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nih/3t3  (ATCC)


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    ATCC nih/3t3
    Nih/3t3, supplied by ATCC, used in various techniques. Bioz Stars score: 99/100, based on 13151 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/mouse+epithelial+adherent+rectal+polyploid+carcinoma+cell+line+cmt93/NIH%2F3T3/custom%40crl-1658%4030838409
    Average 99 stars, based on 13151 article reviews
    nih/3t3 - by Bioz Stars, 2026-09
    99/100 stars

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    Related Articles

    Irradiation:

    Article Title: A multifunctional DECM/PLMA hydrogel incorporated with engineered PRP-derived exosomes enabling PHD2 silencing for skin wound repair
    Article Snippet: (exosome concentration 150 μg/mL) and thoroughly mixed, followed by UV irradiation for 30s to initiate photocrosslinking and subsequent incubation at 37 °C for 1 h to complete gelation. NIH-3T3 cells (ATCC CRL-1658) and HUVECs (ATCC CRL-1730) were cultured in T25 cell culture flasks at 37 °C in a humidified atmosphere containing 95% air and 5% CO 2 . 3T3 fibroblasts and HUVECs were both cultured in

    Incubation:

    Article Title: A multifunctional DECM/PLMA hydrogel incorporated with engineered PRP-derived exosomes enabling PHD2 silencing for skin wound repair
    Article Snippet: (exosome concentration 150 μg/mL) and thoroughly mixed, followed by UV irradiation for 30s to initiate photocrosslinking and subsequent incubation at 37 °C for 1 h to complete gelation. NIH-3T3 cells (ATCC CRL-1658) and HUVECs (ATCC CRL-1730) were cultured in T25 cell culture flasks at 37 °C in a humidified atmosphere containing 95% air and 5% CO 2 . 3T3 fibroblasts and HUVECs were both cultured in

    Cell Culture:

    Article Title: A multifunctional DECM/PLMA hydrogel incorporated with engineered PRP-derived exosomes enabling PHD2 silencing for skin wound repair
    Article Snippet: (exosome concentration 150 μg/mL) and thoroughly mixed, followed by UV irradiation for 30s to initiate photocrosslinking and subsequent incubation at 37 °C for 1 h to complete gelation. NIH-3T3 cells (ATCC CRL-1658) and HUVECs (ATCC CRL-1730) were cultured in T25 cell culture flasks at 37 °C in a humidified atmosphere containing 95% air and 5% CO 2 . 3T3 fibroblasts and HUVECs were both cultured in

    Concentration Assay:

    Article Title: A multifunctional DECM/PLMA hydrogel incorporated with engineered PRP-derived exosomes enabling PHD2 silencing for skin wound repair
    Article Snippet: (exosome concentration 150 μg/mL) and thoroughly mixed, followed by UV irradiation for 30s to initiate photocrosslinking and subsequent incubation at 37 °C for 1 h to complete gelation. NIH-3T3 cells (ATCC CRL-1658) and HUVECs (ATCC CRL-1730) were cultured in T25 cell culture flasks at 37 °C in a humidified atmosphere containing 95% air and 5% CO 2 . 3T3 fibroblasts and HUVECs were both cultured in

    Formulation:

    Article Title: A multifunctional DECM/PLMA hydrogel incorporated with engineered PRP-derived exosomes enabling PHD2 silencing for skin wound repair
    Article Snippet: (exosome concentration 150 μg/mL) and thoroughly mixed, followed by UV irradiation for 30s to initiate photocrosslinking and subsequent incubation at 37 °C for 1 h to complete gelation. NIH-3T3 cells (ATCC CRL-1658) and HUVECs (ATCC CRL-1730) were cultured in T25 cell culture flasks at 37 °C in a humidified atmosphere containing 95% air and 5% CO 2 . 3T3 fibroblasts and HUVECs were both cultured in

    Mouse Assay:

    Article Title: A multifunctional DECM/PLMA hydrogel incorporated with engineered PRP-derived exosomes enabling PHD2 silencing for skin wound repair
    Article Snippet: (exosome concentration 150 μg/mL) and thoroughly mixed, followed by UV irradiation for 30s to initiate photocrosslinking and subsequent incubation at 37 °C for 1 h to complete gelation. NIH-3T3 cells (ATCC CRL-1658) and HUVECs (ATCC CRL-1730) were cultured in T25 cell culture flasks at 37 °C in a humidified atmosphere containing 95% air and 5% CO 2 . 3T3 fibroblasts and HUVECs were both cultured in

    Binding Assay:

    Article Title: A multifunctional DECM/PLMA hydrogel incorporated with engineered PRP-derived exosomes enabling PHD2 silencing for skin wound repair
    Article Snippet: (exosome concentration 150 μg/mL) and thoroughly mixed, followed by UV irradiation for 30s to initiate photocrosslinking and subsequent incubation at 37 °C for 1 h to complete gelation. NIH-3T3 cells (ATCC CRL-1658) and HUVECs (ATCC CRL-1730) were cultured in T25 cell culture flasks at 37 °C in a humidified atmosphere containing 95% air and 5% CO 2 . 3T3 fibroblasts and HUVECs were both cultured in

    Software:

    Article Title: A multifunctional DECM/PLMA hydrogel incorporated with engineered PRP-derived exosomes enabling PHD2 silencing for skin wound repair
    Article Snippet: (exosome concentration 150 μg/mL) and thoroughly mixed, followed by UV irradiation for 30s to initiate photocrosslinking and subsequent incubation at 37 °C for 1 h to complete gelation. NIH-3T3 cells (ATCC CRL-1658) and HUVECs (ATCC CRL-1730) were cultured in T25 cell culture flasks at 37 °C in a humidified atmosphere containing 95% air and 5% CO 2 . 3T3 fibroblasts and HUVECs were both cultured in

    Luciferase:

    Article Title: A multifunctional DECM/PLMA hydrogel incorporated with engineered PRP-derived exosomes enabling PHD2 silencing for skin wound repair
    Article Snippet: (exosome concentration 150 μg/mL) and thoroughly mixed, followed by UV irradiation for 30s to initiate photocrosslinking and subsequent incubation at 37 °C for 1 h to complete gelation. NIH-3T3 cells (ATCC CRL-1658) and HUVECs (ATCC CRL-1730) were cultured in T25 cell culture flasks at 37 °C in a humidified atmosphere containing 95% air and 5% CO 2 . 3T3 fibroblasts and HUVECs were both cultured in

    Lysis:

    Article Title: A multifunctional DECM/PLMA hydrogel incorporated with engineered PRP-derived exosomes enabling PHD2 silencing for skin wound repair
    Article Snippet: (exosome concentration 150 μg/mL) and thoroughly mixed, followed by UV irradiation for 30s to initiate photocrosslinking and subsequent incubation at 37 °C for 1 h to complete gelation. NIH-3T3 cells (ATCC CRL-1658) and HUVECs (ATCC CRL-1730) were cultured in T25 cell culture flasks at 37 °C in a humidified atmosphere containing 95% air and 5% CO 2 . 3T3 fibroblasts and HUVECs were both cultured in



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