The largest database of trusted experimental protocols

Live dead fixable near ir or blue fluorescent dead cell stain kit

Manufactured by BD

The LIVE/DEAD® Fixable Near-IR or Blue fluorescent Dead Cell Stain Kit is a reagent that can be used to label and identify dead cells in a sample. The kit provides a fluorescent dye that selectively binds to proteins in dead cells, allowing them to be distinguished from live cells using flow cytometry or other fluorescence-based analysis methods.

Automatically generated - may contain errors

Lab products found in correlation

2 protocols using live dead fixable near ir or blue fluorescent dead cell stain kit

1

Polychromatic Flow Cytometry for Immune Cell Profiling

Check if the same lab product or an alternative is used in the 5 most similar protocols
Polychromatic Flow Cytometry involved 1–5 × 105 cells being incubated with respective antibodies for 30 min/4 °C and LIVE/DEAD® Fixable Near-IR or Blue fluorescent Dead Cell Stain Kit, washed, optionally incubated with secondary antibodies and acquired at LSRII (BD Biosciences). In tissue-cell-suspensions, CD45 was used to identify leukocytes after exclusion of dead cells and doublets. Myeloid cells were selected based on CD11c (pan-myeloid marker in human) with exclusion of CD3+ T cells. Within CD11c+ cells, ercDCs and macrophages were distinguished as CD209+CD14+ double-positive cells (ercDCs) and CD14 single-positive cells (macrophages). For M1/M2-macrophages, live cells where selected and doublets were excluded before marker analysis. Antibodies are listed in Table S3.
+ Open protocol
+ Expand
2

Comprehensive Myeloid Cell Profiling

Check if the same lab product or an alternative is used in the 5 most similar protocols
1-5 x 10 5 cells were incubated with antibodies for 30 min/4°C and LIVE/DEAD® Fixable Near-IR or Blue fluorescent Dead Cell Stain Kit, washed, optionally incubated with secondary antibodies and acquired at LSRII (BD Biosciences). In tissue-cellsuspensions, CD45 was used to identify leukocytes after exclusion of dead cells and doublets. Myeloid cells were selected based on CD11c (pan-myeloid marker in human)
with exclusion of CD3 + T cells. Within CD11c + cells, ercDCs and macrophages were distinguished as CD209/CD14 double-positive cells (ercDCs) and CD14 singlepositive cells (macrophages). For M1/M2-macrophages, live cells where selected and doublets excluded before marker analysis. Antibodies are listed in table S13.
+ 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!