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rip1  (Cell Signaling Technology Inc)


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    Structured Review

    Cell Signaling Technology Inc rip1
    Rip1, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 96/100, based on 662 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/rip1/RIP+XP+Rabbit+mAb/pm41817888-65-19-22
    Average 96 stars, based on 662 article reviews
    rip1 - by Bioz Stars, 2026-10
    96/100 stars

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    Related Articles

    Saline:

    Article Title: Study on the Function and Mechanism of Neutrophil Extracellular Traps in Regulating Necroptosis Following Traumatic Brain Injury
    Article Snippet: .. The membranes were blocked with 5% skimmed milk prepared in TBST (Tris‐buffered saline with 0.1% Tween‐20) at room temperature for 1 h. They were then incubated overnight at 4°C with the following primary antibodies: PAD4 (1:1000, 214810, Abcam), MPO (1:1000, ab208670, Abcam), Bcl‐2 (1:1000, A0208, Abclonal), Bax (1:1000, A19684, Abclonal), RIP1 (1:1000, #3493, Cell Signaling Technology), RIP3 (1:1000, #95702, Cell Signaling Technology), MLKL (1:1000, #37705, Cell Signaling Technology), P‐RIP1 (1:1000, #31122, Cell Signaling Technology), P‐RIP3 (1:1000, #91702, Cell Signaling Technology), P‐MLKL (1:1000, #37333, Cell Signaling Technology), and GAPDH (1:1000, AB‐P‐R001, GOODHERE Biotech). .. Following the primary antibody incubation, membranes were treated with an HRP‐conjugated secondary antibody (GB23303, Servicebio, 1:10,000) for 1 h at room temperature.

    Incubation:

    Article Title: Study on the Function and Mechanism of Neutrophil Extracellular Traps in Regulating Necroptosis Following Traumatic Brain Injury
    Article Snippet: .. The membranes were blocked with 5% skimmed milk prepared in TBST (Tris‐buffered saline with 0.1% Tween‐20) at room temperature for 1 h. They were then incubated overnight at 4°C with the following primary antibodies: PAD4 (1:1000, 214810, Abcam), MPO (1:1000, ab208670, Abcam), Bcl‐2 (1:1000, A0208, Abclonal), Bax (1:1000, A19684, Abclonal), RIP1 (1:1000, #3493, Cell Signaling Technology), RIP3 (1:1000, #95702, Cell Signaling Technology), MLKL (1:1000, #37705, Cell Signaling Technology), P‐RIP1 (1:1000, #31122, Cell Signaling Technology), P‐RIP3 (1:1000, #91702, Cell Signaling Technology), P‐MLKL (1:1000, #37333, Cell Signaling Technology), and GAPDH (1:1000, AB‐P‐R001, GOODHERE Biotech). .. Following the primary antibody incubation, membranes were treated with an HRP‐conjugated secondary antibody (GB23303, Servicebio, 1:10,000) for 1 h at room temperature.

    Article Title: Sequestosome-1/p62 Mediates TLR4-Induced Inflammatory Program in Dendritic Cells Under Normoxic and Hypoxic Conditions.
    Article Snippet: Equal amounts of total proteins for each sample were separated by 4-42 20% Mini-protean TGX gels (BioRad, Hercules, CA, USA) and transferred onto a 43 nitrocellulose membrane (BioRad, Hercules, CA, USA). .. Membranes were blocked and 44 incubated overnight, at 4°C, with the following primary antibodies: MyD88 (Cell Signaling 45 Technologies,Danvers, MA, 1:1000, Cat.n° 4283); RIP1 (Cell Signaling 46 Technologies,Danvers, MA, 1:1000, Cat.n° 3493); SQSTM1/p62 (Cell Signaling 47 Technologies,Danvers, MA, 1:1000, Cat.n° 5114); ph-p65 (NFκB) (Cell Signaling 48 Technologies,Danvers, MA, 1:1000, Cat.n° 3033); pro-IL-1β (Cell Signaling 49 Technologies,Danvers, MA, 1:1000, Cat.n° 12703); NLRP3 (Cell Signaling 50 Technologies,Danvers, MA, 1:1000, Cat.n° 15101); HIF-1α (BD Biosciences, San Jose, 51 CA, USA, 1:200 Cat.n◦ 610958); and b-actin (Sigma-Aldrich, St. Louis, MO, USA, 52 1:50000, Cat.n° A3854). .. After washing, membranes were incubated with horseradish 53 peroxidase (HRP)-conjugated secondary anti-mouse I anti-rabbit antibodies (Cell Signaling 54 Technologies, Danvers, MA, USA).

    Article Title: Sequestosome-1/p62 Mediates TLR4-Induced Inflammatory Program in Dendritic Cells Under Normoxic and Hypoxic Conditions
    Article Snippet: Equal amounts of total proteins for each sample were separated by 4–20% Mini-protean TGX gels (BioRad, Hercules, CA, USA) and transferred onto a nitrocellulose membrane (BioRad, Hercules, CA, USA). .. Membranes were blocked and incubated overnight, at 4 °C, with the following primary antibodies: MyD88 (Cell Signaling Technologies,Danvers, MA, 1:1000, Cat.n° 4283); RIP1 (Cell Signaling Technologies,Danvers, MA, 1:1000, Cat.n° 3493); SQSTM1/p62 (Cell Signaling Technologies,Danvers, MA, 1:1000, Cat.n° 5114); ph-p65 (NFκB) (Cell Signaling Technologies,Danvers, MA, 1:1000, Cat.n° 3033); pro-IL-1β (Cell Signaling Technologies,Danvers, MA, 1:1000, Cat.n° 12703); NLRP3 (Cell Signaling Technologies,Danvers, MA, 1:1000, Cat.n° 15101); HIF-1α (BD Biosciences, San Jose, CA, USA, 1:200 Cat.n◦ 610958); and b-actin (Sigma-Aldrich, St. Louis, MO, USA, 1:50000, Cat.n° A3854). .. After washing, membranes were incubated with horseradish peroxidase (HRP)-conjugated secondary anti-mouse I anti-rabbit antibodies (Cell Signaling Technologies, Danvers, MA, USA).

    Article Title: RIP1 Exacerbates BBB Disruption by Impairing Autophagy-Mediated A2 Astrocyte Polarization in Hypertension-Induced Cerebral Microhemorrhage in Mice.
    Article Snippet: have been identified as major risk factors contributing to the development of CMHs [2].. The accumulation of multiple CMHs can progressively impair neuronal function and lead to cognitive decline [3, 4].. An animal study further revealed that aging and hypertension interact synergistically to exacerbate the formation of CMHs [5].

    Western Blot:

    Article Title: Mebendazole induces ZBP-1 mediated PANoptosis of acute myeloid leukemia cells by targeting TUBA1A and exerts antileukemia effect
    Article Snippet: Necrostatin-1 (T 1847), Necrosulfonamide (T 6904) and Z-VAD(OMe)-FMK (T 6013) were obtained from TargetMol. .. Primary antibodies for western blot used were as follows: p-MLKL (ab187091, Abcam), MLKL (#14993, CST), p-RIP3 (#93654, CST), RIP3 (#13526, CST), p-RIP1 (#65746, CST), RIP1 (#3493, CST), cleaved caspase-1 (#4199, CST), cleaved caspase-3 (#9661, CST), NLRP3 (#15101, CST), TUBA1A (ab95966, Abcam), GAPDH (AF0006, Beyotime), and β-actin (ACTB) (AF0003, Beyotime). .. Antibodies for flow cytometry used were as follows: human CD45-FITC (304006, Biolegend, USA), CD11b-APC (301310, Biolegend) and CD11c-FITC (337214, Biolegend).



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    Cell Signaling Technology Inc p rip1
    Effects of Cl‐amidine and DNase I on necroptosis‐related protein expression after TBI. (A) Western blot analysis of <t>RIP1,</t> RIP3, MLKL, <t>P‐RIP1,</t> P‐RIP3, and P‐MLKL protein levels in the cortex of mice from Sham, TBI+Vehicle, TBI+Cl‐amidine, and TBI+DNase I groups. GAPDH was used as the loading control ( n = 4 per group). (B–G) Quantification of relative protein levels of RIP1, RIP3, MLKL, P‐RIP1, P‐RIP3, and P‐MLKL, normalized to GAPDH. Data are shown as mean ± SD ( n = 4 per group). Statistical significance is indicated as * p < 0.05, ** p < 0.01, *** p < 0.001, compared with the indicated groups; ns: not significant.
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    Effects of Cl‐amidine and DNase I on necroptosis‐related protein expression after TBI. (A) Western blot analysis of <t>RIP1,</t> RIP3, MLKL, <t>P‐RIP1,</t> P‐RIP3, and P‐MLKL protein levels in the cortex of mice from Sham, TBI+Vehicle, TBI+Cl‐amidine, and TBI+DNase I groups. GAPDH was used as the loading control ( n = 4 per group). (B–G) Quantification of relative protein levels of RIP1, RIP3, MLKL, P‐RIP1, P‐RIP3, and P‐MLKL, normalized to GAPDH. Data are shown as mean ± SD ( n = 4 per group). Statistical significance is indicated as * p < 0.05, ** p < 0.01, *** p < 0.001, compared with the indicated groups; ns: not significant.
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    Cell Signaling Technology Inc α rip1
    Effects of Cl‐amidine and DNase I on necroptosis‐related protein expression after TBI. (A) Western blot analysis of <t>RIP1,</t> RIP3, MLKL, <t>P‐RIP1,</t> P‐RIP3, and P‐MLKL protein levels in the cortex of mice from Sham, TBI+Vehicle, TBI+Cl‐amidine, and TBI+DNase I groups. GAPDH was used as the loading control ( n = 4 per group). (B–G) Quantification of relative protein levels of RIP1, RIP3, MLKL, P‐RIP1, P‐RIP3, and P‐MLKL, normalized to GAPDH. Data are shown as mean ± SD ( n = 4 per group). Statistical significance is indicated as * p < 0.05, ** p < 0.01, *** p < 0.001, compared with the indicated groups; ns: not significant.
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    Image Search Results


    Effects of Cl‐amidine and DNase I on necroptosis‐related protein expression after TBI. (A) Western blot analysis of RIP1, RIP3, MLKL, P‐RIP1, P‐RIP3, and P‐MLKL protein levels in the cortex of mice from Sham, TBI+Vehicle, TBI+Cl‐amidine, and TBI+DNase I groups. GAPDH was used as the loading control ( n = 4 per group). (B–G) Quantification of relative protein levels of RIP1, RIP3, MLKL, P‐RIP1, P‐RIP3, and P‐MLKL, normalized to GAPDH. Data are shown as mean ± SD ( n = 4 per group). Statistical significance is indicated as * p < 0.05, ** p < 0.01, *** p < 0.001, compared with the indicated groups; ns: not significant.

    Journal: Brain and Behavior

    Article Title: Study on the Function and Mechanism of Neutrophil Extracellular Traps in Regulating Necroptosis Following Traumatic Brain Injury

    doi: 10.1002/brb3.71275

    Figure Lengend Snippet: Effects of Cl‐amidine and DNase I on necroptosis‐related protein expression after TBI. (A) Western blot analysis of RIP1, RIP3, MLKL, P‐RIP1, P‐RIP3, and P‐MLKL protein levels in the cortex of mice from Sham, TBI+Vehicle, TBI+Cl‐amidine, and TBI+DNase I groups. GAPDH was used as the loading control ( n = 4 per group). (B–G) Quantification of relative protein levels of RIP1, RIP3, MLKL, P‐RIP1, P‐RIP3, and P‐MLKL, normalized to GAPDH. Data are shown as mean ± SD ( n = 4 per group). Statistical significance is indicated as * p < 0.05, ** p < 0.01, *** p < 0.001, compared with the indicated groups; ns: not significant.

    Article Snippet: The membranes were blocked with 5% skimmed milk prepared in TBST (Tris‐buffered saline with 0.1% Tween‐20) at room temperature for 1 h. They were then incubated overnight at 4°C with the following primary antibodies: PAD4 (1:1000, 214810, Abcam), MPO (1:1000, ab208670, Abcam), Bcl‐2 (1:1000, A0208, Abclonal), Bax (1:1000, A19684, Abclonal), RIP1 (1:1000, #3493, Cell Signaling Technology), RIP3 (1:1000, #95702, Cell Signaling Technology), MLKL (1:1000, #37705, Cell Signaling Technology), P‐RIP1 (1:1000, #31122, Cell Signaling Technology), P‐RIP3 (1:1000, #91702, Cell Signaling Technology), P‐MLKL (1:1000, #37333, Cell Signaling Technology), and GAPDH (1:1000, AB‐P‐R001, GOODHERE Biotech).

    Techniques: Expressing, Western Blot, Control