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ip lysis buffer  (MedChemExpress)


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    MedChemExpress ip lysis buffer
    Ip Lysis Buffer, supplied by MedChemExpress, used in various techniques. Bioz Stars score: 95/100, based on 35 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/ip+lysis+buffer/WB%2FIP+Lysis+Buffer/pm42199156-331-9-12
    Average 95 stars, based on 35 article reviews
    ip lysis buffer - by Bioz Stars, 2026-10
    95/100 stars

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    other:

    Article Title: Comprehensive molecular characterization identifies therapeutic vulnerabilities in ovarian clear cell carcinoma.
    Article Snippet: The libraries were quality controlled with Qubit (Thermo Fisher Scientific, USA) and Qsep100 (BiOptic, China) and sequenced by the Illumina sequencing platform (Nova) on a 150 bp paired-end run.

    Lysis:

    Article Title: Hypoxia‐Induced circPRELID2 Promotes Gastric Cancer Metastasis by Facilitating ZEB2 Translation via PCBP1 O‐GlcNAcylation
    Article Snippet: Then the blots were blocked with 5% non‐fat milk and incubated with primary antibodies at 4 °C overnight, followed by incubation with peroxidase‐labeled secondary antibody at room temperature for 1 h. Finally, the blot signals were detected with an enhanced chemiluminescence (ECL) kit (Vazyme, China) and analyzed with ImageJ software. .. The treated cells were washed three times with 1×PBS, and lysed in IP lysis buffer (20 mM Tris‐HCl, pH 7.4, 150 mM NaCl, 0.5% Triton X‐100, and 2 mM EDTA) supplemented with protease inhibitors (Sparkjade, Shandong, China) and phosphatase inhibitors (MedChemExpress, USA) at 4 °C for 30 min, then the lysates were centrifuged at 13 000 rpm at 4 °C for 15 min. .. The supernatant was incubated with anti‐SAM68/anti‐SFPQ/anti‐PCBP1 antibody at 4 °C overnight followed by incubation with protein A/G or protein A beads (Millipore, USA) at 4 °C for 2–4 h, or incubated with anti‐Flag/Myc/HA affinity gel (Sigma, USA) or anti‐V5 agarose affinity gel (Beyotime, China) at 4 °C for 4 h. Then, the beads were washed and eluted with SDS loading buffer, followed by immunoblotting analysis.

    Article Title: mTORC2 Phosphorylation of GSDME-N Drives Cullin4B-Mediated Proteasomal Degradation to Suppress Pyroptosis and Confer Radioresistance in Small Cell Lung Cancer.
    Article Snippet: Immunoreactive bands were visualized sing the ChemiDoc Imaging System (Bio-Rad, Hercules, CA, SA). dvanced Science, 2026 .. SCLC and HEK293T cells were lysed on ice using IP lysis buffer (MedChemExpress, MCE, NJ, USA) supplemented with protease inhibitors and phosphatase inhibitor cocktail (Selleck, Houston, TX, USA). ..

    Article Title: Discovery of o-aminodiphenyl-based USP7 inhibitor for immune activation and antitumor response in colorectal cancer.
    Article Snippet: Background: Colorectal cancer is a leading cause of cancer mortality, with microsatellite-stable tumors exhibiting poor response to immune checkpoint inhibitors.. Ubiquitin-specific protease 7 (USP7) stabilizes programmed death-ligand 1 (PD-L1), promoting immune evasion.. Methods: Through screening, synthesis, and optimization, we identified an o-aminodiphenyl derivative, U-20, as a potent USP7 inhibitor (IC50 = 83 nM).

    Article Title: High-throughput screening reveals paeoniflorin's efficacy against Apoc2-deficient hypertriglyceridemia via HNF4A/PPARA/LDLR.
    Article Snippet: Hypertriglyceridemia (HTG) is a significant risk factor for cardiovascular disease, fatty liver, and acute pancreatitis, yet remains a therapeutic challenge due to limitations of current treatment options.. To address this unmet clinical need, we screened a natural small-molecule library at an initial concentration of 100 μM to identify effective HTG therapeutic candidates using a CRISPR/Cas9-generated apolipoprotein C2 (apoc2) knockout zebrafish model that resembles human lipid metabolism disorders.. Phenotype-based screening identified paeoniflorin (PAE) from 351 compounds as a potent triglyceride-lowering agent.

    Article Title: Quantitative proteomic analysis identifies the unfolded protein response as a host pathway co-opted by ASFV to promote replication
    Article Snippet: DNA sequencing confirmed the expected specific sequence in the construct (Qingke, Xi'an, China). .. For immunoprecipitation analysis, the HEK293T cells were homogenized with IP lysis buffer (containing 50 mM Tris-Cl [pH = 7.4], 150 mM NaCl, 1%Triton-100, 0.1% SDS, 1% sodium deoxycholate, and protease inhibitor cocktail), centrifuged to remove cell debris, and then the supernatant was collected for immunoprecipitation with Myc (HY-K0206, MCE) and DYKDDDDK magnetic beads (b26103; Selleck Chemicals, USA) at 4°C for 2 h. After washing five times with IP lysis buffer, the protein-bound beads were finally resuspended in SDS-PAGE loading buffer. ..

    Article Title: The AHCY–adenosine complex rewires mRNA methylation to enhance fatty acid biosynthesis and tumorigenesis
    Article Snippet: The antibodies used in this study were anti-AHCY (Proteintech, 10757-2-AP, 1:1000), anti-MAT2A (CST, 84478, 1:1000), anti-Histone H3 (CST, 4499, 1:2000), anti-H3K4me3 (CST, 9751, 1:2000), anti-H3K9me3 (CST, 13969, 1:2000), anti-H3K27me3 (CST, 9733, 1:2000), anti-H3K36me3 (CST, 4909, 1:2000), anti-H3K79me3 (Abways, AB3548, 1:1000), anti-FTO (CST, 45980, 1:1000), anti-actin (CST, 93473, 1:1000), anti-GAPDH (CST, 92310, 1:1000), anti-PARP (CST, 9542, 1:1000), anti-flag (Sigma, F3165, 1:1000), anti-HA (CST, 2367, 1:1000), anti-Myc (CST, 5605, 1:1000), anti-SAHH (Abcam, ab134966, 1:1000), anti-ACC1 (Proteintech, 21923-1-AP, 1:1000), anti-GST (Proteintech, 66001-2-Ig, 1:2000), FASN (Acmec, AC50671, 1:1000), anti-SCD1 (Proteintech, 28678-1-AP, 1:1000), anti-SREBP1 (Santa Cruz, sc-13551, 1:1000), SREBP2 (Santa Cruz, sc-13552, 1:1000), anti-p-AMPK (CST, 9957, 1:1000), anti-AMPK (CST, 9957, 1:1000), anti-p-PI3K (GeneTex, GTX100462S, 1:1000), anti-Akt (CST, 927, 1:10002), anti-EGFR (Proteintech, 66455-1-Ig, 1:1000), anti-Ki67 (Proteintech, 27309-1-AP, 1:1000), anti-ALKBH5 (Proteintech, 16837-1-AP, 1:1000), anti-METTL3 (Proteintech, 15073-1-AP, 1:1000), and anti-METTL14 (Proteintech, 26158-1-AP, 1:1000). .. IP lysis buffer (20 mM Tris-HCl pH 7.4, 1% NP-40, 10% glycerol, 137 mM NaCl, 2 mM EDTA) was supplemented with 1 mM dithiothreitol (DTT), 1 mM phenylmethylsulfonyl fluoride (PMSF) (Beyotime, ST506), and a protease inhibitor cocktail (MCE, HY-K0010). ..

    Article Title: Liquid-liquid phase separation of ATXN2L enhances mRNA translation in hepatocellular carcinoma.
    Article Snippet: After DAPI (S2110, Solarbio, Beijing, China) staining, the slides were observed under a confocal microscope (STELLARIS, Leica, Wetzlar, Germany). .. Cells were collected from a single 10 cm dish for an IP assay, and total proteins were extracted using 500 μL of IP lysis buffer (HYK1000, MedChemExpress, Shanghai, China). .. Antigen retrieval was performed for 16 min, followed by incubation with 3% H 2 O 2 (H755825, Aladdin, Shanghai, China) for 10 min. Tissues were subsequently blocked using 10% goat serum (SL038, Solarbio, Beijing, China) for 30 min. Primary antibodies were then applied and allowed to react for 1 h, followed by incubation with biotin-labeled secondary antibodies for 30 min.

    Protease Inhibitor:

    Article Title: Discovery of o-aminodiphenyl-based USP7 inhibitor for immune activation and antitumor response in colorectal cancer.
    Article Snippet: Background: Colorectal cancer is a leading cause of cancer mortality, with microsatellite-stable tumors exhibiting poor response to immune checkpoint inhibitors.. Ubiquitin-specific protease 7 (USP7) stabilizes programmed death-ligand 1 (PD-L1), promoting immune evasion.. Methods: Through screening, synthesis, and optimization, we identified an o-aminodiphenyl derivative, U-20, as a potent USP7 inhibitor (IC50 = 83 nM).

    Article Title: High-throughput screening reveals paeoniflorin's efficacy against Apoc2-deficient hypertriglyceridemia via HNF4A/PPARA/LDLR.
    Article Snippet: Hypertriglyceridemia (HTG) is a significant risk factor for cardiovascular disease, fatty liver, and acute pancreatitis, yet remains a therapeutic challenge due to limitations of current treatment options.. To address this unmet clinical need, we screened a natural small-molecule library at an initial concentration of 100 μM to identify effective HTG therapeutic candidates using a CRISPR/Cas9-generated apolipoprotein C2 (apoc2) knockout zebrafish model that resembles human lipid metabolism disorders.. Phenotype-based screening identified paeoniflorin (PAE) from 351 compounds as a potent triglyceride-lowering agent.

    Article Title: Quantitative proteomic analysis identifies the unfolded protein response as a host pathway co-opted by ASFV to promote replication
    Article Snippet: DNA sequencing confirmed the expected specific sequence in the construct (Qingke, Xi'an, China). .. For immunoprecipitation analysis, the HEK293T cells were homogenized with IP lysis buffer (containing 50 mM Tris-Cl [pH = 7.4], 150 mM NaCl, 1%Triton-100, 0.1% SDS, 1% sodium deoxycholate, and protease inhibitor cocktail), centrifuged to remove cell debris, and then the supernatant was collected for immunoprecipitation with Myc (HY-K0206, MCE) and DYKDDDDK magnetic beads (b26103; Selleck Chemicals, USA) at 4°C for 2 h. After washing five times with IP lysis buffer, the protein-bound beads were finally resuspended in SDS-PAGE loading buffer. ..

    Article Title: The AHCY–adenosine complex rewires mRNA methylation to enhance fatty acid biosynthesis and tumorigenesis
    Article Snippet: The antibodies used in this study were anti-AHCY (Proteintech, 10757-2-AP, 1:1000), anti-MAT2A (CST, 84478, 1:1000), anti-Histone H3 (CST, 4499, 1:2000), anti-H3K4me3 (CST, 9751, 1:2000), anti-H3K9me3 (CST, 13969, 1:2000), anti-H3K27me3 (CST, 9733, 1:2000), anti-H3K36me3 (CST, 4909, 1:2000), anti-H3K79me3 (Abways, AB3548, 1:1000), anti-FTO (CST, 45980, 1:1000), anti-actin (CST, 93473, 1:1000), anti-GAPDH (CST, 92310, 1:1000), anti-PARP (CST, 9542, 1:1000), anti-flag (Sigma, F3165, 1:1000), anti-HA (CST, 2367, 1:1000), anti-Myc (CST, 5605, 1:1000), anti-SAHH (Abcam, ab134966, 1:1000), anti-ACC1 (Proteintech, 21923-1-AP, 1:1000), anti-GST (Proteintech, 66001-2-Ig, 1:2000), FASN (Acmec, AC50671, 1:1000), anti-SCD1 (Proteintech, 28678-1-AP, 1:1000), anti-SREBP1 (Santa Cruz, sc-13551, 1:1000), SREBP2 (Santa Cruz, sc-13552, 1:1000), anti-p-AMPK (CST, 9957, 1:1000), anti-AMPK (CST, 9957, 1:1000), anti-p-PI3K (GeneTex, GTX100462S, 1:1000), anti-Akt (CST, 927, 1:10002), anti-EGFR (Proteintech, 66455-1-Ig, 1:1000), anti-Ki67 (Proteintech, 27309-1-AP, 1:1000), anti-ALKBH5 (Proteintech, 16837-1-AP, 1:1000), anti-METTL3 (Proteintech, 15073-1-AP, 1:1000), and anti-METTL14 (Proteintech, 26158-1-AP, 1:1000). .. IP lysis buffer (20 mM Tris-HCl pH 7.4, 1% NP-40, 10% glycerol, 137 mM NaCl, 2 mM EDTA) was supplemented with 1 mM dithiothreitol (DTT), 1 mM phenylmethylsulfonyl fluoride (PMSF) (Beyotime, ST506), and a protease inhibitor cocktail (MCE, HY-K0010). ..

    Immunoprecipitation:

    Article Title: Quantitative proteomic analysis identifies the unfolded protein response as a host pathway co-opted by ASFV to promote replication
    Article Snippet: DNA sequencing confirmed the expected specific sequence in the construct (Qingke, Xi'an, China). .. For immunoprecipitation analysis, the HEK293T cells were homogenized with IP lysis buffer (containing 50 mM Tris-Cl [pH = 7.4], 150 mM NaCl, 1%Triton-100, 0.1% SDS, 1% sodium deoxycholate, and protease inhibitor cocktail), centrifuged to remove cell debris, and then the supernatant was collected for immunoprecipitation with Myc (HY-K0206, MCE) and DYKDDDDK magnetic beads (b26103; Selleck Chemicals, USA) at 4°C for 2 h. After washing five times with IP lysis buffer, the protein-bound beads were finally resuspended in SDS-PAGE loading buffer. ..

    Magnetic Beads:

    Article Title: Quantitative proteomic analysis identifies the unfolded protein response as a host pathway co-opted by ASFV to promote replication
    Article Snippet: DNA sequencing confirmed the expected specific sequence in the construct (Qingke, Xi'an, China). .. For immunoprecipitation analysis, the HEK293T cells were homogenized with IP lysis buffer (containing 50 mM Tris-Cl [pH = 7.4], 150 mM NaCl, 1%Triton-100, 0.1% SDS, 1% sodium deoxycholate, and protease inhibitor cocktail), centrifuged to remove cell debris, and then the supernatant was collected for immunoprecipitation with Myc (HY-K0206, MCE) and DYKDDDDK magnetic beads (b26103; Selleck Chemicals, USA) at 4°C for 2 h. After washing five times with IP lysis buffer, the protein-bound beads were finally resuspended in SDS-PAGE loading buffer. ..

    SDS Page:

    Article Title: Quantitative proteomic analysis identifies the unfolded protein response as a host pathway co-opted by ASFV to promote replication
    Article Snippet: DNA sequencing confirmed the expected specific sequence in the construct (Qingke, Xi'an, China). .. For immunoprecipitation analysis, the HEK293T cells were homogenized with IP lysis buffer (containing 50 mM Tris-Cl [pH = 7.4], 150 mM NaCl, 1%Triton-100, 0.1% SDS, 1% sodium deoxycholate, and protease inhibitor cocktail), centrifuged to remove cell debris, and then the supernatant was collected for immunoprecipitation with Myc (HY-K0206, MCE) and DYKDDDDK magnetic beads (b26103; Selleck Chemicals, USA) at 4°C for 2 h. After washing five times with IP lysis buffer, the protein-bound beads were finally resuspended in SDS-PAGE loading buffer. ..



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