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Cd10 bv421

Manufactured by BD
Sourced in United States

The CD10-BV421 is a fluorochrome-conjugated antibody that targets the CD10 cell surface antigen. It is designed for use in flow cytometry applications.

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5 protocols using cd10 bv421

1

Phenotyping Human B Cell Subsets

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B cells are CD3-CD19+ cells with different phenotypes that may be determined by the analysis of the expression of surface markers CD10, CD27 and CD21 (16 (link)): immature or transitional cells (CD10+ CD27-); naïve B cells (CD10-CD27-CD21high); tissue-like memory cells (CD10-CD27-CD21low); resting memory cells (CD10-CD27+CD21high); activated memory cells (CD10-CD27+CD21low); and plasmablasts (CD27++CD20-CD21low) (16 (link)). Antibodies CD3-PE, CD10-BV421, CD19-BV711, CD20-AlexaFluor700, CD21-FITC, CD27-PercP-Cy5.5 were purchased from BD Biosciences (San Jose, CA). Data acquisition and analysis was performed as described above. The gating strategy for acquiring and analyzing the B cell subsets is described in Supplemental Figure 1.
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2

Flow Cytometry Analysis of B Cell Subsets

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Subpopulations of B cells (CD3CD19+) were analyzed by flow cytometry after staining of surface markers CD10, CD27, CD20, and CD21: immature or transitional cells (CD10+ CD27), naïve B cells (CD10CD27CD21high), tissue-like memory cells (CD10CD27CD21low), resting memory cells (CD10CD27+CD21high), activated memory cells (CD10CD27+CD21low), and plasmablasts (CD27++CD20CD21low) [35 (link)]. Antibodies CD3-PE, CD10-BV421, CD19-BV711, CD20-AlexaFluor700, CD21-FITC, and CD27-PercP-Cy5.5 were purchased from BD Biosciences (San Jose, CA, USA). Data acquisition was performed in a BD LSRFortessa X-20 flow cytometer with FACS Diva software (BD Biosciences, San Jose, CA, USA). FlowJo software (Tree Star Inc., Ashland, OR, USA) was used for data analysis.
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3

Characterization of B Cell Subpopulations

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Subpopulations of B cells (CD3-CD19+) were analyzed by flow cytometry after the staining of surface markers CD10, CD27, CD20, and CD21 [12 (link)]. These cells include immature or transitional cells (CD10+ CD27-), naïve B cells (CD10-CD27-CD21high), tissue-like memory cells (CD10-CD27-CD21low), resting memory cells (CD10-CD27+CD21high), activated memory cells (CD10-CD27+CD21low), and plasmablasts (CD27++CD20-CD21low). Antibodies CD3-PE, CD10-BV421, CD19-BV711, CD20-AlexaFluor700, CD21-FITC, and CD27-PercP-Cy5.5 were purchased from BD Biosciences (San Jose, CA, USA). Data acquisition was performed in BD LSRFortessa X-20 flow cytometer with FACS Diva software (BD Biosciences, San Jose, CA, USA). FlowJo software (Tree Star Inc., Ashland, OR, USA) was used for data analysis.
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4

Comprehensive B-cell Subset Profiling

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B-cell subpopulations (CD3CD19+) were differentiated via flow cytometry after staining the surface markers of CD10, CD27, CD20, and CD21 as follows: immature or transitional cells (CD10+CD27); naïve B cells (CD10CD27CD21high); tissue-like memory cells (CD10CD27CD21low); resting memory cells (CD10CD27+CD21high); activated memory cells (CD10CD27+CD21low); and plasmablasts (CD27++CD20CD21low). Antibodies CD3-PE, CD10-BV421, CD19-BV711, CD20-AlexaFluor700, CD21-FITC, and CD27-PercPCy5.5 were purchased from BD Biosciences (San Jose, CA, USA). Data acquisition was performed in a BD LSRFortessa X-20 flow cytometer with FACS Diva software v7.0 (BD Biosciences, San Jose, CA, USA). FlowJo software v10 (Tree Star Inc., Ashland, OR, USA) was used for data analysis.
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5

Characterization of B Cell Subsets by Flow Cytometry

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Subpopulations of B cells (CD3CD19+) were analyzed by flow cytometry after staining of surface markers CD10, CD27, CD20, and CD21 as follows: immature or transitional cells (CD10+CD27); naïve B cells (CD10CD27CD21high); tissue-like memory cells (CD10CD27CD21low); resting memory cells (CD10CD27+CD21high); activated memory cells (CD10CD27+CD21low); and plasmablasts (CD27++CD20CD21low) [31 (link)]. Antibodies CD3-PE, CD10-BV421, CD19-BV711, CD20-AlexaFluor700, CD21-FITC, and CD27-PercP-Cy5.5 were purchased from BD Biosciences (San Jose, CA). Data acquisition was performed in a BD LSRFortessa X-20 flow cytometer and FACS Diva software v6.0 (BD Biosciences, San Jose, CA, USA). FlowJo software v10.8 (Tree Star Inc., Ashland, OR, USA) was used for data analysis.
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