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kb2145  (Krishgen Biosystems)


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    Structured Review

    Krishgen Biosystems kb2145
    Kb2145, supplied by Krishgen Biosystems, used in various techniques. Bioz Stars score: 94/100, based on 94 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/kb2145/GENLISA+Mouse+Tumor+Necrosis+Factor+Alpha+(TNF-A+%2F+TNFA)+ELISA/10__1186_slash_s41936___026___00580___8-77-35-46
    Average 94 stars, based on 94 article reviews
    kb2145 - by Bioz Stars, 2026-09
    94/100 stars

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    other:

    Article Title: Teriflunomide mitigates pain-depression dyad in mice: Modulation of PI3K-mediated defensive signaling
    Article Snippet: No. KB2145) was procured from Krishgen Biosystems, Maharashtra, India.

    Enzyme-linked Immunosorbent Assay:

    Article Title: Andrographolide mitigates lipopolysaccharide-induced mastitis in a mouse model: role of oxidative stress, inflammation, and mitochondrial dysfunction
    Article Snippet: Estimation of signalling/transcription factor in mammary homogenate Signalling factor (NF-κB) (catalogue no.-KBH11868) in tissue homogenates was estimated using commercially available ELISA kits (Krishgen biosystem, USA). .. Estimation of inflammatory cytokines in mammary homogenate and serum Mammary tissue homogenates and corresponding serum samples were used for inflammatory cytokine estimation using a commercially available ELISA kit [Tumor necrosis factor alpha (TNF-α), catalogue no.- KB2145; interleukin-6 (IL-6), catalogue no.- KB2068; interleukin-10 (IL-10), catalogue no.- KB2072], Krishgen biosystem, USA] as per manufacturers’ instructions. ..

    Article Title: Loss of Protection by Antiepileptic Drugs in Lipopolysaccharide-primed Pilocarpine-induced Status Epilepticus is Mediated via Inflammatory Signalling.
    Article Snippet: The evidences from various studies show the association of peripheral and neuronal inflammation with complex pathophysiology of status epilepticus (SE).. In this view, the present work attempted to develop a model of neuronal inflammation mediated SE by combining both epileptic and inflammatory components of the disease and also to mimic SE co-morbid with systemic inflammation by peripheral administration of the lipopolysaccharide (LPS) 2 hours prior to the pilocarpine induction in C57BL/6 mice.. We evaluated the anticonvulsant and neuroprotective effects of 7-day prophylactic treatment with three conventional anti-epileptic drugs (Sodium valproate, SVP 300 mg/kg p.o.; Carbamazepine CBZ 100 mg/kg p.o.; Levetiracetam; LEV 200 mg/kg p.o.) of widespread clinical use.

    In Vivo:

    Article Title: Loss of Protection by Antiepileptic Drugs in Lipopolysaccharide-primed Pilocarpine-induced Status Epilepticus is Mediated via Inflammatory Signalling.
    Article Snippet: The evidences from various studies show the association of peripheral and neuronal inflammation with complex pathophysiology of status epilepticus (SE).. In this view, the present work attempted to develop a model of neuronal inflammation mediated SE by combining both epileptic and inflammatory components of the disease and also to mimic SE co-morbid with systemic inflammation by peripheral administration of the lipopolysaccharide (LPS) 2 hours prior to the pilocarpine induction in C57BL/6 mice.. We evaluated the anticonvulsant and neuroprotective effects of 7-day prophylactic treatment with three conventional anti-epileptic drugs (Sodium valproate, SVP 300 mg/kg p.o.; Carbamazepine CBZ 100 mg/kg p.o.; Levetiracetam; LEV 200 mg/kg p.o.) of widespread clinical use.



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    In vivo validation of allium PDNV-mediated suppression of psoriatic inflammation via NRF2-IL-17 axis (A–C) (A) qRT-PCR validation of selected genes in IMQ and PDNV-treated murine skin samples. Relative IL-17A, TNF-α, and IL-23 protein abundance in mice skin (B) or serum (C) quantified by <t>ELISA</t> ( n = 6). (D) Relative transcript abundance of NRF2 targets, HMOX1 , and NQO1 in IMQ and PDNV-treated murine skin samples. n = 6; error bar denotes mean ± SD. One-way ANOVA with Turkey’s multiple comparison test was used for post hoc analysis. (ns, non-significant, ∗ p < 0.05, ∗∗ p < 0.01, ∗∗∗ p < 0.001, and ∗∗∗∗ p < 0.0001). (E) Dorsal skin sections from mice were stained with antibodies against NRF2 (green) by immunohistochemistry and counterstained with DAPI (in blue). Scale bar,100 μm.
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    In vivo validation of allium PDNV-mediated suppression of psoriatic inflammation via NRF2-IL-17 axis (A–C) (A) qRT-PCR validation of selected genes in IMQ and PDNV-treated murine skin samples. Relative IL-17A, TNF-α, and IL-23 protein abundance in mice skin (B) or serum (C) quantified by <t>ELISA</t> ( n = 6). (D) Relative transcript abundance of NRF2 targets, HMOX1 , and NQO1 in IMQ and PDNV-treated murine skin samples. n = 6; error bar denotes mean ± SD. One-way ANOVA with Turkey’s multiple comparison test was used for post hoc analysis. (ns, non-significant, ∗ p < 0.05, ∗∗ p < 0.01, ∗∗∗ p < 0.001, and ∗∗∗∗ p < 0.0001). (E) Dorsal skin sections from mice were stained with antibodies against NRF2 (green) by immunohistochemistry and counterstained with DAPI (in blue). Scale bar,100 μm.
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    Image Search Results


    In vivo validation of allium PDNV-mediated suppression of psoriatic inflammation via NRF2-IL-17 axis (A–C) (A) qRT-PCR validation of selected genes in IMQ and PDNV-treated murine skin samples. Relative IL-17A, TNF-α, and IL-23 protein abundance in mice skin (B) or serum (C) quantified by ELISA ( n = 6). (D) Relative transcript abundance of NRF2 targets, HMOX1 , and NQO1 in IMQ and PDNV-treated murine skin samples. n = 6; error bar denotes mean ± SD. One-way ANOVA with Turkey’s multiple comparison test was used for post hoc analysis. (ns, non-significant, ∗ p < 0.05, ∗∗ p < 0.01, ∗∗∗ p < 0.001, and ∗∗∗∗ p < 0.0001). (E) Dorsal skin sections from mice were stained with antibodies against NRF2 (green) by immunohistochemistry and counterstained with DAPI (in blue). Scale bar,100 μm.

    Journal: iScience

    Article Title: Natural plant-derived nanovesicles for effective psoriasis therapy via dual modulation of IL-17 and NRF2 pathway

    doi: 10.1016/j.isci.2025.112556

    Figure Lengend Snippet: In vivo validation of allium PDNV-mediated suppression of psoriatic inflammation via NRF2-IL-17 axis (A–C) (A) qRT-PCR validation of selected genes in IMQ and PDNV-treated murine skin samples. Relative IL-17A, TNF-α, and IL-23 protein abundance in mice skin (B) or serum (C) quantified by ELISA ( n = 6). (D) Relative transcript abundance of NRF2 targets, HMOX1 , and NQO1 in IMQ and PDNV-treated murine skin samples. n = 6; error bar denotes mean ± SD. One-way ANOVA with Turkey’s multiple comparison test was used for post hoc analysis. (ns, non-significant, ∗ p < 0.05, ∗∗ p < 0.01, ∗∗∗ p < 0.001, and ∗∗∗∗ p < 0.0001). (E) Dorsal skin sections from mice were stained with antibodies against NRF2 (green) by immunohistochemistry and counterstained with DAPI (in blue). Scale bar,100 μm.

    Article Snippet: TNF-α ELISA kit , Krishgen , Cat#KB2145.

    Techniques: In Vivo, Biomarker Discovery, Quantitative RT-PCR, Quantitative Proteomics, Enzyme-linked Immunosorbent Assay, Comparison, Staining, Immunohistochemistry