human protein atlas list Search Results


human protein atlas list  (Human Protein Atlas)
86
Human Protein Atlas human protein atlas list
Human Protein Atlas List, supplied by Human Protein Atlas, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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surface marker gene list  (Human Protein Atlas)
86
Human Protein Atlas surface marker gene list
( A ) A schematic illustrating the experimental design: CD45 − CD71 + TER119 + CD44 + erythroblasts (total Erys) from spleens of CTRL mice or mice with advanced AML were sorted by flow cytometry and processed for scRNA-Seq on the 10x Genomics platform. ( B ) UMAP plot showing the cell cluster distribution for AML Erys and CTRL Erys. ( C ) Top 5 <t>gene</t> ontology terms and their corresponding P values in the identified clusters. ( D ) Pseudotime analysis illustrating the differentiation trajectory of C1–C4 (top) and the distribution of each cluster (bottom). ( E ) Relative proportions of AML Erys (red) and CTRL Erys (blue) in each cluster. ( F and G ) Directional network plots showing the number of incoming ( F ) and outgoing ( G ) interactions for AML C1 Erys and other cells in the AML microenvironment, including AML cells, endothelial cells (ECs), pericytes, Tcf21 + fibroblasts, and Tcf21 + mesenchymal stem cells (MSCs). ( H ) Venn diagram illustrating the intersection of C1 signature genes and a <t>list</t> of <t>surface</t> <t>marker</t> genes . The 14 identified genes are listed in the box below the Venn diagram. ( I ) Expression levels of the top 5 C1 surface marker genes across C1–C4. ( J ) Expression of Cd81 in C1 versus in C2–C4. ( K ) Representative Wright-Giemsa staining of the sorted CD81 + Erys and CD81 − Erys from the spleens of AML mice. Scale bar: 20 μm. ( L ) Cell counts and frequencies of CD81 + Erys in the spleens of CTRL mice and mice at different stages of AML ( n = 4). Data are presented as the mean ± SEM. The results are representative of 1 of 3 independent experiments with consistent trends. * P < 0.05 and *** P < 0.001, by 1-way ANOVA ( L ).
Surface Marker Gene List, supplied by Human Protein Atlas, 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/human+protein+atlas+list/pmc12700549-61-19-26?v=Human+Protein+Atlas
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reference secretome list  (Human Protein Atlas)
86
Human Protein Atlas reference secretome list
( A ) A schematic illustrating the experimental design: CD45 − CD71 + TER119 + CD44 + erythroblasts (total Erys) from spleens of CTRL mice or mice with advanced AML were sorted by flow cytometry and processed for scRNA-Seq on the 10x Genomics platform. ( B ) UMAP plot showing the cell cluster distribution for AML Erys and CTRL Erys. ( C ) Top 5 <t>gene</t> ontology terms and their corresponding P values in the identified clusters. ( D ) Pseudotime analysis illustrating the differentiation trajectory of C1–C4 (top) and the distribution of each cluster (bottom). ( E ) Relative proportions of AML Erys (red) and CTRL Erys (blue) in each cluster. ( F and G ) Directional network plots showing the number of incoming ( F ) and outgoing ( G ) interactions for AML C1 Erys and other cells in the AML microenvironment, including AML cells, endothelial cells (ECs), pericytes, Tcf21 + fibroblasts, and Tcf21 + mesenchymal stem cells (MSCs). ( H ) Venn diagram illustrating the intersection of C1 signature genes and a <t>list</t> of <t>surface</t> <t>marker</t> genes . The 14 identified genes are listed in the box below the Venn diagram. ( I ) Expression levels of the top 5 C1 surface marker genes across C1–C4. ( J ) Expression of Cd81 in C1 versus in C2–C4. ( K ) Representative Wright-Giemsa staining of the sorted CD81 + Erys and CD81 − Erys from the spleens of AML mice. Scale bar: 20 μm. ( L ) Cell counts and frequencies of CD81 + Erys in the spleens of CTRL mice and mice at different stages of AML ( n = 4). Data are presented as the mean ± SEM. The results are representative of 1 of 3 independent experiments with consistent trends. * P < 0.05 and *** P < 0.001, by 1-way ANOVA ( L ).
Reference Secretome List, supplied by Human Protein Atlas, 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/human+protein+atlas+list/pm41074024-62-7-17?v=Human+Protein+Atlas
Average 86 stars, based on 1 article reviews
reference secretome list - by Bioz Stars, 2026-08
86/100 stars
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Image Search Results


( A ) A schematic illustrating the experimental design: CD45 − CD71 + TER119 + CD44 + erythroblasts (total Erys) from spleens of CTRL mice or mice with advanced AML were sorted by flow cytometry and processed for scRNA-Seq on the 10x Genomics platform. ( B ) UMAP plot showing the cell cluster distribution for AML Erys and CTRL Erys. ( C ) Top 5 gene ontology terms and their corresponding P values in the identified clusters. ( D ) Pseudotime analysis illustrating the differentiation trajectory of C1–C4 (top) and the distribution of each cluster (bottom). ( E ) Relative proportions of AML Erys (red) and CTRL Erys (blue) in each cluster. ( F and G ) Directional network plots showing the number of incoming ( F ) and outgoing ( G ) interactions for AML C1 Erys and other cells in the AML microenvironment, including AML cells, endothelial cells (ECs), pericytes, Tcf21 + fibroblasts, and Tcf21 + mesenchymal stem cells (MSCs). ( H ) Venn diagram illustrating the intersection of C1 signature genes and a list of surface marker genes . The 14 identified genes are listed in the box below the Venn diagram. ( I ) Expression levels of the top 5 C1 surface marker genes across C1–C4. ( J ) Expression of Cd81 in C1 versus in C2–C4. ( K ) Representative Wright-Giemsa staining of the sorted CD81 + Erys and CD81 − Erys from the spleens of AML mice. Scale bar: 20 μm. ( L ) Cell counts and frequencies of CD81 + Erys in the spleens of CTRL mice and mice at different stages of AML ( n = 4). Data are presented as the mean ± SEM. The results are representative of 1 of 3 independent experiments with consistent trends. * P < 0.05 and *** P < 0.001, by 1-way ANOVA ( L ).

Journal: The Journal of Clinical Investigation

Article Title: Leukemia-expanded splenic CD81 + erythroblasts potentiate disease progression in mice by reshaping leukemic cell metabolism

doi: 10.1172/JCI193082

Figure Lengend Snippet: ( A ) A schematic illustrating the experimental design: CD45 − CD71 + TER119 + CD44 + erythroblasts (total Erys) from spleens of CTRL mice or mice with advanced AML were sorted by flow cytometry and processed for scRNA-Seq on the 10x Genomics platform. ( B ) UMAP plot showing the cell cluster distribution for AML Erys and CTRL Erys. ( C ) Top 5 gene ontology terms and their corresponding P values in the identified clusters. ( D ) Pseudotime analysis illustrating the differentiation trajectory of C1–C4 (top) and the distribution of each cluster (bottom). ( E ) Relative proportions of AML Erys (red) and CTRL Erys (blue) in each cluster. ( F and G ) Directional network plots showing the number of incoming ( F ) and outgoing ( G ) interactions for AML C1 Erys and other cells in the AML microenvironment, including AML cells, endothelial cells (ECs), pericytes, Tcf21 + fibroblasts, and Tcf21 + mesenchymal stem cells (MSCs). ( H ) Venn diagram illustrating the intersection of C1 signature genes and a list of surface marker genes . The 14 identified genes are listed in the box below the Venn diagram. ( I ) Expression levels of the top 5 C1 surface marker genes across C1–C4. ( J ) Expression of Cd81 in C1 versus in C2–C4. ( K ) Representative Wright-Giemsa staining of the sorted CD81 + Erys and CD81 − Erys from the spleens of AML mice. Scale bar: 20 μm. ( L ) Cell counts and frequencies of CD81 + Erys in the spleens of CTRL mice and mice at different stages of AML ( n = 4). Data are presented as the mean ± SEM. The results are representative of 1 of 3 independent experiments with consistent trends. * P < 0.05 and *** P < 0.001, by 1-way ANOVA ( L ).

Article Snippet: To determine the function of AML-expanded C1 Erys, we next intersected the signature genes of C1 with a curated surface marker gene list obtained from The Human Protein Atlas ( ) ( ).

Techniques: Flow Cytometry, Marker, Expressing, Staining