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2 protocols using ab128919

1

Immunostaining of Mitotic Proteins

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Primary antibodies used for immunostaining were anti-TRF1 (Abcam, ab192629, 1:100), anti-BubR1 (Abcam, ab28193, 1:100), anti-Zw10 (Abcam, ab21582, 1:100), anti-acetylated-α-tubulin (Sigma Aldrich, T7451, 1:500; Abcam, ab179484, 1:500), anti-centromere (Antibodies Incorporated, 15-234, 1:100), anti-CENP-A (Cell Signaling, #2048, 1:100), anti-Survivin (Cell Signaling, #2808, 1:100), anti-Hec1 (Santa Cruz Biotechnology, sc-515550, 1:100), anti-H3T3ph (Upstate, 07-424, 1:100), anti-SMC3 (Abcam, ab128919, 1:100), anti-SMC4 (Novus Biologicals, NBP1-86635, 1:100), and anti-TRF2 (Abcam, ab13579, 1:100). Secondary antibodies were Alexa Fluor 488-conjugated anti-mouse (Jackson ImmunoResearch, 115-545-144 1:500), Alexa Fluor 594-conjugated anti-mouse (Jackson ImmunoResearch, 111-585-146, 1:500), Alexa Fluor 488-conjugated anti-rabbit (Jackson ImmunoResearch, 115-545-144 1:500), Alexa Fluor 594-conjugated anti-rabbit (Jackson ImmunoResearch, 111-585-144, 1:500), and Alexa Fluor 488-conjugated anti-sheep antibodies (Abcam, ab150177, 1:500).
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2

Immunofluorescence Staining of Mitotic Markers

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The following primary antibodies were used: anti‐γ‐H2AX (Abcam, ab22551, 1:250), anti‐MDC1 (Abcam, ab241048, 1:100), anti‐acetylated‐α‐tubulin (Sigma‐Aldrich, T7451, 1:500; Abcam, ab179484, 1:500), anti‐Mad2 (Abcam, ab70383, 1:100), anti‐BubR1 (Abcam, ab28193, 1:100), anti‐centromere (ACA; Antibodies Incorporated, 15–234, 1:100), anti‐SMC3 (Abcam, ab128919, 1:100), anti‐SMC4 (Novus Biologicals, NBP1‐86635, 1:100) and anti‐CENP‐A (Cell Signaling, #2048, 1:250). Alexa Fluor 488‐conjugated anti‐mouse (Jackson ImmunoResearch, 115‐545‐144, 1:500), Alexa Fluor 488‐conjugated anti‐rabbit (Jackson ImmunoResearch, 115‐545‐144 1:500), Alexa Fluor 594‐conjugated anti‐rabbit (Jackson ImmunoResearch, 111‐585‐144, 1:500) and Rhodamine (TRITC) ‐conjugated anti‐human (Jackson ImmunoResearch, 109‐025‐088, 1:100) were used as secondary antibodies.
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