The largest database of trusted experimental protocols

Fluorescein isothiocyanate fitc cd90

Manufactured by BioLegend
Sourced in United States

Fluorescein Isothiocyanate (FITC)-CD90 is a fluorescently labeled antibody that binds to the CD90 (Thy-1) cell surface antigen. CD90 is a glycosylphosphatidylinositol (GPI)-anchored glycoprotein expressed on various cell types, including hematopoietic stem cells, mesenchymal stem cells, and certain subsets of T cells.

Automatically generated - may contain errors

2 protocols using fluorescein isothiocyanate fitc cd90

1

Flow Cytometry Analysis of Stem Cell Markers

Check if the same lab product or an alternative is used in the 5 most similar protocols
Expression of stem cell surface markers in DPCs was determined by fluorescence-activated cell sorting (FACS) analysis. The cells were detached using trypsin in 0.25% elhylene diamine tetraacetic acid (EDTA). After neutralization, single-cell suspensions were washed with phosphate-buffered saline supplemented with 2% FBS and 0.01% NaN3 (FACS buffer). Quantities of 1 × 105 cells were incubated with the conjugated antibody for 20 min on ice in the dark. After washing, fluorescence intensity was measured on FACS Aria II cell sorter (BD Biosciences, San Jose, CA, USA). The following antibodies were used: Phycoerythrin (PE)-CD271 (Miltenyi Biotec, Auburn, CA, USA), Fluorescein Isothiocyanate (FITC)-CD90 (Biolegend, San Diego, CA, USA), allophycocyanin (APC)-CD106 (Biolegend, San Diego, CA, USA) or dual color combinations APC-STRO-1/PE-CD146 (Both from: Biolegend, San Diego, CA, USA), and PE-CD51 (Biolegend, San Diego, CA, USA)/APC-CD140α (BD Biosciences, San Jose, CA, USA). PE-IgG was used as a negative control.
+ Open protocol
+ Expand
2

Stem Cell Surface Marker Expression Analysis

Check if the same lab product or an alternative is used in the 5 most similar protocols
Expression of stem cell surface markers in PDLCs was determined by fluorescent activated cell sorting (FACS) analysis. The cells were detached using trypsin in 0.25% ethylenediaminetetraacetic acid (EDTA). After neutralization, single-cell suspensions were washed with phosphate-buffered saline (PBS) supplemented with 2% FBS and 0.01% NaN3 (FACS buffer). Quantities of 1 × 106 cells were incubated with direct conjugated antibodies for 20 min on ice in the dark. After washing, fluorescence intensity was measured on FACS Aria II cell sorter (BD Biosciences, San Jose, CA, USA). The following anti-human antibodies were used: phycoerythrin (PE)-CD271 (Miltenyi Biotec, Auburn, CA, USA), fluorescein isothiocyanate (FITC)-CD90 (BioLegend, San Diego, CA, USA), allophycocyanin (APC)-CD106 (BioLegend, San Diego, CA, USA) or dual color combinations APC-STRO-1/PE-CD146 (Both from: BioLegend, San Diego, CA, USA), and PE-CD51 (BioLegend, San Diego, CA, USA)/APC-CD140α (BD Biosciences, San Jose, CA, USA). PE-IgG was used as a negative control.
+ 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!