mass Search Results


ms grade  (New England Biolabs)
95
New England Biolabs ms grade
Ms Grade, supplied by New England Biolabs, used in various techniques. Bioz Stars score: 95/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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msmls library  (IROA Technologies LLC)
96
IROA Technologies LLC msmls library
Msmls Library, supplied by IROA Technologies LLC, 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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timstof pro 2 mass spectrometer  (Bruker Corporation)
99
Bruker Corporation timstof pro 2 mass spectrometer
Timstof Pro 2 Mass Spectrometer, supplied by Bruker Corporation, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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liquid chromatography tandem mass spectrometry analysis  (Proteintech)
96
Proteintech liquid chromatography tandem mass spectrometry analysis
Liquid Chromatography Tandem Mass Spectrometry Analysis, 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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imaging mass cytometry  (fluidigm)
98
fluidigm imaging mass cytometry
Fig. 7. Spatial-seq reinforces the effects of IFN-producing interfollicular KCs on CD16+ DCs and FBs in the superficial dermis. N = 4 biological replicates; data are shown for the most complex sample as defined by the highest number of spots after quality control steps. (A) Hematoxylin and eosin staining of DLE tissue section cor- responding to spatial-seq data below. Scale bars, 200 m (A to F). (B) Spatial scatter pie plot showing cell type composition based on detection of scRNA-seq signatures corre- sponding to seven cell types. Each spot is represented as a pie chart showing relative cell type proportions. Spot coordinates correspond to tissue location. (C) Spatial heatmap of the IFN FB subset gene signature. Color, scaled expression of each subset gene signature. Only spots meeting an FB prediction score threshold of 0.25 are shown. (D) Spatial heatmap of the LC subset gene signature. All spots are shown. (E) Spatial heatmap of the pDC subset gene signature. All spots are shown. (F) Spatial heatmap of the CD16+ DC subset gene signature. All spots are shown. (G) Representative image of a DLE skin section showing the localization of CD16+ DCs (as indicated by the CD14+CD11c+CD16+ immunophenotype) generated by imaging mass <t>cytometry.</t> Scale bar, 100 m. Insets, subepidermal enrichment of CD16+ DCs. (H) Heatmap depicting the number of the indicated cell types (columns) located within 4 m of each of the CD16+ DCs (rows) located across six DLE (N = 16 CD16+ DCs) and two sub- acute CLE (SCLE; N = 5 CD16+ DCs) sections. Color scale, number of neighboring cells.
Imaging Mass Cytometry, supplied by fluidigm, used in various techniques. Bioz Stars score: 98/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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arsenic concentrations  (National Research Council Canada)
93
National Research Council Canada arsenic concentrations
Fig. 7. Spatial-seq reinforces the effects of IFN-producing interfollicular KCs on CD16+ DCs and FBs in the superficial dermis. N = 4 biological replicates; data are shown for the most complex sample as defined by the highest number of spots after quality control steps. (A) Hematoxylin and eosin staining of DLE tissue section cor- responding to spatial-seq data below. Scale bars, 200 m (A to F). (B) Spatial scatter pie plot showing cell type composition based on detection of scRNA-seq signatures corre- sponding to seven cell types. Each spot is represented as a pie chart showing relative cell type proportions. Spot coordinates correspond to tissue location. (C) Spatial heatmap of the IFN FB subset gene signature. Color, scaled expression of each subset gene signature. Only spots meeting an FB prediction score threshold of 0.25 are shown. (D) Spatial heatmap of the LC subset gene signature. All spots are shown. (E) Spatial heatmap of the pDC subset gene signature. All spots are shown. (F) Spatial heatmap of the CD16+ DC subset gene signature. All spots are shown. (G) Representative image of a DLE skin section showing the localization of CD16+ DCs (as indicated by the CD14+CD11c+CD16+ immunophenotype) generated by imaging mass <t>cytometry.</t> Scale bar, 100 m. Insets, subepidermal enrichment of CD16+ DCs. (H) Heatmap depicting the number of the indicated cell types (columns) located within 4 m of each of the CD16+ DCs (rows) located across six DLE (N = 16 CD16+ DCs) and two sub- acute CLE (SCLE; N = 5 CD16+ DCs) sections. Color scale, number of neighboring cells.
Arsenic Concentrations, supplied by National Research Council Canada, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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triple quadruple mass spectrometer  (Bruker Corporation)
96
Bruker Corporation triple quadruple mass spectrometer
Fig. 7. Spatial-seq reinforces the effects of IFN-producing interfollicular KCs on CD16+ DCs and FBs in the superficial dermis. N = 4 biological replicates; data are shown for the most complex sample as defined by the highest number of spots after quality control steps. (A) Hematoxylin and eosin staining of DLE tissue section cor- responding to spatial-seq data below. Scale bars, 200 m (A to F). (B) Spatial scatter pie plot showing cell type composition based on detection of scRNA-seq signatures corre- sponding to seven cell types. Each spot is represented as a pie chart showing relative cell type proportions. Spot coordinates correspond to tissue location. (C) Spatial heatmap of the IFN FB subset gene signature. Color, scaled expression of each subset gene signature. Only spots meeting an FB prediction score threshold of 0.25 are shown. (D) Spatial heatmap of the LC subset gene signature. All spots are shown. (E) Spatial heatmap of the pDC subset gene signature. All spots are shown. (F) Spatial heatmap of the CD16+ DC subset gene signature. All spots are shown. (G) Representative image of a DLE skin section showing the localization of CD16+ DCs (as indicated by the CD14+CD11c+CD16+ immunophenotype) generated by imaging mass <t>cytometry.</t> Scale bar, 100 m. Insets, subepidermal enrichment of CD16+ DCs. (H) Heatmap depicting the number of the indicated cell types (columns) located within 4 m of each of the CD16+ DCs (rows) located across six DLE (N = 16 CD16+ DCs) and two sub- acute CLE (SCLE; N = 5 CD16+ DCs) sections. Color scale, number of neighboring cells.
Triple Quadruple Mass Spectrometer, supplied by Bruker Corporation, 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/result/triple quadruple mass spectrometer/product/Bruker Corporation
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pip3 mass elisa kit  (Echelon Biosciences)
95
Echelon Biosciences pip3 mass elisa kit
Fig. 7. Spatial-seq reinforces the effects of IFN-producing interfollicular KCs on CD16+ DCs and FBs in the superficial dermis. N = 4 biological replicates; data are shown for the most complex sample as defined by the highest number of spots after quality control steps. (A) Hematoxylin and eosin staining of DLE tissue section cor- responding to spatial-seq data below. Scale bars, 200 m (A to F). (B) Spatial scatter pie plot showing cell type composition based on detection of scRNA-seq signatures corre- sponding to seven cell types. Each spot is represented as a pie chart showing relative cell type proportions. Spot coordinates correspond to tissue location. (C) Spatial heatmap of the IFN FB subset gene signature. Color, scaled expression of each subset gene signature. Only spots meeting an FB prediction score threshold of 0.25 are shown. (D) Spatial heatmap of the LC subset gene signature. All spots are shown. (E) Spatial heatmap of the pDC subset gene signature. All spots are shown. (F) Spatial heatmap of the CD16+ DC subset gene signature. All spots are shown. (G) Representative image of a DLE skin section showing the localization of CD16+ DCs (as indicated by the CD14+CD11c+CD16+ immunophenotype) generated by imaging mass <t>cytometry.</t> Scale bar, 100 m. Insets, subepidermal enrichment of CD16+ DCs. (H) Heatmap depicting the number of the indicated cell types (columns) located within 4 m of each of the CD16+ DCs (rows) located across six DLE (N = 16 CD16+ DCs) and two sub- acute CLE (SCLE; N = 5 CD16+ DCs) sections. Color scale, number of neighboring cells.
Pip3 Mass Elisa Kit, supplied by Echelon Biosciences, used in various techniques. Bioz Stars score: 95/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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k 12 science education  (National Research Council Canada)
94
National Research Council Canada k 12 science education
Fig. 7. Spatial-seq reinforces the effects of IFN-producing interfollicular KCs on CD16+ DCs and FBs in the superficial dermis. N = 4 biological replicates; data are shown for the most complex sample as defined by the highest number of spots after quality control steps. (A) Hematoxylin and eosin staining of DLE tissue section cor- responding to spatial-seq data below. Scale bars, 200 m (A to F). (B) Spatial scatter pie plot showing cell type composition based on detection of scRNA-seq signatures corre- sponding to seven cell types. Each spot is represented as a pie chart showing relative cell type proportions. Spot coordinates correspond to tissue location. (C) Spatial heatmap of the IFN FB subset gene signature. Color, scaled expression of each subset gene signature. Only spots meeting an FB prediction score threshold of 0.25 are shown. (D) Spatial heatmap of the LC subset gene signature. All spots are shown. (E) Spatial heatmap of the pDC subset gene signature. All spots are shown. (F) Spatial heatmap of the CD16+ DC subset gene signature. All spots are shown. (G) Representative image of a DLE skin section showing the localization of CD16+ DCs (as indicated by the CD14+CD11c+CD16+ immunophenotype) generated by imaging mass <t>cytometry.</t> Scale bar, 100 m. Insets, subepidermal enrichment of CD16+ DCs. (H) Heatmap depicting the number of the indicated cell types (columns) located within 4 m of each of the CD16+ DCs (rows) located across six DLE (N = 16 CD16+ DCs) and two sub- acute CLE (SCLE; N = 5 CD16+ DCs) sections. Color scale, number of neighboring cells.
K 12 Science Education, supplied by National Research Council Canada, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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amazon speed etd ion trap mass spectrometer  (Bruker Corporation)
96
Bruker Corporation amazon speed etd ion trap mass spectrometer
Fig. 7. Spatial-seq reinforces the effects of IFN-producing interfollicular KCs on CD16+ DCs and FBs in the superficial dermis. N = 4 biological replicates; data are shown for the most complex sample as defined by the highest number of spots after quality control steps. (A) Hematoxylin and eosin staining of DLE tissue section cor- responding to spatial-seq data below. Scale bars, 200 m (A to F). (B) Spatial scatter pie plot showing cell type composition based on detection of scRNA-seq signatures corre- sponding to seven cell types. Each spot is represented as a pie chart showing relative cell type proportions. Spot coordinates correspond to tissue location. (C) Spatial heatmap of the IFN FB subset gene signature. Color, scaled expression of each subset gene signature. Only spots meeting an FB prediction score threshold of 0.25 are shown. (D) Spatial heatmap of the LC subset gene signature. All spots are shown. (E) Spatial heatmap of the pDC subset gene signature. All spots are shown. (F) Spatial heatmap of the CD16+ DC subset gene signature. All spots are shown. (G) Representative image of a DLE skin section showing the localization of CD16+ DCs (as indicated by the CD14+CD11c+CD16+ immunophenotype) generated by imaging mass <t>cytometry.</t> Scale bar, 100 m. Insets, subepidermal enrichment of CD16+ DCs. (H) Heatmap depicting the number of the indicated cell types (columns) located within 4 m of each of the CD16+ DCs (rows) located across six DLE (N = 16 CD16+ DCs) and two sub- acute CLE (SCLE; N = 5 CD16+ DCs) sections. Color scale, number of neighboring cells.
Amazon Speed Etd Ion Trap Mass Spectrometer, supplied by Bruker Corporation, 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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pi 3 4 p2 levels  (Echelon Biosciences)
93
Echelon Biosciences pi 3 4 p2 levels
Fig. 7. Spatial-seq reinforces the effects of IFN-producing interfollicular KCs on CD16+ DCs and FBs in the superficial dermis. N = 4 biological replicates; data are shown for the most complex sample as defined by the highest number of spots after quality control steps. (A) Hematoxylin and eosin staining of DLE tissue section cor- responding to spatial-seq data below. Scale bars, 200 m (A to F). (B) Spatial scatter pie plot showing cell type composition based on detection of scRNA-seq signatures corre- sponding to seven cell types. Each spot is represented as a pie chart showing relative cell type proportions. Spot coordinates correspond to tissue location. (C) Spatial heatmap of the IFN FB subset gene signature. Color, scaled expression of each subset gene signature. Only spots meeting an FB prediction score threshold of 0.25 are shown. (D) Spatial heatmap of the LC subset gene signature. All spots are shown. (E) Spatial heatmap of the pDC subset gene signature. All spots are shown. (F) Spatial heatmap of the CD16+ DC subset gene signature. All spots are shown. (G) Representative image of a DLE skin section showing the localization of CD16+ DCs (as indicated by the CD14+CD11c+CD16+ immunophenotype) generated by imaging mass <t>cytometry.</t> Scale bar, 100 m. Insets, subepidermal enrichment of CD16+ DCs. (H) Heatmap depicting the number of the indicated cell types (columns) located within 4 m of each of the CD16+ DCs (rows) located across six DLE (N = 16 CD16+ DCs) and two sub- acute CLE (SCLE; N = 5 CD16+ DCs) sections. Color scale, number of neighboring cells.
Pi 3 4 P2 Levels, supplied by Echelon Biosciences, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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anti lmp2 psmb9  (Proteintech)
93
Proteintech anti lmp2 psmb9
Fig. 7. Spatial-seq reinforces the effects of IFN-producing interfollicular KCs on CD16+ DCs and FBs in the superficial dermis. N = 4 biological replicates; data are shown for the most complex sample as defined by the highest number of spots after quality control steps. (A) Hematoxylin and eosin staining of DLE tissue section cor- responding to spatial-seq data below. Scale bars, 200 m (A to F). (B) Spatial scatter pie plot showing cell type composition based on detection of scRNA-seq signatures corre- sponding to seven cell types. Each spot is represented as a pie chart showing relative cell type proportions. Spot coordinates correspond to tissue location. (C) Spatial heatmap of the IFN FB subset gene signature. Color, scaled expression of each subset gene signature. Only spots meeting an FB prediction score threshold of 0.25 are shown. (D) Spatial heatmap of the LC subset gene signature. All spots are shown. (E) Spatial heatmap of the pDC subset gene signature. All spots are shown. (F) Spatial heatmap of the CD16+ DC subset gene signature. All spots are shown. (G) Representative image of a DLE skin section showing the localization of CD16+ DCs (as indicated by the CD14+CD11c+CD16+ immunophenotype) generated by imaging mass <t>cytometry.</t> Scale bar, 100 m. Insets, subepidermal enrichment of CD16+ DCs. (H) Heatmap depicting the number of the indicated cell types (columns) located within 4 m of each of the CD16+ DCs (rows) located across six DLE (N = 16 CD16+ DCs) and two sub- acute CLE (SCLE; N = 5 CD16+ DCs) sections. Color scale, number of neighboring cells.
Anti Lmp2 Psmb9, supplied by Proteintech, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Image Search Results


Fig. 7. Spatial-seq reinforces the effects of IFN-producing interfollicular KCs on CD16+ DCs and FBs in the superficial dermis. N = 4 biological replicates; data are shown for the most complex sample as defined by the highest number of spots after quality control steps. (A) Hematoxylin and eosin staining of DLE tissue section cor- responding to spatial-seq data below. Scale bars, 200 m (A to F). (B) Spatial scatter pie plot showing cell type composition based on detection of scRNA-seq signatures corre- sponding to seven cell types. Each spot is represented as a pie chart showing relative cell type proportions. Spot coordinates correspond to tissue location. (C) Spatial heatmap of the IFN FB subset gene signature. Color, scaled expression of each subset gene signature. Only spots meeting an FB prediction score threshold of 0.25 are shown. (D) Spatial heatmap of the LC subset gene signature. All spots are shown. (E) Spatial heatmap of the pDC subset gene signature. All spots are shown. (F) Spatial heatmap of the CD16+ DC subset gene signature. All spots are shown. (G) Representative image of a DLE skin section showing the localization of CD16+ DCs (as indicated by the CD14+CD11c+CD16+ immunophenotype) generated by imaging mass cytometry. Scale bar, 100 m. Insets, subepidermal enrichment of CD16+ DCs. (H) Heatmap depicting the number of the indicated cell types (columns) located within 4 m of each of the CD16+ DCs (rows) located across six DLE (N = 16 CD16+ DCs) and two sub- acute CLE (SCLE; N = 5 CD16+ DCs) sections. Color scale, number of neighboring cells.

Journal: Science translational medicine

Article Title: Nonlesional lupus skin contributes to inflammatory education of myeloid cells and primes for cutaneous inflammation.

doi: 10.1126/scitranslmed.abn2263

Figure Lengend Snippet: Fig. 7. Spatial-seq reinforces the effects of IFN-producing interfollicular KCs on CD16+ DCs and FBs in the superficial dermis. N = 4 biological replicates; data are shown for the most complex sample as defined by the highest number of spots after quality control steps. (A) Hematoxylin and eosin staining of DLE tissue section cor- responding to spatial-seq data below. Scale bars, 200 m (A to F). (B) Spatial scatter pie plot showing cell type composition based on detection of scRNA-seq signatures corre- sponding to seven cell types. Each spot is represented as a pie chart showing relative cell type proportions. Spot coordinates correspond to tissue location. (C) Spatial heatmap of the IFN FB subset gene signature. Color, scaled expression of each subset gene signature. Only spots meeting an FB prediction score threshold of 0.25 are shown. (D) Spatial heatmap of the LC subset gene signature. All spots are shown. (E) Spatial heatmap of the pDC subset gene signature. All spots are shown. (F) Spatial heatmap of the CD16+ DC subset gene signature. All spots are shown. (G) Representative image of a DLE skin section showing the localization of CD16+ DCs (as indicated by the CD14+CD11c+CD16+ immunophenotype) generated by imaging mass cytometry. Scale bar, 100 m. Insets, subepidermal enrichment of CD16+ DCs. (H) Heatmap depicting the number of the indicated cell types (columns) located within 4 m of each of the CD16+ DCs (rows) located across six DLE (N = 16 CD16+ DCs) and two sub- acute CLE (SCLE; N = 5 CD16+ DCs) sections. Color scale, number of neighboring cells.

Article Snippet: Imaging mass cytometry of tissue sections Formalin-fixed, paraffin-embedded skin biopsy tissue sections from lesional skin of patients with SCLE or DLE were analyzed using a Hyperion imaging cytometry by time of flight system (CyTOF) (Fluidigm) as previously described (34) with modifications of the antibody panel.

Techniques: Control, Staining, Expressing, Generated, Imaging, Mass Cytometry