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B 5 1 2

Manufactured by Santa Cruz Biotechnology
Sourced in United States

B-5-1-2 is a laboratory instrument designed for the separation and purification of biological molecules. It is capable of performing centrifugation at high speeds to isolate specific components from complex samples. The core function of this product is to facilitate the extraction and concentration of target analytes for further analysis or downstream processing.

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9 protocols using b 5 1 2

1

Western Blot Analysis of Cellular Proteins

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Cells were lysed in lysis buffer (50 mM Tris-HCl pH 7.4, 150 mM NaCl, 1% Triton X-100) with protease- and phosphatase inhibitors (Roche), except for the WABS fibroblasts (Fig. 3a, c), which were directly scraped in sample buffer. Proteins were separated by 3–8%, 4–15% or 8–16% SDS-PAGE (NU-PAGE or BioRad) and transferred to immobilon-P membranes (Millipore). Membranes were blocked in 5% dry milk in TBST-T (10 mM Tris-HCl pH 7.4, 150 mM NaCl, 0.04% Tween-20), incubated with primary and peroxidase-conjugated secondary antibodies (DAKO Glostrup, Denmark; 1:10000) and bands were visualized by chemoluminescence (Amersham). Antibodies used for detection are mouse-anti-DDX11 (B01P, Abnova; 1:250–1:1000), goat-anti-β-actin (I-19, Santa Cruz; 1:1000), mouse-anti-α-tubulin (B-5-1-2, Santa Cruz #sc-23948; 1:2000), mouse-anti-CDC6 (Santa Cruz #sc-9964; 1:500), mouse-anti-p62 (D5L7G, cell signaling; 1:1000), mouse-anti-Flag (M2, Sigma; 1:10000), mouse-anti-p53 (DO-1, Santa Cruz #sc-126; 1:1000), mouse-anti-vinculin (H-10, Santa Cruz #sc-25336; 1:2000), guinea pig anti-ESCO2 (1:50083 (link)). Uncropped western blots are provided in Supplementary Fig. 13.
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2

Chromatin-Bound Protein Extraction and Western Blot

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Cells were lysed in lysis buffer (50 mM Tris-HCl pH 7.4, 150 mM NaCl, 1% Triton X-100) with protease- and phosphatase inhibitors (Roche). For DNA-bound protein fractions, cells were lysed in lysis buffer for 10 min and centrifuged at 1300 g for 10 min. The pellet was subsequently lysed in lysis buffer containing 5 units/μL benzonase nuclease (Sigma) for 1 h and centrifuged at maximum speed for 5 min. Proteins were separated by 3–8% or 8–16% SDS-PAGE (NU-PAGE or BioRad) and transferred to immobilon-P membranes (Millipore). Membranes were blocked in 5% dry milk in TBST-T (10 mM Tris-HCl pH 7.4, 150 mM NaCl, 0.04% Tween-20), incubated with primary and peroxidase-conjugated secondary antibodies (DAKO Glostrup, Denmark) and bands were visualized by chemoluminescence (Amersham). Antibodies used for detection are mouse anti-DDX11 (B01P, Abnova), mouse anti-α-tubulin (B-5-1-2, Santa Cruz #sc-23948), mouse anti-vinculin (H-10, Santa Cruz sc-25336), guinea pig anti-ESCO2 [36 (link)], mouse anti-ESCO1 (gift from JM Peters), rabbit anti-PARP (9542, Cell signaling), AcSM3 (gift from K Shirahige), rabbit anti-SMC3 (A300-060A, Bethyl), rabbit anti-WAPL (A300-268, Bethyl), mouse anti-vinculin (H-10, sc-25336, Santa Cruz).
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3

Western Blot Analysis of DNA Repair Proteins

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Cells were lysed in 2× sample buffer and boiled for 10 min at 95°C. The proteins were subsequently separated by SDS-PAGE and transferred to PVDF membranes (0.45 μm). Membranes were blocked with 5% BSA in PBS-T (PBS containing 0.05% Tween 20) for 1 h at room temperature (RT) and blotted with the following primary antibodies: CPD-PL and 6-4PP-PL (rabbit polyclonal, 1:500) (58 (link),59 (link)), RFP mCherry (rat monoclonal, 1:1000, 5F8, Chromotek), DDB2 (rabbit monoclonal, 1:1000, EPR981, abcam), Ku70 (goat polyclonal, 1:1000, M-19, sc-1487, Santa Cruz), tubulin (mouse monoclonal, 1:3000, B-5-1-2, sc-23948, Santa Cruz), XPC (rabbit polyclonal, 1:1000, A301-122A, Bethyl) or XPF (mouse monoclonal, 1:500, 3F2/3, sc-136153, Santa Cruz). After five times washing with PBS-T, the membranes were blotted with the following corresponding secondary antibodies from Sigma Aldrich: CF™ 680 Goat anti-Rabbit IgG (1:5000) and CF™ 770 Goat anti-Mouse IgG (1:5000). The blots were imaged with the Odyssey CLx Infrared Imaging System (LI-COR Biosciences).
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4

Immunodetection of Cytoskeletal Proteins

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Mouse monoclonal antibody against α-Tubulin (B-5-1-2; Cat. No.23948) was procured from Santacruz Biotechnology company, whereas mouse monoclonal antibodies against β-tubulin (Cat. No. T7816) and GFP (GF28R; Cat. No.MA5-15256) were purchased from Sigma and Invitrogen, respectively.
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5

Immunoblotting Protein Isolation and Detection

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Proteins were isolated in lysis buffer (50 mM Tris-HCl pH 7.4, 150 mM NaCl, 1% Triton X-100) with protease- and phosphatase inhibitors, separated by 3–8% or 8–16% SDS-PAGE (NU-PAGE), blotted onto polyvinylidene fluoride transfer membranes, incubated with the appropriate primary and secondary antibodies, and bands were visualized by chemoluminescence (Amersham). Antibodies used for detection are mouse anti-DDX11 (Abnova #H00001663-B01P, dilution 1:1,000), mouse anti-vinculin (H-10, Santa Cruz #sc-25336, dilution 1:1,000), rabbit anti-APC2 (kind gift from J. Pines, dilution 1:5,00), mouse anti-α-tubulin (B-5-1-2, Santa Cruz #sc-23948, dilution 1:5,000), mouse anti-APC3 (BD Transduction laboratories, #610454, dilution 1:1,000), goat anti-APC4 (C-18, Santa Cruz #SC-21414, dilution 1:500), rabbit anti-p31comet (Abcam #ab150363, dilution 1:1,000), guinea pig anti-ESCO2 (ref. 40 (link)) (dilution 1:1,000), mouse anti-Rad21 (Oncogene #NA80, dilution 1:1,000) and rabbit anti-WAPL (Bethyl #A300-268 A, dilution 1:1,000). Uncropped images of western blots are provided in Supplementary Fig. 9.
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6

Western Blot Analysis of Cell Proteins

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Cells were lysed in lysis buffer [50 mM tris-HCl (pH 7.4), 150 mM NaCl, and 1% Triton X-100] with protease and phosphatase inhibitors (Roche). Proteins were separated by 4 to 15% SDS–polyacrylamide gel electrophoresis (Bio-Rad) and transferred to Immobilon-P membranes (Millipore). Membranes were blocked in 5% dry milk in TBST-T [10 mM tris-HCl (pH 7.4), 150 mM NaCl, and 0.04% Tween 20] and incubated with primary and peroxidase-conjugated secondary antibodies (1:10,000; DAKO, Glostrup, Denmark), and bands were visualized by chemiluminescence (Amersham). Antibodies used for detection are rabbit anti-BUB1 (1:1000; A300-373A, Bethyl and ab9000, Abcam), sheep anti-BUB1 (1:500; SB1.3, gift from S. Taylor), mouse anti–α-tubulin (1:2000; B-5-1-2, #sc-23948, Santa Cruz Biotechnology), and mouse anti-CDC6 (1:500; #sc-9964, Santa Cruz Biotechnology).
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7

Western Blot Analysis of Protein Expression

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Briefly, total proteins from cells were lysed in RIPA buffer supplemented with protease inhibitor cocktail, PIC (88266, Thermo Fisher Scientific) for 20 min on ice. The protein concentration was determined using a Bradford protein assay kit (Bio-Rad). The following antibodies and dilutions were used for western blot analysis. Mouse anti-Sugt1 (1:500, sc-81822, Santa Cruz), mouse anti-α-Tubulin (1:5000, B-5-1-2, Santa Cruz), mouse anti-Flag (1:1000, F1804, Sigma), mouse anti-Ub (1:5000, sc-8017, Santa Cruz), mouse anti-HA (1:1000, sc-7392, Santa Cruz), rabbit anti-Hnrnpl (1:1000, sc-28726, Santa Cruz), mouse anti-Dnmt 3a (1:1000, ab-13888, Abcam); rabbit anti-Dnmt 3b (1:1000, ab-2851, Abcam); and rabbit anti-Hec1 antibody9 (link) (1:5000) a very kind gift from Dr. Robert Benezra, Memorial Sloan Kettering Cancer Center, USA). The relative band intensities were quantified using ImageJ 1.50i (National Institutes of Health).
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8

Immunoblot Analysis of Protein Expression

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Immunoblotting was essentially performed as described35 (link). Proteins were detected on nitrocellulose membranes (Bio-Rad, #1620115) using the following primary antibodies: α−6*His-tag (clone 4A4 or 2F12, source: antibody facility of the Helmholtz Center Munich, hybridoma supernatants were used at a 1:10 dilution)75 (link), α-TRAF6 (H-274, Santa Cruz Biotech., #sc-7221, used at 1:1000), α-HA-tag (12CA5, Sigma-Aldrich, #11583816001, used at 0.4 µg per mL), α-IκBα (C-21, Santa Cruz Biotech., #sc-371, used at 1:500) and α-Tubulin (B-5-1-2, Santa Cruz Biotech., #sc-23948, used at 1:500). Horseradish peroxidase-coupled antibodies were used as secondary antibodies (Cell Signalling Technology, #7074 or #7076, respectively, both used at 1:5000). ECL signals were captured on X-ray films (Agfa Healthcare) and quantified by densitometry using the ImageJ software. Uncropped scans of immunoblots indicating molecular weights are provided in Supplementary Fig. 6.
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9

Comprehensive Immunofluorescence and Western Blot Protocol

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For immunofluorescence (IF) and Western blot (WB) assays, we used the following antibodies and dilutions: VEGF [(1:100 dilution (IF), 1:500 dilution (WB), RM 9128-S0; NeoMarkers)]; Bevacizumab (1:100 dilution (IF), Genentech); MCT1 [(1:200 dilution, AB3538P; Chemicon International (IF)), (1:500 dilution; H-1, sc-365501; Santa Cruz Biotechnology (WB))]; MCT4 (1:500 dilution; H-90; sc-50329; Santa Cruz Biotechnology); CD147 (1:500 dilution, 1.BB.218, sc-71038; Santa Cruz Biotechnology); HKII (1:4000 dilution, ab104836, Abcam); GLUT-1 (1:500 dilution, ab15309, Abcam); HIF-1α [(1:100 dilution (IF); 1:500 dilution (WB), 610958, BD Biosciences), LDHA (1:1000 dilution, E9, sc-137243, Santa Cruz Biotechnology), CAIX (1:2000 dilution, ab15086, Abcam); LC3A/B (1:1000 dilution, 4108, Cell Signaling Technology); p62 (1:1000 dilution, sc-28359, Santa Cruz Biotechnology); IRF1 (1:1000 dilution, sc-135952, Santa Cruz Biotechnology); α-Tubulin (1:5000 dilution, B-5-1-2, sc-2394, Santa Cruz Biotechnology) and GAPDH (1:1000 dilution, sc-69778, Santa Cruz Biotechnology).
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