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Pseudotime analysis identifies regulators of differentiation, including AP-1 genes, that play a role in pre-leukemic B-1-cell identity. ( A ) B cell-specified common lymphoid progenitors (CLPs) progress through multiple stages of development to become immature B cells after undergoing V(D)J antigen receptor heavy (H) and light (L) chain recombination. B-2 cell development occurs in the bone marrow, whereas B-1 cell development occurs in the fetal liver. Early B-1 progenitor cells have been identified in the yolk sac as early as E8.25. Immature B-1 cells differentiate into <t>CD5</t> + B-1a or CD5- B-1b cells in the periphery, predominantly in serous cavities (e.g. pleural, peritoneal cavities). Expression of defining cell surface markers are indicated below each cell type. Cell surface markers expressed during B-1 cell development are not well defined. sIgM, surface immunoglobulin M. Created with BioRender.com. ( B ) B-1 (left) or B-2 (right) signature gene sets from Fitch et al. . Expression of signature genes in scRNA-seq data from Prdm14 -expressing pre-leukemic B cells is indicated, with significant differentially expressed genes highlighted in green (up-regulated) or orange (down-regulated). ( C ) Gene Ontology analysis of down-regulated genes in sorted pre-leukemia cells relative to immunophenotype-matched controls. ( D ) Pseudotime analysis was restricted to one manifold which included B cell-associated clusters 0, 1, 2, 11, and 17. One lineage was identified, beginning at cluster 11 and ending at cluster 1. ( E ) Thirty transcription factors were significantly differentially expressed along the pseudotime axis. ( F ) GO analysis of the 30 transcription factors identified enrichment of various biological processes.
Cd5 Apc Antibody, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Thermo Fisher cd5 rat igg2" mouse apc-efluor780 53-7.3
Pseudotime analysis identifies regulators of differentiation, including AP-1 genes, that play a role in pre-leukemic B-1-cell identity. ( A ) B cell-specified common lymphoid progenitors (CLPs) progress through multiple stages of development to become immature B cells after undergoing V(D)J antigen receptor heavy (H) and light (L) chain recombination. B-2 cell development occurs in the bone marrow, whereas B-1 cell development occurs in the fetal liver. Early B-1 progenitor cells have been identified in the yolk sac as early as E8.25. Immature B-1 cells differentiate into <t>CD5</t> + B-1a or CD5- B-1b cells in the periphery, predominantly in serous cavities (e.g. pleural, peritoneal cavities). Expression of defining cell surface markers are indicated below each cell type. Cell surface markers expressed during B-1 cell development are not well defined. sIgM, surface immunoglobulin M. Created with BioRender.com. ( B ) B-1 (left) or B-2 (right) signature gene sets from Fitch et al. . Expression of signature genes in scRNA-seq data from Prdm14 -expressing pre-leukemic B cells is indicated, with significant differentially expressed genes highlighted in green (up-regulated) or orange (down-regulated). ( C ) Gene Ontology analysis of down-regulated genes in sorted pre-leukemia cells relative to immunophenotype-matched controls. ( D ) Pseudotime analysis was restricted to one manifold which included B cell-associated clusters 0, 1, 2, 11, and 17. One lineage was identified, beginning at cluster 11 and ending at cluster 1. ( E ) Thirty transcription factors were significantly differentially expressed along the pseudotime axis. ( F ) GO analysis of the 30 transcription factors identified enrichment of various biological processes.
Cd5 Rat Igg2" Mouse Apc Efluor780 53 7.3, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Biogems International anti human cd56 apc flow antibody
Pseudotime analysis identifies regulators of differentiation, including AP-1 genes, that play a role in pre-leukemic B-1-cell identity. ( A ) B cell-specified common lymphoid progenitors (CLPs) progress through multiple stages of development to become immature B cells after undergoing V(D)J antigen receptor heavy (H) and light (L) chain recombination. B-2 cell development occurs in the bone marrow, whereas B-1 cell development occurs in the fetal liver. Early B-1 progenitor cells have been identified in the yolk sac as early as E8.25. Immature B-1 cells differentiate into <t>CD5</t> + B-1a or CD5- B-1b cells in the periphery, predominantly in serous cavities (e.g. pleural, peritoneal cavities). Expression of defining cell surface markers are indicated below each cell type. Cell surface markers expressed during B-1 cell development are not well defined. sIgM, surface immunoglobulin M. Created with BioRender.com. ( B ) B-1 (left) or B-2 (right) signature gene sets from Fitch et al. . Expression of signature genes in scRNA-seq data from Prdm14 -expressing pre-leukemic B cells is indicated, with significant differentially expressed genes highlighted in green (up-regulated) or orange (down-regulated). ( C ) Gene Ontology analysis of down-regulated genes in sorted pre-leukemia cells relative to immunophenotype-matched controls. ( D ) Pseudotime analysis was restricted to one manifold which included B cell-associated clusters 0, 1, 2, 11, and 17. One lineage was identified, beginning at cluster 11 and ending at cluster 1. ( E ) Thirty transcription factors were significantly differentially expressed along the pseudotime axis. ( F ) GO analysis of the 30 transcription factors identified enrichment of various biological processes.
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Cytek Biosciences cd5

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Thermo Fisher anti-mouse cd5 apc-cy7

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Thermo Fisher rat anti-canine cd5, clone ykix322.3, apc-efluor780

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Thermo Fisher anti-cd5-apc clone 53-7.3

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Pseudotime analysis identifies regulators of differentiation, including AP-1 genes, that play a role in pre-leukemic B-1-cell identity. ( A ) B cell-specified common lymphoid progenitors (CLPs) progress through multiple stages of development to become immature B cells after undergoing V(D)J antigen receptor heavy (H) and light (L) chain recombination. B-2 cell development occurs in the bone marrow, whereas B-1 cell development occurs in the fetal liver. Early B-1 progenitor cells have been identified in the yolk sac as early as E8.25. Immature B-1 cells differentiate into CD5 + B-1a or CD5- B-1b cells in the periphery, predominantly in serous cavities (e.g. pleural, peritoneal cavities). Expression of defining cell surface markers are indicated below each cell type. Cell surface markers expressed during B-1 cell development are not well defined. sIgM, surface immunoglobulin M. Created with BioRender.com. ( B ) B-1 (left) or B-2 (right) signature gene sets from Fitch et al. . Expression of signature genes in scRNA-seq data from Prdm14 -expressing pre-leukemic B cells is indicated, with significant differentially expressed genes highlighted in green (up-regulated) or orange (down-regulated). ( C ) Gene Ontology analysis of down-regulated genes in sorted pre-leukemia cells relative to immunophenotype-matched controls. ( D ) Pseudotime analysis was restricted to one manifold which included B cell-associated clusters 0, 1, 2, 11, and 17. One lineage was identified, beginning at cluster 11 and ending at cluster 1. ( E ) Thirty transcription factors were significantly differentially expressed along the pseudotime axis. ( F ) GO analysis of the 30 transcription factors identified enrichment of various biological processes.

Journal: Scientific Reports

Article Title: Functional and molecular single-cell analyses implicate PRDM14 in the initiation of B cell leukemia in mice

doi: 10.1038/s41598-025-93043-z

Figure Lengend Snippet: Pseudotime analysis identifies regulators of differentiation, including AP-1 genes, that play a role in pre-leukemic B-1-cell identity. ( A ) B cell-specified common lymphoid progenitors (CLPs) progress through multiple stages of development to become immature B cells after undergoing V(D)J antigen receptor heavy (H) and light (L) chain recombination. B-2 cell development occurs in the bone marrow, whereas B-1 cell development occurs in the fetal liver. Early B-1 progenitor cells have been identified in the yolk sac as early as E8.25. Immature B-1 cells differentiate into CD5 + B-1a or CD5- B-1b cells in the periphery, predominantly in serous cavities (e.g. pleural, peritoneal cavities). Expression of defining cell surface markers are indicated below each cell type. Cell surface markers expressed during B-1 cell development are not well defined. sIgM, surface immunoglobulin M. Created with BioRender.com. ( B ) B-1 (left) or B-2 (right) signature gene sets from Fitch et al. . Expression of signature genes in scRNA-seq data from Prdm14 -expressing pre-leukemic B cells is indicated, with significant differentially expressed genes highlighted in green (up-regulated) or orange (down-regulated). ( C ) Gene Ontology analysis of down-regulated genes in sorted pre-leukemia cells relative to immunophenotype-matched controls. ( D ) Pseudotime analysis was restricted to one manifold which included B cell-associated clusters 0, 1, 2, 11, and 17. One lineage was identified, beginning at cluster 11 and ending at cluster 1. ( E ) Thirty transcription factors were significantly differentially expressed along the pseudotime axis. ( F ) GO analysis of the 30 transcription factors identified enrichment of various biological processes.

Article Snippet: CD5-APC , eBioscience , 53 − 7.3.

Techniques: Expressing

Antibodies used for the CyTOF experiments.

Journal: Scientific Reports

Article Title: Functional and molecular single-cell analyses implicate PRDM14 in the initiation of B cell leukemia in mice

doi: 10.1038/s41598-025-93043-z

Figure Lengend Snippet: Antibodies used for the CyTOF experiments.

Article Snippet: CD5-APC , eBioscience , 53 − 7.3.

Techniques:

Antibodies used for the flow cytometry experiments.

Journal: Scientific Reports

Article Title: Functional and molecular single-cell analyses implicate PRDM14 in the initiation of B cell leukemia in mice

doi: 10.1038/s41598-025-93043-z

Figure Lengend Snippet: Antibodies used for the flow cytometry experiments.

Article Snippet: CD5-APC , eBioscience , 53 − 7.3.

Techniques: Flow Cytometry

Journal: STAR Protocols

Article Title: Protocol to induce cell labeling in vivo and to trace labeled hematopoietic cells using mouse models

doi: 10.1016/j.xpro.2024.103408

Figure Lengend Snippet:

Article Snippet: CD5 53-7.3 , Tonbo , 20-0051.

Techniques: Recombinant

Examples: Staining 5 samples of peritoneal cells for B-1 cell identification

Journal: STAR Protocols

Article Title: Protocol to induce cell labeling in vivo and to trace labeled hematopoietic cells using mouse models

doi: 10.1016/j.xpro.2024.103408

Figure Lengend Snippet: Examples: Staining 5 samples of peritoneal cells for B-1 cell identification

Article Snippet: CD5 53-7.3 , Tonbo , 20-0051.

Techniques: Staining

Journal: iScience

Article Title: Arginine methylation of the p30 C/EBPα oncoprotein regulates progenitor proliferation and myeloid differentiation

doi: 10.1016/j.isci.2024.111199

Figure Lengend Snippet:

Article Snippet: CD5 APC (Lineage cocktail) , eBioscience , #17-0051-82.

Techniques: Magnetic Beads, Virus, Retroviral, Recombinant, Red Blood Cell Lysis, Mutagenesis, Transformation Assay, Derivative Assay, Plasmid Preparation, Software, Imaging