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Alert : The site is undergoing maintenance. Some functionality including sign-in may be impacted
Saturday, February 21, 3:00 pm through Tuesday, March 03, 9:00 pm (PST), 2026
Ordering can continue through fax and phone.
Contact usAlert : The site is undergoing maintenance. Some functionality including sign-in may be impacted
Saturday, February 21, 3:00 pm through Tuesday, March 03, 9:00 pm (PST), 2026
.Ordering can continue through fax and phone.
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The BD Rhapsody™ Express System enables single-cell capture and barcoding of hundreds to thousands of single cells for analysis of genomic and proteomic information, using proprietary, gentle, robust microwell-based single-cell partitioning technology. The BD Rhapsody™ Express System can be used for lower scale experiments or throughput needs versus the NEW BD Rhapsody™ HT Xpress System, our NEW platform for flexible and scalable experimental design and higher throughput cell and sample inputs. The BD Rhapsody™ Express System is also ideal for routine use with familiar cell systems that do not require visual QC or troubleshooting.
Get more information from the BD Rhapsody™ Express System brochure.
Features
High correlation in gene expression and minimal batch effects seen in data obtained from beads stored up to 12 weeks.
Reliable, reproducible results from gentle, gravity-based single-cell partitioning without microfluidics
High correlation in gene expression seen between technical and biological replicates and between users and sites.
Performance
The system offers superior cell capture rates and low multiplet rates with a variety of cell types as compared to other systems
Strong correlation of all mRNA and protein markers identifies similar T-cell populations between cartridges
Equivalent data from biological replicates
Equivalent data from subsampled beads
Similar proportions of each cell type are recovered from WTA and targeted analysis on subsampled beads
Differential gene expression and differential protein expression analysis were performed on three main Treg subsets identified based on manual gating and bivariate analysis of CD45RA and HLA-DR sorted Treg samples. Differential gene expression analysis was performed using the BD Rhapsody™ Targeted Human Immune Response Panel (399 genes). Upregulated genes (>1.25X) are shown in the heat map above. Differential protein expression of 22 proteins was performed simultaneously using BD® AbSeq Oligo-Conjugated Antibodies.
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Expression of 12 proteins and genes that are significantly upregulated at day 14 of chronic simulation of CD8+ T cells. Two populations (red and green boxes) emerged based on the expression level of markers. Co-expression patterns were discerned for CD38, CD39 and CD94.
Differential protein and gene expression at the single-cell level. Heterogeneity was observed in major ILC subsets.
Clusters are well defined using simultaneous mRNA and protein analysis. Samples from healthy donors cluster similarly. CLL samples cluster separately and uniquely.
A powerful, high-throughput, microwell-based single-cell partitioning system
For Research Use Only. Not for use in diagnostic or therapeutic procedures.
Results shown are not guaranteed and may not be representative.
Dynabeads is a trademark of Thermo Fisher Scientific.