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rana amurensis 57 helix a549 n d bcap 37 n d bel7402 n d bgc 823 n d h446 n d hela n d ho 8910 n d ht 29 n d  (ATCC)


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    Structured Review

    ATCC rana amurensis 57 helix a549 n d bcap 37 n d bel7402 n d bgc 823 n d h446 n d hela n d ho 8910 n d ht 29 n d
    Rana Amurensis 57 Helix A549 N D Bcap 37 N D Bel7402 N D Bgc 823 N D H446 N D Hela N D Ho 8910 N D Ht 29 N D, supplied by ATCC, used in various techniques. Bioz Stars score: 99/100, based on 9102 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/n-185/A549/pm41892485-104-27-57
    Average 99 stars, based on 9102 article reviews
    rana amurensis 57 helix a549 n d bcap 37 n d bel7402 n d bgc 823 n d h446 n d hela n d ho 8910 n d ht 29 n d - by Bioz Stars, 2026-10
    99/100 stars

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    Related Articles

    Sequencing:

    Article Title: Frog Skin Peptides: Nature's Dual-Action Weapons Against Infection and Cancer.
    Article Snippet: .. Peptide Name and Sequence Frog Species Hydrophobic Residues (%) a 3D Structure a AC Activity AB Activity Ref. Frenatin 2.1S GLVGTLLGHIGKAILG Sphaenorhynchus lacteus 50 Helix A549 (LC50 80–140 μM) 4T1 (n.d.) S. aureus ATCC 25293 (MIC 8 μM) MRSA 127/08, 145/08, 274/08, S908, T4/6, V4180 clinical isolates (MIC 8–16 μM) S. epidermidis RP62A biofilm producer, RP62A/1 biofilm non-producer variant of RP62A, T6/19 and T37/8 clinical isolates (MIC 8–16 μM) E. coli ATCC 25726 (MIC 125 μM) K. pneumoniae ATCC 700603 (MIC 250 μM) P. aeruginosa ATCC 27853 (MIC 250 μM) E. faecalis ATCC 29212 (MIC 62.5 μM) A. baumannii NM8, NM35, NM75, NM109, NM124 clinical isolates (MIC 62.5–125 μM) S. maltophilia B32/1, B32/4, B5/5, B6/2, U8708 clinical isolates (MIC 31.3–62.5 μM) X. axonopodis pv. vesicatoria (MIC 3.1–6.2 μM) * [103,104] Frenatin 2.2S GLVGTLLGHIGKAILS Sphaenorhynchus lacteus 50 Helix A549 (LC50 65 μM) S. aureus ATCC 25293 (MIC 16 μM) MRSA 127/08, 145/08, 274/08, S908, T4/6, V4180 clinical isolates (MIC 8–16 μM) S. epidermidis RP62A biofilm producer, RP62A/1 biofilm non-producer variant of RP62A, T6/19 and T37/8 clinical isolates (MIC 8–16 μM) A. baumannii NM8, NM35, NM75, NM109, NM124 clinical isolates (MIC 62.5–125 μM) S. maltophilia B32/1, B32/4, B5/5, B6/2, U8708 clinical isolates (MIC 31.3–62.5 μM) E. coli ATCC 25726 (MIC 125 μM) K. pneumoniae ATCC 700603 (MIC 250 μM) P. aeruginosa ATCC 27853 (MIC 250 μM) E. faecalis ATCC 29212 (MIC 62.5 μM) X. axonopodis pv. vesicatoria (MIC 6.2–12.5 μM) * X. arboricola pv. pruni (MIC 6.2–12.5 μM) * [103] Hylin PL FLGLIPALAGAIGNLIK Boana platanera 65 Helix A549 (LC50 58 μg/mL) HT-29 (LC50 68 μg/mL) MDA-MB-231 (LC50 58 μg/mL) E. coli DSM 787 (MIC 100 μg/mL) S. aureus ATCC 43300 (MIC 100 μg/mL) S. epidermidis DSM 28319 (MIC > 100 μg/mL) P. aeruginosa DSM 50071 (MIC > 100 μg/mL) K. pneumoniae ATCC BAA1705 (MIC > 100 μg/mL) A. baumannii DSM 30008 (MIC 100 μg/mL) E. faecalis MF 06036 (MIC 100 μg/mL) E. faecium NCTC 12201 (MIC 50 μg/mL) C. difficile R20291 or 630 BAA1382 (MIC 25–50 μg/mL) [102] https://doi.org/10.3390/antibiotics15030324 Table 1. ..

    Activity Assay:

    Article Title: Frog Skin Peptides: Nature's Dual-Action Weapons Against Infection and Cancer.
    Article Snippet: .. Peptide Name and Sequence Frog Species Hydrophobic Residues (%) a 3D Structure a AC Activity AB Activity Ref. Frenatin 2.1S GLVGTLLGHIGKAILG Sphaenorhynchus lacteus 50 Helix A549 (LC50 80–140 μM) 4T1 (n.d.) S. aureus ATCC 25293 (MIC 8 μM) MRSA 127/08, 145/08, 274/08, S908, T4/6, V4180 clinical isolates (MIC 8–16 μM) S. epidermidis RP62A biofilm producer, RP62A/1 biofilm non-producer variant of RP62A, T6/19 and T37/8 clinical isolates (MIC 8–16 μM) E. coli ATCC 25726 (MIC 125 μM) K. pneumoniae ATCC 700603 (MIC 250 μM) P. aeruginosa ATCC 27853 (MIC 250 μM) E. faecalis ATCC 29212 (MIC 62.5 μM) A. baumannii NM8, NM35, NM75, NM109, NM124 clinical isolates (MIC 62.5–125 μM) S. maltophilia B32/1, B32/4, B5/5, B6/2, U8708 clinical isolates (MIC 31.3–62.5 μM) X. axonopodis pv. vesicatoria (MIC 3.1–6.2 μM) * [103,104] Frenatin 2.2S GLVGTLLGHIGKAILS Sphaenorhynchus lacteus 50 Helix A549 (LC50 65 μM) S. aureus ATCC 25293 (MIC 16 μM) MRSA 127/08, 145/08, 274/08, S908, T4/6, V4180 clinical isolates (MIC 8–16 μM) S. epidermidis RP62A biofilm producer, RP62A/1 biofilm non-producer variant of RP62A, T6/19 and T37/8 clinical isolates (MIC 8–16 μM) A. baumannii NM8, NM35, NM75, NM109, NM124 clinical isolates (MIC 62.5–125 μM) S. maltophilia B32/1, B32/4, B5/5, B6/2, U8708 clinical isolates (MIC 31.3–62.5 μM) E. coli ATCC 25726 (MIC 125 μM) K. pneumoniae ATCC 700603 (MIC 250 μM) P. aeruginosa ATCC 27853 (MIC 250 μM) E. faecalis ATCC 29212 (MIC 62.5 μM) X. axonopodis pv. vesicatoria (MIC 6.2–12.5 μM) * X. arboricola pv. pruni (MIC 6.2–12.5 μM) * [103] Hylin PL FLGLIPALAGAIGNLIK Boana platanera 65 Helix A549 (LC50 58 μg/mL) HT-29 (LC50 68 μg/mL) MDA-MB-231 (LC50 58 μg/mL) E. coli DSM 787 (MIC 100 μg/mL) S. aureus ATCC 43300 (MIC 100 μg/mL) S. epidermidis DSM 28319 (MIC > 100 μg/mL) P. aeruginosa DSM 50071 (MIC > 100 μg/mL) K. pneumoniae ATCC BAA1705 (MIC > 100 μg/mL) A. baumannii DSM 30008 (MIC 100 μg/mL) E. faecalis MF 06036 (MIC 100 μg/mL) E. faecium NCTC 12201 (MIC 50 μg/mL) C. difficile R20291 or 630 BAA1382 (MIC 25–50 μg/mL) [102] https://doi.org/10.3390/antibiotics15030324 Table 1. ..

    Variant Assay:

    Article Title: Frog Skin Peptides: Nature's Dual-Action Weapons Against Infection and Cancer.
    Article Snippet: .. Peptide Name and Sequence Frog Species Hydrophobic Residues (%) a 3D Structure a AC Activity AB Activity Ref. Frenatin 2.1S GLVGTLLGHIGKAILG Sphaenorhynchus lacteus 50 Helix A549 (LC50 80–140 μM) 4T1 (n.d.) S. aureus ATCC 25293 (MIC 8 μM) MRSA 127/08, 145/08, 274/08, S908, T4/6, V4180 clinical isolates (MIC 8–16 μM) S. epidermidis RP62A biofilm producer, RP62A/1 biofilm non-producer variant of RP62A, T6/19 and T37/8 clinical isolates (MIC 8–16 μM) E. coli ATCC 25726 (MIC 125 μM) K. pneumoniae ATCC 700603 (MIC 250 μM) P. aeruginosa ATCC 27853 (MIC 250 μM) E. faecalis ATCC 29212 (MIC 62.5 μM) A. baumannii NM8, NM35, NM75, NM109, NM124 clinical isolates (MIC 62.5–125 μM) S. maltophilia B32/1, B32/4, B5/5, B6/2, U8708 clinical isolates (MIC 31.3–62.5 μM) X. axonopodis pv. vesicatoria (MIC 3.1–6.2 μM) * [103,104] Frenatin 2.2S GLVGTLLGHIGKAILS Sphaenorhynchus lacteus 50 Helix A549 (LC50 65 μM) S. aureus ATCC 25293 (MIC 16 μM) MRSA 127/08, 145/08, 274/08, S908, T4/6, V4180 clinical isolates (MIC 8–16 μM) S. epidermidis RP62A biofilm producer, RP62A/1 biofilm non-producer variant of RP62A, T6/19 and T37/8 clinical isolates (MIC 8–16 μM) A. baumannii NM8, NM35, NM75, NM109, NM124 clinical isolates (MIC 62.5–125 μM) S. maltophilia B32/1, B32/4, B5/5, B6/2, U8708 clinical isolates (MIC 31.3–62.5 μM) E. coli ATCC 25726 (MIC 125 μM) K. pneumoniae ATCC 700603 (MIC 250 μM) P. aeruginosa ATCC 27853 (MIC 250 μM) E. faecalis ATCC 29212 (MIC 62.5 μM) X. axonopodis pv. vesicatoria (MIC 6.2–12.5 μM) * X. arboricola pv. pruni (MIC 6.2–12.5 μM) * [103] Hylin PL FLGLIPALAGAIGNLIK Boana platanera 65 Helix A549 (LC50 58 μg/mL) HT-29 (LC50 68 μg/mL) MDA-MB-231 (LC50 58 μg/mL) E. coli DSM 787 (MIC 100 μg/mL) S. aureus ATCC 43300 (MIC 100 μg/mL) S. epidermidis DSM 28319 (MIC > 100 μg/mL) P. aeruginosa DSM 50071 (MIC > 100 μg/mL) K. pneumoniae ATCC BAA1705 (MIC > 100 μg/mL) A. baumannii DSM 30008 (MIC 100 μg/mL) E. faecalis MF 06036 (MIC 100 μg/mL) E. faecium NCTC 12201 (MIC 50 μg/mL) C. difficile R20291 or 630 BAA1382 (MIC 25–50 μg/mL) [102] https://doi.org/10.3390/antibiotics15030324 Table 1. ..

    Multiple Displacement Amplification:

    Article Title: Frog Skin Peptides: Nature's Dual-Action Weapons Against Infection and Cancer.
    Article Snippet: .. Peptide Name and Sequence Frog Species Hydrophobic Residues (%) a 3D Structure a AC Activity AB Activity Ref. Frenatin 2.1S GLVGTLLGHIGKAILG Sphaenorhynchus lacteus 50 Helix A549 (LC50 80–140 μM) 4T1 (n.d.) S. aureus ATCC 25293 (MIC 8 μM) MRSA 127/08, 145/08, 274/08, S908, T4/6, V4180 clinical isolates (MIC 8–16 μM) S. epidermidis RP62A biofilm producer, RP62A/1 biofilm non-producer variant of RP62A, T6/19 and T37/8 clinical isolates (MIC 8–16 μM) E. coli ATCC 25726 (MIC 125 μM) K. pneumoniae ATCC 700603 (MIC 250 μM) P. aeruginosa ATCC 27853 (MIC 250 μM) E. faecalis ATCC 29212 (MIC 62.5 μM) A. baumannii NM8, NM35, NM75, NM109, NM124 clinical isolates (MIC 62.5–125 μM) S. maltophilia B32/1, B32/4, B5/5, B6/2, U8708 clinical isolates (MIC 31.3–62.5 μM) X. axonopodis pv. vesicatoria (MIC 3.1–6.2 μM) * [103,104] Frenatin 2.2S GLVGTLLGHIGKAILS Sphaenorhynchus lacteus 50 Helix A549 (LC50 65 μM) S. aureus ATCC 25293 (MIC 16 μM) MRSA 127/08, 145/08, 274/08, S908, T4/6, V4180 clinical isolates (MIC 8–16 μM) S. epidermidis RP62A biofilm producer, RP62A/1 biofilm non-producer variant of RP62A, T6/19 and T37/8 clinical isolates (MIC 8–16 μM) A. baumannii NM8, NM35, NM75, NM109, NM124 clinical isolates (MIC 62.5–125 μM) S. maltophilia B32/1, B32/4, B5/5, B6/2, U8708 clinical isolates (MIC 31.3–62.5 μM) E. coli ATCC 25726 (MIC 125 μM) K. pneumoniae ATCC 700603 (MIC 250 μM) P. aeruginosa ATCC 27853 (MIC 250 μM) E. faecalis ATCC 29212 (MIC 62.5 μM) X. axonopodis pv. vesicatoria (MIC 6.2–12.5 μM) * X. arboricola pv. pruni (MIC 6.2–12.5 μM) * [103] Hylin PL FLGLIPALAGAIGNLIK Boana platanera 65 Helix A549 (LC50 58 μg/mL) HT-29 (LC50 68 μg/mL) MDA-MB-231 (LC50 58 μg/mL) E. coli DSM 787 (MIC 100 μg/mL) S. aureus ATCC 43300 (MIC 100 μg/mL) S. epidermidis DSM 28319 (MIC > 100 μg/mL) P. aeruginosa DSM 50071 (MIC > 100 μg/mL) K. pneumoniae ATCC BAA1705 (MIC > 100 μg/mL) A. baumannii DSM 30008 (MIC 100 μg/mL) E. faecalis MF 06036 (MIC 100 μg/mL) E. faecium NCTC 12201 (MIC 50 μg/mL) C. difficile R20291 or 630 BAA1382 (MIC 25–50 μg/mL) [102] https://doi.org/10.3390/antibiotics15030324 Table 1. ..

    other:

    Article Title: Nanobody-Conjugated Theranostic Prodrug Targeting α v β 3 Integrin Enables Precision Cancer Therapy With Real-Time Imaging.
    Article Snippet: SKOV3 (ovarian carcinoma, catalog numberHTB-77), A549 (lung adenocarcinoma, catalog number CCL-185), and U87MG (human glioblastoma, catalog number HTB-14) cell lines were purchased from the American Type Culture Collection (ATCC, Manassas, VA, USA).



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    Quantification of reactive oxygen species (ROS) induced by blue light irradiation. A549 cells were pretreated for 1 h with the indicated concentrations of Ir­(III) complexes. Cells were then irradiated for 1 h with blue light. Intracellular ROS were quantified using the CellRox Green probe and analyzed via flow cytometry. ROS levels are normalized to irradiated, untreated control samples. Data represent the mean ± standard deviation from three independent experiments, with duplicate samples in each run.

    Journal: Journal of Medicinal Chemistry

    Article Title: Novel 2‑(2′-Benzothiazolyl)-benzimidazole-Based Iridium(III) Photocatalysts Exhibit Antiproliferative Effects in 2D and 3D Cancer Cells to Bypass Hypoxia-Induced Resistance

    doi: 10.1021/acs.jmedchem.5c03280

    Figure Lengend Snippet: Quantification of reactive oxygen species (ROS) induced by blue light irradiation. A549 cells were pretreated for 1 h with the indicated concentrations of Ir­(III) complexes. Cells were then irradiated for 1 h with blue light. Intracellular ROS were quantified using the CellRox Green probe and analyzed via flow cytometry. ROS levels are normalized to irradiated, untreated control samples. Data represent the mean ± standard deviation from three independent experiments, with duplicate samples in each run.

    Article Snippet: Elemental analysis (C, H, N, and S) of the ancillary ligand and the iridium (III) complexes was conducted in a TruSpec Leco microanalyzer equipped with nondispersive IR detectors for C, H, and S, and a thermal conductivity detector for N. A549 and HCC827 lung adenocarcinoma cell lines were from ATCC and colon carcinoma HCT-116 cells were from ECACC.

    Techniques: Irradiation, Flow Cytometry, Control, Standard Deviation

    Intracellular colocalization studies of iridium complexes 4 and 5 in A549 cells. A549 cells were incubated with 5 μM iridium complexes for 2 h, followed by costaining with specific cell trackers for mitochondria, endoplasmic reticulum, and lysosomes. Confocal microscopy was used for imaging. Scale bars represent 20 μm.

    Journal: Journal of Medicinal Chemistry

    Article Title: Novel 2‑(2′-Benzothiazolyl)-benzimidazole-Based Iridium(III) Photocatalysts Exhibit Antiproliferative Effects in 2D and 3D Cancer Cells to Bypass Hypoxia-Induced Resistance

    doi: 10.1021/acs.jmedchem.5c03280

    Figure Lengend Snippet: Intracellular colocalization studies of iridium complexes 4 and 5 in A549 cells. A549 cells were incubated with 5 μM iridium complexes for 2 h, followed by costaining with specific cell trackers for mitochondria, endoplasmic reticulum, and lysosomes. Confocal microscopy was used for imaging. Scale bars represent 20 μm.

    Article Snippet: Elemental analysis (C, H, N, and S) of the ancillary ligand and the iridium (III) complexes was conducted in a TruSpec Leco microanalyzer equipped with nondispersive IR detectors for C, H, and S, and a thermal conductivity detector for N. A549 and HCC827 lung adenocarcinoma cell lines were from ATCC and colon carcinoma HCT-116 cells were from ECACC.

    Techniques: Incubation, Confocal Microscopy, Imaging

    Intracellular NADH depletion in A549 cells. A549 cells were treated with the respective complexes at their IC 50 concentrations for 2 h (1 h incubation in the dark followed by 1 h irradiation with blue light, 420 nm, 58 W/m 2 ). Experiments were performed in duplicate with triplicate samples per condition. Data are shown as mean ± SD. Statistical significance between dark-incubated and irradiated samples was assessed using a two-tailed t test. Significance levels are indicated as follows: * P ≤ 0.05, ** P ≤ 0.01; “ns” denotes a nonsignificant difference.

    Journal: Journal of Medicinal Chemistry

    Article Title: Novel 2‑(2′-Benzothiazolyl)-benzimidazole-Based Iridium(III) Photocatalysts Exhibit Antiproliferative Effects in 2D and 3D Cancer Cells to Bypass Hypoxia-Induced Resistance

    doi: 10.1021/acs.jmedchem.5c03280

    Figure Lengend Snippet: Intracellular NADH depletion in A549 cells. A549 cells were treated with the respective complexes at their IC 50 concentrations for 2 h (1 h incubation in the dark followed by 1 h irradiation with blue light, 420 nm, 58 W/m 2 ). Experiments were performed in duplicate with triplicate samples per condition. Data are shown as mean ± SD. Statistical significance between dark-incubated and irradiated samples was assessed using a two-tailed t test. Significance levels are indicated as follows: * P ≤ 0.05, ** P ≤ 0.01; “ns” denotes a nonsignificant difference.

    Article Snippet: Elemental analysis (C, H, N, and S) of the ancillary ligand and the iridium (III) complexes was conducted in a TruSpec Leco microanalyzer equipped with nondispersive IR detectors for C, H, and S, and a thermal conductivity detector for N. A549 and HCC827 lung adenocarcinoma cell lines were from ATCC and colon carcinoma HCT-116 cells were from ECACC.

    Techniques: Incubation, Irradiation, Two Tailed Test