rabbit anti tnfα  (Proteintech)

Journal: JPRAS Open

Article Title: Effects of extremely low-frequency sinusoidal electromagnetic field therapy on survival and vascularization in a rat random-pattern skin flap model

doi: 10.1016/j.jpra.2026.05.040

Figure Lengend Snippet: Immunohistochemical localization of TNF-α in skin flaps of experimental groups. Representative sections showing TNF-α expression in the control (A), low-dose EMF (B), and high-dose EMF (C) groups. Black arrows indicate TNF-α immunoreactivity in keratinocytes, fibroblasts, and inflammatory cells. Stronger cytoplasmic immunoreactivity was observed in the control and high-dose EMF groups compared with the low-dose EMF group. Scale bar: 50 μm; magnification × 40.

Article Snippet: Sections were incubated overnight at 4 °C with rabbit polyclonal anti-TNF-α antibody (Affinity Biosciences, catalog no AF7014; dilution 1:100).

Techniques: Immunohistochemical staining, Expressing, Control

Journal: JOR Spine

Article Title: Intradiscal Cutibacterium acnes Sustains Modic Type 1‐Like Lesions Over Time in a Rat Lumbar Endplate Injury Model

doi: 10.1002/jsp2.70182

Figure Lengend Snippet: Schematic overview of the study design and experimental timeline. The surgery involved (1) an anterior abdominal approach, followed by (2) EP injury, and (3) intradiscal injection of either TNF‐α or C. acnes , such that all outcome measures reflect the combined effects of both the EP injury and the respective injectate. Pain‐like behavior was evaluated biweekly using the von Frey assay to assess hind paw mechanical allodynia. Post‐euthanasia assessments included ex vivo spinal MRI using T1w and T2w sequences as well as histological analysis of spine and spinal cord. The timeline depicts the three experimental cohorts and the corresponding analyses time points. C. acnes, Cutibacterium acnes ; EP, endplate; MRI, magnetic resonance imaging; T1w, T1‐weighted.

Article Snippet: Sections were then incubated for 1 h at room temperature with one of the following primary antibodies: (i) rabbit polyclonal antibody against rat TNF‐α (1:500 dilution, #NBP1‐19532, Novus Biologics, MN, USA), (ii) rabbit recombinant multiclonal antibody against rat NE (1:500 dilution, #ab314916, Abcam, Waltham, MA, USA), or (iii) rabbit recombinant polyclonal antibody against rat CD19 (1:150 dilution, #27949‐1‐AP, ThermoFisher, Waltham, MA, USA).

Techniques: Injection, Ex Vivo, Magnetic Resonance Imaging

Journal: JOR Spine

Article Title: Intradiscal Cutibacterium acnes Sustains Modic Type 1‐Like Lesions Over Time in a Rat Lumbar Endplate Injury Model

doi: 10.1002/jsp2.70182

Figure Lengend Snippet: Degree of disc degeneration was increased in both EP injury + C. acnes and EP injury + TNF‐α discs compared to Sham without difference between injury groups. (A) Representative T1w and T2w MRI of discs per group and timepoint. (B) Both EP injury + C. acnes and EP injury + TNF‐α discs were significantly more degenerated than Sham at 8‐ and 14 weeks post‐injury, with no differences between the two injury groups at any time point. Disc degeneration increased over time in the EP injury + C. acnes group. Bars represent median with IQR. Significance bars represent results of Tukey's post hoc analysis of pairwise comparisons after detecting main effects with a two‐way ANOVA. Timepoints week 1, 8, and 14: Sham: N = 8 discs, EP injury + TNF‐α: N = 12–14 discs, EP injury + C. acnes : N = 10–12 discs. (C) Representative histological images of whole discs per group and timepoint, SafO/F/H staining. (D) Quantification of histological disc degeneration score. Discs from both EP injury groups were significantly more degenerated than Sham at all‐time points (weeks 1, 8, and 14). No significant differences were observed between EP injury + TNF‐α versus EP injury + C. acnes groups at any time point. Bars represent median with IQR. Significance bars represent results of Tukey's post hoc analysis of pairwise comparisons after detecting main effects with a two‐way ANOVA. Timepoints week 1, 8, and 14: Sham: N = 6–7 discs, EP injury + TNF‐α: N = 10–12 discs, EP injury + C. acnes : N = 9–12 discs. ANOVA, analysis of variance; C. acnes , Cutibacterium acnes ; EP, endplate; IQR, interquartile range; SafO/F/H, Safranin‐O/fastgreen/hematoxylin; T1w, T1‐weighted.

Article Snippet: Sections were then incubated for 1 h at room temperature with one of the following primary antibodies: (i) rabbit polyclonal antibody against rat TNF‐α (1:500 dilution, #NBP1‐19532, Novus Biologics, MN, USA), (ii) rabbit recombinant multiclonal antibody against rat NE (1:500 dilution, #ab314916, Abcam, Waltham, MA, USA), or (iii) rabbit recombinant polyclonal antibody against rat CD19 (1:150 dilution, #27949‐1‐AP, ThermoFisher, Waltham, MA, USA).

Techniques: Staining

Journal: JOR Spine

Article Title: Intradiscal Cutibacterium acnes Sustains Modic Type 1‐Like Lesions Over Time in a Rat Lumbar Endplate Injury Model

doi: 10.1002/jsp2.70182

Figure Lengend Snippet: Intradiscal injectate following EP injury determined MC subtype prevalence over time. (A) Representative T1w and T2w MR images showing MC1‐ (top), MC2‐ (middle), and MC3‐like (bottom) lesions in EP injury + TNF‐α (left) or EP injury + C. acnes (right) discs. All 3 different MC subtypes developed in both EP injury + TNF‐α and EP injury + C. acnes groups. MC1‐like lesions: T1w: Hypo‐, or isointense; T2w: Hyperintense. MC2‐like lesions: T1w and T2w: Hyperintense. MC3‐like lesions: T1w and T2w: Hypointense. Red arrows surround bone marrow lesions. Images are from time points 8‐ and 14‐weeks post‐injury. (B) Representative histological images of features associated with MC1 (cellular infiltrates), MC2 (fatty replacement of normal bone marrow), and MC3 (sclerotic bone) in EP injury + TNF‐α and EP injury + C. acnes groups. In both injury groups, all 3 histological features of MC subtypes were found. #: Normal bone marrow region. 1: Cellular infiltrates; 2: Fatty replacement of normal bone marrow; 3: Increased bone structure. SafO/F/H staining. (C) Quantification of MC1‐like lesion prevalence (% of total number of EPs: L6 cranial, L5 caudal, L5 cranial, L4 caudal) revealed that EP injury + intradiscal C. acnes injection resulted in a significantly higher prevalence of MC1‐like lesions across all 3 time points compared to both EP injury + TNF‐α and Sham. The EP injury + TNF‐α group tended to have significantly more MC1‐like lesions compared to Sham. (D) MC2‐like lesions increased in the EP injury + TNF‐α group over time and were significantly higher than EP injury + C. acnes and Sham at 14‐weeks post‐injury. (E) MC3‐like lesions increased over time in the EP injury + C. acnes group. Bars represent median with IQR. Significance bars represent pairwise comparisons from Tukey's post hoc analysis following two‐way ANOVA. Timepoints week 1, 8, and 14: Sham: N = 4 rats, EP injury + TNF‐α: N = 5–7 rats, EP injury + C. acnes : N = 5–6 rats. * p < 0.05, ** p < 0.01, *** p < 0.001. ANOVA, analysis of variance; C. acnes , Cutibacterium acnes ; EP, endplate; IQR, interquartile range; MC, modic change; SafO/F/H, Safranin‐O/fastgreen/hematoxylin; T1w, T1‐weighted.

Article Snippet: Sections were then incubated for 1 h at room temperature with one of the following primary antibodies: (i) rabbit polyclonal antibody against rat TNF‐α (1:500 dilution, #NBP1‐19532, Novus Biologics, MN, USA), (ii) rabbit recombinant multiclonal antibody against rat NE (1:500 dilution, #ab314916, Abcam, Waltham, MA, USA), or (iii) rabbit recombinant polyclonal antibody against rat CD19 (1:150 dilution, #27949‐1‐AP, ThermoFisher, Waltham, MA, USA).

Techniques: Staining, Injection

Journal: JOR Spine

Article Title: Intradiscal Cutibacterium acnes Sustains Modic Type 1‐Like Lesions Over Time in a Rat Lumbar Endplate Injury Model

doi: 10.1002/jsp2.70182

Figure Lengend Snippet: Intradiscal C. acnes versus TNF‐α injection following EP injury determined adjacent bone marrow lesion immune cell response. (A) Representative images of intradiscal inflammatory burden measured as TNF‐α‐ir in Sham (left), TNF‐α (middle) and C. acnes (right)‐injected discs. Upper right images represent magnified areas of the overview section. Arrows indicate TNF‐α positive cells. (B) Both EP injury + TNF‐α and EP injury + C. acnes groups led to increased discal TNF‐α‐ir at all 3 time points without a difference between injury groups. Bars represent median with IQR. Significance bars represent pairwise comparisons from Tukey's post hoc analysis. Timepoints week 1, 8, and 14: Sham: N = 6–8 discs, EP injury + TNF‐α: N = 8–10 discs, EP injury + C. acnes : 10–12 discs. (C) Representative images of NE‐ir (top) and CD19‐ir (bottom). Red arrows indicate NE‐positive cells, orange arrows indicate CD19‐positive cells. (D) Bone marrow lesions adjacent to EP injury + C. acnes ‐ versus EP injury + TNF‐α‐ discs showed increased NE‐ir and CD19‐ir. Bars represent median with IQR. Significance bars represent results from Mann–Whitney U ‐test. All time points combined: EP injury + TNF‐α: N = 12 bone marrow lesions, EP injury + C. acnes : N = 16 bone marrow lesions. * p < 0.05, ** p < 0.01, *** p < 0.001. C. acnes , Cutibacterium acnes ; IQR, interquartile range; NE, neutrophil elastase.

Article Snippet: Sections were then incubated for 1 h at room temperature with one of the following primary antibodies: (i) rabbit polyclonal antibody against rat TNF‐α (1:500 dilution, #NBP1‐19532, Novus Biologics, MN, USA), (ii) rabbit recombinant multiclonal antibody against rat NE (1:500 dilution, #ab314916, Abcam, Waltham, MA, USA), or (iii) rabbit recombinant polyclonal antibody against rat CD19 (1:150 dilution, #27949‐1‐AP, ThermoFisher, Waltham, MA, USA).

Techniques: Injection, MANN-WHITNEY

Journal: JOR Spine

Article Title: Intradiscal Cutibacterium acnes Sustains Modic Type 1‐Like Lesions Over Time in a Rat Lumbar Endplate Injury Model

doi: 10.1002/jsp2.70182

Figure Lengend Snippet: Pain‐like behavior and spinal cord sensitization was increased in both EP injury groups and SubP was significantly higher in the EP injury + C. acnes group. (A) Normalized hind paw withdrawal thresholds (% baseline) measured using von Frey testing over 13 weeks following EP injury with TNF‐α (blue squares) or C. acnes (pink triangles) injection, or sham surgery (black circles). Both EP injury groups demonstrated a significant and sustained reduction in mechanical thresholds compared to Sham, indicating long‐lasting mechanical hypersensitivity. No significant difference was observed between the EP injury + TNF‐α and EP injury + C. acnes groups. Data are shown as mean ± SD. Mixed‐effect analysis with Tukey post hoc analysis. * p < 0.05 for EP injury + TNF‐α versus Sham; # p < 0.05 for EP injury + C. acnes versus Sham. Time points 1–13 weeks: Sham: N = 4–12 rats, EP injury + TNF‐α: 6–19 rats, EP injury + C. acnes : 6–18 rats. (B) Random forest model showed that MC1‐like presence and area contributed strongest to pain‐like behavior. Graph shows %IncMSE. p values are FDR‐adjusted permutation‐based values. Black bars: p < 0.05. (C) Representative images of SubP expression spinal cord dorsal horn. (D) Quantification of SubP‐ir in the spinal cord dorsal horn area at 1‐, 8‐, and 14‐weeks. SubP levels were significantly increased in EP injury + TNF‐α and EP injury + C. acnes groups compared to Sham at 8‐ and 14‐weeks. SubP was significantly higher in EP injury + C. acnes versus EP injury + TNF‐α groups at 14‐WKs post‐injury. Significance bars represent results from Tukey's post hoc analysis. Time points weeks 1, 8, 14: Sham: N = 4, EP injury + TNF‐α: N = 6–7, EP injury + C. acnes : N = 5–6 spinal cords. (E) Representative images of GFAP expression in spinal cord dorsal horn. (F) Quantification of GFAP‐ir in the spinal cord dorsal horn area at 1‐, 8‐, and 14‐weeks. GFAP expression increased significantly in both EP injury + TNF‐α and EP injury + C . acnes groups compared to Sham, with a progressive increase from week 1 to week 14. There was no difference between injury groups. Significance bars represent results from Tukey post hoc analysis. Time points weeks 1, 8, 14: Sham: N = 4, EP injury + TNF‐α: N = 6–7, EP injury + C. acnes : N = 5–6. Bars represent mean ± SD. * p < 0.05, ** p < 0.01, *** p < 0.001. C. acnes , Cutibacterium acnes ; EP, endplate; GFAP, glial fibrillary acidic protein; IncMSE, percent increase in mean standard error; IQR, interquartile range; MC, modic change; SubP, substance P.

Article Snippet: Sections were then incubated for 1 h at room temperature with one of the following primary antibodies: (i) rabbit polyclonal antibody against rat TNF‐α (1:500 dilution, #NBP1‐19532, Novus Biologics, MN, USA), (ii) rabbit recombinant multiclonal antibody against rat NE (1:500 dilution, #ab314916, Abcam, Waltham, MA, USA), or (iii) rabbit recombinant polyclonal antibody against rat CD19 (1:150 dilution, #27949‐1‐AP, ThermoFisher, Waltham, MA, USA).

Techniques: Injection, Expressing

Journal: Materials Today Bio

Article Title: Intravesical folate-conjugated hydroxyethyl starch micelles for pH-triggered co-delivery of epirubicin and TLR7 agonist toward synergistic chemoimmunotherapy of bladder cancer

doi: 10.1016/j.mtbio.2026.102835

Figure Lengend Snippet: (A) CLSM images of RAW 264.7 cells after treatment with LPS + IFN-γ and IL-4. Cell nuclei were stained with DAPI (blue), CD86 fluorescence displayed in green and CD206 fluorescence displayed in red. Scale bar: 10 μm; (B) Confocal imaging of CD86 and CD206 expression in M2-TAMs treated with free IMQ, FA-HES-EPI, and FA-HES-EPI/IMQ micelles. Cell nuclei were stained with DAPI (blue), CD86 fluorescence displayed in green and CD206 fluorescence displayed in red. Scale bar: 10 μm; (C) FCM analysis of expression of CD86 and CD206 after co-culturing M2-TAMs with different formulations; (D) Mean fluorescence intensity of CD86 and CD206 in M2-TAMs treated with different formulations. (n = 3), n.s.: p > 0.05, **p < 0.01and ****p < 0.0001 vs. the IL-4 group; ##p < 0.01and ####p < 0.0001 vs. the IL-4 group; (E) Expression levels of IL-6 and TNF-α in RAW264.7 cells treated with free IMQ and FA-HES-EPI/IMQ micelles. (n = 3), n.s.: p > 0.05, ***p < 0.001 and ****p < 0.0001; ####p < 0.0001; (F) Western blot analysis of TLR7/MyD88/NF-κB signaling in RAW 264.7 cells treated with free IMQ or FA-HES-EPI/IMQ micelles.

Article Snippet: Rabbit anti-CD86 polyclonal antibody, rabbit anti-CD206 polyclonal antibody, FITC goat anti-rabbit antibody, IgG/Alexa Fluor555 goat anti-rabbit antibody, APC anti-mouse CD206 antibody, PE anti-mouse CD86 antibody, purified anti-mouse CD16/32 antibody, intracellular Fixation/Permeabilization buffer kit, IL-6 ELISA kit and TNF-α ELISA kit were all purchased from Elabscience Biotechnology (Wuhan, China).

Techniques: Staining, Fluorescence, Imaging, Expressing, Western Blot

Journal: Journal of Neuroinflammation

Article Title: TNF-α impairs the stria vascularis by inducing pericyte apoptosis via the NF-κB pathway in gentamicin-induced hearing loss

doi: 10.1186/s12974-026-03787-2

Figure Lengend Snippet: TNF-α in supernatant(GM) induces apoptosis of pericytes. A ELISA measurement of TNF-α concentrations in supernatant(PBS) and supernatant(GM) ( n = 4 for each group). B CCK-8 assay assessing the viability of pericytes treated with medium containing 0, 1, 2, 3, 4, or 5 ng/ml recombinant TNF-α ( n = 3 for each group). C , D Western blot analysis of c-casp3 and GAPDH in pericytes treated with medium containing 0, 1, 2, 3, 4, or 5 ng/ml recombinant TNF-α, with quantification of protein band intensities ( n = 3 for each group). E RT-qPCR analysis of TNFR1 expression in the Empty, pericyte, and RAW264.7 groups, with quantification of relative TNFR1 mRNA levels ( n = 3 for each group). F RT-qPCR analysis of TNFR1 expression in the control, TNFR1 siRNA, and Control siRNA groups, with quantification of relative TNFR1 mRNA levels ( n = 3 for each group). G , H Western blot analysis of c-casp3 and GAPDH in pericytes from the control, TNF-α, TNF-α+TNFR1 siRNA, and TNF-α+Control siRNA groups, with quantification of protein band intensities ( n = 3 for each group). I ELISA measurement of TNF-α concentrations in supernatant(PBS), supernatant(GM), supernatant(GM)+Anti-TNF-α, or supernatant(GM)+Rabbit IgG ( n = 3 for each group). J CCK-8 assay assessment of pericyte viability after treatment with supernatant(PBS), supernatant(GM), supernatant(GM)+Anti-TNF-α, or supernatant(GM)+Rabbit IgG ( n = 3 for each group). K , L Annexin V/PI staining followed by flow cytometry analysis of apoptosis in pericytes treated with supernatant(PBS), supernatant(GM), supernatant(GM)+Anti-TNF-α, or supernatant(GM)+Rabbit IgG, with quantification of Annexin V-positive cells ( n = 5 for each group). M , N Fluorescence images of TUNEL staining in pericytes cultured in supernatant(PBS), supernatant(GM), supernatant(GM)+Anti-TNF-α, or supernatant(GM)+Rabbit IgG, and the proportion of TUNEL-positive pericytes was quantified ( n = 5 for each group). Scale bar: 50 µm. Data are presented as mean ± SEM. * P < 0.05, ** P < 0.01, *** P < 0.001, one-way ANOVA followed by Bonferroni post hoc tests

Article Snippet: The sections were then placed in a humidified chamber and incubated overnight at 4°C with following primary antibody: rabbit polyclonal anti-IL-1β (Abcam, ab283818; 1:200), rabbit polyclonal anti-IL-6 (Abcam, ab290735; 1:200), rabbit polyclonal anti-TNF-α (signalway antibody, 41504; 1:200).

Techniques: Enzyme-linked Immunosorbent Assay, CCK-8 Assay, Recombinant, Western Blot, Quantitative RT-PCR, Expressing, Control, Staining, Flow Cytometry, Fluorescence, TUNEL Assay, Cell Culture

Journal: Journal of Neuroinflammation

Article Title: TNF-α impairs the stria vascularis by inducing pericyte apoptosis via the NF-κB pathway in gentamicin-induced hearing loss

doi: 10.1186/s12974-026-03787-2

Figure Lengend Snippet: JSH-23 pretreatment inhibits the NF-κB activation and reduces apoptosis of pericytes cultured in the supernatant(GM). A , B Western blot analysis of p-p38, p38, p-JNK, JNK, p-p65, p65, β-actin, and GAPDH in pericytes treated with supernatant(PBS), supernatant(GM), supernatant(GM)+Anti-TNF-α, or supernatant(GM)+Rabbit IgG, with quantification of protein band intensities ( n = 3 for each group). C , D Western blot analysis of c-casp3, p-p38, p38, p-p65, p65, β-actin, and GAPDH in pericytes treated with the supernatant(PBS), supernatant(GM), supernatant(GM)+JSH-23, or supernatant(GM)+SB202190, with quantification of protein band intensities ( n = 3 for each group). E , F Apoptosis analysis by Annexin V/PI staining followed by flow cytometry in pericytes treated with supernatant(PBS), supernatant(GM), supernatant(GM)+JSH-23, or supernatant(GM)+SB202190, with quantification of Annexin V-positive cells ( n = 5 for each group). Data are presented as mean ± SEM. * P < 0.05, ** P < 0.01, *** P < 0.001, one-way ANOVA followed by Bonferroni post hoc tests

Article Snippet: The sections were then placed in a humidified chamber and incubated overnight at 4°C with following primary antibody: rabbit polyclonal anti-IL-1β (Abcam, ab283818; 1:200), rabbit polyclonal anti-IL-6 (Abcam, ab290735; 1:200), rabbit polyclonal anti-TNF-α (signalway antibody, 41504; 1:200).

Techniques: Activation Assay, Cell Culture, Western Blot, Staining, Flow Cytometry