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Ha conjugated magnetic beads

Manufactured by Cell Signaling Technology

HA-conjugated magnetic beads are a type of lab equipment used for various biological and biochemical applications. These beads are composed of a magnetic core with a surface that has been conjugated with the HA (Hemagglutinin) epitope tag. The magnetic properties of the beads allow for easy separation and manipulation using a magnetic field, while the HA tag enables specific capture and purification of HA-tagged proteins or other molecules.

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2 protocols using ha conjugated magnetic beads

1

HA-tagged Protein Immunoprecipitation and RNase Treatment

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2 × 106 iSLK.KSHV219 cells were transfected with eF4E2-HA, eIF4E1-HA and HIF2α-HA 24 h prior reactivation. Then, 24 h or 48 h post-reactivation, cells were washed with 1X PBS and harvested with IP buffer (ThermoFisher Scientific) containing phosphatase and protease inhibitors (Sigma). 5% of input sample was removed before IP. Then, IgG XP Isotype magnetic beads (Cell Signaling) and HA-conjugated magnetic beads (Cell Signaling) were added to the respective sample following manufacture’s recommendation. The samples containing beads were rotated at 4°C for 6 h. Then beads were washed 4 times prior to RNase treatment. The beads were treated with RNase or left untreated for 20 min at 25°C with rotation. After RNase incubation, the beads were washed 4 additional times and resuspended in 50 μL of 2X Laemmli buffer containing BME, boiled for 5 min and resolved in SDS-PAGE gel.
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2

HA-tagged Protein Immunoprecipitation and RNase Treatment

Check if the same lab product or an alternative is used in the 5 most similar protocols
2 × 106 iSLK.KSHV219 cells were transfected with eF4E2-HA, eIF4E1-HA and HIF2α-HA 24 h prior reactivation. Then, 24 h or 48 h post-reactivation, cells were washed with 1X PBS and harvested with IP buffer (ThermoFisher Scientific) containing phosphatase and protease inhibitors (Sigma). 5% of input sample was removed before IP. Then, IgG XP Isotype magnetic beads (Cell Signaling) and HA-conjugated magnetic beads (Cell Signaling) were added to the respective sample following manufacture’s recommendation. The samples containing beads were rotated at 4°C for 6 h. Then beads were washed 4 times prior to RNase treatment. The beads were treated with RNase or left untreated for 20 min at 25°C with rotation. After RNase incubation, the beads were washed 4 additional times and resuspended in 50 μL of 2X Laemmli buffer containing BME, boiled for 5 min and resolved in SDS-PAGE gel.
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