Results shown for selected experiment:
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Contents identified in selected experiment:
Top 200 abundant gene(s) for selected experiment:
Other experiments from same study (PubMed ID):
PubMed ID | Species | Experiment description | Sample | Sample name | Identifications | Isolation methods | Vesicle type | MISEV | Quantification | |
1 | 33638284 | Canis lupus familiaris | Transglutaminase-2, RNA-binding proteins and mitochondrial proteins selectively traffic to MDCK cell-derived microvesicles following H-Ras-induced epithelial-mesenchymal transition | Kidney cells | MDCK - 10K pellet | Protein | Differential centrifugation | Microvesicles | Large EVs | EVQuant |
2 | 33638284 | Canis lupus familiaris | Transglutaminase-2, RNA-binding proteins and mitochondrial proteins selectively traffic to MDCK cell-derived microvesicles following H-Ras-induced epithelial-mesenchymal transition | Kidney cells | MDCK (21D1) - 10K pellet | Protein | Differential centrifugation | Microvesicles | Large EVs | EVQuant |
Experiments in which KRTCAP3 is identified:
PubMed ID | Species | Experiment description | Sample | Sample name | Identifications | Isolation methods | Vesicle type | MISEV | Quantification | |
1 | 33638284 | Canis lupus familiaris | Transglutaminase-2, RNA-binding proteins and mitochondrial proteins selectively traffic to MDCK cell-derived microvesicles following H-Ras-induced epithelial-mesenchymal transition | Kidney cells | MDCK - 10K pellet | Protein | Differential centrifugation | Microvesicles | Large EVs | EVQuant |
2 | 33638284 | Canis lupus familiaris | Transglutaminase-2, RNA-binding proteins and mitochondrial proteins selectively traffic to MDCK cell-derived microvesicles following H-Ras-induced epithelial-mesenchymal transition | Kidney cells | MDCK (21D1) - 10K pellet | Protein | Differential centrifugation | Microvesicles | Large EVs | EVQuant |