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inf2 c terminal  (Proteintech)


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    Proteintech inf2 c terminal
    Inf2 C Terminal, supplied by Proteintech, used in various techniques. Bioz Stars score: 94/100, based on 49 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/anti+inf2+antibody/INF2+Antibody/pmc12569161-15-0-3
    Average 94 stars, based on 49 article reviews
    inf2 c terminal - by Bioz Stars, 2026-09
    94/100 stars

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    Related Articles

    Incubation:

    Article Title: Targeting INF2 with DiosMetin 7-O-β-D-Glucuronide: a new stratagem for colorectal cancer therapy.
    Article Snippet: Following antigen retrieval using 100 mM sodium citrate (ZSGB-BIO, Beijing, China), the tissue sections were blocked with 3% hydrogen peroxide (Sinopharm, Beijing, China) and 5% bovine serum albumin (Boster, Wuhan, China) at room temperature. .. Subsequently, the sections were incubated with an anti-INF2 antibody (1:1000; cat no. 20466–1-AP, Proteintech, Wuhan, China), anti-KI67 (1:4000; cat no. 27309–1-AP, Proteintech), and antiPCNA (1:5000; cat no. 27309–1-AP, Proteintech) overnight at 4 °C. .. After this incubation period, the sections were treated with a secondary antibody for 2 h. The slides were then stained using a Cell and Tissue Staining HRP3,3′-diaminobenzidine kit (ZSGB-BIO, Beijing, China), followed by nuclear counterstaining with 0.2% hematoxylin (ZSGB-BIO, Beijing, China) for 1 min.

    Article Title: Targeting INF2 with DiosMetin 7-O-β-D-Glucuronide: a new stratagem for colorectal cancer therapy
    Article Snippet: Following antigen retrieval using 100 mM sodium citrate (ZSGB-BIO, Beijing, China), the tissue sections were blocked with 3% hydrogen peroxide (Sinopharm, Beijing, China) and 5% bovine serum albumin (Boster, Wuhan, China) at room temperature. .. Subsequently, the sections were incubated with an anti-INF2 antibody (1:1000; cat no. 20466–1-AP, Proteintech, Wuhan, China), anti-KI67 (1:4000; cat no. 27309–1-AP, Proteintech), and anti-PCNA (1:5000; cat no. 27309–1-AP, Proteintech) overnight at 4 °C. .. After this incubation period, the sections were treated with a secondary antibody for 2 h. The slides were then stained using a Cell and Tissue Staining HRP-3,3′-diaminobenzidine kit (ZSGB-BIO, Beijing, China), followed by nuclear counterstaining with 0.2% hematoxylin (ZSGB-BIO, Beijing, China) for 1 min.



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    ( A ) Western blot for VAP-B and myc-tag showing VAP-B expression in control and myc-VAP-B overexpressed U2OS cells. <t>INF2</t> is used as loading control. Molecular weight in kDa. ( B ) Quantification of CCCP-induced actin polymerization in control and myc-VAP-B-overexpressing U2OS cells. Data with 65 cells (control) and 53 cells (overexpressing myc-VAP-B) from 3 independent runs. Error ± SEM. ( C ) Averaged traces showing mitochondrial calcium fold change (MitoGCamp6f) following histamine stimulation (at time 0) in control (ER-RFP expressing), ER-RFP-mito (ER-Mito linker) and PM-RFP-Mito (PM-Mito-linker) transfected HeLa cells. Data from 2 independent experiments comprising of 4 individual traces for each condition. Error: ±SEM. ( D ) Dot plot of peak fold change in mitochondrial calcium following histamine stimulation from individual traces as in Fig S4C. Data for 32 cells (Control- ER-RFP); 32 cells (ER-RFP-Mito); 28 cells (PM-RFP-Mito) for 3 independent runs. Error: ±s.d. P = 0.0213 (*) for Control Vs ER-RFP-Mito, P = 0.0439 (*) for Control Vs PM-RFP-Mito and P = 0.0001 (****) for ER-RFP-Mito Vs PM-RFP-Mito, One-way ANOVA used. ( E ) Graph showing actin filaments intensity (GFP-Ftractin) from HeLa cells transiently expressing either ER-RFP-Mito (magenta) or PM-RFP-Mito or ER-RFP, treated with 20 µM CCCP. Data from 28 cells (ER-RFP); 27 cells (ER-RFP-Mito) and 23 cells (PM-RFP-Mito) from 4 independent experiments. Error: ±SEM.
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    Image Search Results


    ( A ) Western blot for VAP-B and myc-tag showing VAP-B expression in control and myc-VAP-B overexpressed U2OS cells. INF2 is used as loading control. Molecular weight in kDa. ( B ) Quantification of CCCP-induced actin polymerization in control and myc-VAP-B-overexpressing U2OS cells. Data with 65 cells (control) and 53 cells (overexpressing myc-VAP-B) from 3 independent runs. Error ± SEM. ( C ) Averaged traces showing mitochondrial calcium fold change (MitoGCamp6f) following histamine stimulation (at time 0) in control (ER-RFP expressing), ER-RFP-mito (ER-Mito linker) and PM-RFP-Mito (PM-Mito-linker) transfected HeLa cells. Data from 2 independent experiments comprising of 4 individual traces for each condition. Error: ±SEM. ( D ) Dot plot of peak fold change in mitochondrial calcium following histamine stimulation from individual traces as in Fig S4C. Data for 32 cells (Control- ER-RFP); 32 cells (ER-RFP-Mito); 28 cells (PM-RFP-Mito) for 3 independent runs. Error: ±s.d. P = 0.0213 (*) for Control Vs ER-RFP-Mito, P = 0.0439 (*) for Control Vs PM-RFP-Mito and P = 0.0001 (****) for ER-RFP-Mito Vs PM-RFP-Mito, One-way ANOVA used. ( E ) Graph showing actin filaments intensity (GFP-Ftractin) from HeLa cells transiently expressing either ER-RFP-Mito (magenta) or PM-RFP-Mito or ER-RFP, treated with 20 µM CCCP. Data from 28 cells (ER-RFP); 27 cells (ER-RFP-Mito) and 23 cells (PM-RFP-Mito) from 4 independent experiments. Error: ±SEM.

    Journal: EMBO Reports

    Article Title: Peri-mitochondrial actin filaments inhibit Parkin assembly by disrupting ER-mitochondria contacts

    doi: 10.1038/s44319-025-00561-y

    Figure Lengend Snippet: ( A ) Western blot for VAP-B and myc-tag showing VAP-B expression in control and myc-VAP-B overexpressed U2OS cells. INF2 is used as loading control. Molecular weight in kDa. ( B ) Quantification of CCCP-induced actin polymerization in control and myc-VAP-B-overexpressing U2OS cells. Data with 65 cells (control) and 53 cells (overexpressing myc-VAP-B) from 3 independent runs. Error ± SEM. ( C ) Averaged traces showing mitochondrial calcium fold change (MitoGCamp6f) following histamine stimulation (at time 0) in control (ER-RFP expressing), ER-RFP-mito (ER-Mito linker) and PM-RFP-Mito (PM-Mito-linker) transfected HeLa cells. Data from 2 independent experiments comprising of 4 individual traces for each condition. Error: ±SEM. ( D ) Dot plot of peak fold change in mitochondrial calcium following histamine stimulation from individual traces as in Fig S4C. Data for 32 cells (Control- ER-RFP); 32 cells (ER-RFP-Mito); 28 cells (PM-RFP-Mito) for 3 independent runs. Error: ±s.d. P = 0.0213 (*) for Control Vs ER-RFP-Mito, P = 0.0439 (*) for Control Vs PM-RFP-Mito and P = 0.0001 (****) for ER-RFP-Mito Vs PM-RFP-Mito, One-way ANOVA used. ( E ) Graph showing actin filaments intensity (GFP-Ftractin) from HeLa cells transiently expressing either ER-RFP-Mito (magenta) or PM-RFP-Mito or ER-RFP, treated with 20 µM CCCP. Data from 28 cells (ER-RFP); 27 cells (ER-RFP-Mito) and 23 cells (PM-RFP-Mito) from 4 independent experiments. Error: ±SEM.

    Article Snippet: Primary antibody: anti-myc-tag antibody (Abcam, ab32 used 1:1000) anti-INF2 antibody (CST #41081; used at 1:1000) anti-VAP-B antibody (Proteintech #14477-1-AP; used at 1:5000 at RT) anti-LC3B antibody (CST #12741S; used at 1:1000) anti-Parkin antibody (CST #2132S; used at 1:1000) anti-Parkin(phospho S65) antibody (Abcam #315376; used at 1:1000) anti-Pink1 antibody (CST #6946S; used at 1:1000) anti-β-actin antibody (CST #3700S; used at 1:10,000) anti-Mfn2 antibody (CST #9482S; used at 1:1000) anti-VDAC antibody (Invitrogen #MA5-41088; used at 1:1000) anti-Phospho ubiquitin (Ser65) (CST #62802S; used at 1:1000).

    Techniques: Western Blot, Expressing, Control, Molecular Weight, Transfection