The largest database of trusted experimental protocols

Anti cd49b antibody

Manufactured by BioLegend
Sourced in United States

The Anti-CD49b antibody is a tool used for the detection and identification of CD49b, also known as the integrin alpha 2 subunit (ITGA2) or very late antigen-2 (VLA-2). CD49b is a cell surface marker expressed on various cell types, including platelets, natural killer cells, and some T cells. This antibody can be used in flow cytometry, immunohistochemistry, and other immunological applications to study the expression and distribution of CD49b in biological samples.

Automatically generated - may contain errors

4 protocols using anti cd49b antibody

1

ScRNA-seq Analysis of Murine Basophils

Check if the same lab product or an alternative is used in the 5 most similar protocols
For scRNA-seq in Fig. 1, BMBAs generated by culturing bone marrow cells in the presence of IL-3 (0.3 ng/mL: BioLegend) for 7 days were subjected to scRNA-seq analysis. BMBAs generated from 5 mice were pooled to generate scRNA-seq data. For scRNA-seq in Fig. 2, single-cell samples were prepared from the bone marrow and spleen of Mcpt8GFP transgenic mice and depleted of lineage-positive cells by using biotinylated lineage antibodies (anti-CD4, anti-CD8a, anti-CD19, anti-B220, anti-Gr-1 and anti-TER-119, dilution 1:400) and EasySep Mouse Streptavidin RapidSpheres Isolation Kit (Stemcell Technologies, catalog #: ST-19860). GFP-positive cells were sort-purified from lineage-negative cells. Basophils isolated from 5 mice were pooled to generate scRNA-seq data. For scRNA-seq in Fig. 5, single-cell suspensions were prepared from the bone marrow and infected skin and subjected to positive selection of CD49b-positive cells by using biotinylated anti-CD49b antibody (BioLegend; clone: DX5, catalog #: 108904, dilution 1:400) and EasySep mouse Biotin Positive Selection Kit II (Stemcell Technologies, catalog #: ST-17665) followed by the isolation of CD200R3+cKit- cells by cell sorting. Basophils isolated from 5 mice were pooled to generate scRNA-seq data.
+ Open protocol
+ Expand
2

Comprehensive Tumor Immune Profiling

Check if the same lab product or an alternative is used in the 5 most similar protocols
Experimental mice were sacrificed, and tumor tissues were collected for single‐cell dissociation. The tumor‐infiltrating immune cell population was measured by flow cytometry. The T‐cell population was identified using anti‐CD45 (304032; BioLegend, CA, USA), anti‐CD3 (100320; BioLegend), anti‐CD4 (100526; BioLegend), anti‐CD8 (100750; BioLegend), anti‐FoxP3 (12‐5773‐82; eBioscience, MA, USA), anti‐CD25 (102049; BioLegend) and anti‐PD‐1 (135218; BioLegend) antibodies. Dendritic cells were identified using anti‐H2 (33A15443; Invitrogen), anti‐CD11c (117343; BioLegend), anti‐CD80 (47‐4801‐82; eBioscience) and anti‐CD86 (104729; BioLegend) antibodies. M1 and M2 macrophages were identified using anti‐F4/80 (47‐4801‐82; eBioscience), anti‐CD206 (17‐2061‐80; eBioscience), anti‐CD11c, anti‐CD80 and anti‐CD86 antibodies. MDSCs were identified using anti‐CD11b (101216; BioLegend) and anti‐Ly‐6G (127606; BioLegend) antibodies, whereas NK cells were identified using anti‐CD49b antibody (108906; BioLegend). For staining, the standard intra‐nucleus staining protocol provided with the BioLegend kit was used (424401; BioLegend). All antibody‐stained tumor‐dissociated cells were detected on an LSR2 flow cytometer (BD Bioscience, NJ, USA) and analysed using FlowJo software (FlowJo LLC, OR, USA).
+ Open protocol
+ Expand
3

Nanoparticle-based Immunostimulant Delivery

Check if the same lab product or an alternative is used in the 5 most similar protocols
Folate (FA), monomethoxyl poly (ethylene glycol) (MPEG), ε-CL and 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyl tetrazoliumbromide (MTT) were purchased from Sigma–Aldrich (Darmstadt, Germany). 1,2-Dioleoyl-3-trimethylammonium-propane (DOTAP) was purchased from Avanti Polar Lipids (AL, USA). Dulbecco's modified Eagle's medium (DMEM) and fetal bovine serum (FBS) were both purchased from Gibco (NY, USA). The antibodies used in this study were summarized: rat anti-mouse CD31 polyclonal antibody, rat anti-mouse Ki67 polyclonal antibody, rat anti-mouse horseradish peroxidase (HRP)-conjugated secondary antibody (Servicebio, Wuhan, China); The anti-CD4 antibody, anti-CD8 antibody, anti-CD69 antibody, anti-CD11c antibody, anti-CD80 antibody, anti-CD86 antibody, anti-MHCII antiobody, anti-CD45 antibody, anti-CD11b antibody and anti-IFN-γ antibody (BD Pharmingen, NJ, USA); The anti-CD11b antibody, anti-CD206 antibody, anti-F480 antibody, anti-CD107a antibody, anti-CD49b antibody, anti-CD274 (PDL-1) antibody (Biolegend, CA, USA). The pvax and pIL-12 were extracted and purified using a QIAGEN Endofree Plasmid Mega Kit (Hulsterweg, Netherlands). The contents of murine IFN-γ, TNF-α and IL-12 p70 were detected by corresponding ELISA kits from Invitrogen (CA, USA).7-AAD/Annexin-V apoptosis kit was purchased from BD, Pharmingen (CA, USA).
+ Open protocol
+ Expand
4

Characterization of Immune Landscape in 4T1 Tumor Model

Check if the same lab product or an alternative is used in the 5 most similar protocols
The livers and bone marrow cells were harvested from sham and 4T1 cancer-bearing animals 14 days after transplantation. Red blood cells (RBCs) were lysed with RBC lysis buffer (BD Bioscience). The obtained cells were then stained with the following antibodies (BioLegend, CA, USA) for 30 min at 4 °C: anti-CD45 antibody (Clone: 30-F11), anti-CD19 antibody (Clone: 6D5), anti-TCRβ antibody (Clone: H57-597), anti-CD11b antibody (Clone: M1/70), anti-Ly6G antibody (Clone: 1A8), anti-FCεR1a antibody (Clone: MAR-1), anti-CD117 antibody (Clone: 2B8), anti-CD123 (Clone: 5B11), anti-CD49b antibody (Clone: DX5), anti-CD3 antibody (Clone: 17A2), anti-CD11c antibody (Clone: N418), anti-TER-119 antibody, or anti-CD34 antibody (Clone: HM34). Non-viable cells were stained with Propidium Iodide Solution (PI) and gated out. Data were acquired using FACS Aria (BD Bioscience) and analyzed using FlowJo software (v10.8.1, BD Biosciences). Gating strategy is shown in Supplementary Fig. 14.
+ 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!