F54557 Search Results


91
Lifespan Biosciences mouse endostatin elisa commercial kit
Mouse Endostatin Elisa Commercial Kit, supplied by Lifespan Biosciences, used in various techniques. Bioz Stars score: 91/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/mouse endostatin elisa commercial kit/product/Lifespan Biosciences
Average 91 stars, based on 1 article reviews
mouse endostatin elisa commercial kit - by Bioz Stars, 2026-02
91/100 stars
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86
Lifespan Biosciences mouse trem2 trem 2 elisa kit
Effects of taxifolin on the accumulation of cells expressing Iba-1, TNF-α, or <t>TREM2</t> in the hippocampus or cortex of Tg-SwDI mice. The histograms and representative images are for Tg-SwDI mice that received the control diet (control group, n = 3) or chow containing taxifolin (taxifolin group, n = 3) for 7 mo. The various cells were detected immunohistochemically, and the total cells were visualized by counterstaining with hematoxylin. Representative images are shown for the control group (Left) and taxifolin group (Right). [Scale bars, 500 μm for the low-power field (Left) and 20 μm for the high-power field (Right).] The proportion of positive cells was obtained by dividing the number of immunohistochemically positive cells by the total number of cells. (A–D) Immunohistochemical analyses of Iba-1–expressing cells in the hippocampus (A and C) and cortex (B and D) of the control group (A and B) and taxifolin group (C and D). (E–H) Immunohistochemical analyses of TNF-α–positive cells in the hippocampus (E and G) and cortex (F and H) of the control group (E and F) and taxifolin group (G and H) (n = 3). (I–L) Immunohistochemical analyses of cells positive for TREM2 in the hippocampus (I and K) and cortex (J and L) of the control group (I and J) and taxifolin group (K and L). Data are expressed as mean ± SEM (control, n = 3; taxifolin, n = 3). P values were determined by Student’s t test. *P < 0.05; **P < 0.01.
Mouse Trem2 Trem 2 Elisa Kit, supplied by Lifespan Biosciences, 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/result/mouse trem2 trem 2 elisa kit/product/Lifespan Biosciences
Average 86 stars, based on 1 article reviews
mouse trem2 trem 2 elisa kit - by Bioz Stars, 2026-02
86/100 stars
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This gene encodes the prototype of the membrane-associated guanylate kinase (MAGUK) family proteins. MAGUKs interact with the cytoskeleton and regulate cell proliferation, signaling pathways, and intercellular junctions. The encoded protein is an extensively palmitoylated membrane
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This gene encodes a member of the F-box protein family, members of which are characterized by an approximately 40 amino acid motif, the F-box. The F-box proteins constitute one of the four subunits of ubiquitin
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Cysteine protease required for the cytoplasm to vacuole transport (Cvt) and autophagy. Cleaves the C-terminal amino acid of ATG8 family proteins to reveal a C-terminal glycine. Exposure of the glycine at the C-terminus is essential
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Ubiquitous transcription factor required for a diverse set of processes. It is a component of the CCR4 complex involved in the control of gene expression (By similarity).
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The protein encoded by this gene is a type I transmembrane protein identified as a subunit of the interleukin 12 receptor complex. The coexpression of this and IL12RB1 proteins was shown to lead to the
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The protein encoded by this gene, a member of the G protein-coupled receptor family 1, is an integral plasma membrane protein which binds melanin-concentrating hormone. The encoded protein can inhibit cAMP accumulation and stimulate intracellular
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Forms part of a macromolecular complex that catalyzes the attachment of specific amino acids to cognate tRNAs during protein synthesis. Modulates the secretion of AIMP1 and may be involved in generation of the inflammatory cytokine
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ARL8A plays a role in lysosome motility. [UniProt]
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Image Search Results


Effects of taxifolin on the accumulation of cells expressing Iba-1, TNF-α, or TREM2 in the hippocampus or cortex of Tg-SwDI mice. The histograms and representative images are for Tg-SwDI mice that received the control diet (control group, n = 3) or chow containing taxifolin (taxifolin group, n = 3) for 7 mo. The various cells were detected immunohistochemically, and the total cells were visualized by counterstaining with hematoxylin. Representative images are shown for the control group (Left) and taxifolin group (Right). [Scale bars, 500 μm for the low-power field (Left) and 20 μm for the high-power field (Right).] The proportion of positive cells was obtained by dividing the number of immunohistochemically positive cells by the total number of cells. (A–D) Immunohistochemical analyses of Iba-1–expressing cells in the hippocampus (A and C) and cortex (B and D) of the control group (A and B) and taxifolin group (C and D). (E–H) Immunohistochemical analyses of TNF-α–positive cells in the hippocampus (E and G) and cortex (F and H) of the control group (E and F) and taxifolin group (G and H) (n = 3). (I–L) Immunohistochemical analyses of cells positive for TREM2 in the hippocampus (I and K) and cortex (J and L) of the control group (I and J) and taxifolin group (K and L). Data are expressed as mean ± SEM (control, n = 3; taxifolin, n = 3). P values were determined by Student’s t test. *P < 0.05; **P < 0.01.

Journal: Proceedings of the National Academy of Sciences of the United States of America

Article Title: Pleiotropic neuroprotective effects of taxifolin in cerebral amyloid angiopathy

doi: 10.1073/pnas.1901659116

Figure Lengend Snippet: Effects of taxifolin on the accumulation of cells expressing Iba-1, TNF-α, or TREM2 in the hippocampus or cortex of Tg-SwDI mice. The histograms and representative images are for Tg-SwDI mice that received the control diet (control group, n = 3) or chow containing taxifolin (taxifolin group, n = 3) for 7 mo. The various cells were detected immunohistochemically, and the total cells were visualized by counterstaining with hematoxylin. Representative images are shown for the control group (Left) and taxifolin group (Right). [Scale bars, 500 μm for the low-power field (Left) and 20 μm for the high-power field (Right).] The proportion of positive cells was obtained by dividing the number of immunohistochemically positive cells by the total number of cells. (A–D) Immunohistochemical analyses of Iba-1–expressing cells in the hippocampus (A and C) and cortex (B and D) of the control group (A and B) and taxifolin group (C and D). (E–H) Immunohistochemical analyses of TNF-α–positive cells in the hippocampus (E and G) and cortex (F and H) of the control group (E and F) and taxifolin group (G and H) (n = 3). (I–L) Immunohistochemical analyses of cells positive for TREM2 in the hippocampus (I and K) and cortex (J and L) of the control group (I and J) and taxifolin group (K and L). Data are expressed as mean ± SEM (control, n = 3; taxifolin, n = 3). P values were determined by Student’s t test. *P < 0.05; **P < 0.01.

Article Snippet: Quantification of sTREM2 in Brain Tissue Extracts. sTREM2 levels in the hippocampal and cortical tissues of the mice were quantified using a Mouse TREM2/TREM-2 ELISA Kit (LifeSpan BioSciences, Inc.), according to the manufacturer’s instructions.

Techniques: Expressing, Immunohistochemical staining

Beneficial effects of taxifolin on proinflammatory phenotypes of microglia in the hippocampus of Tg-SwDI mice. The histograms and graphs show results for the hippocampal tissue of 14-wk-old Tg-SwDI mice that received either the control diet (n = 4) or chow containing taxifolin (n = 5) for 13 mo. mRNA expression levels were measured by quantitative RT-PCR and normalized to GAPDH. (A–C) Hippocampal mRNA expression levels of Iba-1 (A), TREM2 (B), and ADAM10 (C). (D) Concentration of sTREM2. (E and F) Activation levels of proinflammatory signaling pathways. The relative amounts of phospho-p38 (Thr180/Tyr182) to total p38 (E) and phospho-NF-κB p65 (Ser536) to total NF-κB p65 (F) were determined by Western blot and densitometry. Representative images are shown at the Upper Left. (G–M) Relationships between expression levels of TREM2 and levels of Iba-1 (G), ADAM10 (H), TNF-α (I), IL-6 (J), IL-1β (K), glutamate (L), and lipid peroxidation (M) in the hippocampal tissue. In A–F, data are expressed as mean ± SEM (control, n = 4; taxifolin, n = 5); P values were determined by Student’s t test; *P < 0.05; **P < 0.01. In G–M, Pearson’s correlation coefficients (r) were used to test the associations of interest.

Journal: Proceedings of the National Academy of Sciences of the United States of America

Article Title: Pleiotropic neuroprotective effects of taxifolin in cerebral amyloid angiopathy

doi: 10.1073/pnas.1901659116

Figure Lengend Snippet: Beneficial effects of taxifolin on proinflammatory phenotypes of microglia in the hippocampus of Tg-SwDI mice. The histograms and graphs show results for the hippocampal tissue of 14-wk-old Tg-SwDI mice that received either the control diet (n = 4) or chow containing taxifolin (n = 5) for 13 mo. mRNA expression levels were measured by quantitative RT-PCR and normalized to GAPDH. (A–C) Hippocampal mRNA expression levels of Iba-1 (A), TREM2 (B), and ADAM10 (C). (D) Concentration of sTREM2. (E and F) Activation levels of proinflammatory signaling pathways. The relative amounts of phospho-p38 (Thr180/Tyr182) to total p38 (E) and phospho-NF-κB p65 (Ser536) to total NF-κB p65 (F) were determined by Western blot and densitometry. Representative images are shown at the Upper Left. (G–M) Relationships between expression levels of TREM2 and levels of Iba-1 (G), ADAM10 (H), TNF-α (I), IL-6 (J), IL-1β (K), glutamate (L), and lipid peroxidation (M) in the hippocampal tissue. In A–F, data are expressed as mean ± SEM (control, n = 4; taxifolin, n = 5); P values were determined by Student’s t test; *P < 0.05; **P < 0.01. In G–M, Pearson’s correlation coefficients (r) were used to test the associations of interest.

Article Snippet: Quantification of sTREM2 in Brain Tissue Extracts. sTREM2 levels in the hippocampal and cortical tissues of the mice were quantified using a Mouse TREM2/TREM-2 ELISA Kit (LifeSpan BioSciences, Inc.), according to the manufacturer’s instructions.

Techniques: Expressing, Quantitative RT-PCR, Concentration Assay, Activation Assay, Western Blot