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mdbk ccl 22 cells  (ATCC)


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    ATCC mdbk ccl 22 cells
    Mdbk Ccl 22 Cells, supplied by ATCC, used in various techniques. Bioz Stars score: 96/100, based on 1631 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/mdbk+cells/MDBK/pm42277020-259-7-18
    Average 96 stars, based on 1631 article reviews
    mdbk ccl 22 cells - by Bioz Stars, 2026-10
    96/100 stars

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    Related Articles

    Virus:

    Article Title: Complete genome sequence of a Bangladesh-developed live-attenuated goatpox (GTPV) vaccine strain.
    Article Snippet: .. The virus was attenuated through serial passaging: initially in primary lamb testis cells (five passages), followed by 35 passages in Vero cells (American Type Culture Collection [ATCC] CCL-81, USA) and 25 passages in MDBK cells (ATCC CCL-22, USA). ..

    Passaging:

    Article Title: Complete genome sequence of a Bangladesh-developed live-attenuated goatpox (GTPV) vaccine strain.
    Article Snippet: .. The virus was attenuated through serial passaging: initially in primary lamb testis cells (five passages), followed by 35 passages in Vero cells (American Type Culture Collection [ATCC] CCL-81, USA) and 25 passages in MDBK cells (ATCC CCL-22, USA). ..

    Incubation:

    Article Title: Anticoccidial composition comprising ginkgo leaves and use thereof
    Article Snippet: .. 100,000 MDBK cells (purchased from ATCC) were aliquoted in a 24-well plate, and then incubated at a temperature of 37° C. for 12 hours. ..

    other:

    Article Title: A single PA-X mutation in bovine-origin H5N1 influenza virus reduces pathogenicity in mice
    Article Snippet: For the puromycin incorporation assay, NP and β-actin were detected using the same HT103 and AC-15 mouse monoclonal antibodies, and puromycin-labeled proteins were detected using the mouse anti-puromycin antibody 12D10 (Sigma).



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    A : 0.24, 2.4 or 24 μg hPBAE, with or without diRNA (at a 40:1 hPBAE:RNA weight ratio), with or without pseudouridin modification (ψ), were delivered to ( A ) Vero, ( B ) Calu-3, or ( C ) A549 cells and cell viability was measured by MTT assay. D : hPBAE–diRNA nanoparticles (0.3 μg of RNA) were delivered to MDBK cells 1 h after exposure to BCoV (MOI of 1), and the amount of BCoV genomic RNA and diRNA in cell extracts and in supernatants were measured after 1 or 24 h.

    Journal: bioRxiv

    Article Title: Delivery of defective interfering RNA antivirals using hyperbranched poly(beta-amino ester) nanoparticles

    doi: 10.64898/2026.05.29.721911

    Figure Lengend Snippet: A : 0.24, 2.4 or 24 μg hPBAE, with or without diRNA (at a 40:1 hPBAE:RNA weight ratio), with or without pseudouridin modification (ψ), were delivered to ( A ) Vero, ( B ) Calu-3, or ( C ) A549 cells and cell viability was measured by MTT assay. D : hPBAE–diRNA nanoparticles (0.3 μg of RNA) were delivered to MDBK cells 1 h after exposure to BCoV (MOI of 1), and the amount of BCoV genomic RNA and diRNA in cell extracts and in supernatants were measured after 1 or 24 h.

    Article Snippet: Eagle’s Minimum Essential Medium (EMEM) supplemented with 10% FBS was used for human hepatocellular carcinoma HepG2 cells (ATCC #HB-8065), human glioblastoma U-87 MG cells (ATCC #HTB-14), human airway epithelial Calu-3 cells (ATCC #HTB-55), human breast adenocarcinoma MCF-7 cells (ATCC #HTB-22), and bovine kidney epithelial MDBK cells (ATCC #CCL-22).

    Techniques: Modification, MTT Assay