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e7o4e rabbit anti ngf  (Cell Signaling Technology Inc)


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    Structured Review

    Cell Signaling Technology Inc e7o4e rabbit anti ngf
    E7o4e Rabbit Anti Ngf, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/rabbit+anti+ngf/bio_rxiv__64898__2026__01__15__699724-263-0-3
    Average 86 stars, based on 1 article reviews
    e7o4e rabbit anti ngf - by Bioz Stars, 2026-10
    86/100 stars

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    Related Articles

    other:

    Article Title: Neuroprotective effects of bajijiasu against cognitive impairment induced by amyloid-β in APP/PS1 mice
    Article Snippet: Rabbit anti-APP (1:4000; Abcam: ab32136), rabbit anti-PS1 (1:1000; Abcam: ab134195), rabbit anti-NEP (1:1000; Abcam: ab126593), rabbit anti-IDE (1:1000; Abcam: ab133561), mouse anti-BACE1 (1:500; Abcam: ab183612), rabbit anti-BDNF (1:1000; Abcam: ab101747), rabbit anti-NGF (1:1000; Abcam:ab68151), rabbit anti-NF-κB (1:1000; Cell Signaling Technology: #8242), rabbit anti-Iba1 (1:1000; Abcam: ab178847), rabbit anti-CD40 (1:1000; Abcam: ab65853) rabbit anti-Synaptophysin (1:1000; Cell Signaling: #4329), rabbit anti-PSD-93 (1:1000; Cell Signaling: #9445), rabbit anti-PSD-95 (1:1000; Cell Signaling: #2507), and mouse anti-β-actin (1:60000; Sigma:A5441).

    Article Title: Engineered Exosomes Derived From Primary M2 Macrophages With Anti-inflammatory And Neuroprotective Properties For The Treatment of Spinal Cord Injury.
    Article Snippet: The primary antibodies used were as follows: rabbit anti-CD9 (1:1000, Abcam, Cambridge, UK), rabbit anti-TSG101 (1:1000, Abcam, Page 13/28 Cambridge, UK), rabbit anti-CD206 (1:1000, Cell Signaling Technology, MA, USA), rabbit anti-IL10 (1:1000, Cell Signaling Technology, MA, USA), rabbit anti-CCR2 (1:1000, Cell Signaling Technology, MA, USA), rabbit anti-ARG-1 (1:1000, Cell Signaling Technology, MA, USA), rabbit anti-NGF (1:1000, Cell Signaling Technology, MA, USA), and mouse anti-β-actin (1:1000, Abcam, Cambridge, UK).

    Article Title: Engineered extracellular vesicles derived from primary M2 macrophages with anti-inflammatory and neuroprotective properties for the treatment of spinal cord injury
    Article Snippet: The primary antibodies used were as follows: rabbit anti-CD9 (1:1000, Abcam, Cambridge, UK), rabbit anti-TSG101 (1:1000, Abcam, Cambridge, UK), rabbit anti-CD206 (1:1000, Cell Signaling Technology, MA, USA), rabbit anti-IL10 (1:1000, Cell Signaling Technology, MA, USA), rabbit anti-CCR2 (1:1000, Cell Signaling Technology, MA, USA), rabbit anti-ARG-1 (1:1000, Cell Signaling Technology, MA, USA), rabbit anti-NGF (1:1000, Cell Signaling Technology, MA, USA), and mouse anti-β-actin (1:1000, Abcam, Cambridge, UK).



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    Alomone Labs rabbit anti brain derived neurotrophic factor bdnf
    Mature <t>BDNF</t> and proBDNF levels were measured by Western blot in brain lysates derived from mice exposed to either vehicle or DFP (4.0 mg/kg), followed by treatment with saline, GM1, or GD3 (5 mg/kg/day for 7 days). (A) Representative blot illustrating proBDNF (32 kDa) and BDNF (14 kDa). CTX, cortex; PFC, prefrontal cortex; HIP, hippocampus; SVZ, subventricular zone. (B) The data presented in the bar graphs were obtained from densitometry measurements of the bands for proBDNF, BDNF, and actin . Ratios of proBDNF and BDNF to actin were calculated for each replicate sample. Results are expressed as means ± S.E.M. of ≥3 replicates per condition. *P < 0.05 and **P < 0.01 indicates significant differences between indicated groups, as calculated using one-way ANOVA with Tukey’s multiple comparison test.
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    Image Search Results


    Protein expression of molecules from the BDNF signaling pathway determined by Western Blot and representative membranes. (A)mBDNF. (B)TrkB. (C)proBDNF. (D)p75 for yogurt treated mice after 4 weeks. (E–F) Representative membranes showing signals for TrkB, mBDNF, pro-BDNF, and p75 in Control and fatty acids-treated mice. Data are expressed as mean ± SD, n =5−6/group. # 0.05 < p < 0.10; *p < 0.05; **p < 0.01; ***p < 0.001.

    Journal: bioRxiv

    Article Title: Nanoliposomal Omega-3 Fatty Acids Promote Adult Hippocampal Neurogenesis through the BDNF/TrkB Pathway in C57BL/6 Mice

    doi: 10.64898/2026.02.24.707750

    Figure Lengend Snippet: Protein expression of molecules from the BDNF signaling pathway determined by Western Blot and representative membranes. (A)mBDNF. (B)TrkB. (C)proBDNF. (D)p75 for yogurt treated mice after 4 weeks. (E–F) Representative membranes showing signals for TrkB, mBDNF, pro-BDNF, and p75 in Control and fatty acids-treated mice. Data are expressed as mean ± SD, n =5−6/group. # 0.05 < p < 0.10; *p < 0.05; **p < 0.01; ***p < 0.001.

    Article Snippet: Samples (50 μgr in 5× loading buffer) were then loaded into SDS-PAGE gels (12 or 15%) and transferred onto nitrocellulose membranes using the Mini-PROTEAN ® Tetra System (BIO-RAD) for 1 h. Membranes were incubated for 1 h with blocking solution (5% milk in TBST) and then probed overnight at 4°C with mouse anti-BDNF (1:2000; Icosagen; 327-100 clone 3C11), rabbit anti-p75 (1:700; Alomone Labs; ANT-007), rabbit anti-TrkB (1:700; Alomone Labs; ANT-019), and rabbit anti-proBDNF (1:2500; Genocopoeia) in TBST.

    Techniques: Expressing, Western Blot, Control

    Mature BDNF and proBDNF levels were measured by Western blot in brain lysates derived from mice exposed to either vehicle or DFP (4.0 mg/kg), followed by treatment with saline, GM1, or GD3 (5 mg/kg/day for 7 days). (A) Representative blot illustrating proBDNF (32 kDa) and BDNF (14 kDa). CTX, cortex; PFC, prefrontal cortex; HIP, hippocampus; SVZ, subventricular zone. (B) The data presented in the bar graphs were obtained from densitometry measurements of the bands for proBDNF, BDNF, and actin . Ratios of proBDNF and BDNF to actin were calculated for each replicate sample. Results are expressed as means ± S.E.M. of ≥3 replicates per condition. *P < 0.05 and **P < 0.01 indicates significant differences between indicated groups, as calculated using one-way ANOVA with Tukey’s multiple comparison test.

    Journal: bioRxiv

    Article Title: GM1 and GD3 Gangliosides Attenuate NGF-TrkA and BDNF-TrkB Signaling Dysfunction Associated with Acute Diisopropylfluorophosphate Exposure in Mouse Brain

    doi: 10.1101/2025.03.31.646417

    Figure Lengend Snippet: Mature BDNF and proBDNF levels were measured by Western blot in brain lysates derived from mice exposed to either vehicle or DFP (4.0 mg/kg), followed by treatment with saline, GM1, or GD3 (5 mg/kg/day for 7 days). (A) Representative blot illustrating proBDNF (32 kDa) and BDNF (14 kDa). CTX, cortex; PFC, prefrontal cortex; HIP, hippocampus; SVZ, subventricular zone. (B) The data presented in the bar graphs were obtained from densitometry measurements of the bands for proBDNF, BDNF, and actin . Ratios of proBDNF and BDNF to actin were calculated for each replicate sample. Results are expressed as means ± S.E.M. of ≥3 replicates per condition. *P < 0.05 and **P < 0.01 indicates significant differences between indicated groups, as calculated using one-way ANOVA with Tukey’s multiple comparison test.

    Article Snippet: For this study, the following antibodies were purchased: rabbit anti-TrkA (RRID:AB_310180; Millipore Millipore, St. Louis, MO, USA, #06-574), mouse anti-NeuN (RRID:AB_2298772; Sigma-Aldrich, St. Louis, MO, USA, #MAB377), rabbit anti-p75 neurotrophin receptor (p75 NTR , RRID:AB_310649; Millipore #07-476), rabbit anti-sortilin (RRID:AB_2192606; Abcam, Cambridge, MA, USA, #ab16640), goat anti-TrkB (RRID:AB_2155263; R&D Systems, Minneapolis, MN, USA, #BAF1494), rabbit anti-actin (RRID:AB_476693; Sigma #A2066), rabbit anti-NGF (RRID:AB_2040019, Alomone Labs, Jerusalem, Israel, #AN-240), rabbit anti-brain-derived neurotrophic factor (BDNF) (RRID:AB_2039756, Alomone Labs #ANT-010), and rabbit anti-phospho-Trk (RRID:AB_2298805; Cell Signaling Technology, Danvers, MA, USA, #9141).

    Techniques: Western Blot, Derivative Assay, Saline, Comparison