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axiovert 135m microscope  (Carl Zeiss)


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    Structured Review

    Carl Zeiss axiovert 135m microscope
    Axiovert 135m Microscope, supplied by Carl Zeiss, 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/microscope+axiovert+135m/135+axiovert+microscope/pm39775697-74-16-16
    Average 90 stars, based on 1 article reviews
    axiovert 135m microscope - by Bioz Stars, 2026-10
    90/100 stars

    Images

    Related Articles

    other:

    Article Title: The fd phage and a peptide derived from its p8 coat protein interact with the HIV-1 Tat-NLS and inhibit its biological functions.
    Article Snippet: Filamentous fd bacteriophages are used to construct phage-display peptide libraries, which have been instrumental in selecting peptides that interact with specific domains within target molecules.. Here we demonstrate that the fd bacteriophage itself, as well as NTP8 – a synthetic peptide derived from it and bearing amino acids 1–20 of the phage p8 protein – interact with the nuclear localization signal (NLS) of the HIV-1 T i o t N t ©

    Article Title: Prestress in the extracellular matrix sensitizes latent TGF-β1 for activation
    Article Snippet: Images were taken on a microscope (Axiovert 135M; Carl Zeiss) with a camera (C10600 ORCA-R2; Hamamatsu Photonics).

    Article Title: Translocation of histone proteins across lipid bilayers and Mycoplasma membranes.
    Article Snippet: 0022-2836/$ see front matter q 2004 E Abbreviations used: Antp, Drosop protein; ARM, arginine-rich motif; BSA; B-histone, histone molecules l BSA, bovine serum albumin; chl, ch penetrating protein or peptide; LUV vesicle; MLV, multilamellar vesicle; capricolum; PTD, protein transductio E-mail address of the correspond loyter@mail.ls.huji.ac.il We show that the three core histones H2A, H3 and H4 can transverse lipid bilayers of large unilamellar vesicles (LUVs) and multilamellar vesicles (MLVs).. In contrast, the histone H2B, although able to bind to the liposomes, fails to penetrate the unilamellar and the multilamellar vesicles.. Translocation across the lipid bilayer was determined using biotin-labeled histones and an ELISA-based system.

    Article Title: Prestress in the extracellular matrix sensitizes latent TGF-β1 for activation
    Article Snippet: LTBP-1 organization by myofibroblasts on DOC-insoluble ECM. hDMfs were seeded on top of DOC-insoluble ECM produced by LTBP-1–EGFP-expressing HEK293 and allowed to adhere for 4 h. LTBP-1–EGFP (black dots) organization was recorded at 488 nm for 220 min with images taken every 15 s. Images were taken on a microscope (Axiovert 135M; Carl Zeiss) with a camera (C10600 ORCA-R2; Hamamatsu Photonics).

    Microscopy:

    Article Title: Physiological responses to pH in the freshwater microalga Limnomonas gaiensis.
    Article Snippet: .. Culture coloration was systematically and qualitatively monitored, organismal morphology and swimming behavior were regularly checked under the microscope (Axiovert 135M, Zeiss), and the cell abundances evaluated at the start and after a week of incubation using flow cytometry. .. A volume of 200 μL of homogenized culture was sampled and analyzed using a NovoCyte 3000 equipped with a 405, 488, and 640 nm laser (Agilent, Santa Clara, CA).

    Article Title: Transport of sodium and chloride across earthworm skin in vitro.
    Article Snippet: We present a new invertebrate model for the study of epithelial sodium transport in tight epithelia, the earthworm integument.. Dissected segments of earthworm integument were mounted in modified Ussing chambers and perfused with either pond water (PW) or earthworm ringer solution (ERS) on the apical side.. In order to investigate ion transport under near-in vivo physiological conditions, measurements were performed under current-clamp conditions by monitoring the transepithelial potential (VT), as well as the transepithelial resistance (RT).

    Article Title: Postnatal constriction, ATP depletion, and cell death in the mature and immature ductus arteriosus.
    Article Snippet: Max Levin, Don McCurnin, Steven R. Seidner, Bradley Yoder, Nahid Waleh, Seth Goldbarg, Christine Roman, Bao Mei Liu, Jan Borén, and Ronald I. Clyman Cardiovascular Research Institute and Department of Pediatrics, University of California, San Francisco; Wallenberg Laboratory for Cardiovascular Research, Göteborg University, Göteborg, Sweden, Departments of Pediatrics and Pathology, University of Texas Health Science Center, San Antonio, Texas; SRI International, Menlo Park, California

    Article Title: Prestress in the extracellular matrix sensitizes latent TGF-β1 for activation
    Article Snippet: Images in were taken on Zeiss-1 with a Plan Fluar objective (20×, NA 0.75 at RT; Carl Zeiss), and images were taken live with Zeiss-1 and a water immersion Apochromat objective (40×, NA 1.0 at RT; Carl Zeiss). images are obtained from Video 1 processed with MetaMorph software (Molecular Devices). .. Video 1 was taken on a microscope (Axiovert 135M; Carl Zeiss) with a camera (C10600 ORCA-R2; Hamamatsu Photonics) and a Plan Fluar objective (10×, NA 0.5 at RT; Carl Zeiss). .. Fig. S4 B images were taken on Confocal-1 with a Plan Fluar objective (40×, NA 1.30, oil immersion at RT; Nikon).

    Incubation:

    Article Title: Physiological responses to pH in the freshwater microalga Limnomonas gaiensis.
    Article Snippet: .. Culture coloration was systematically and qualitatively monitored, organismal morphology and swimming behavior were regularly checked under the microscope (Axiovert 135M, Zeiss), and the cell abundances evaluated at the start and after a week of incubation using flow cytometry. .. A volume of 200 μL of homogenized culture was sampled and analyzed using a NovoCyte 3000 equipped with a 405, 488, and 640 nm laser (Agilent, Santa Clara, CA).

    Flow Cytometry:

    Article Title: Physiological responses to pH in the freshwater microalga Limnomonas gaiensis.
    Article Snippet: .. Culture coloration was systematically and qualitatively monitored, organismal morphology and swimming behavior were regularly checked under the microscope (Axiovert 135M, Zeiss), and the cell abundances evaluated at the start and after a week of incubation using flow cytometry. .. A volume of 200 μL of homogenized culture was sampled and analyzed using a NovoCyte 3000 equipped with a 405, 488, and 640 nm laser (Agilent, Santa Clara, CA).



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