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transwell dishes with pore polyester membrane inserts corning 3460  (Corning Life Sciences)

 
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    Corning Life Sciences transwell dishes with pore polyester membrane inserts corning 3460
    Transwell Dishes With Pore Polyester Membrane Inserts Corning 3460, supplied by Corning Life Sciences, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/transwell+dishes/pmc10945765__pnas__2316544121__sapp-14-2-11?v=Corning+Life+Sciences
    Average 90 stars, based on 1 article reviews
    transwell dishes with pore polyester membrane inserts corning 3460 - by Bioz Stars, 2026-07
    90/100 stars

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    transwell dishes with pore polyester membrane inserts corning 3460  (Corning Life Sciences)
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    transwell petri dishes with or without matrigel coating  (Corning Life Sciences)
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    transwell dishes  (Thermo Fisher)
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    Knockdown of ITGA5 in vitro antagonizes the oncogenic effects of F. nucleatum . (A) Western blot of integrin α5 expression in colorectal cancer (CRC) cells. (B) CCK‐8 assay of proliferation at the indicated times after treatment. (C) Colony formation assay. (D) <t>Transwell</t> assay of invasion ability. (E) Wound healing assay of migration ability. (F) Western blot to assess phosphorylation of FAK, PI3K, and Akt1 in CRC cells. ** p < 0.01, *** p < 0.001.
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    transwell petri dishes with or without matrigel  (Corning Life Sciences)
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    Knockdown of ITGA5 in vitro antagonizes the oncogenic effects of F. nucleatum . (A) Western blot of integrin α5 expression in colorectal cancer (CRC) cells. (B) CCK‐8 assay of proliferation at the indicated times after treatment. (C) Colony formation assay. (D) <t>Transwell</t> assay of invasion ability. (E) Wound healing assay of migration ability. (F) Western blot to assess phosphorylation of FAK, PI3K, and Akt1 in CRC cells. ** p < 0.01, *** p < 0.001.
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    transwell dishes corning 0.4 μm polycarbonate membrane 24 well plate  (Corning Life Sciences)
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    Corning Life Sciences transwell dishes corning 0.4 μm polycarbonate membrane 24 well plate
    Knockdown of ITGA5 in vitro antagonizes the oncogenic effects of F. nucleatum . (A) Western blot of integrin α5 expression in colorectal cancer (CRC) cells. (B) CCK‐8 assay of proliferation at the indicated times after treatment. (C) Colony formation assay. (D) <t>Transwell</t> assay of invasion ability. (E) Wound healing assay of migration ability. (F) Western blot to assess phosphorylation of FAK, PI3K, and Akt1 in CRC cells. ** p < 0.01, *** p < 0.001.
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    transwell dishes  (Corning Life Sciences)
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    Knockdown of ITGA5 in vitro antagonizes the oncogenic effects of F. nucleatum . (A) Western blot of integrin α5 expression in colorectal cancer (CRC) cells. (B) CCK‐8 assay of proliferation at the indicated times after treatment. (C) Colony formation assay. (D) <t>Transwell</t> assay of invasion ability. (E) Wound healing assay of migration ability. (F) Western blot to assess phosphorylation of FAK, PI3K, and Akt1 in CRC cells. ** p < 0.01, *** p < 0.001.
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    collagen-coated transwell culture dishes #3401  (Corning Life Sciences)
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    Corning Life Sciences collagen-coated transwell culture dishes #3401
    Schematic design of the study. A We detected CB1R and CB2R expression in TF-1, TF-1a and THP-1 cells. B We prepared the nanoparticles using the emulsion evaporation method and characterized them by analyzing their PDI, zeta potential, surface charge, size, morphology, EE, release profile and invasion profile using DLS, SEM, LC‒MS/MS and in vitro invasion assays, respectively. C We analyzed the effect of nanoparticles on TF-1, TF-1a and THP-1 cell viability using SEM, TEM and MTT assays. D We detected the migratory effect of nanoparticles on TF-1, TF-1a and THP-1 cells using a <t>transwell</t> migration assay
    Collagen Coated Transwell Culture Dishes #3401, supplied by Corning Life Sciences, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Image Search Results


    Knockdown of ITGA5 in vitro antagonizes the oncogenic effects of F. nucleatum . (A) Western blot of integrin α5 expression in colorectal cancer (CRC) cells. (B) CCK‐8 assay of proliferation at the indicated times after treatment. (C) Colony formation assay. (D) Transwell assay of invasion ability. (E) Wound healing assay of migration ability. (F) Western blot to assess phosphorylation of FAK, PI3K, and Akt1 in CRC cells. ** p < 0.01, *** p < 0.001.

    Journal: MedComm

    Article Title: Fusobacterium nucleatum Promotes the Growth and Metastasis of Colorectal Cancer by Activating E‐Cadherin/Krüppel‐Like Factor 4/Integrin α5 Signaling in a Calcium‐Dependent Manner

    doi: 10.1002/mco2.70137

    Figure Lengend Snippet: Knockdown of ITGA5 in vitro antagonizes the oncogenic effects of F. nucleatum . (A) Western blot of integrin α5 expression in colorectal cancer (CRC) cells. (B) CCK‐8 assay of proliferation at the indicated times after treatment. (C) Colony formation assay. (D) Transwell assay of invasion ability. (E) Wound healing assay of migration ability. (F) Western blot to assess phosphorylation of FAK, PI3K, and Akt1 in CRC cells. ** p < 0.01, *** p < 0.001.

    Article Snippet: For invasion assay, Matrigel (Corning, USA) was added to the upper chamber of transwell dishes (Thermo Fisher Scientific, USA), and incubated for 1 h at 37°C.

    Techniques: Knockdown, In Vitro, Western Blot, Expressing, CCK-8 Assay, Colony Assay, Transwell Assay, Wound Healing Assay, Migration, Phospho-proteomics

    Schematic design of the study. A We detected CB1R and CB2R expression in TF-1, TF-1a and THP-1 cells. B We prepared the nanoparticles using the emulsion evaporation method and characterized them by analyzing their PDI, zeta potential, surface charge, size, morphology, EE, release profile and invasion profile using DLS, SEM, LC‒MS/MS and in vitro invasion assays, respectively. C We analyzed the effect of nanoparticles on TF-1, TF-1a and THP-1 cell viability using SEM, TEM and MTT assays. D We detected the migratory effect of nanoparticles on TF-1, TF-1a and THP-1 cells using a transwell migration assay

    Journal: Stem Cell Research & Therapy

    Article Title: 2-AG-loaded and bone marrow-targeted PCL nanoparticles as nanoplatforms for hematopoietic cell line mobilization

    doi: 10.1186/s13287-024-03902-1

    Figure Lengend Snippet: Schematic design of the study. A We detected CB1R and CB2R expression in TF-1, TF-1a and THP-1 cells. B We prepared the nanoparticles using the emulsion evaporation method and characterized them by analyzing their PDI, zeta potential, surface charge, size, morphology, EE, release profile and invasion profile using DLS, SEM, LC‒MS/MS and in vitro invasion assays, respectively. C We analyzed the effect of nanoparticles on TF-1, TF-1a and THP-1 cell viability using SEM, TEM and MTT assays. D We detected the migratory effect of nanoparticles on TF-1, TF-1a and THP-1 cells using a transwell migration assay

    Article Snippet: hCMEC/D3 cells were expanded on the filter of collagen-coated transwell culture dishes (#3401, Corning) for 5 days.

    Techniques: Expressing, Emulsion, Evaporation, Zeta Potential Analyzer, In Vitro, Transwell Migration Assay