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Anti lamin b1 12987 1 ap

Manufactured by Proteintech

Anti-lamin B1 (12987-1-AP) is a primary antibody that recognizes the lamin B1 protein. Lamin B1 is a structural protein that is a component of the nuclear lamina, which provides mechanical support and organization to the cell nucleus. This antibody can be used to detect and study the expression and localization of lamin B1 in various biological samples.

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4 protocols using anti lamin b1 12987 1 ap

1

Western Blot Analysis of Histone Proteins

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Western blot analysis was performed as described previously (16 (link)). Briefly, cells were suspended in RIPA buffer (50 mM Tris–HCl (pH 8.0), 420 mM NaCl, 0.5% sodium deoxycholate, 0.1% Sodium dodecyl sulfate, 1% NP-40) and sonicated. The extract was incubated for 30 min on ice, and then incubated at 95°C for 5 min. The extract was loaded and run on SDS-PAGE gel as standard protocols. For histone proteins, intensity was analyzed by OdysseyR CLx Imagins System(LI-COR). Anti-lamin B1 (12987-1-AP, Proteintech), anti-lamin A/C (3A6-4C11, Diagenode), anti-H2Aub (D27C4), anti-Ring1B (monoclonal antibody kindly gifted from Dr Koseki, RIKEN), anti-Ring1A (#2820, CST) were used.
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2

Antibody Panel for Cellular Signaling

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The following antibodies were used in this study: anti-PGAM1 (NBP1-49532; Novus Biologicals), anti-CtIP (sc-271339; Santa Cruz Biotechnology, Inc.), anti-Mre11 (ab214; Abcam), anti–H2AX-pS139 (9718; Cell Signaling Technology), anti–β-actin (60008-1-Ig; Proteintech), anti–Lamin B1 (12987-1-AP; Proteintech), anti-GAPDH (60004-1-Ig; Proteintech), anti-RPA32 (ab2175; Abcam), anti–RPA32-pS4S8 (NBP1-23017; Novus Biologicals), anti-BrdU (5292; Cell Signaling Technology), anti-Cdh1 (ab3242; Abcam), anti-p21 (2947; Cell Signaling Technology), anti-RAD51 (sc-8349; Santa Cruz Biotechnology, Inc.), anti-PGD (sc-398977; Santa Cruz Biotechnology, Inc.), anti-PHGDH (ab57030; Abcam), anti-IgG (2729; Cell Signaling Technology), anti-Histone H3 (4620; Cell Signaling Technology), anti-p53 (9282; Cell Signaling Technology), anti-p73 (ab202474; Abcam), and anti–Cleaved Caspase-3 (9661; Cell Signaling Technology).
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3

Ferroptosis-related Molecular Mechanisms

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Erastin (HY-15763), ferrosatatin-1 (HY-100579), N-acetylcystein (HY–B0215) and MitoSOX Red (HY-D1055) were purchased from MedChem Express (Monmouth Junction, NJ). All-trans retinoic acid (ATRA, R2625), 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT, M2003) and 4′,6-diamidino-2-phenylindole (DAPI, D9542) were from Merck KGaA (Darmstadt, Germany). Anti-CYTL1 (ab129767) antibody was purchased from Abcam (Cambridge, UK). Anti-CSE (12217-1-AP), anti-ATG5 (10181-2-AP), anti-Keap1 (10503-2-AP), anti-Lamin B1 (12987-1-AP) and anti-p53 (10442-1-AP) antibodies were from Proteintech (Chicago, IL). Anti-HA (3724), anti-LC3B (3868), anti-Myc (2276) and anti-SQSTM1/p62 (8025) antibodies were from Cell Signaling Technology (Beverly, MA). Anti-GAPDH (sc-47724), anti-β-tubulin (sc-5274), anti-β-actin (sc-47778), anti-CBS (sc-133154), anti-Nrf2 (sc-365949), and anti-GPX4 (sc-166570) antibodies were from Santa Cruz Biotechnology (Santa Cruz, CA). Lipofectamine 3000 (L3000), Lipofectamine RNAi MAX (13778), the lysosome-specific dye LysoTraker Red (L7528), and Alexa Fluor 488 goat anti-rabbit IgG (R37116) were purchased from Thermo Fisher Scientific (Waltham, MA). All other chemicals were purchased from Sigma-Aldrich (St. Louis, MO).
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4

Protein Expression Analysis by Western Blot

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Cells were collected and lysed by RIPA lysis buffer (Beyotime), put on ice for 20 min and harvested the supernatant after centrifuged at 12,000 × g, 4 °C for 20 min. The concentration of protein samples were detected by BCA Protein Assay Kit (Beyotime). Then, the protein samples were standardized, subjected to SDS–PAGE, transferred to PVDF membrane (Millipore), immunoblotted, and exposed by ECL (Thermo). Primary antibodies of anti-PIN1 (10495-1-AP) and anti-LaminB1 (12987-1-AP) were purchased from Proteintech. Anti-cyclin D1 (55506 S), anti-MMP2 (40994 S), anti-MMP9 (13667 S), anti-β-catenin (8480 S), anti-E-cadherin (14472 S), anti-N-cadherin (13116 S), and anti-XPO5 (12565 S) were from CST. The β-actin expression was applied as control for normalization (CST, 3700). The HRP-conjugated goat anti-rabbit IgG antibody (ZB-2301) and HRP-conjugated goat anti-mouse IgG antibody (ZB-2305) were from ZSGB-Bio.
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