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bcl2 rabbit ab  (Bioss)


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    Bioss bcl2 rabbit ab
    The mRNA expression of ITGAV, FAK, PLC, PKC, p65, ERK, JNK, p38, PI3K, Akt, Bax, <t>Bcl2</t> , and Caspase 3 in E.tenella host cells.
    Bcl2 Rabbit Ab, supplied by Bioss, used in various techniques. Bioz Stars score: 95/100, based on 155 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/bcl2 rabbit ab/product/Bioss
    Average 95 stars, based on 155 article reviews
    bcl2 rabbit ab - by Bioz Stars, 2026-06
    95/100 stars

    Images

    1) Product Images from "Pathogenic mechanism of Eimeria tenella Et MIC2 promotes Eimeria tenella invasion and inhibits host cell apoptosis through binding to the ITGAV receptor"

    Article Title: Pathogenic mechanism of Eimeria tenella Et MIC2 promotes Eimeria tenella invasion and inhibits host cell apoptosis through binding to the ITGAV receptor

    Journal: Poultry Science

    doi: 10.1016/j.psj.2026.106922

    The mRNA expression of ITGAV, FAK, PLC, PKC, p65, ERK, JNK, p38, PI3K, Akt, Bax, Bcl2 , and Caspase 3 in E.tenella host cells.
    Figure Legend Snippet: The mRNA expression of ITGAV, FAK, PLC, PKC, p65, ERK, JNK, p38, PI3K, Akt, Bax, Bcl2 , and Caspase 3 in E.tenella host cells.

    Techniques Used: Expressing

    The protein activity changes of ITGAV, FAK, PLC, PKC, p65, ERK, JNK, p38, PI3K, Akt, Bax, Bcl2, and Caspase 3 in E.tenella host cells.
    Figure Legend Snippet: The protein activity changes of ITGAV, FAK, PLC, PKC, p65, ERK, JNK, p38, PI3K, Akt, Bax, Bcl2, and Caspase 3 in E.tenella host cells.

    Techniques Used: Activity Assay



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    NRP2 mediates the FAK signaling pathway to regulate the malignant progression of GBM cells. (A): NRP2 expression levels in patients from the GSE4290 and GSE68848 data sets. (B): The knockdown effect of sh-NRP2 in U251 and T98G cells was detected by qRT-PCR. (C): WB was used to detect the expressions of pY297-FAK and FAK. (D): The CCK-8 method was used to detect the cell viability of GBM cells in different treatment groups (sh-NC, sh-NRP2, sh-NRP2 + adhesamine). Adhesamine is a FAK activator. (E): The colony formation experiment was used to detect the number of colony formations of GBM cells in different treatment groups; (F): The scratch healing experiment was used to detect the migration ability of GBM cells in different treatment groups; (G): The Transwell experiment was used to detect the invasion ability of GBM cells in different treatment groups; (H): The Annexin V/PI double staining method was used to detect the apoptosis level of cells in different treatment groups. (I): Western blot was used to detect the protein expression of pro-apoptotic indicators clever-caspase3, clever-PARP, BAX and pro-apoptotic indicator <t>BCL2</t> in different treatment groups. * indicates P < 0.05, **** indicates P < 0.0001.
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    Image Search Results


    The mRNA expression of ITGAV, FAK, PLC, PKC, p65, ERK, JNK, p38, PI3K, Akt, Bax, Bcl2 , and Caspase 3 in E.tenella host cells.

    Journal: Poultry Science

    Article Title: Pathogenic mechanism of Eimeria tenella Et MIC2 promotes Eimeria tenella invasion and inhibits host cell apoptosis through binding to the ITGAV receptor

    doi: 10.1016/j.psj.2026.106922

    Figure Lengend Snippet: The mRNA expression of ITGAV, FAK, PLC, PKC, p65, ERK, JNK, p38, PI3K, Akt, Bax, Bcl2 , and Caspase 3 in E.tenella host cells.

    Article Snippet: Bcl2 Rabbit Ab , Bioss , bs-0032R , 1: 1500.

    Techniques: Expressing

    The protein activity changes of ITGAV, FAK, PLC, PKC, p65, ERK, JNK, p38, PI3K, Akt, Bax, Bcl2, and Caspase 3 in E.tenella host cells.

    Journal: Poultry Science

    Article Title: Pathogenic mechanism of Eimeria tenella Et MIC2 promotes Eimeria tenella invasion and inhibits host cell apoptosis through binding to the ITGAV receptor

    doi: 10.1016/j.psj.2026.106922

    Figure Lengend Snippet: The protein activity changes of ITGAV, FAK, PLC, PKC, p65, ERK, JNK, p38, PI3K, Akt, Bax, Bcl2, and Caspase 3 in E.tenella host cells.

    Article Snippet: Bcl2 Rabbit Ab , Bioss , bs-0032R , 1: 1500.

    Techniques: Activity Assay

    Relative gene expression levels of various mRNAs in the FaDu cells transfected with angiopoietin-like 4 small interfering RNA were determined by reverse transcription-quantitative PCR. The angiopoietin-like 4 level decreased by 38%, and MKI67 expression increased significantly. The expression of BAX decreased, and that of BCL2 increased. CASP3 expression also increased in the angiopoietin-like 4 knockdown cells.

    Journal: Oncology Reports

    Article Title: Inhibitory role of angiopoietin-like 4 for cancer progression in oropharyngeal squamous cell carcinoma

    doi: 10.3892/or.2026.9122

    Figure Lengend Snippet: Relative gene expression levels of various mRNAs in the FaDu cells transfected with angiopoietin-like 4 small interfering RNA were determined by reverse transcription-quantitative PCR. The angiopoietin-like 4 level decreased by 38%, and MKI67 expression increased significantly. The expression of BAX decreased, and that of BCL2 increased. CASP3 expression also increased in the angiopoietin-like 4 knockdown cells.

    Article Snippet: The primers and probes were procured from Applied Biosystems (TaqMan ® Gene Expression Assays) and had the following IDs: ANGPTL4 (Hs01101127_m1), ACTB (Hs01060665_g1), MKI67 (Hs04260396_g1), BAX (Hs0018269_m1), BCL2 (Hs00608023_m1), and CASP3 (Hs00234387_m1).

    Techniques: Gene Expression, Transfection, Small Interfering RNA, Reverse Transcription, Real-time Polymerase Chain Reaction, Expressing, Knockdown

    SC suppresses apoptosis in vivo . Ovarian Granulosa Cells intervene in multiple pathophysiological indicators. Examination of apoptosis in laying hens by TUNEL assay. (A-B) Results revealed that treatment with different doses of SC resulted in decreased apoptosis. (C-J) The protein and mRNA expression of Bax, Cyt c, Cleaved Caspase-3, and Bcl-2.

    Journal: Poultry Science

    Article Title: Dietary semen cuscuta improves laying performance by stabilizing mitochondria-associated membranes (MAMs) and inhibiting granulosa cell apoptosis in laying hens

    doi: 10.1016/j.psj.2026.106749

    Figure Lengend Snippet: SC suppresses apoptosis in vivo . Ovarian Granulosa Cells intervene in multiple pathophysiological indicators. Examination of apoptosis in laying hens by TUNEL assay. (A-B) Results revealed that treatment with different doses of SC resulted in decreased apoptosis. (C-J) The protein and mRNA expression of Bax, Cyt c, Cleaved Caspase-3, and Bcl-2.

    Article Snippet: The membranes underwent blocking with 5% skimmed milk diluted in PBS, and afterwards incubated employing primary antibodies against β-actin (GB15001, Servicebio, Wuhan, China), IP3R (GB11742, Servicebio, Wuhan, China), GRP75 (GB11852, Servicebio, Wuhan, China), VDAC1 ( GB111939 , Servicebio, Wuhan, China), Bcl-2 (26593-1-AP, Proteintech, Wuhan, China), Bax (50599-2-Ig, Proteintech, Wuhan, China), Cyt c (WL02410, Wanleibio, Shenyang, China), Cleaved Caspase-3 (WL01992, Wanleibio, Shenyang, China), GPR41 ( OM184469 , Omnimabs, California, United States), GPR43 ( OM255320 , Omnimabs, California, United States), Occludin (WL01996, Wanleibio, Shenyang, China) and ZO-1(21773-1-AP, Proteintech, Wuhan, China) overnight at 4°C with gentle shaking.

    Techniques: In Vivo, TUNEL Assay, Expressing

    NRP2 mediates the FAK signaling pathway to regulate the malignant progression of GBM cells. (A): NRP2 expression levels in patients from the GSE4290 and GSE68848 data sets. (B): The knockdown effect of sh-NRP2 in U251 and T98G cells was detected by qRT-PCR. (C): WB was used to detect the expressions of pY297-FAK and FAK. (D): The CCK-8 method was used to detect the cell viability of GBM cells in different treatment groups (sh-NC, sh-NRP2, sh-NRP2 + adhesamine). Adhesamine is a FAK activator. (E): The colony formation experiment was used to detect the number of colony formations of GBM cells in different treatment groups; (F): The scratch healing experiment was used to detect the migration ability of GBM cells in different treatment groups; (G): The Transwell experiment was used to detect the invasion ability of GBM cells in different treatment groups; (H): The Annexin V/PI double staining method was used to detect the apoptosis level of cells in different treatment groups. (I): Western blot was used to detect the protein expression of pro-apoptotic indicators clever-caspase3, clever-PARP, BAX and pro-apoptotic indicator BCL2 in different treatment groups. * indicates P < 0.05, **** indicates P < 0.0001.

    Journal: Translational Oncology

    Article Title: The brain imaging feature-related gene NRP2 drives the malignant progression of glioblastoma through the FAK pathway: a Mendelian randomization study

    doi: 10.1016/j.tranon.2026.102732

    Figure Lengend Snippet: NRP2 mediates the FAK signaling pathway to regulate the malignant progression of GBM cells. (A): NRP2 expression levels in patients from the GSE4290 and GSE68848 data sets. (B): The knockdown effect of sh-NRP2 in U251 and T98G cells was detected by qRT-PCR. (C): WB was used to detect the expressions of pY297-FAK and FAK. (D): The CCK-8 method was used to detect the cell viability of GBM cells in different treatment groups (sh-NC, sh-NRP2, sh-NRP2 + adhesamine). Adhesamine is a FAK activator. (E): The colony formation experiment was used to detect the number of colony formations of GBM cells in different treatment groups; (F): The scratch healing experiment was used to detect the migration ability of GBM cells in different treatment groups; (G): The Transwell experiment was used to detect the invasion ability of GBM cells in different treatment groups; (H): The Annexin V/PI double staining method was used to detect the apoptosis level of cells in different treatment groups. (I): Western blot was used to detect the protein expression of pro-apoptotic indicators clever-caspase3, clever-PARP, BAX and pro-apoptotic indicator BCL2 in different treatment groups. * indicates P < 0.05, **** indicates P < 0.0001.

    Article Snippet: BCL2 , Proteintech , China , 12,789-1-AP , Rabbit , 1:9000.

    Techniques: Expressing, Knockdown, Quantitative RT-PCR, CCK-8 Assay, Migration, Double Staining, Western Blot

    NRP2 promotes the malignant progression of GBM by activating FAK. U251 and T98G cell groups: sh-NC, sh-NRP2, sh-NRP2 + oe-FAK. (A): qRT-PCR was used to detect the mRNA level of FAK; (B): WB was used to detect the protein expression of pY397-FAK and FAK; (C): CCK-8 was used to detect cell viability; (D): Scratch test was used to detect the migration ability of cells; (E): Transwell test was used to detect the invasion ability of cells; (F): WB was used to detect the protein expression of apoptotic proteins clever-caspase3, clever-PARP, BAX and anti-apoptotic protein BCL2. * indicates P < 0.05.

    Journal: Translational Oncology

    Article Title: The brain imaging feature-related gene NRP2 drives the malignant progression of glioblastoma through the FAK pathway: a Mendelian randomization study

    doi: 10.1016/j.tranon.2026.102732

    Figure Lengend Snippet: NRP2 promotes the malignant progression of GBM by activating FAK. U251 and T98G cell groups: sh-NC, sh-NRP2, sh-NRP2 + oe-FAK. (A): qRT-PCR was used to detect the mRNA level of FAK; (B): WB was used to detect the protein expression of pY397-FAK and FAK; (C): CCK-8 was used to detect cell viability; (D): Scratch test was used to detect the migration ability of cells; (E): Transwell test was used to detect the invasion ability of cells; (F): WB was used to detect the protein expression of apoptotic proteins clever-caspase3, clever-PARP, BAX and anti-apoptotic protein BCL2. * indicates P < 0.05.

    Article Snippet: BCL2 , Proteintech , China , 12,789-1-AP , Rabbit , 1:9000.

    Techniques: Quantitative RT-PCR, Expressing, CCK-8 Assay, Migration

    The nude mouse experiment demonstrates that NRP2 mediates the Focal-adhesion pathway to regulate the formation of GBM tumors. (A): Nude mice were subcutaneously injected with sh-NRP2 and sh-NC stably transfected T98G cells. Comparison of tumor size in sh-NRP2 nude mice treated with FAK activator adhesamine. (B): Tumor weights of different treatment groups of nude mice. (C): Tumor volumes of different treatment groups of nude mice. (D): IHC detection of the expression of Ki67, BCL2 and BAX in tumor tissues; (E): WB detection of the expression of pY297-FAK and FAK in tumor tissues.

    Journal: Translational Oncology

    Article Title: The brain imaging feature-related gene NRP2 drives the malignant progression of glioblastoma through the FAK pathway: a Mendelian randomization study

    doi: 10.1016/j.tranon.2026.102732

    Figure Lengend Snippet: The nude mouse experiment demonstrates that NRP2 mediates the Focal-adhesion pathway to regulate the formation of GBM tumors. (A): Nude mice were subcutaneously injected with sh-NRP2 and sh-NC stably transfected T98G cells. Comparison of tumor size in sh-NRP2 nude mice treated with FAK activator adhesamine. (B): Tumor weights of different treatment groups of nude mice. (C): Tumor volumes of different treatment groups of nude mice. (D): IHC detection of the expression of Ki67, BCL2 and BAX in tumor tissues; (E): WB detection of the expression of pY297-FAK and FAK in tumor tissues.

    Article Snippet: BCL2 , Proteintech , China , 12,789-1-AP , Rabbit , 1:9000.

    Techniques: Injection, Stable Transfection, Transfection, Comparison, Expressing