The largest database of trusted experimental protocols

4 protocols using cd11c pb

1

Multiparameter Flow Cytometry Profiling

Check if the same lab product or an alternative is used in the 5 most similar protocols
All stains were performed in 96 well u-bottom plates in a volume of 100 μl. 1×105–1×106 cells were plated and blocked with Fc receptor block (BD, Biosciences, San Jose, CA) for 15 min at 4°C and subsequently incubated with antibodies for 1 h at 4°C. Cells were then washed and fixed in 5% formalin for 15 min at room temperature. Flow cytometry was acquired using a FACSCanto RUO system (BD Biosciences). Data analysis was performed using FlowJo (Treestar, Ashland OR). Antibodies included: Siglec F PE (BD), Ly6G APC, Ly6G FITC, CD11b PE-Cy7, CD11c PB, CD71 PerCP Cy5.5, CD206 BV605, ICAM1 FITC, CD45 APC-Cy7, MHCII BV510, CD103 APC (Biolegend).
+ Open protocol
+ Expand
2

Immunophenotyping of Leukocyte Subsets

Check if the same lab product or an alternative is used in the 5 most similar protocols
Leucocytes subsets were identified using an antibody panel containing CD45‐PO (Life Technologies) for lymphocytes; CD123‐PerCPCy5.5 (BD Pharmingen), CD203c APC (Sony), HLA‐DR‐PB (Sony), and CD41‐PE‐Cy7 for basophils; and CD45‐PO (Life Technologies) and CD14‐APC‐H7 (BD Pharmingen) for monocytes. To distinguish between the three different subsets of dendritic cells (DCs), an antibody panel containing HLA‐DR‐PE‐CY7 (BioLegend), CD11c‐PB (BioLegend), and CD123 PerCP Cy5.5 (BD Pharmingen) was used for plasmacytoid dendritic cells (pDCs). For two subsets of myeloid dendritic cells (mDCs), CD14‐V500 (BD), HLA‐DR‐PE‐CY7 (BioLegend), CD1c‐APC‐Cy7 (BioLegend), and CD141‐APC (Miltenyi) were used. Leucocyte subset quantities were depicted as the percentage of cells within the total leucocyte measures/numbers.
+ Open protocol
+ Expand
3

Multiparameter Flow Cytometry Profiling

Check if the same lab product or an alternative is used in the 5 most similar protocols
Isolation of lung cells and splenocytes was performed as described elsewhere [8 (link)]. Cell phenotyping was performed on LSRII flow cytometer using FACS Diva software (BD Bioscience, Heidelberg, Germany) and Flowjo software 9.6.6 (Tree Star Inc, San Carlos, CA, USA) with the following anti-mouse monoclonal antibodies: CD45 Peridinin-Chlorophyll-protein (PerCP), CD11b Allophycocyanin-cyanine dye 7 (APC-Cy7), NK1.1 phycoerythrin (PE), CD19 Fluorescein (FITC), CD3 APC, CD4 Alexa Fluor 700 (A700), CD8 Pacific-Blue (PB), Gr1PE, CD11bPE-Cy7, F480 APC, Siglec F APC-Cy7, CD11 c PB (Biolegend, San Diego, CA, USA).
+ Open protocol
+ Expand
4

Multiparametric Flow Cytometry for Immune Cell Profiling

Check if the same lab product or an alternative is used in the 5 most similar protocols
Lung cells and splenocytes were isolated as described elsewhere (Engel et al., 2015) and stained with the following anti-mouse monoclonal antibodies for 20 min at 4 • C in the dark: CD45 PerCP, CD11b APC-Cy7, NK1.1 PE, CD19 FITC, CD3 APC, CD4 A700, CD8 PB, Gr1 PE, CD11b PE-Cy7, F4/80 APC, Siglec F APC-Cy7, CD11c PB (Biolegend, San Diego, USA or BD Bioscience, Heidelberg, Germany). Cell phenotyping was performed on LSRII flow cytometer using FACS Diva software (BD Bioscience, Heidelberg, Germany) and analyzed using FlowJo software (Tree Star Inc). Leukocytes were analyzed as follows: Neutrophils in spleen and lung (CD45+/CD11b high /Gr1 high ), Lymphocytes in spleen and lung (B cells: CD45+/CD11b-/CD19+; T cells: CD45+/CD11b-/ CD3+; NK cells: CD45+/NK1.1+/CD3-; NKT cells: CD45+/NK1.1+/ CD3+), alveolar macrophages (CD45+/Gr1-/SiglecF+/CD11c+), macrophages in spleen (CD45+/Gr1-/CD11b+/CD11c-).
+ Open protocol
+ Expand

About PubCompare

Our mission is to provide scientists with the largest repository of trustworthy protocols and intelligent analytical tools, thereby offering them extensive information to design robust protocols aimed at minimizing the risk of failures.

We believe that the most crucial aspect is to grant scientists access to a wide range of reliable sources and new useful tools that surpass human capabilities.

However, we trust in allowing scientists to determine how to construct their own protocols based on this information, as they are the experts in their field.

Ready to get started?

Sign up for free.
Registration takes 20 seconds.
Available from any computer
No download required

Sign up now

Revolutionizing how scientists
search and build protocols!