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human gfap  (R&D Systems)


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    R&D Systems human gfap
    Human Gfap, supplied by R&D Systems, used in various techniques. Bioz Stars score: 93/100, based on 18 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/dy2594+05/Human+GFAP+DuoSet+ELISA/10__1016_slash_j__cej__2025__161118-297-7-9
    Average 93 stars, based on 18 article reviews
    human gfap - by Bioz Stars, 2026-10
    93/100 stars

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    Related Articles

    Clinical Proteomics:

    Article Title: Plasma β-III tubulin, neurofilament light chain and glial fibrillary acidic protein are associated with neurodegeneration and progression in schizophrenia
    Article Snippet: .. GFAP levels of plasma samples of patients and healthy controls were measured by sandwich enzyme-linked immunosorbent assay (ELISA) using a commercial kit (Human GFAP DuoSet ELISA Kit, DY2594-05, Lot P22599, R&D Systems, Minneapolis, USA) according to the manufacturer’s instructions. ..

    Enzyme-linked Immunosorbent Assay:

    Article Title: Plasma β-III tubulin, neurofilament light chain and glial fibrillary acidic protein are associated with neurodegeneration and progression in schizophrenia
    Article Snippet: .. GFAP levels of plasma samples of patients and healthy controls were measured by sandwich enzyme-linked immunosorbent assay (ELISA) using a commercial kit (Human GFAP DuoSet ELISA Kit, DY2594-05, Lot P22599, R&D Systems, Minneapolis, USA) according to the manufacturer’s instructions. ..

    Article Title: The Evaluation of AREG, MMP-2, CHI3L1, GFAP, and OPN Serum Combined Value in Astrocytic Glioma Patients’ Diagnosis and Prognosis
    Article Snippet: .. The protein expression in blood serum was analyzed using commercial ELISA kits: for AREG protein expression, the Ray BioTech kit (Cat. No ELH-AR) was used; for OPN, the Abcam ab192143 kit; for MMP-2, the Thermo Fisher Scientific kit KHC3081; and for CHI3L1 and GFAP, R&DSystems kits DY2599 and DY2594-05, respectively. ..

    Expressing:

    Article Title: The Evaluation of AREG, MMP-2, CHI3L1, GFAP, and OPN Serum Combined Value in Astrocytic Glioma Patients’ Diagnosis and Prognosis
    Article Snippet: .. The protein expression in blood serum was analyzed using commercial ELISA kits: for AREG protein expression, the Ray BioTech kit (Cat. No ELH-AR) was used; for OPN, the Abcam ab192143 kit; for MMP-2, the Thermo Fisher Scientific kit KHC3081; and for CHI3L1 and GFAP, R&DSystems kits DY2599 and DY2594-05, respectively. ..



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    Inclusion procedure of double negative atypical IDD, MS, AQP4‐IgG + NMOSD, and MOGAD. Of the 298 patients initially enrolled, 98 double‐negative atypical IDD, 73 AQP4‐IgG‐positive NMOSD, 23 MOGAD, and 63 MS patients were finally included in the analysis after rigorous screening. AQP4, aquaporin‐4; <t>GFAP,</t> glial fibrillary acidic protein; IDD, inflammatory demyelinating diseases; MOG, myelin oligodendrocyte glycoprotein; MOGAD, myelin oligodendrocyte glycoprotein antibody associated disease; MS, multiple sclerosis; NMOSD, neuromyelitis optica spectrum disorders.
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    Inclusion procedure of double negative atypical IDD, MS, AQP4‐IgG + NMOSD, and MOGAD. Of the 298 patients initially enrolled, 98 double‐negative atypical IDD, 73 AQP4‐IgG‐positive NMOSD, 23 MOGAD, and 63 MS patients were finally included in the analysis after rigorous screening. AQP4, aquaporin‐4; GFAP, glial fibrillary acidic protein; IDD, inflammatory demyelinating diseases; MOG, myelin oligodendrocyte glycoprotein; MOGAD, myelin oligodendrocyte glycoprotein antibody associated disease; MS, multiple sclerosis; NMOSD, neuromyelitis optica spectrum disorders.

    Journal: Annals of Clinical and Translational Neurology

    Article Title: Clinical characteristics of double negative atypical inflammatory demyelinating disease: A prospective study

    doi: 10.1002/acn3.52191

    Figure Lengend Snippet: Inclusion procedure of double negative atypical IDD, MS, AQP4‐IgG + NMOSD, and MOGAD. Of the 298 patients initially enrolled, 98 double‐negative atypical IDD, 73 AQP4‐IgG‐positive NMOSD, 23 MOGAD, and 63 MS patients were finally included in the analysis after rigorous screening. AQP4, aquaporin‐4; GFAP, glial fibrillary acidic protein; IDD, inflammatory demyelinating diseases; MOG, myelin oligodendrocyte glycoprotein; MOGAD, myelin oligodendrocyte glycoprotein antibody associated disease; MS, multiple sclerosis; NMOSD, neuromyelitis optica spectrum disorders.

    Article Snippet: Serum GFAP of double negative atypical IDD patients was quantified using commercial Human GFAP DuoSet ELISA (R&D Systems Minneapolis, MN, USA) by an independent investigator who was blinded to the result of TBA.

    Techniques:

    The specificity and sensitivity of the TBA using a rat brain indirect immunofluorescence. (A) The TBA results of the specimens that positive for AQP4‐IgG or GFAP‐IgG determined by CBA. (B) The TBA results of the specimens tested negative for AQP4‐IgG, GFAP‐IgG, and MOG‐IgG determined by CBA. AQP4, aquaporin‐4; CNS, central nervous system; IDD, inflammatory demyelinating diseases; MOGAD, myelin oligodendrocyte glycoprotein antibody‐associated disease; MS, multiple sclerosis; NIE, noninflammatory encephalopathy; NIM, noninflammatory myelopathy; NIPN, noninflammatory peripheral neuropathy; NMOSD, neuromyelitis optica spectrum disorders.

    Journal: Annals of Clinical and Translational Neurology

    Article Title: Clinical characteristics of double negative atypical inflammatory demyelinating disease: A prospective study

    doi: 10.1002/acn3.52191

    Figure Lengend Snippet: The specificity and sensitivity of the TBA using a rat brain indirect immunofluorescence. (A) The TBA results of the specimens that positive for AQP4‐IgG or GFAP‐IgG determined by CBA. (B) The TBA results of the specimens tested negative for AQP4‐IgG, GFAP‐IgG, and MOG‐IgG determined by CBA. AQP4, aquaporin‐4; CNS, central nervous system; IDD, inflammatory demyelinating diseases; MOGAD, myelin oligodendrocyte glycoprotein antibody‐associated disease; MS, multiple sclerosis; NIE, noninflammatory encephalopathy; NIM, noninflammatory myelopathy; NIPN, noninflammatory peripheral neuropathy; NMOSD, neuromyelitis optica spectrum disorders.

    Article Snippet: Serum GFAP of double negative atypical IDD patients was quantified using commercial Human GFAP DuoSet ELISA (R&D Systems Minneapolis, MN, USA) by an independent investigator who was blinded to the result of TBA.

    Techniques: Immunofluorescence

    TBA immunofluorescence patterns of autoantibodies against astrocytes, neurons, or oligodendrocyte in double negative atypical IDD patients. (A) An immunofluorescence pattern of antibodies from patients with double negative atypical IDD binding to astrocytes at rat cerebral cortex (green), similar to commercial AQP4‐IgG (red). (B) An immunofluorescence pattern of antibodies from patients with double negative atypical IDD binding to astrocytes at rat cerebral cortex (green), similar to commercial GFAP‐IgG (red). (C) An immunofluorescence pattern of antibodies from patients with double negative atypical IDD binding to neurons at rat cerebral cortex (green), similar to commercial NeuN‐IgG (red). (D) An immunofluorescence pattern of antibodies from patients with double negative atypical IDD binding to oligodendrocytes at rat cerebellum (green), similar to commercial MOG‐IgG (red). (E) Seronegative immunofluorescence pattern. Nuclei were counterstained with 4′,6‐diamidino‐2‐phenylindole (DAPI) (blue). Scale bars: 100 μm. AQP4, aquaporin‐4; GFAP, glial fibrillary acidic protein; MOG, myelin oligodendrocyte glycoprotein; NeuN, neuronal nucleus.

    Journal: Annals of Clinical and Translational Neurology

    Article Title: Clinical characteristics of double negative atypical inflammatory demyelinating disease: A prospective study

    doi: 10.1002/acn3.52191

    Figure Lengend Snippet: TBA immunofluorescence patterns of autoantibodies against astrocytes, neurons, or oligodendrocyte in double negative atypical IDD patients. (A) An immunofluorescence pattern of antibodies from patients with double negative atypical IDD binding to astrocytes at rat cerebral cortex (green), similar to commercial AQP4‐IgG (red). (B) An immunofluorescence pattern of antibodies from patients with double negative atypical IDD binding to astrocytes at rat cerebral cortex (green), similar to commercial GFAP‐IgG (red). (C) An immunofluorescence pattern of antibodies from patients with double negative atypical IDD binding to neurons at rat cerebral cortex (green), similar to commercial NeuN‐IgG (red). (D) An immunofluorescence pattern of antibodies from patients with double negative atypical IDD binding to oligodendrocytes at rat cerebellum (green), similar to commercial MOG‐IgG (red). (E) Seronegative immunofluorescence pattern. Nuclei were counterstained with 4′,6‐diamidino‐2‐phenylindole (DAPI) (blue). Scale bars: 100 μm. AQP4, aquaporin‐4; GFAP, glial fibrillary acidic protein; MOG, myelin oligodendrocyte glycoprotein; NeuN, neuronal nucleus.

    Article Snippet: Serum GFAP of double negative atypical IDD patients was quantified using commercial Human GFAP DuoSet ELISA (R&D Systems Minneapolis, MN, USA) by an independent investigator who was blinded to the result of TBA.

    Techniques: Immunofluorescence, Binding Assay