anti tumor necrosis factor alpha  (ProSci Incorporated)


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    ProSci Incorporated anti tumor necrosis factor alpha
    Anti Tumor Necrosis Factor Alpha, supplied by ProSci Incorporated, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    anti tumor necrosis factor alpha  (ProSci Incorporated)


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    ProSci Incorporated anti tumor necrosis factor alpha
    Anti Tumor Necrosis Factor Alpha, supplied by ProSci Incorporated, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    ProSci Incorporated goat anti htnf
    Goat Anti Htnf, supplied by ProSci Incorporated, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    anti tnf α  (ProSci Incorporated)


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    ProSci Incorporated anti tnf α
    At 2 weeks Pi, pre‐inflammatory factors COX‐2 (A–E, immunostaining, counterstained with hematoxylin), NFκB (F–J, immunostaining, counterstained with <t>hematoxylin),</t> <t>TNF‐α</t> (K–O, red color immunofluorescence staining, nuclei of all cells were stained with blue color of Hoechst 33342) and GAP‐43 (P–T, green color immunofluorescence staining) exhibited visible expression levels in the lumbar spinal cord anterior horn. Scale bar: 100 μm. COX‐2, NF‐κB <t>and</t> <t>TNF‐α</t> were all significantly increased in vehicle‐treated EAE rats, while the C+A, Reg‐2 and C+A+R treatments could markedly reduce the expression of those factors. Moreover, treatment with C+A, Reg‐2 and C+A+R upregulated the expression of GAP‐43.
    Anti Tnf α, supplied by ProSci Incorporated, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Images

    1) Product Images from "Role of C16, angiopoietin‐1 and regeneration gene protein 2 in attenuating inflammation in an experimental rat model of autoimmune encephalomyelitis"

    Article Title: Role of C16, angiopoietin‐1 and regeneration gene protein 2 in attenuating inflammation in an experimental rat model of autoimmune encephalomyelitis

    Journal: Journal of Anatomy

    doi: 10.1111/joa.12541

    At 2 weeks Pi, pre‐inflammatory factors COX‐2 (A–E, immunostaining, counterstained with hematoxylin), NFκB (F–J, immunostaining, counterstained with hematoxylin), TNF‐α (K–O, red color immunofluorescence staining, nuclei of all cells were stained with blue color of Hoechst 33342) and GAP‐43 (P–T, green color immunofluorescence staining) exhibited visible expression levels in the lumbar spinal cord anterior horn. Scale bar: 100 μm. COX‐2, NF‐κB and TNF‐α were all significantly increased in vehicle‐treated EAE rats, while the C+A, Reg‐2 and C+A+R treatments could markedly reduce the expression of those factors. Moreover, treatment with C+A, Reg‐2 and C+A+R upregulated the expression of GAP‐43.
    Figure Legend Snippet: At 2 weeks Pi, pre‐inflammatory factors COX‐2 (A–E, immunostaining, counterstained with hematoxylin), NFκB (F–J, immunostaining, counterstained with hematoxylin), TNF‐α (K–O, red color immunofluorescence staining, nuclei of all cells were stained with blue color of Hoechst 33342) and GAP‐43 (P–T, green color immunofluorescence staining) exhibited visible expression levels in the lumbar spinal cord anterior horn. Scale bar: 100 μm. COX‐2, NF‐κB and TNF‐α were all significantly increased in vehicle‐treated EAE rats, while the C+A, Reg‐2 and C+A+R treatments could markedly reduce the expression of those factors. Moreover, treatment with C+A, Reg‐2 and C+A+R upregulated the expression of GAP‐43.

    Techniques Used: Immunostaining, Immunofluorescence, Staining, Expressing

    anti tnf α  (ProSci Incorporated)


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  • 86

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    ProSci Incorporated anti tnf α
    At 2 weeks Pi, pre‐inflammatory factors COX‐2 (A–E, immunostaining, counterstained with hematoxylin), NFκB (F–J, immunostaining, counterstained with <t>hematoxylin),</t> <t>TNF‐α</t> (K–O, red color immunofluorescence staining, nuclei of all cells were stained with blue color of Hoechst 33342) and GAP‐43 (P–T, green color immunofluorescence staining) exhibited visible expression levels in the lumbar spinal cord anterior horn. Scale bar: 100 μm. COX‐2, NF‐κB <t>and</t> <t>TNF‐α</t> were all significantly increased in vehicle‐treated EAE rats, while the C+A, Reg‐2 and C+A+R treatments could markedly reduce the expression of those factors. Moreover, treatment with C+A, Reg‐2 and C+A+R upregulated the expression of GAP‐43.
    Anti Tnf α, supplied by ProSci Incorporated, 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/anti tnf α/product/ProSci Incorporated
    Average 86 stars, based on 1 article reviews
    Price from $9.99 to $1999.99
    anti tnf α - by Bioz Stars, 2024-04
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    Images

    1) Product Images from "Role of C16, angiopoietin‐1 and regeneration gene protein 2 in attenuating inflammation in an experimental rat model of autoimmune encephalomyelitis"

    Article Title: Role of C16, angiopoietin‐1 and regeneration gene protein 2 in attenuating inflammation in an experimental rat model of autoimmune encephalomyelitis

    Journal: Journal of Anatomy

    doi: 10.1111/joa.12541

    At 2 weeks Pi, pre‐inflammatory factors COX‐2 (A–E, immunostaining, counterstained with hematoxylin), NFκB (F–J, immunostaining, counterstained with hematoxylin), TNF‐α (K–O, red color immunofluorescence staining, nuclei of all cells were stained with blue color of Hoechst 33342) and GAP‐43 (P–T, green color immunofluorescence staining) exhibited visible expression levels in the lumbar spinal cord anterior horn. Scale bar: 100 μm. COX‐2, NF‐κB and TNF‐α were all significantly increased in vehicle‐treated EAE rats, while the C+A, Reg‐2 and C+A+R treatments could markedly reduce the expression of those factors. Moreover, treatment with C+A, Reg‐2 and C+A+R upregulated the expression of GAP‐43.
    Figure Legend Snippet: At 2 weeks Pi, pre‐inflammatory factors COX‐2 (A–E, immunostaining, counterstained with hematoxylin), NFκB (F–J, immunostaining, counterstained with hematoxylin), TNF‐α (K–O, red color immunofluorescence staining, nuclei of all cells were stained with blue color of Hoechst 33342) and GAP‐43 (P–T, green color immunofluorescence staining) exhibited visible expression levels in the lumbar spinal cord anterior horn. Scale bar: 100 μm. COX‐2, NF‐κB and TNF‐α were all significantly increased in vehicle‐treated EAE rats, while the C+A, Reg‐2 and C+A+R treatments could markedly reduce the expression of those factors. Moreover, treatment with C+A, Reg‐2 and C+A+R upregulated the expression of GAP‐43.

    Techniques Used: Immunostaining, Immunofluorescence, Staining, Expressing

    tnf α  (ProSci Incorporated)


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    ProSci Incorporated tnf α
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    rabbit anti mouse tnf α  (ProSci Incorporated)


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    ProSci Incorporated rabbit anti mouse tnf α
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    tnf-a antibody  (ProSci Incorporated)


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    ProSci Incorporated tnf-a antibody
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    anti tumor necrosis factor alpha  (ProSci Incorporated)


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    ProSci Incorporated anti tumor necrosis factor alpha
    Anti Tumor Necrosis Factor Alpha, supplied by ProSci Incorporated, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    anti tumor necrosis factor alpha  (ProSci Incorporated)


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    ProSci Incorporated anti tumor necrosis factor alpha
    Anti Tumor Necrosis Factor Alpha, supplied by ProSci Incorporated, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    anti tnf  (ProSci Incorporated)


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    ProSci Incorporated anti tnf
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    ProSci Incorporated anti tumor necrosis factor alpha
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    At 2 weeks Pi, pre‐inflammatory factors COX‐2 (A–E, immunostaining, counterstained with hematoxylin), NFκB (F–J, immunostaining, counterstained with <t>hematoxylin),</t> <t>TNF‐α</t> (K–O, red color immunofluorescence staining, nuclei of all cells were stained with blue color of Hoechst 33342) and GAP‐43 (P–T, green color immunofluorescence staining) exhibited visible expression levels in the lumbar spinal cord anterior horn. Scale bar: 100 μm. COX‐2, NF‐κB <t>and</t> <t>TNF‐α</t> were all significantly increased in vehicle‐treated EAE rats, while the C+A, Reg‐2 and C+A+R treatments could markedly reduce the expression of those factors. Moreover, treatment with C+A, Reg‐2 and C+A+R upregulated the expression of GAP‐43.
    Anti Tnf α, supplied by ProSci Incorporated, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    At 2 weeks Pi, pre‐inflammatory factors COX‐2 (A–E, immunostaining, counterstained with hematoxylin), NFκB (F–J, immunostaining, counterstained with <t>hematoxylin),</t> <t>TNF‐α</t> (K–O, red color immunofluorescence staining, nuclei of all cells were stained with blue color of Hoechst 33342) and GAP‐43 (P–T, green color immunofluorescence staining) exhibited visible expression levels in the lumbar spinal cord anterior horn. Scale bar: 100 μm. COX‐2, NF‐κB <t>and</t> <t>TNF‐α</t> were all significantly increased in vehicle‐treated EAE rats, while the C+A, Reg‐2 and C+A+R treatments could markedly reduce the expression of those factors. Moreover, treatment with C+A, Reg‐2 and C+A+R upregulated the expression of GAP‐43.
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    At 2 weeks Pi, pre‐inflammatory factors COX‐2 (A–E, immunostaining, counterstained with hematoxylin), NFκB (F–J, immunostaining, counterstained with <t>hematoxylin),</t> <t>TNF‐α</t> (K–O, red color immunofluorescence staining, nuclei of all cells were stained with blue color of Hoechst 33342) and GAP‐43 (P–T, green color immunofluorescence staining) exhibited visible expression levels in the lumbar spinal cord anterior horn. Scale bar: 100 μm. COX‐2, NF‐κB <t>and</t> <t>TNF‐α</t> were all significantly increased in vehicle‐treated EAE rats, while the C+A, Reg‐2 and C+A+R treatments could markedly reduce the expression of those factors. Moreover, treatment with C+A, Reg‐2 and C+A+R upregulated the expression of GAP‐43.
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    At 2 weeks Pi, pre‐inflammatory factors COX‐2 (A–E, immunostaining, counterstained with hematoxylin), NFκB (F–J, immunostaining, counterstained with <t>hematoxylin),</t> <t>TNF‐α</t> (K–O, red color immunofluorescence staining, nuclei of all cells were stained with blue color of Hoechst 33342) and GAP‐43 (P–T, green color immunofluorescence staining) exhibited visible expression levels in the lumbar spinal cord anterior horn. Scale bar: 100 μm. COX‐2, NF‐κB <t>and</t> <t>TNF‐α</t> were all significantly increased in vehicle‐treated EAE rats, while the C+A, Reg‐2 and C+A+R treatments could markedly reduce the expression of those factors. Moreover, treatment with C+A, Reg‐2 and C+A+R upregulated the expression of GAP‐43.
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    At 2 weeks Pi, pre‐inflammatory factors COX‐2 (A–E, immunostaining, counterstained with hematoxylin), NFκB (F–J, immunostaining, counterstained with <t>hematoxylin),</t> <t>TNF‐α</t> (K–O, red color immunofluorescence staining, nuclei of all cells were stained with blue color of Hoechst 33342) and GAP‐43 (P–T, green color immunofluorescence staining) exhibited visible expression levels in the lumbar spinal cord anterior horn. Scale bar: 100 μm. COX‐2, NF‐κB <t>and</t> <t>TNF‐α</t> were all significantly increased in vehicle‐treated EAE rats, while the C+A, Reg‐2 and C+A+R treatments could markedly reduce the expression of those factors. Moreover, treatment with C+A, Reg‐2 and C+A+R upregulated the expression of GAP‐43.
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    Image Search Results


    At 2 weeks Pi, pre‐inflammatory factors COX‐2 (A–E, immunostaining, counterstained with hematoxylin), NFκB (F–J, immunostaining, counterstained with hematoxylin), TNF‐α (K–O, red color immunofluorescence staining, nuclei of all cells were stained with blue color of Hoechst 33342) and GAP‐43 (P–T, green color immunofluorescence staining) exhibited visible expression levels in the lumbar spinal cord anterior horn. Scale bar: 100 μm. COX‐2, NF‐κB and TNF‐α were all significantly increased in vehicle‐treated EAE rats, while the C+A, Reg‐2 and C+A+R treatments could markedly reduce the expression of those factors. Moreover, treatment with C+A, Reg‐2 and C+A+R upregulated the expression of GAP‐43.

    Journal: Journal of Anatomy

    Article Title: Role of C16, angiopoietin‐1 and regeneration gene protein 2 in attenuating inflammation in an experimental rat model of autoimmune encephalomyelitis

    doi: 10.1111/joa.12541

    Figure Lengend Snippet: At 2 weeks Pi, pre‐inflammatory factors COX‐2 (A–E, immunostaining, counterstained with hematoxylin), NFκB (F–J, immunostaining, counterstained with hematoxylin), TNF‐α (K–O, red color immunofluorescence staining, nuclei of all cells were stained with blue color of Hoechst 33342) and GAP‐43 (P–T, green color immunofluorescence staining) exhibited visible expression levels in the lumbar spinal cord anterior horn. Scale bar: 100 μm. COX‐2, NF‐κB and TNF‐α were all significantly increased in vehicle‐treated EAE rats, while the C+A, Reg‐2 and C+A+R treatments could markedly reduce the expression of those factors. Moreover, treatment with C+A, Reg‐2 and C+A+R upregulated the expression of GAP‐43.

    Article Snippet: After rinsing in 0.01 m Tris‐buffered saline (TBS) for 10 min, sections were permeabilized and blocked with 0.3% Triton X‐100/10% normal goat serum in 0.01 m PBS for 30 min, then incubated with the following polyclonal rabbit antibodies: anti‐Olig1 (1 : 500; Santa Cruz, Dallas, TX, USA), anti‐NF‐κB p65 (1 : 500; Abcam, MA, USA), anti‐cyclooxygenase‐2 (COX‐2; 1 : 1000; BioVision, Milpitas, CA, USA) and anti‐TNF‐α (1 : 1000; ProSci, CA, USA) overnight at 4 °C.

    Techniques: Immunostaining, Immunofluorescence, Staining, Expressing