The largest database of trusted experimental protocols

Fitc anti human thy1

Manufactured by BioLegend

The FITC anti-human THY1 is a lab equipment product that can be used to detect the presence of the THY1 antigen in human samples. THY1, also known as CD90, is a cell surface glycoprotein expressed on various cell types. The FITC (Fluorescein Isothiocyanate) conjugate allows for the visualization and identification of THY1-positive cells using flow cytometry or other fluorescence-based detection methods.

Automatically generated - may contain errors

2 protocols using fitc anti human thy1

1

Basal Cell Isolation and Profiling

Check if the same lab product or an alternative is used in the 5 most similar protocols
Single-cell suspensions in FACS Buffer (HBSS [ThermoFisher 14170161, Ca/Mg-free] supplemented with 2% FCS) were pre-incubated with Fc-Block (BD 564220) before staining for surface antigens. The following antibodies were used to identify basal cells via flow cytometry: FITC anti-human THY1 (Biolegend, clone 5E10), Brilliant Violet 421 anti-human CD45 (Biolegend, clone HI30), Brilliant Violet 650 anti-human EPCAM (Biolegend, clone 9C4), APC/Cy7 anti-human ITGA6 (Biolegend, clone GoH3), PE/Cy7 anti-human NGFR (Biolegend, clone ME20.4), APC anti-human PDPN (Biolegend, clone NC-08). Cells were stained for 30 minutes on ice in FACS buffer and then washed for immediate sorting. Cells were sorted on a BD FACSAria Fusion cell sorter using BD FACSDiva software. Up to 10,000 Basal cells were sorted into 100 μL BAM banker (Wako chemicals) for Omni-ATAC-seq and cooled to −80°C using a “Mr. Frosty” freezing container (Thermo scientific). Samples were stored at −80°C until thawed for Omni-ATAC-seq. 1,000 Basal cells for bulk RNAseq were sorted directly into 5 μL TCL buffer (Qiagen). FlowJo v10 by TreeStar was used to generate plots.
+ Open protocol
+ Expand
2

Basal Cell Isolation and Profiling

Check if the same lab product or an alternative is used in the 5 most similar protocols
Single-cell suspensions in FACS Buffer (HBSS [ThermoFisher 14170161, Ca/Mg-free] supplemented with 2% FCS) were pre-incubated with Fc-Block (BD 564220) before staining for surface antigens. The following antibodies were used to identify basal cells via flow cytometry: FITC anti-human THY1 (Biolegend, clone 5E10), Brilliant Violet 421 anti-human CD45 (Biolegend, clone HI30), Brilliant Violet 650 anti-human EPCAM (Biolegend, clone 9C4), APC/Cy7 anti-human ITGA6 (Biolegend, clone GoH3), PE/Cy7 anti-human NGFR (Biolegend, clone ME20.4), APC anti-human PDPN (Biolegend, clone NC-08). Cells were stained for 30 minutes on ice in FACS buffer and then washed for immediate sorting. Cells were sorted on a BD FACSAria Fusion cell sorter using BD FACSDiva software. Up to 10,000 Basal cells were sorted into 100 μL BAM banker (Wako chemicals) for Omni-ATAC-seq and cooled to −80°C using a “Mr. Frosty” freezing container (Thermo scientific). Samples were stored at −80°C until thawed for Omni-ATAC-seq. 1,000 Basal cells for bulk RNAseq were sorted directly into 5 μL TCL buffer (Qiagen). FlowJo v10 by TreeStar was used to generate plots.
+ 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!