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3x blue loading buffer  (Cell Signaling Technology Inc)


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    Structured Review

    Cell Signaling Technology Inc 3x blue loading buffer
    3x Blue Loading Buffer, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 96/100, based on 222 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/3x+loading+buffer/Blue+Loading+Buffer+Pack/pm38566168-53-24-29
    Average 96 stars, based on 222 article reviews
    3x blue loading buffer - by Bioz Stars, 2026-09
    96/100 stars

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    Related Articles

    Protein Concentration:

    Article Title: CK2 inhibitor, CX-4945, enhances BH3 priming and promotes apoptosis of venetoclax-resistant AML by targeting antiapoptotic proteins
    Article Snippet: The AML cell lines were seeded at a density of 4 × 10 5 cells/mL in a 6-well plate and left untreated or treated with vehicle (DMSO), CX-4945, VEN, CX+VEN at indicated doses for 24 h. The cells were collected by centrifugation, washed with ice-cold PBS and then whole-cell lysates were prepared using 1X cell lysis buffer (#9803; Cell Signaling, Danvers, MA) supplemented with 1 mM of PMSF protease Inhibitor (#36978; Thermo Scientific) and phosphatase inhibitor cocktail (#P5726; Sigma-Aldrich). .. After quantification of protein concentration using BCA assay kit (#23225; Thermo Fisher Scientific), an equal amount of protein (10-20 μg) from each sample was denatured at 95°C for 5 min in reducing SDS loading buffer (#7722; Cell Signaling), subjected to gel electrophoresis using 4–20% mini-PROTEAN TGX precast protein gels (Bio-Rad Laboratories, Hercules, CA) and transferred to Immobilon-FL PVDF membrane (#IPFL00010; Millipore Sigma). ..

    BIA-KA:

    Article Title: CK2 inhibitor, CX-4945, enhances BH3 priming and promotes apoptosis of venetoclax-resistant AML by targeting antiapoptotic proteins
    Article Snippet: The AML cell lines were seeded at a density of 4 × 10 5 cells/mL in a 6-well plate and left untreated or treated with vehicle (DMSO), CX-4945, VEN, CX+VEN at indicated doses for 24 h. The cells were collected by centrifugation, washed with ice-cold PBS and then whole-cell lysates were prepared using 1X cell lysis buffer (#9803; Cell Signaling, Danvers, MA) supplemented with 1 mM of PMSF protease Inhibitor (#36978; Thermo Scientific) and phosphatase inhibitor cocktail (#P5726; Sigma-Aldrich). .. After quantification of protein concentration using BCA assay kit (#23225; Thermo Fisher Scientific), an equal amount of protein (10-20 μg) from each sample was denatured at 95°C for 5 min in reducing SDS loading buffer (#7722; Cell Signaling), subjected to gel electrophoresis using 4–20% mini-PROTEAN TGX precast protein gels (Bio-Rad Laboratories, Hercules, CA) and transferred to Immobilon-FL PVDF membrane (#IPFL00010; Millipore Sigma). ..

    Nucleic Acid Electrophoresis:

    Article Title: CK2 inhibitor, CX-4945, enhances BH3 priming and promotes apoptosis of venetoclax-resistant AML by targeting antiapoptotic proteins
    Article Snippet: The AML cell lines were seeded at a density of 4 × 10 5 cells/mL in a 6-well plate and left untreated or treated with vehicle (DMSO), CX-4945, VEN, CX+VEN at indicated doses for 24 h. The cells were collected by centrifugation, washed with ice-cold PBS and then whole-cell lysates were prepared using 1X cell lysis buffer (#9803; Cell Signaling, Danvers, MA) supplemented with 1 mM of PMSF protease Inhibitor (#36978; Thermo Scientific) and phosphatase inhibitor cocktail (#P5726; Sigma-Aldrich). .. After quantification of protein concentration using BCA assay kit (#23225; Thermo Fisher Scientific), an equal amount of protein (10-20 μg) from each sample was denatured at 95°C for 5 min in reducing SDS loading buffer (#7722; Cell Signaling), subjected to gel electrophoresis using 4–20% mini-PROTEAN TGX precast protein gels (Bio-Rad Laboratories, Hercules, CA) and transferred to Immobilon-FL PVDF membrane (#IPFL00010; Millipore Sigma). ..

    Membrane:

    Article Title: CK2 inhibitor, CX-4945, enhances BH3 priming and promotes apoptosis of venetoclax-resistant AML by targeting antiapoptotic proteins
    Article Snippet: The AML cell lines were seeded at a density of 4 × 10 5 cells/mL in a 6-well plate and left untreated or treated with vehicle (DMSO), CX-4945, VEN, CX+VEN at indicated doses for 24 h. The cells were collected by centrifugation, washed with ice-cold PBS and then whole-cell lysates were prepared using 1X cell lysis buffer (#9803; Cell Signaling, Danvers, MA) supplemented with 1 mM of PMSF protease Inhibitor (#36978; Thermo Scientific) and phosphatase inhibitor cocktail (#P5726; Sigma-Aldrich). .. After quantification of protein concentration using BCA assay kit (#23225; Thermo Fisher Scientific), an equal amount of protein (10-20 μg) from each sample was denatured at 95°C for 5 min in reducing SDS loading buffer (#7722; Cell Signaling), subjected to gel electrophoresis using 4–20% mini-PROTEAN TGX precast protein gels (Bio-Rad Laboratories, Hercules, CA) and transferred to Immobilon-FL PVDF membrane (#IPFL00010; Millipore Sigma). ..

    Western Blot:

    Article Title: Mechanisms of HIV Latency in Hematopoietic Progenitors: GFI1 as a Key Regulator
    Article Snippet: .. For western blot analysis, cells were lysed in Blue Loading Buffer (cat# 7722, Cell Signaling Technology), sonicated with a Misonix sonicator (Qsonica, LLC. ..

    Article Title: Energy stress-induced PKCζ S-glutathionylation is essential for LKB1 cytoplasmic translocation and AMPK activation
    Article Snippet: .. For western blot analysis, cells were collected, washed twice with cold PBS, and lysed in 1 × SDS Sample Buffer (#7722, Cell Signaling Technology, USA) according to the manufacturer’s protocol supplemented with proteasome inhibitor cocktail. .. Equal amounts of protein were loaded, separated by SDS-PAGE, and transferred to PVDF membranes (Millipore, Darmstadt, Germany).

    Sonication:

    Article Title: Mechanisms of HIV Latency in Hematopoietic Progenitors: GFI1 as a Key Regulator
    Article Snippet: .. For western blot analysis, cells were lysed in Blue Loading Buffer (cat# 7722, Cell Signaling Technology), sonicated with a Misonix sonicator (Qsonica, LLC. ..

    SDS Page:

    Article Title: Largely Distinct Post-Translational Modifications Differentiate Skeletal Muscle Wasting Caused by Cancer, Dexamethasone and Aging.
    Article Snippet: TA muscles were homogenized in 200 μL NP40 cell lysis buffer (Invitrogen, #FNN0021), and the protein extracts were quantified by using the Bradford assay (Bio- Rad protein assay dye reagent concentrate, #5000006). .. Protein samples were prepared for SDS- PAGE by adding SDS- Blue loading buffer (Cell Signalling, #7722) and 0.1 M DTT (Cell Signalling, #1425 S) and by heating the samples at 95°C for 5 min. .. Samples were then run on 4%–20% gradient SDS- PAGE gels (Bio- Rad, #4561096) alongside a molecular weight ladder (Bio- Rad, #1610374) and transferred to PVDF membranes (Millipore, #IPVH00010), which were blocked with either 5% milk powder or 5% BSA for 1 h. Subsequently, the membranes were sequentially incubated overnight at 4°C with primary antibodies (at 1:1000) for PGC- 1α (Invitrogen, #PA5- 72948) and α- tubulin (Cell Signalling, #2125).

    Article Title: Perturbation of multiprotein complexes in skeletal muscle induces protective proteases in the CNS that degrade pathogenic proteins
    Article Snippet: .. To this purpose, the samples were heated to 95 °C for four minutes with SDS-Blue loading buffer (Cell Signaling Technology, #7722) and DTT (Cell Signaling Technology, #1425S), and analyzed by 4–20% SDS-PAGE gels (Mini-PROTEAN TGX pre-cast gels; Bio-Rad, #4561096). .. Western blots were probed sequentially with rabbit anti-GFP primary antibodies (1:1000 dilution, Cell Signaling Technology, #2956) and HRP-linked anti-rabbit secondary antibodies (1:2000 dilution, Cell Signaling Technology, #7074), then with rat anti-myosin primary antibodies (1:10,000 dilution, Babraham Institute Enterprise) and HRP-linked anti-rat secondary antibodies (1:5000 dilution for the insoluble fraction and 1:2000 dilution for the soluble fraction; Cell Signaling Technology #7077) in 5% skim milk powder in TBST (tris-buffered saline with Tween 20).



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