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- Cedarlane
- CLAS15-2934
- 2025年07月09日
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999
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100 µg
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文献和实验- or triple-labeling immunofluorescence, it is necessary to use primary antibodies raised in different host species such as mouse, rabbit, and goat. However, in many cases, suitable primary antibodies raised in different species are unavailable
Immunofluorescent Staining of Mouse and Rat Leukocytes
(or 50 µl wash buffer for negative controls). Mix by gently vortexing or tapping. Incubate at 4°C for 20-40 min in the dark. Wash 2X with 200 µl wash buffer (or 3X if a biotin-conjugated primary antibody is used). After each centrifugation, 350 x g
Use of Flow Cytometric Methods to Quantify Protein‐Protein Interactions
Introduction Characterizing Protein‐Protein Binding Using the Flow Cytometry Protein‐Protein Interaction Assay Basic Protocol 1: Saturation Analysis of Biotin‐RGS with Alexa Fluor532‐Gαo
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