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cdk4  (Cell Signaling Technology Inc)


Bioz Verified Symbol Cell Signaling Technology Inc is a verified supplier
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    Structured Review

    Cell Signaling Technology Inc cdk4
    Cdk4, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 96/100, based on 972 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/cdk4/CDK4+Rabbit+mAb/pm42855461-330-20-21
    Average 96 stars, based on 972 article reviews
    cdk4 - by Bioz Stars, 2026-11
    96/100 stars

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    Related Articles

    Cell-Signaling:

    Article Title: GSK3i combinatorial treatments affect CDK4/6 and compensatory pathways in 3D preclinical models of pancreatic neuroendocrine tumors
    Article Snippet: Cyclin D1 , 55506, Cell Signaling Technology (Danvers, MA, USA) , 1:500. .. CDK4 , 12790, Cell Signaling Technology (Danvers, MA, USA) , 1:500. .. CDK6 , sc-7961, Santa Cruz Biotechnology (USA) , 1:100.

    Article Title: GSK3i combinatorial treatments affect CDK4/6 and compensatory pathways in 3D preclinical models of pancreatic neuroendocrine tumors
    Article Snippet: .. The antibodies (Abs) used were: CDK4 (#12790, 1:50) and CDK6 (#30483, 1:30), both from Cell Signaling Technology. .. The secondary Ab (anti-rabbit HRP) and enhanced chemiluminescence (ECL) reagents were used according to the kit's instructions (anti-rabbit detection module chemiluminescence; ProteinSimple , Bio-Techne).

    Histone Deacetylase Assay:

    Article Title: Exploratory Proteomic Profiling Reveals Potential Mediators of 5-FU Response under p53 Deficiency in Colon Cancer Cells
    Article Snippet: Membranes were blocked with 5% blotting-grade blocker (Bio-Rad Laboratories, Hercules, CA, USA) at RT for 1 h and incubated with primary antibodies at 4°C overnight. .. The primary antibodies used were: p53 (BP53-12, monoclonal, 1:1,000, P5813, Sigma-Aldrich), p21 (CP74, monoclunal, 1:2,000, P38936 , Sigma-Aldrich), phospho-p53 (p-p53, F-11, monoclonal, sc-377561), cyclin E (E-4, monoclonal, sc-377100), cyclin A (B-8, monoclonal, sc-271682), histone deacetylase 2 (HDAC2, C-8, monoclonal, sc-9959), and tissue factor (TF, F3, H-9, monoclonal, sc-374441) (1:1,000, Santa Cruz Biotechnology, TX, USA), cyclin B1 (V152, monoclonal, #4135), cyclin D1 (monoclonal, #2922), cyclin-dependent kinase (CDK)1 (POH1, monoclonal, #9116), CDK2 (78B2, monoclonal, #2546), CDK4 (D9G3E, monoclonal, #12790), CDK 6 (D4S8S, monoclonal, #13331)(1:1,000, Cell signaling, MA, USA), and aldehyde dehydrogenase family 1 member A4 (ALDH1A3, GT926, monoclonal, #MA5-27727) (1:1,000, Thermo Fisher Scientific) ( Lee et al ., 2022 ). .. The membranes were washed and incubated with goat anti-mouse IgG-HRP conjugate and goat anti-rabbit IgG-HRP conjugate (1:3,000, Bio-Rad Laboratories) secondary antibodies at RT for 3 h. Specific protein expression was visualized using an enhanced chemiluminescence solution and detected using ImageQuant LAS 500 (Cytiva Sweden AB, Uppsala, Sweden).

    Multiple Displacement Amplification:

    Article Title: WNT inhibition activates interferon stimulated gene expression by alleviating epigenetic repression of endogenous retroviruses.
    Article Snippet: For Western Blot analysis, protein quantification was determined by BCA assay and lysate was combined with reducing 6X Laemmli SDS sample buffer and ran on a NovexTM4-20% Tris Glycine gel (Invitrogen) in SDS-PAGE. .. Antibodies against c-Myc (5605), CDK4 (12790), CDK2 (18048), ISG20 (79004), OAS1(4498),CTNNB1(9562), phospho-Stat1 (9167), Stat1(9172), ISG15(2758), GBP2 (53311), phospho-TBK1/NAK (5483), TBK1/NAK (3504), phospho-IRF-3 (37829), MDA-5 (5321), RIG-I (3743), P-STING (19781),STING (13647), LSD1 (2184), DNMT1 (5032), EZH2 (5246), ERK (4695), phospho-ERK (4370 ) were purchased from Cell Signaling Technologies and used at 1:500 in 1% milk. .. Primary antibody against Axin2 (ab109307), GBP2 (ab179829), and IRF3 (ab68481) was purchased from Abcam and used at 1:500 in 1% milk.



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    Image Search Results


    Effects of single and combined inhibitors targeting PI3K, FGFR, and CDK4/6 on the viability of CU-OP spheroids For each cell line, (A) CU-OP-2, (B) CU-OP-3, (C) CU-OP-20, and (D) CU-OP-17, subimages (i)–(v) show viability following treatment with the indicated single/combined agents (i, BYL719; ii, JNJ-42756493; iii, PD-0332991; iv, BYL719 + JNJ-42756493; and v, BYL719 + PD-0332991). Subimages (vi) and (vii) display synergy analyses for the combinations BYL719 + JNJ-42756493 (vi) and BYL719 + PD-0332991 (vii). The data is presented as mean ± SD.

    Journal: Molecular Therapy Oncology

    Article Title: Dual targeting of PI3K and FGFR or CDK4/6 reveals synergistic responses in HPV-positive and HPV-negative oropharyngeal cancer spheroids

    doi: 10.1016/j.omton.2026.201283

    Figure Lengend Snippet: Effects of single and combined inhibitors targeting PI3K, FGFR, and CDK4/6 on the viability of CU-OP spheroids For each cell line, (A) CU-OP-2, (B) CU-OP-3, (C) CU-OP-20, and (D) CU-OP-17, subimages (i)–(v) show viability following treatment with the indicated single/combined agents (i, BYL719; ii, JNJ-42756493; iii, PD-0332991; iv, BYL719 + JNJ-42756493; and v, BYL719 + PD-0332991). Subimages (vi) and (vii) display synergy analyses for the combinations BYL719 + JNJ-42756493 (vi) and BYL719 + PD-0332991 (vii). The data is presented as mean ± SD.

    Article Snippet: The PI3K, FGFR, and CDK4/6 inhibitors BYL719 (alpelisib), JNJ-42756493 (erdafitinib), and PD-0332991 (palbociclib), respectively, were purchased from TargetMol (San Diego, California, US) at a concentration of 10 mM in DMSO.

    Techniques: Spheroids

    Effects of single chemotherapeutic agents and their combination with a PI3K inhibitor on the viability of CU-OP spheroids For each cell line, (A) CU-OP-2, (B) CU-OP-3, (C) CU-OP-20, and (D) CU-OP-17, subimages (i)–(v) show viability following treatment with the indicated single/combined agents (i, BYL719; ii, cisplatin; iii, docetaxel; iv, BYL719 + cisplatin; and v, BYL719 + docetaxel). Subimages (vi) and (vii) display synergy analyses for the combinations BYL719 + cisplatin (vi) and BYL719 + docetaxel (vii). The data is presented as mean ± SD.

    Journal: Molecular Therapy Oncology

    Article Title: Dual targeting of PI3K and FGFR or CDK4/6 reveals synergistic responses in HPV-positive and HPV-negative oropharyngeal cancer spheroids

    doi: 10.1016/j.omton.2026.201283

    Figure Lengend Snippet: Effects of single chemotherapeutic agents and their combination with a PI3K inhibitor on the viability of CU-OP spheroids For each cell line, (A) CU-OP-2, (B) CU-OP-3, (C) CU-OP-20, and (D) CU-OP-17, subimages (i)–(v) show viability following treatment with the indicated single/combined agents (i, BYL719; ii, cisplatin; iii, docetaxel; iv, BYL719 + cisplatin; and v, BYL719 + docetaxel). Subimages (vi) and (vii) display synergy analyses for the combinations BYL719 + cisplatin (vi) and BYL719 + docetaxel (vii). The data is presented as mean ± SD.

    Article Snippet: The PI3K, FGFR, and CDK4/6 inhibitors BYL719 (alpelisib), JNJ-42756493 (erdafitinib), and PD-0332991 (palbociclib), respectively, were purchased from TargetMol (San Diego, California, US) at a concentration of 10 mM in DMSO.

    Techniques: Spheroids

    Effects of single PI3K, FGFR, and CDK4/6 inhibitors and chemotherapeutic agents and their combination with a PI3K inhibitor on CU-OP-2 spheroid growth Representative images of spheroid growth at 72 h after treatment with: (A) PBS (control); (B) single treatment with BYL719 (BYL), JNJ-42756493 (JNJ), PD-0332991 (PD), cisplatin (CIS), and docetaxel (DOC); and (C) their combination with BYL719. The scale bars represent 400 μm.

    Journal: Molecular Therapy Oncology

    Article Title: Dual targeting of PI3K and FGFR or CDK4/6 reveals synergistic responses in HPV-positive and HPV-negative oropharyngeal cancer spheroids

    doi: 10.1016/j.omton.2026.201283

    Figure Lengend Snippet: Effects of single PI3K, FGFR, and CDK4/6 inhibitors and chemotherapeutic agents and their combination with a PI3K inhibitor on CU-OP-2 spheroid growth Representative images of spheroid growth at 72 h after treatment with: (A) PBS (control); (B) single treatment with BYL719 (BYL), JNJ-42756493 (JNJ), PD-0332991 (PD), cisplatin (CIS), and docetaxel (DOC); and (C) their combination with BYL719. The scale bars represent 400 μm.

    Article Snippet: The PI3K, FGFR, and CDK4/6 inhibitors BYL719 (alpelisib), JNJ-42756493 (erdafitinib), and PD-0332991 (palbociclib), respectively, were purchased from TargetMol (San Diego, California, US) at a concentration of 10 mM in DMSO.

    Techniques: Control

    Effects of single PI3K, FGFR, and CDK4/6 inhibitors and chemotherapeutic agents and their combination with a PI3K inhibitor on CU-OP-3 spheroid growth Representative images of spheroid growth at 72 h after treatment with: (A) PBS (control); (B) single treatment with BYL719 (BYL), JNJ-42756493 (JNJ), PD-0332991 (PD), cisplatin (CIS), and docetaxel (DOC); and (C) their combination with BYL719. The scale bars represent 400 μm.

    Journal: Molecular Therapy Oncology

    Article Title: Dual targeting of PI3K and FGFR or CDK4/6 reveals synergistic responses in HPV-positive and HPV-negative oropharyngeal cancer spheroids

    doi: 10.1016/j.omton.2026.201283

    Figure Lengend Snippet: Effects of single PI3K, FGFR, and CDK4/6 inhibitors and chemotherapeutic agents and their combination with a PI3K inhibitor on CU-OP-3 spheroid growth Representative images of spheroid growth at 72 h after treatment with: (A) PBS (control); (B) single treatment with BYL719 (BYL), JNJ-42756493 (JNJ), PD-0332991 (PD), cisplatin (CIS), and docetaxel (DOC); and (C) their combination with BYL719. The scale bars represent 400 μm.

    Article Snippet: The PI3K, FGFR, and CDK4/6 inhibitors BYL719 (alpelisib), JNJ-42756493 (erdafitinib), and PD-0332991 (palbociclib), respectively, were purchased from TargetMol (San Diego, California, US) at a concentration of 10 mM in DMSO.

    Techniques: Control

    Effects of single PI3K, FGFR, and CDK4/6 inhibitors and their combination with a PI3K inhibitor on CU-OP-2 spheroid migration Representative images of spheroid migration 72 h after treatment with PBS, single BYL719 (BYL), JNJ-42756493 (JNJ), and PD-0332991 (PD) or their combination with BYL719. The scale bars represent 1 mm.

    Journal: Molecular Therapy Oncology

    Article Title: Dual targeting of PI3K and FGFR or CDK4/6 reveals synergistic responses in HPV-positive and HPV-negative oropharyngeal cancer spheroids

    doi: 10.1016/j.omton.2026.201283

    Figure Lengend Snippet: Effects of single PI3K, FGFR, and CDK4/6 inhibitors and their combination with a PI3K inhibitor on CU-OP-2 spheroid migration Representative images of spheroid migration 72 h after treatment with PBS, single BYL719 (BYL), JNJ-42756493 (JNJ), and PD-0332991 (PD) or their combination with BYL719. The scale bars represent 1 mm.

    Article Snippet: The PI3K, FGFR, and CDK4/6 inhibitors BYL719 (alpelisib), JNJ-42756493 (erdafitinib), and PD-0332991 (palbociclib), respectively, were purchased from TargetMol (San Diego, California, US) at a concentration of 10 mM in DMSO.

    Techniques: Migration

    Effects of single PI3K, FGFR, and CDK4/6 inhibitors and their combination with a PI3K inhibitor on proliferation and apoptosis in CU-OP-2 and -3 IHC staining of Ki-67 and cleaved caspase-3 in (A) CU-OP-2 and (B) CU-OP-3 spheroids collected 72 h after treatment with PBS, single BYL719 (BYL), JNJ-42756493 (JNJ), and PD-0332991 (PD) or their combination with BYL719. The scale bars represent 100 μm.

    Journal: Molecular Therapy Oncology

    Article Title: Dual targeting of PI3K and FGFR or CDK4/6 reveals synergistic responses in HPV-positive and HPV-negative oropharyngeal cancer spheroids

    doi: 10.1016/j.omton.2026.201283

    Figure Lengend Snippet: Effects of single PI3K, FGFR, and CDK4/6 inhibitors and their combination with a PI3K inhibitor on proliferation and apoptosis in CU-OP-2 and -3 IHC staining of Ki-67 and cleaved caspase-3 in (A) CU-OP-2 and (B) CU-OP-3 spheroids collected 72 h after treatment with PBS, single BYL719 (BYL), JNJ-42756493 (JNJ), and PD-0332991 (PD) or their combination with BYL719. The scale bars represent 100 μm.

    Article Snippet: The PI3K, FGFR, and CDK4/6 inhibitors BYL719 (alpelisib), JNJ-42756493 (erdafitinib), and PD-0332991 (palbociclib), respectively, were purchased from TargetMol (San Diego, California, US) at a concentration of 10 mM in DMSO.

    Techniques: Immunohistochemistry, Spheroids

    Journal: Molecular Therapy Oncology

    Article Title: Dual targeting of PI3K and FGFR or CDK4/6 reveals synergistic responses in HPV-positive and HPV-negative oropharyngeal cancer spheroids

    doi: 10.1016/j.omton.2026.201283

    Figure Lengend Snippet:

    Article Snippet: The PI3K, FGFR, and CDK4/6 inhibitors BYL719 (alpelisib), JNJ-42756493 (erdafitinib), and PD-0332991 (palbociclib), respectively, were purchased from TargetMol (San Diego, California, US) at a concentration of 10 mM in DMSO.

    Techniques: