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microglia a9 cells  (ATCC)


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    ATCC microglia a9 cells
    Microglia A9 Cells, supplied by ATCC, used in various techniques. Bioz Stars score: 96/100, based on 133 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/crl+3265/SIM-A9/pm42019888-52-2-22
    Average 96 stars, based on 133 article reviews
    microglia a9 cells - by Bioz Stars, 2026-09
    96/100 stars

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    Related Articles

    In Vitro:

    Article Title: Antioxidant and Anti-Inflammatory Activity of N-acylethanolamines of Omega-3 Polyunsaturated Fatty Acids in Vitro.
    Article Snippet: acids.. Among them, ethanolamides of docosahexaenoic acid (DHEA, FA 22:6(n-3)-EA), eicosapentaenoic acid (EPEA, FA 20:5(n-3)-EA), and stearidonic acid (SDEA, FA 18:4(n-3)-EA) stand out due to their potential role in modulating inflammatory processes, oxidative stress, and cellular metabolism [1].. These ethanolamides do not exist in the brain in isolation but participate in complex metabolic pathways that ensure their interconversion and maintenance of lipid homeostasis.

    Cell Culture:

    Article Title: Antioxidant and Anti-Inflammatory Activity of N-acylethanolamines of Omega-3 Polyunsaturated Fatty Acids in Vitro.
    Article Snippet: acids.. Among them, ethanolamides of docosahexaenoic acid (DHEA, FA 22:6(n-3)-EA), eicosapentaenoic acid (EPEA, FA 20:5(n-3)-EA), and stearidonic acid (SDEA, FA 18:4(n-3)-EA) stand out due to their potential role in modulating inflammatory processes, oxidative stress, and cellular metabolism [1].. These ethanolamides do not exist in the brain in isolation but participate in complex metabolic pathways that ensure their interconversion and maintenance of lipid homeostasis.



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    Image Search Results


    Journal: bioRxiv

    Article Title: HAPI Cells are SIM-A9-related Mouse Microglial Cells Useful for In Vitro Modeling of Microglial Immunometabolism

    doi: 10.64898/2026.02.11.705385

    Figure Lengend Snippet:

    Article Snippet: The number of repeats varies greatly among cell lines, making STRs highly useful for identification by providing a cell line “fingerprint.” STR profiling revealed that HAPI cells are a 100% STR match for SIM-A9 cells, a mouse microglial cell line in the ATCC database that was reported to originate from a postnatal day 1 primary mouse microglial culture through spontaneous immortalization ( ) ( ; Figure S1).

    Techniques:

    HAPI cells express microglia-selective markers. (A) Representative image of HAPI cells immunostained for TMEM119. (B) Detection of Tmem119 polymerase chain reaction (PCR) product in sample prepared from HAPI cells, SIM-A9 cells, mouse cortex tissue, mouse bone marrow-derived macrophages (BMDMs), or Neuro2a cells. An arrow designates the band corresponding to the predicted product size of 119 base pairs (bp). (C) Detection of Cx3cr1 PCR product in the same samples evaluated in B. An arrow designates the band corresponding to the predicted 109 bp product.

    Journal: bioRxiv

    Article Title: HAPI Cells are SIM-A9-related Mouse Microglial Cells Useful for In Vitro Modeling of Microglial Immunometabolism

    doi: 10.64898/2026.02.11.705385

    Figure Lengend Snippet: HAPI cells express microglia-selective markers. (A) Representative image of HAPI cells immunostained for TMEM119. (B) Detection of Tmem119 polymerase chain reaction (PCR) product in sample prepared from HAPI cells, SIM-A9 cells, mouse cortex tissue, mouse bone marrow-derived macrophages (BMDMs), or Neuro2a cells. An arrow designates the band corresponding to the predicted product size of 119 base pairs (bp). (C) Detection of Cx3cr1 PCR product in the same samples evaluated in B. An arrow designates the band corresponding to the predicted 109 bp product.

    Article Snippet: The number of repeats varies greatly among cell lines, making STRs highly useful for identification by providing a cell line “fingerprint.” STR profiling revealed that HAPI cells are a 100% STR match for SIM-A9 cells, a mouse microglial cell line in the ATCC database that was reported to originate from a postnatal day 1 primary mouse microglial culture through spontaneous immortalization ( ) ( ; Figure S1).

    Techniques: Polymerase Chain Reaction, Derivative Assay