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Ab155091

Manufactured by Abcam

Ab155091 is a laboratory equipment product offered by Abcam. It is a high-quality, durable and reliable tool designed for use in various scientific and research applications. The core function of this product is to facilitate specific tasks or procedures within a laboratory setting. However, a detailed description of its intended use or application cannot be provided in an unbiased and factual manner without the risk of extrapolation.

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3 protocols using ab155091

1

Immunoblotting Analysis of Immune Proteins

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Cells were washed with PBS, lysed in sample buffer, boiled for 3 min, resolved by SDS-PAGE and analyzed by immunoblotting using primary antibodies specific for human MX2 (sc-47197 (N-17), Santa Cruz Biotechnology), human TRIM5α (ab4389, Abcam), human PSMB8 (ab3329, Abcam), human PSMB9 (ab3328, Abcam), human PSMB10 (ab77735, Abcam), human PA28A (ab155091, Abcam), human PA28B (ab183727, Abcam), FLAG (HRP-conjugated M2, Sigma), HA (HRP-conjugated 3F10, Sigma) or human α-tubulin (DM1A, Sigma), and detected using either horseradish peroxidase-conjugated secondary antibodies and chemiluminescence (ECL+ western blotting substrate, Pierce) or IRDye®-800CW-labelled secondary antibodies and the LI-COR infrared imaging technology (LI-COR UK LTD).
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2

Immunoblotting Analysis of Immune Proteins

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Cells were washed with PBS, lysed in sample buffer, boiled for 3 min, resolved by SDS-PAGE and analyzed by immunoblotting using primary antibodies specific for human MX2 (sc-47197 (N-17), Santa Cruz Biotechnology), human TRIM5α (ab4389, Abcam), human PSMB8 (ab3329, Abcam), human PSMB9 (ab3328, Abcam), human PSMB10 (ab77735, Abcam), human PA28A (ab155091, Abcam), human PA28B (ab183727, Abcam), FLAG (HRP-conjugated M2, Sigma), HA (HRP-conjugated 3F10, Sigma) or human α-tubulin (DM1A, Sigma), and detected using either horseradish peroxidase-conjugated secondary antibodies and chemiluminescence (ECL+ western blotting substrate, Pierce) or IRDye®-800CW-labelled secondary antibodies and the LI-COR infrared imaging technology (LI-COR UK LTD).
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3

Proteasome Subunit Quantification by Western Blot

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Proteins were transferred to PVDF membranes using a Bio-Rad mini-protean transfer system containing a buffer of 25 mM Tris base, 192 mM glycine, 0.1% SDS. Proteins were transferred for 6h at 40V at 4°C. Membranes with transferred proteins were blocked with a 1:1 mixture of Li-COR blocking buffer and PBS. Membranes were then incubated in blocking solution for 1 h and primary Abs (1:1000) applied for 16 h at 4°C. Membranes were washed and incubated with secondary Abs (IR Dye® 800CW goat anti-mouse IgG (H+L) or IR Dye 680CW donkey anti-rabbit IgG (H+L), and imaged using an Odyssey Li-Cor platform. Antibodies used were rabbit anti-PSMB5 polyclonal (Abcam, ab90867), rabbit monoclonal to anti-PSME1 (EPR10967, Abcam, ab155091), rabbit monoclonal to anti-PSME2 (EPR14931, Abcam, ab183727), rabbit anti-LMP2 polyclonal (PSMB9, Abcam, ab42987), rabbit anti-PSMB10 polyclonal (Abcam, ab77735), rabbit anti-LMP7 monoclonal (EPR14482, PSMB8, Abcam, ab180606), rabbit anti-PSMA6 polyclonal (Cell Signaling 2459), rabbit anti-PSMB1 polyclonal (Abcam, ab196623), rabbit anti-PSMB2 polyclonal (Abcam, ab140426), mouse anti-Rpn5 monoclonal (PSMD12, clone H3, Santa Cruz Biotechnology, sc-398279), mouse anti-α-tubulin monoclonal (DM1a, Abcam, ab7291), and rabbit anti-histone 3 polyclonal (Abcam, ab1791).
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