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an extracellular region
Int J Cell Cloning
Dropwise 1×DAPI Working solution onto the sample
Add the primary antibody: gently shake off the blocking solution
AO/PI Double Staining Size:100T an extracellular regionProduct Specification Usage 1. Reagent preparation: (1) PBS buffer (pH7. 4) (2) or HbSS (hank's balanced salt solution) 2. Consumables preparation (1) centrifuge tube (2) suction tip (3) disposable gloves 3. Dyeing working solution preparation: (1) according to the number of samples, prepare the staining buffer according to the following ratio. Take 100 L reagent C used 900 Dilute with L pure water and mix well to form staining buffer (2) every 500
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