : an Open Access Journal from MDPI

Article Title: Proteomic Analysis of Differentially Expressed Plasma Exosome Proteins in Heat-Stressed Holstein cows

doi: 10.3390/ani15152286

Figure Lengend Snippet: Isolation and characterization of plasma exosomes. ( A ) Transmission electron microscopy (TEM) image of plasma exosomes. ( B ) Western blot analysis of exosome protein markers (CD63, CD81, TSG101, and Calnexin C). BMECs denote bovine mammary epithelial cells. ( C , D ) Nanoparticle tracking analysis (NTA) of plasma exosomes.

Article Snippet: The membrane was blocked with 5% skim milk for 1 h and then incubated with primary antibodies (CD81, TSG101, CD63, an Calnexin; Proteintech, Rosemont, IL, USA) overnight at 4 °C.

Techniques: Isolation, Clinical Proteomics, Transmission Assay, Electron Microscopy, Western Blot

Characterization of hucMSCs, sEVs, and CFs. (a) The surface markers of hucMSCs measured by flow cytometry. (b) Morphology of hucMSCs. Scale bar: 1000 μ m (i) and 500 μ m (ii). (c) Morphology of sEVs observed by TEM. Scale bar: 200 nm. (d) Particle size distribution of sEVs measured by NTA. (e) Brownian motion image of hucMSCs. (f) Protein expression of CD9, TSG101, CD81, and calnexin in hucMSCs and sEVs. (g, h) The expression of α -SMA, vimentin, collagen I, periostin, and CD31 on primary CFs was measured by immunofluorescence (g) and western blotting (h). Scale bar: 50 μ m.

Journal: Stem Cells International

Article Title: Small Extracellular Vesicles Derived from Human Umbilical Cord Mesenchymal Stem Cells Enhanced Proangiogenic Potential of Cardiac Fibroblasts via Angiopoietin-Like 4

doi: 10.1155/2022/3229289

Figure Lengend Snippet: Characterization of hucMSCs, sEVs, and CFs. (a) The surface markers of hucMSCs measured by flow cytometry. (b) Morphology of hucMSCs. Scale bar: 1000 μ m (i) and 500 μ m (ii). (c) Morphology of sEVs observed by TEM. Scale bar: 200 nm. (d) Particle size distribution of sEVs measured by NTA. (e) Brownian motion image of hucMSCs. (f) Protein expression of CD9, TSG101, CD81, and calnexin in hucMSCs and sEVs. (g, h) The expression of α -SMA, vimentin, collagen I, periostin, and CD31 on primary CFs was measured by immunofluorescence (g) and western blotting (h). Scale bar: 50 μ m.

Article Snippet: Next, the PVDF membranes were blocked with 5% milk for 1 h and incubated overnight at 4°C with primary antibodies against CD9 (1 : 1,000; Cell Signaling Technology), TSG101 (1 : 1,000; Boster), CD81 (1 : 800; Proteintech), calnexin (1 : 1,000; Boster), α -SMA (1 : 1,000; Boster), vimentin (1 : 1,000; Cell Signaling Technology), collagen I (1 : 1,000; Boster), periostin (1 : 1,000; Proteintech), CD31 (1 : 1,000; Arigo), Angptl4 (1 : 800; Cell Signaling Technology), cyclin D1 (1 : 800; Cell Signaling Technology), β -catenin (1 : 800; Cell Signaling Technology), and GAPDH (1 : 2,000; Cell Signaling Technology).

Techniques: Flow Cytometry, Expressing, Immunofluorescence, Western Blot