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adult normal human brain tissue lysates  (Novus Biologicals)


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    Structured Review

    Novus Biologicals adult normal human brain tissue lysates
    a Comparison of CHSY1 gene expression in glioma subtypes and <t>normal</t> <t>brain</t> <t>tissue</t> in the REMBRANDT glioma microarray database. ** P < 0.01, **** P < 0.0001. b High expression of CHSY1 was associated with worse overall survival in glioma patients. The high and low expression groups were divided by median expression level of CHSY1 in 329 cases. These data were from the REMBRANDT database ( http://www.betastasis.com/glioma/rembrandt/ ). c Immunohistochemistry of CHSY1 (upper panel) and CS56 (lower panel) on tissue array contains 85 primary glioma cases. The staining was visualized in brown color with a 3,3-diaminobenzidine liquid substrate system. All sections were counterstained with hematoxylin. Representative images of four glioma cases with different staining intensities are shown. Amplified images are shown at the bottom right of each image. Scale bars, 50 μm. Arrows indicate positive stained glioma cells. d Representative images of CHSY1 staining on normal brain tissue ( n = 5). e Statistical analysis of immunohistochemistry in glioma tissue array. Mann–Whitney U -test was used. P -values are shown at top. f Expression of CHSY1 in glioma cell lines and normal <t>human</t> brain tissue. The protein expression was analyzed by western blotting. Total loading protein is shown at bottom. Relative expression levels to total brain tissue form three independent blots are shown at the right.
    Adult Normal Human Brain Tissue Lysates, supplied by Novus Biologicals, used in various techniques. Bioz Stars score: 93/100, based on 2 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Average 93 stars, based on 2 article reviews
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    Images

    1) Product Images from "Chondroitin sulfate synthase 1 enhances proliferation of glioblastoma by modulating PDGFRA stability"

    Article Title: Chondroitin sulfate synthase 1 enhances proliferation of glioblastoma by modulating PDGFRA stability

    Journal: Oncogenesis

    doi: 10.1038/s41389-020-0197-0

    a Comparison of CHSY1 gene expression in glioma subtypes and normal brain tissue in the REMBRANDT glioma microarray database. ** P < 0.01, **** P < 0.0001. b High expression of CHSY1 was associated with worse overall survival in glioma patients. The high and low expression groups were divided by median expression level of CHSY1 in 329 cases. These data were from the REMBRANDT database ( http://www.betastasis.com/glioma/rembrandt/ ). c Immunohistochemistry of CHSY1 (upper panel) and CS56 (lower panel) on tissue array contains 85 primary glioma cases. The staining was visualized in brown color with a 3,3-diaminobenzidine liquid substrate system. All sections were counterstained with hematoxylin. Representative images of four glioma cases with different staining intensities are shown. Amplified images are shown at the bottom right of each image. Scale bars, 50 μm. Arrows indicate positive stained glioma cells. d Representative images of CHSY1 staining on normal brain tissue ( n = 5). e Statistical analysis of immunohistochemistry in glioma tissue array. Mann–Whitney U -test was used. P -values are shown at top. f Expression of CHSY1 in glioma cell lines and normal human brain tissue. The protein expression was analyzed by western blotting. Total loading protein is shown at bottom. Relative expression levels to total brain tissue form three independent blots are shown at the right.
    Figure Legend Snippet: a Comparison of CHSY1 gene expression in glioma subtypes and normal brain tissue in the REMBRANDT glioma microarray database. ** P < 0.01, **** P < 0.0001. b High expression of CHSY1 was associated with worse overall survival in glioma patients. The high and low expression groups were divided by median expression level of CHSY1 in 329 cases. These data were from the REMBRANDT database ( http://www.betastasis.com/glioma/rembrandt/ ). c Immunohistochemistry of CHSY1 (upper panel) and CS56 (lower panel) on tissue array contains 85 primary glioma cases. The staining was visualized in brown color with a 3,3-diaminobenzidine liquid substrate system. All sections were counterstained with hematoxylin. Representative images of four glioma cases with different staining intensities are shown. Amplified images are shown at the bottom right of each image. Scale bars, 50 μm. Arrows indicate positive stained glioma cells. d Representative images of CHSY1 staining on normal brain tissue ( n = 5). e Statistical analysis of immunohistochemistry in glioma tissue array. Mann–Whitney U -test was used. P -values are shown at top. f Expression of CHSY1 in glioma cell lines and normal human brain tissue. The protein expression was analyzed by western blotting. Total loading protein is shown at bottom. Relative expression levels to total brain tissue form three independent blots are shown at the right.

    Techniques Used: Comparison, Gene Expression, Microarray, Expressing, Immunohistochemistry, Staining, Amplification, MANN-WHITNEY, Western Blot

    Related Articles

    In Situ Hybridization:

    Article Title: FIN-Seq: transcriptional profiling of specific cell types from frozen archived tissue of the human central nervous system
    Article Snippet: FFPE adult human cerebral cortex tissue from a 54-year-old female was obtained from Abcam (ab4296). .. Chromogenic double in situ hybridization was performed for the human brain tissue using the RNAscope 2.5 HD Duplex Assay (Advanced Cell Diagnostics) according to the manufacturer's protocol. .. A Fluorescent Multiplex assay was used for the human retina tissue according to the manufacturer's protocol (Advanced Cell Diagnostics).

    Article Title: FIN-Seq: Transcriptional profiling of specific cell types in frozen archived tissue from the human central nervous system
    Article Snippet: FFPE adult human cerebral cortex tissue from a 54-year-old female was obtained from Abcam (ab4296). .. Chromogenic double in situ hybridization was performed for the human brain tissue using the RNAscope 2.5 HD Duplex Assay (Advanced Cell Diagnostics) according to protocol. .. Fluorescent Multiplex assay was used for the human retina tissue according to protocol (Advanced Cell Diagnostics).

    RNAscope:

    Article Title: FIN-Seq: transcriptional profiling of specific cell types from frozen archived tissue of the human central nervous system
    Article Snippet: FFPE adult human cerebral cortex tissue from a 54-year-old female was obtained from Abcam (ab4296). .. Chromogenic double in situ hybridization was performed for the human brain tissue using the RNAscope 2.5 HD Duplex Assay (Advanced Cell Diagnostics) according to the manufacturer's protocol. .. A Fluorescent Multiplex assay was used for the human retina tissue according to the manufacturer's protocol (Advanced Cell Diagnostics).

    Article Title: Transcriptomic analysis of the human habenula in schizophrenia
    Article Snippet: .. smFISH experiments were performed on postmortem human brain tissue using RNAScope Multiplex Fluorescent Reagent Kit v2 (Advanced Cell Diagnostics) and 4-Plex Ancillary Kit as previously described . ..

    Article Title: FIN-Seq: Transcriptional profiling of specific cell types in frozen archived tissue from the human central nervous system
    Article Snippet: FFPE adult human cerebral cortex tissue from a 54-year-old female was obtained from Abcam (ab4296). .. Chromogenic double in situ hybridization was performed for the human brain tissue using the RNAscope 2.5 HD Duplex Assay (Advanced Cell Diagnostics) according to protocol. .. Fluorescent Multiplex assay was used for the human retina tissue according to protocol (Advanced Cell Diagnostics).

    Labeling:

    Article Title: Isoglutaminyl cyclase contributes to CCL2-driven neuroinflammation in Alzheimer’s disease
    Article Snippet: .. In human brain tissue, the goat antiserum sc-1784 and the mouse monoclonal antibody MAB2791 (R&D Systems) demonstrated distinct neuronal CCL2 labeling comparable to the staining pattern observed in mouse brain. ..

    Staining:

    Article Title: Isoglutaminyl cyclase contributes to CCL2-driven neuroinflammation in Alzheimer’s disease
    Article Snippet: .. In human brain tissue, the goat antiserum sc-1784 and the mouse monoclonal antibody MAB2791 (R&D Systems) demonstrated distinct neuronal CCL2 labeling comparable to the staining pattern observed in mouse brain. ..

    Multiplex Assay:

    Article Title: Transcriptomic analysis of the human habenula in schizophrenia
    Article Snippet: .. smFISH experiments were performed on postmortem human brain tissue using RNAScope Multiplex Fluorescent Reagent Kit v2 (Advanced Cell Diagnostics) and 4-Plex Ancillary Kit as previously described . ..



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    Image Search Results


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    Journal: bioRxiv

    Article Title: Viral Microglia Reprogramming Clears Oligomeric Neurotoxic Debris

    doi: 10.64898/2026.04.06.716590

    Figure Lengend Snippet: PVSRIPO directs infection of, non-cytopathogenic vRNA replication in, and IFN-I signaling in the microglial compartment in vivo . (A-C) Flow cytometry analyses of microglia before/after CD11b + -bead isolation from hCD155 -tg mouse (A, C) or human brain tissue (B) . The same kit and identical procedures were used to process human/mouse brain tissue samples (see Materials and methods ). Consistently, ∼90-95% of CD45 hi , CD11b + , MERTK + , Cx3cx1 + (A, B) and Tmem119 + (C) cells were recovered from brain tissue of either species. (D) RT-qPCR analyses of total RNA from hCD155 -tg murine or human microglia as shown. Microglia were either infected ex vivo [multiplicity of infection (MOI) 10; left and middle panels], or CD11b + -bead isolated after infection in vivo [single intracerebral inoculation of PVSRIPO (5 x 10 7 pfu); right panel]. Ipsilateral (to the site of virus inoculation) and contralateral hemispheres were processed separately. vRNA levels in mouse microglia were analyzed by two-tailed Mann-Whitney test on ΔΔCt values at 8 weeks pi (n=5; left panel); the same test was used to analyze vRNA levels in human microglia at 72hpi (n=3; right middle panel). (E) HCR-FISH analyses of vRNA species in human CD11b + -bead isolated microglia infected ex vivo with PVSRIPO (MOI 10). Two individual microglia cells at 24 and 72hpi, each, are shown. (F-G) IF and HCR-FISH analyses in non-tumor-bearing hCD155 -tg mouse brains 48h post single intracerebral PVSRIPO infusion (5 x 10 7 pfu). Tmem119 + microglia stain positive for (-)strand vRNA (F) with widespread ISG15 induction in the microglial compartment (G) .

    Article Snippet: Microglia were isolated from freshly dissected mouse brains or from epilepsy surgery human brain tissues using a CD11b + -bead isolation kit (Miltenyi MicroBeads, human & mouse; #130-097-142) as described in detail previously ( ).

    Techniques: Infection, In Vivo, Flow Cytometry, Isolation, Quantitative RT-PCR, Ex Vivo, Virus, Two Tailed Test, MANN-WHITNEY, Staining