mouse vcam Search Results


mouse vcam 1 cd106 mab  (R&D Systems)
93
R&D Systems mouse vcam 1 cd106 mab
Mouse Vcam 1 Cd106 Mab, supplied by R&D Systems, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/mouse+vcam/Mouse+VCAM-1%2FCD106+Antibody/pmc06778015-8-0-7
Average 93 stars, based on 1 article reviews
mouse vcam 1 cd106 mab - by Bioz Stars, 2026-10
93/100 stars
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quantikine elisa kit  (R&D Systems)
93
R&D Systems quantikine elisa kit
Quantikine Elisa Kit, supplied by R&D Systems, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/mouse+vcam/Mouse+VCAM-1%2FCD106+Quantikine+ELISA+Kit/pm26414017-81-31-34
Average 93 stars, based on 1 article reviews
quantikine elisa kit - by Bioz Stars, 2026-10
93/100 stars
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mouse vcam  (R&D Systems)
94
R&D Systems mouse vcam
Mouse Vcam, supplied by R&D Systems, 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/mouse+vcam/Mouse+VCAM-1%2FCD106+Quantikine+ELISA+Kit/pmc08833245-82-24-31
Average 94 stars, based on 1 article reviews
mouse vcam - by Bioz Stars, 2026-10
94/100 stars
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invivo mab anti mouse cd106 vcam 1  (Bio X Cell)
94
Bio X Cell invivo mab anti mouse cd106 vcam 1
Representative IHC staining of tumor core and adjacent region in PDAC patient (stage II) for <t>CD106</t> + . The corresponding magnification insets of the tumor core (red dotted line) or adjacent region (green dotted line) are displayed on the right. Scale bar, 500 μm in gross, 20 μm in magnification. Immunofluorescence staining of the pancreas obtained from a 2.5‐month‐old KC mouse for CD106 (red), α‐SMA (green) or CK19 (green), and DAPI (blue). Scale bar, 50 μm, 10 μm. Gating strategy for the identification of the CD106 + CD24 + CD44 + population in KC and WT mice. FACS analysis of the percentage of CD106 + among CD45 − CD31 − cells; each dot represents one mouse. The bars are representing the mean. The P ‐values were calculated using Student's t ‐test. Immunofluorescence staining of pancreases obtained from a KC mouse (left) and a 2.5‐month‐old KPC mouse (right) for CD44 (green), CD24 (red), and DAPI (blue). Scale bar, 50, 10 μm. Source data are available online for this figure.
Invivo Mab Anti Mouse Cd106 Vcam 1, supplied by Bio X Cell, 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/mouse+vcam/InVivoMAb+anti-mouse+CD106/pmc10074138-78-0-6
Average 94 stars, based on 1 article reviews
invivo mab anti mouse cd106 vcam 1 - by Bioz Stars, 2026-10
94/100 stars
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vascular cell adhesion molecule 1 vcam 1  (R&D Systems)
94
R&D Systems vascular cell adhesion molecule 1 vcam 1
Representative IHC staining of tumor core and adjacent region in PDAC patient (stage II) for <t>CD106</t> + . The corresponding magnification insets of the tumor core (red dotted line) or adjacent region (green dotted line) are displayed on the right. Scale bar, 500 μm in gross, 20 μm in magnification. Immunofluorescence staining of the pancreas obtained from a 2.5‐month‐old KC mouse for CD106 (red), α‐SMA (green) or CK19 (green), and DAPI (blue). Scale bar, 50 μm, 10 μm. Gating strategy for the identification of the CD106 + CD24 + CD44 + population in KC and WT mice. FACS analysis of the percentage of CD106 + among CD45 − CD31 − cells; each dot represents one mouse. The bars are representing the mean. The P ‐values were calculated using Student's t ‐test. Immunofluorescence staining of pancreases obtained from a KC mouse (left) and a 2.5‐month‐old KPC mouse (right) for CD44 (green), CD24 (red), and DAPI (blue). Scale bar, 50, 10 μm. Source data are available online for this figure.
Vascular Cell Adhesion Molecule 1 Vcam 1, supplied by R&D Systems, 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/mouse+vcam/Mouse+VCAM-1%2FCD106+DuoSet+ELISA/pm39414727-94-9-15
Average 94 stars, based on 1 article reviews
vascular cell adhesion molecule 1 vcam 1 - by Bioz Stars, 2026-10
94/100 stars
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goat anti mouse vcam 1 antibody  (R&D Systems)
91
R&D Systems goat anti mouse vcam 1 antibody
Representative IHC staining of tumor core and adjacent region in PDAC patient (stage II) for <t>CD106</t> + . The corresponding magnification insets of the tumor core (red dotted line) or adjacent region (green dotted line) are displayed on the right. Scale bar, 500 μm in gross, 20 μm in magnification. Immunofluorescence staining of the pancreas obtained from a 2.5‐month‐old KC mouse for CD106 (red), α‐SMA (green) or CK19 (green), and DAPI (blue). Scale bar, 50 μm, 10 μm. Gating strategy for the identification of the CD106 + CD24 + CD44 + population in KC and WT mice. FACS analysis of the percentage of CD106 + among CD45 − CD31 − cells; each dot represents one mouse. The bars are representing the mean. The P ‐values were calculated using Student's t ‐test. Immunofluorescence staining of pancreases obtained from a KC mouse (left) and a 2.5‐month‐old KPC mouse (right) for CD44 (green), CD24 (red), and DAPI (blue). Scale bar, 50, 10 μm. Source data are available online for this figure.
Goat Anti Mouse Vcam 1 Antibody, supplied by R&D Systems, used in various techniques. Bioz Stars score: 91/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/mouse+vcam/Mouse+VCAM-1%2FCD106+Biotinylated+Antibody/pm17328072-84-37-41
Average 91 stars, based on 1 article reviews
goat anti mouse vcam 1 antibody - by Bioz Stars, 2026-10
91/100 stars
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recombinant mouse vcam 1 fc chimera  (R&D Systems)
94
R&D Systems recombinant mouse vcam 1 fc chimera
Representative IHC staining of tumor core and adjacent region in PDAC patient (stage II) for <t>CD106</t> + . The corresponding magnification insets of the tumor core (red dotted line) or adjacent region (green dotted line) are displayed on the right. Scale bar, 500 μm in gross, 20 μm in magnification. Immunofluorescence staining of the pancreas obtained from a 2.5‐month‐old KC mouse for CD106 (red), α‐SMA (green) or CK19 (green), and DAPI (blue). Scale bar, 50 μm, 10 μm. Gating strategy for the identification of the CD106 + CD24 + CD44 + population in KC and WT mice. FACS analysis of the percentage of CD106 + among CD45 − CD31 − cells; each dot represents one mouse. The bars are representing the mean. The P ‐values were calculated using Student's t ‐test. Immunofluorescence staining of pancreases obtained from a KC mouse (left) and a 2.5‐month‐old KPC mouse (right) for CD44 (green), CD24 (red), and DAPI (blue). Scale bar, 50, 10 μm. Source data are available online for this figure.
Recombinant Mouse Vcam 1 Fc Chimera, supplied by R&D Systems, 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/mouse+vcam/Recombinant+Mouse+VCAM-1%2FCD106+Fc+Chimera+Protein%2C+CF/pmc02118716-117-20-24
Average 94 stars, based on 1 article reviews
recombinant mouse vcam 1 fc chimera - by Bioz Stars, 2026-10
94/100 stars
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antibody goat anticd106 vcam r  (R&D Systems)
95
R&D Systems antibody goat anticd106 vcam r
Representative IHC staining of tumor core and adjacent region in PDAC patient (stage II) for <t>CD106</t> + . The corresponding magnification insets of the tumor core (red dotted line) or adjacent region (green dotted line) are displayed on the right. Scale bar, 500 μm in gross, 20 μm in magnification. Immunofluorescence staining of the pancreas obtained from a 2.5‐month‐old KC mouse for CD106 (red), α‐SMA (green) or CK19 (green), and DAPI (blue). Scale bar, 50 μm, 10 μm. Gating strategy for the identification of the CD106 + CD24 + CD44 + population in KC and WT mice. FACS analysis of the percentage of CD106 + among CD45 − CD31 − cells; each dot represents one mouse. The bars are representing the mean. The P ‐values were calculated using Student's t ‐test. Immunofluorescence staining of pancreases obtained from a KC mouse (left) and a 2.5‐month‐old KPC mouse (right) for CD44 (green), CD24 (red), and DAPI (blue). Scale bar, 50, 10 μm. Source data are available online for this figure.
Antibody Goat Anticd106 Vcam R, supplied by R&D Systems, used in various techniques. Bioz Stars score: 95/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/mouse+vcam/Mouse+VCAM-1%2FCD106+Antibody/10__7554_slash_elife__35816-200-129-133
Average 95 stars, based on 1 article reviews
antibody goat anticd106 vcam r - by Bioz Stars, 2026-10
95/100 stars
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goat anti vascular cell adhesion protein 1  (R&D Systems)
93
R&D Systems goat anti vascular cell adhesion protein 1
Representative IHC staining of tumor core and adjacent region in PDAC patient (stage II) for <t>CD106</t> + . The corresponding magnification insets of the tumor core (red dotted line) or adjacent region (green dotted line) are displayed on the right. Scale bar, 500 μm in gross, 20 μm in magnification. Immunofluorescence staining of the pancreas obtained from a 2.5‐month‐old KC mouse for CD106 (red), α‐SMA (green) or CK19 (green), and DAPI (blue). Scale bar, 50 μm, 10 μm. Gating strategy for the identification of the CD106 + CD24 + CD44 + population in KC and WT mice. FACS analysis of the percentage of CD106 + among CD45 − CD31 − cells; each dot represents one mouse. The bars are representing the mean. The P ‐values were calculated using Student's t ‐test. Immunofluorescence staining of pancreases obtained from a KC mouse (left) and a 2.5‐month‐old KPC mouse (right) for CD44 (green), CD24 (red), and DAPI (blue). Scale bar, 50, 10 μm. Source data are available online for this figure.
Goat Anti Vascular Cell Adhesion Protein 1, supplied by R&D Systems, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/mouse+vcam/Mouse+VCAM-1%2FCD106+Antibody/pmc12519545-245-66-77
Average 93 stars, based on 1 article reviews
goat anti vascular cell adhesion protein 1 - by Bioz Stars, 2026-10
93/100 stars
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vcam 1  (R&D Systems)
94
R&D Systems vcam 1
Representative IHC staining of tumor core and adjacent region in PDAC patient (stage II) for <t>CD106</t> + . The corresponding magnification insets of the tumor core (red dotted line) or adjacent region (green dotted line) are displayed on the right. Scale bar, 500 μm in gross, 20 μm in magnification. Immunofluorescence staining of the pancreas obtained from a 2.5‐month‐old KC mouse for CD106 (red), α‐SMA (green) or CK19 (green), and DAPI (blue). Scale bar, 50 μm, 10 μm. Gating strategy for the identification of the CD106 + CD24 + CD44 + population in KC and WT mice. FACS analysis of the percentage of CD106 + among CD45 − CD31 − cells; each dot represents one mouse. The bars are representing the mean. The P ‐values were calculated using Student's t ‐test. Immunofluorescence staining of pancreases obtained from a KC mouse (left) and a 2.5‐month‐old KPC mouse (right) for CD44 (green), CD24 (red), and DAPI (blue). Scale bar, 50, 10 μm. Source data are available online for this figure.
Vcam 1, supplied by R&D Systems, 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/mouse+vcam/Recombinant+Mouse+VCAM-1%2FCD106+Fc+Chimera+Protein%2C+CF/pm26232433-113-54-67
Average 94 stars, based on 1 article reviews
vcam 1 - by Bioz Stars, 2026-10
94/100 stars
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pe conjugated mab anti cd106  (R&D Systems)
93
R&D Systems pe conjugated mab anti cd106
Representative IHC staining of tumor core and adjacent region in PDAC patient (stage II) for <t>CD106</t> + . The corresponding magnification insets of the tumor core (red dotted line) or adjacent region (green dotted line) are displayed on the right. Scale bar, 500 μm in gross, 20 μm in magnification. Immunofluorescence staining of the pancreas obtained from a 2.5‐month‐old KC mouse for CD106 (red), α‐SMA (green) or CK19 (green), and DAPI (blue). Scale bar, 50 μm, 10 μm. Gating strategy for the identification of the CD106 + CD24 + CD44 + population in KC and WT mice. FACS analysis of the percentage of CD106 + among CD45 − CD31 − cells; each dot represents one mouse. The bars are representing the mean. The P ‐values were calculated using Student's t ‐test. Immunofluorescence staining of pancreases obtained from a KC mouse (left) and a 2.5‐month‐old KPC mouse (right) for CD44 (green), CD24 (red), and DAPI (blue). Scale bar, 50, 10 μm. Source data are available online for this figure.
Pe Conjugated Mab Anti Cd106, supplied by R&D Systems, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/mouse+vcam/Mouse+VCAM-1%2FCD106+PE-conjugated+Antibody/10__1681_slash_asn__2014010057-101-12-16
Average 93 stars, based on 1 article reviews
pe conjugated mab anti cd106 - by Bioz Stars, 2026-10
93/100 stars
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mab6434  (R&D Systems)
94
R&D Systems mab6434
Primary and secondary antibodies used in this study
Mab6434, supplied by R&D Systems, 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/mouse+vcam/Mouse+VCAM-1%2FCD106+Antibody/pmc09120697-4-9-5
Average 94 stars, based on 1 article reviews
mab6434 - by Bioz Stars, 2026-10
94/100 stars
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Image Search Results


Representative IHC staining of tumor core and adjacent region in PDAC patient (stage II) for CD106 + . The corresponding magnification insets of the tumor core (red dotted line) or adjacent region (green dotted line) are displayed on the right. Scale bar, 500 μm in gross, 20 μm in magnification. Immunofluorescence staining of the pancreas obtained from a 2.5‐month‐old KC mouse for CD106 (red), α‐SMA (green) or CK19 (green), and DAPI (blue). Scale bar, 50 μm, 10 μm. Gating strategy for the identification of the CD106 + CD24 + CD44 + population in KC and WT mice. FACS analysis of the percentage of CD106 + among CD45 − CD31 − cells; each dot represents one mouse. The bars are representing the mean. The P ‐values were calculated using Student's t ‐test. Immunofluorescence staining of pancreases obtained from a KC mouse (left) and a 2.5‐month‐old KPC mouse (right) for CD44 (green), CD24 (red), and DAPI (blue). Scale bar, 50, 10 μm. Source data are available online for this figure.

Journal: EMBO Reports

Article Title: Pericyte stem cells induce Ly6G + cell accumulation and immunotherapy resistance in pancreatic cancer

doi: 10.15252/embr.202256524

Figure Lengend Snippet: Representative IHC staining of tumor core and adjacent region in PDAC patient (stage II) for CD106 + . The corresponding magnification insets of the tumor core (red dotted line) or adjacent region (green dotted line) are displayed on the right. Scale bar, 500 μm in gross, 20 μm in magnification. Immunofluorescence staining of the pancreas obtained from a 2.5‐month‐old KC mouse for CD106 (red), α‐SMA (green) or CK19 (green), and DAPI (blue). Scale bar, 50 μm, 10 μm. Gating strategy for the identification of the CD106 + CD24 + CD44 + population in KC and WT mice. FACS analysis of the percentage of CD106 + among CD45 − CD31 − cells; each dot represents one mouse. The bars are representing the mean. The P ‐values were calculated using Student's t ‐test. Immunofluorescence staining of pancreases obtained from a KC mouse (left) and a 2.5‐month‐old KPC mouse (right) for CD44 (green), CD24 (red), and DAPI (blue). Scale bar, 50, 10 μm. Source data are available online for this figure.

Article Snippet: InVivo Mab anti‐mouse CD106 (VCAM‐1) , Bio X Cell , Cat# BE0027, RRID:AB_1107572.

Techniques: Immunohistochemistry, Immunofluorescence, Staining

Representative IHC staining for CD106 + in normal pancreas. Scale bar, 50 μm. Representative IHC staining for CD106 + in IPMN+PanIN I‐III and IPMT human samples. The adjacent region (above) and tumor core (below) were paired from the same patient respectively, corresponding to the diagnosis. The red arrow indicated the CD106 + spindle‐like cells. Scale bar, 50 μm. Representative IHC staining of pancreatic lesions of human TMA for CD106 + . The magnification region indicates representative CD106 + cells. Scale bar, 200, 50 μm. Quantification of CD106 expression in pancreatitis, PanIN and PDAC lesions according to patients' pathological references of TMA (Appendix Table ). * P < 0.05 and ** P < 0.01. **** P < 0.0001. The P ‐values were calculated using Student's t ‐test. Representative IF staining of the PeSC cell line on a coverslip for CD106 (green), mCherry (red), and DAPI (blue). Scale bar, 50 μm.

Journal: EMBO Reports

Article Title: Pericyte stem cells induce Ly6G + cell accumulation and immunotherapy resistance in pancreatic cancer

doi: 10.15252/embr.202256524

Figure Lengend Snippet: Representative IHC staining for CD106 + in normal pancreas. Scale bar, 50 μm. Representative IHC staining for CD106 + in IPMN+PanIN I‐III and IPMT human samples. The adjacent region (above) and tumor core (below) were paired from the same patient respectively, corresponding to the diagnosis. The red arrow indicated the CD106 + spindle‐like cells. Scale bar, 50 μm. Representative IHC staining of pancreatic lesions of human TMA for CD106 + . The magnification region indicates representative CD106 + cells. Scale bar, 200, 50 μm. Quantification of CD106 expression in pancreatitis, PanIN and PDAC lesions according to patients' pathological references of TMA (Appendix Table ). * P < 0.05 and ** P < 0.01. **** P < 0.0001. The P ‐values were calculated using Student's t ‐test. Representative IF staining of the PeSC cell line on a coverslip for CD106 (green), mCherry (red), and DAPI (blue). Scale bar, 50 μm.

Article Snippet: InVivo Mab anti‐mouse CD106 (VCAM‐1) , Bio X Cell , Cat# BE0027, RRID:AB_1107572.

Techniques: Immunohistochemistry, Biomarker Discovery, Expressing, Staining

Experimental protocol for bone marrow chimeras. One month old KC mice were sublethally irradiated and reconstituted with bone marrow cells from a Tomato expressing mouse. After reconstitution, the chimeras were sacrificed on day 60. Representative dot plots of reconstituted bone marrow cells (Tomato + ) in KC chimeras compared to the nonreconstituted KC mice as control by FACS analysis. Quantification of reconstituted cells (Tomato + ) among CD45 + immune cells in either pancreas or periphery of KC chimeras compared to the control. Three mice in each condition. Representative dot plots and gating strategy of distinguishing the reconstituted CD106 + cells (Tomato + ) and nonreconstituted CD106 + cells (Tomato − ) in KC chimeras. Three mice in the group, each dot represents one mouse. Representative IF staining for CD106 (green) and Tomato (red) in the pancreas of chimera mice. Inset shows colocalization of CD106‐ and Tomato‐stained cells. Scale bar, 50 μm (upper), 10 μm (lower). Data information: ns not significant, * P < 0.05, ** P < 0.01, *** P < 0.001 and **** P < 0.0001. The P ‐values were calculated using Student's t ‐test.

Journal: EMBO Reports

Article Title: Pericyte stem cells induce Ly6G + cell accumulation and immunotherapy resistance in pancreatic cancer

doi: 10.15252/embr.202256524

Figure Lengend Snippet: Experimental protocol for bone marrow chimeras. One month old KC mice were sublethally irradiated and reconstituted with bone marrow cells from a Tomato expressing mouse. After reconstitution, the chimeras were sacrificed on day 60. Representative dot plots of reconstituted bone marrow cells (Tomato + ) in KC chimeras compared to the nonreconstituted KC mice as control by FACS analysis. Quantification of reconstituted cells (Tomato + ) among CD45 + immune cells in either pancreas or periphery of KC chimeras compared to the control. Three mice in each condition. Representative dot plots and gating strategy of distinguishing the reconstituted CD106 + cells (Tomato + ) and nonreconstituted CD106 + cells (Tomato − ) in KC chimeras. Three mice in the group, each dot represents one mouse. Representative IF staining for CD106 (green) and Tomato (red) in the pancreas of chimera mice. Inset shows colocalization of CD106‐ and Tomato‐stained cells. Scale bar, 50 μm (upper), 10 μm (lower). Data information: ns not significant, * P < 0.05, ** P < 0.01, *** P < 0.001 and **** P < 0.0001. The P ‐values were calculated using Student's t ‐test.

Article Snippet: InVivo Mab anti‐mouse CD106 (VCAM‐1) , Bio X Cell , Cat# BE0027, RRID:AB_1107572.

Techniques: Irradiation, Expressing, Control, Staining

A, B In vivo neutralization of CD106: (A) Experiment setting. (B) Tumor weight, FACS analysis of % PeSC + among CD45 − cells, % Epi + among CD45 − cells, % CD11b + among CD45 + cells, % Ly6G + CD11b + among CD45 + cells, % CD11b + F4/80 + among CD45 + cells, % CD11b + F4/80 + CD103 + among CD45 + cells (eight mice in each group, five for FACS analysis, and three for histological analysis. Quantification of PeSCs and Epi cells were cumulative from two FACS panels as technical duplicates). C–L In vivo depletion of CCL5 impact the macrophages differentiation: (C) Experimental setting. (D) Tumor weight of the grafts formed by Epi + PeSC in CCL5‐depleted conditions compared with undepleted conditions. FACS analysis of the percentage of CD11b + cells (E), Ly6G + CD11b + (F), F4/80 + CD11b + (G), F4/80 + CSFR1 + (H), F4/80 + CD163 + (I), F4/80 + CD11b + CD103 + (J), F4/80 + CD11b + PD‐L1 + (K) and CD8 + cells (L) among CD45 + cells derived from the tumor grafts. Ten mice in each group, six for FACS analysis and four for histological analysis. Data information: * P < 0.05, ** P < 0.01, *** P < 0.001, and **** P < 0.0001. The P ‐values were calculated using Student's t ‐test.

Journal: EMBO Reports

Article Title: Pericyte stem cells induce Ly6G + cell accumulation and immunotherapy resistance in pancreatic cancer

doi: 10.15252/embr.202256524

Figure Lengend Snippet: A, B In vivo neutralization of CD106: (A) Experiment setting. (B) Tumor weight, FACS analysis of % PeSC + among CD45 − cells, % Epi + among CD45 − cells, % CD11b + among CD45 + cells, % Ly6G + CD11b + among CD45 + cells, % CD11b + F4/80 + among CD45 + cells, % CD11b + F4/80 + CD103 + among CD45 + cells (eight mice in each group, five for FACS analysis, and three for histological analysis. Quantification of PeSCs and Epi cells were cumulative from two FACS panels as technical duplicates). C–L In vivo depletion of CCL5 impact the macrophages differentiation: (C) Experimental setting. (D) Tumor weight of the grafts formed by Epi + PeSC in CCL5‐depleted conditions compared with undepleted conditions. FACS analysis of the percentage of CD11b + cells (E), Ly6G + CD11b + (F), F4/80 + CD11b + (G), F4/80 + CSFR1 + (H), F4/80 + CD163 + (I), F4/80 + CD11b + CD103 + (J), F4/80 + CD11b + PD‐L1 + (K) and CD8 + cells (L) among CD45 + cells derived from the tumor grafts. Ten mice in each group, six for FACS analysis and four for histological analysis. Data information: * P < 0.05, ** P < 0.01, *** P < 0.001, and **** P < 0.0001. The P ‐values were calculated using Student's t ‐test.

Article Snippet: InVivo Mab anti‐mouse CD106 (VCAM‐1) , Bio X Cell , Cat# BE0027, RRID:AB_1107572.

Techniques: In Vivo, Neutralization, Derivative Assay

Journal: EMBO Reports

Article Title: Pericyte stem cells induce Ly6G + cell accumulation and immunotherapy resistance in pancreatic cancer

doi: 10.15252/embr.202256524

Figure Lengend Snippet:

Article Snippet: InVivo Mab anti‐mouse CD106 (VCAM‐1) , Bio X Cell , Cat# BE0027, RRID:AB_1107572.

Techniques: Recombinant, Purification, Plasmid Preparation, Control, Mutagenesis, Sequencing, SYBR Green Assay, Saline, Modification, Membrane, Activation Assay, Concentration Assay, Staining, Western Blot

Primary and secondary antibodies used in this study

Journal: Neural Regeneration Research

Article Title: ADAM10 facilitates rapid neural stem cell cycling and proper positioning within the subventricular zone niche via JAMC/RAP1Gap signaling

doi: 10.4103/1673-5374.339007

Figure Lengend Snippet: Primary and secondary antibodies used in this study

Article Snippet: Rat monoclonal anti- mouseVCAM1 , R and D Systems, MAB6434 , AB_2214050.

Techniques: