pe cy7 cd45 Search Results


cd45 antibody, anti-human, pe  (Miltenyi Biotec)
96
Miltenyi Biotec cd45 antibody, anti-human, pe
Cd45 Antibody, Anti Human, Pe, supplied by Miltenyi Biotec, 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/cd45 antibody, anti-human, pe/product/Miltenyi Biotec
Average 96 stars, based on 1 article reviews
cd45 antibody, anti-human, pe - by Bioz Stars, 2026-04
96/100 stars
  Buy from Supplier
cd45 2 pe cy7  (R&D Systems)
96
R&D Systems cd45 2 pe cy7
Cd45 2 Pe Cy7, supplied by R&D Systems, 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/cd45 2 pe cy7/product/R&D Systems
Average 96 stars, based on 1 article reviews
cd45 2 pe cy7 - by Bioz Stars, 2026-04
96/100 stars
  Buy from Supplier
pe cy7 conjugated anti mouse cd45 antibody  (Novus Biologicals)
93
Novus Biologicals pe cy7 conjugated anti mouse cd45 antibody
Pe Cy7 Conjugated Anti Mouse Cd45 Antibody, supplied by Novus Biologicals, 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/result/pe cy7 conjugated anti mouse cd45 antibody/product/Novus Biologicals
Average 93 stars, based on 1 article reviews
pe cy7 conjugated anti mouse cd45 antibody - by Bioz Stars, 2026-04
93/100 stars
  Buy from Supplier
pe cy7  (Biorbyt)
91
Biorbyt pe cy7
Interaction between BMECs and HCC cells enhances tumor growth in the spine. (A) si-CX3CL1 was transfected into BMECs to construct CX3CL1 low BMECs. Transwell assays were used to examine recruitment of BMECs co-cultured with or without HMCC97H cells. The number of the recruited cells was quantified. n=3. Cell recruitment were analyzed using ANOVA test. (B) Cell vitality of BMECs was assessed using CCK-8 assay; n=3. Data were analyzed using ANOVA followed by Tukey's test. (C) Tumor size was measured based on the volume. n=5. Scale bar, 5 mm. Data were analyzed using an unpaired t-test. (D) Samples from 2 groups were examined using immunofluorescence. Magnification, ×20. The result was analyzed using an unpaired t-test. Gray bars represent the CX3CL1 nor BMECs group and black bars represent the CX3CL1 low BMECs group (E) Flow cytometry revealed the percentage and number of F4/80 + CD11b + cells; n=5. (F) Flow cytometry was used for detecting expression of M2 macrophage surface markers, CX3CR1, MRC1 and CD163; n=5. Cells were selected based on higher expression of <t>CD45</t> for macrophages. Subsequently, CD11b and F4/80 expression were used for further characterization of macrophages. FACS (fluorescent-activated cell sorting) data were analyzed using a Kruskal Wallis test followed by Dunn's non-parametric post hoc test. HCC, hepatocellular carcinoma; BMECs, bone marrow endothelial cells; si, small interfering; CCK-8, Cell Counting kit-8; CX3CL1, C-X3-C motif chemokine ligand 1.
Pe Cy7, supplied by Biorbyt, 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/result/pe cy7/product/Biorbyt
Average 91 stars, based on 1 article reviews
pe cy7 - by Bioz Stars, 2026-04
91/100 stars
  Buy from Supplier
fivecolor (cd45-percp-cy5.5, cd19-pe-cy7, cd38fitc, cd138-apc, cd56-pe) flow cytometry  (Partec)
90
Partec fivecolor (cd45-percp-cy5.5, cd19-pe-cy7, cd38fitc, cd138-apc, cd56-pe) flow cytometry
Interaction between BMECs and HCC cells enhances tumor growth in the spine. (A) si-CX3CL1 was transfected into BMECs to construct CX3CL1 low BMECs. Transwell assays were used to examine recruitment of BMECs co-cultured with or without HMCC97H cells. The number of the recruited cells was quantified. n=3. Cell recruitment were analyzed using ANOVA test. (B) Cell vitality of BMECs was assessed using CCK-8 assay; n=3. Data were analyzed using ANOVA followed by Tukey's test. (C) Tumor size was measured based on the volume. n=5. Scale bar, 5 mm. Data were analyzed using an unpaired t-test. (D) Samples from 2 groups were examined using immunofluorescence. Magnification, ×20. The result was analyzed using an unpaired t-test. Gray bars represent the CX3CL1 nor BMECs group and black bars represent the CX3CL1 low BMECs group (E) Flow cytometry revealed the percentage and number of F4/80 + CD11b + cells; n=5. (F) Flow cytometry was used for detecting expression of M2 macrophage surface markers, CX3CR1, MRC1 and CD163; n=5. Cells were selected based on higher expression of <t>CD45</t> for macrophages. Subsequently, CD11b and F4/80 expression were used for further characterization of macrophages. FACS (fluorescent-activated cell sorting) data were analyzed using a Kruskal Wallis test followed by Dunn's non-parametric post hoc test. HCC, hepatocellular carcinoma; BMECs, bone marrow endothelial cells; si, small interfering; CCK-8, Cell Counting kit-8; CX3CL1, C-X3-C motif chemokine ligand 1.
Fivecolor (Cd45 Percp Cy5.5, Cd19 Pe Cy7, Cd38fitc, Cd138 Apc, Cd56 Pe) Flow Cytometry, supplied by Partec, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/fivecolor (cd45-percp-cy5.5, cd19-pe-cy7, cd38fitc, cd138-apc, cd56-pe) flow cytometry/product/Partec
Average 90 stars, based on 1 article reviews
fivecolor (cd45-percp-cy5.5, cd19-pe-cy7, cd38fitc, cd138-apc, cd56-pe) flow cytometry - by Bioz Stars, 2026-04
90/100 stars
  Buy from Supplier
cd45 polyclonal antibody, pe-cy7 conjugated  (Bioss)
N/A
Protein tyrosine-protein phosphatase required for T-cell activation through the antigen receptor. Acts as a positive regulator of T-cell coactivation upon binding to DPP4. The first PTPase domain has enzymatic activity, while the second one seems
   Buy from Supplier
pe cy7 anti human cd45 hi30 antibody  (Abcepta)
N/A
The HI30 antibody reacts with human CD45 one of the most abundant hematopoietic markers and one that is expressed on all leukocytes the Leukocyte Common Antigen LCA CD45 is a protein tyrosine phosphatase existing in
   Buy from Supplier
pe cy 7 rat anti mouse cd45  (BD Biosciences)
N/A
   Buy from Supplier
cd45 antibody (998209) [pe/cy7]  (Novus Biologicals)
N/A
The CD45 Antibody (998209) [PE/Cy7] from Novus is a CD45 antibody to CD45. This antibody reacts with Human. The CD45 antibody has been validated for the following applications: Flow Cytometry.
   Buy from Supplier
mouse cd45 pe-cy7  (Bioss)
N/A
Enables several functions, including heparan sulfate proteoglycan binding activity; heparin binding activity; and protein tyrosine phosphatase activity. Involved in several processes, including lymphocyte differentiation; positive regulation of macromolecule metabolic process; and regulation of signal transduction.
   Buy from Supplier
pe cy7 anti mouse cd45 1  (Tonbo Biosciences)
N/A
PE Cy7 Anti Mouse CD45 1 A20
   Buy from Supplier
pe/cy7 anti-mouse cd45  (BioLegend)
N/A
PE/Cy7 anti-mouse CD45 [30-F11]; Isotype: Rat IgG2b, κ; Reactivity: Mouse; Apps: FC; Size: 25 μg
   Buy from Supplier

Image Search Results


Interaction between BMECs and HCC cells enhances tumor growth in the spine. (A) si-CX3CL1 was transfected into BMECs to construct CX3CL1 low BMECs. Transwell assays were used to examine recruitment of BMECs co-cultured with or without HMCC97H cells. The number of the recruited cells was quantified. n=3. Cell recruitment were analyzed using ANOVA test. (B) Cell vitality of BMECs was assessed using CCK-8 assay; n=3. Data were analyzed using ANOVA followed by Tukey's test. (C) Tumor size was measured based on the volume. n=5. Scale bar, 5 mm. Data were analyzed using an unpaired t-test. (D) Samples from 2 groups were examined using immunofluorescence. Magnification, ×20. The result was analyzed using an unpaired t-test. Gray bars represent the CX3CL1 nor BMECs group and black bars represent the CX3CL1 low BMECs group (E) Flow cytometry revealed the percentage and number of F4/80 + CD11b + cells; n=5. (F) Flow cytometry was used for detecting expression of M2 macrophage surface markers, CX3CR1, MRC1 and CD163; n=5. Cells were selected based on higher expression of CD45 for macrophages. Subsequently, CD11b and F4/80 expression were used for further characterization of macrophages. FACS (fluorescent-activated cell sorting) data were analyzed using a Kruskal Wallis test followed by Dunn's non-parametric post hoc test. HCC, hepatocellular carcinoma; BMECs, bone marrow endothelial cells; si, small interfering; CCK-8, Cell Counting kit-8; CX3CL1, C-X3-C motif chemokine ligand 1.

Journal: International Journal of Oncology

Article Title: ADAM17-regulated CX3CL1 expression produced by bone marrow endothelial cells promotes spinal metastasis from hepatocellular carcinoma

doi: 10.3892/ijo.2020.5045

Figure Lengend Snippet: Interaction between BMECs and HCC cells enhances tumor growth in the spine. (A) si-CX3CL1 was transfected into BMECs to construct CX3CL1 low BMECs. Transwell assays were used to examine recruitment of BMECs co-cultured with or without HMCC97H cells. The number of the recruited cells was quantified. n=3. Cell recruitment were analyzed using ANOVA test. (B) Cell vitality of BMECs was assessed using CCK-8 assay; n=3. Data were analyzed using ANOVA followed by Tukey's test. (C) Tumor size was measured based on the volume. n=5. Scale bar, 5 mm. Data were analyzed using an unpaired t-test. (D) Samples from 2 groups were examined using immunofluorescence. Magnification, ×20. The result was analyzed using an unpaired t-test. Gray bars represent the CX3CL1 nor BMECs group and black bars represent the CX3CL1 low BMECs group (E) Flow cytometry revealed the percentage and number of F4/80 + CD11b + cells; n=5. (F) Flow cytometry was used for detecting expression of M2 macrophage surface markers, CX3CR1, MRC1 and CD163; n=5. Cells were selected based on higher expression of CD45 for macrophages. Subsequently, CD11b and F4/80 expression were used for further characterization of macrophages. FACS (fluorescent-activated cell sorting) data were analyzed using a Kruskal Wallis test followed by Dunn's non-parametric post hoc test. HCC, hepatocellular carcinoma; BMECs, bone marrow endothelial cells; si, small interfering; CCK-8, Cell Counting kit-8; CX3CL1, C-X3-C motif chemokine ligand 1.

Article Snippet: To stain for the cell surface markers, cells were incubated with following fluorescence-labeled monoclonal antibodies for 30 min on ice respectively: PE-conjugated anti-CD11b (cat. no. 333142; BD Biosciences; 1:300), FITC-conjugated anti-F4/80 (cat. no. orb223773; Biorbyt; 1:300), PE-Cy7-conjugated-CD45 (cat. no. 147703; BioLegend; 1:300), APC-conjugated CX3CR1 (cat. no. 341609; BioLegend; 1:300), PE-Cy3-conjugated MRC1 (cat. no. sc-376232; Santa Cruz Biotechnology, Inc.; 1:300) and PE-Cy5-CD163 (cat. no. sc-33715; Santa Cruz Biotechnology, Inc.; 1:300) antibodies.

Techniques: Transfection, Construct, Cell Culture, CCK-8 Assay, Immunofluorescence, Flow Cytometry, Expressing, FACS, Cell Counting