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Invitrogen™ BrdU (5-Bromo-2'-Deoxyuridine)
Description
Cells can naturally incorporate the thymidine analog BrdU into their cells during cell division, making this nucleoside analog an excellent marker of by cell cycle and proliferation. Analysis of incorporated BrdU can be with an anti-BrdU antibody.
Apoptosis, Cell Analysis, Cell Cycle, Cell Proliferation, Cell Viability, Proliferation and Function, DNA Fragmentation, Flow Cytometry, Flow Cytometry Apoptosis Assays, Flow Cytometry Cell Proliferation, Flow Cytometry of Cellular Processes
Order Info
Shipping Condition: Room temperature
Specifications
Specifications
| Product Type | BrdU |
| Content And Storage | Store in freezer -5°C to -30°C and protect from light. |
| Shipping Condition | Room Temperature |
| Label or Dye | BrdU |
| Quantity | 100 mg |
Frequently Asked Questions (FAQs)
Yes, EdU and BrdU labeling can be combined for dual-pulse labeling of cell proliferation in cultured cells and in vivo. BrdU will be preferentially incorporated into DNA, so perform the EdU incubation first followed by the BrdU incubation. Removal of EdU from the media is not required in cultured cells when BrdU is added as the second label. Perform an alcohol fixation followed by some method of DNA denaturation as required for the BrdU detection protocol and then perform the click labeling reaction for detection of EdU followed by antibody labeling for detection of BrdU. Be sure to select a BrdU antibody that does not have cross-reactivity to EdU, such as our MoBU-1 clone (Cat. No. B35141). Many BrdU antibodies have been shown to have some amount of cross-reactivity with incorporated EdU. Here is a link (http://www.thermofisher.com/us/en/home/references/protocols/cell-and-tissue-analysis/flow-cytometry-protocol/cell-proliferation/dual-pulse-labeling-of-cell-proliferation-using-edu-and-brdu-incorporation.html) to an example protocol for dual-pulse labeling using EdU and BrdU.
For Research Use Only. Not for use in diagnostic procedures.