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inverted microscope hoffman modulation contrast equipment  (Nikon)


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    Nikon inverted microscope hoffman modulation contrast equipment
    Inverted Microscope Hoffman Modulation Contrast Equipment, supplied by Nikon, 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/hoffman+modulation+contrast+microscope/te2000/pmc04793165-72-26-30
    Average 90 stars, based on 1 article reviews
    inverted microscope hoffman modulation contrast equipment - by Bioz Stars, 2026-09
    90/100 stars

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    Related Articles

    Microscopy:

    Article Title: Phytophthora infestans RXLR effector AVR1 disturbs the growth of Physcomitrium patens without affecting Sec5 localization
    Article Snippet: .. Phenotyping was performed using a Nikon Hoffman modulation contrast microscope equipped with an Axiocam MRc5 with Axiovision software and 4 x (Leitz Wetzlar, NA 0.12) or 20 x (Nikon MC2, NA 0.4) objectives. .. Fluorescent live-cell imaging was performed on a Roper spinning disk microscope system composed of a Nikon Ti eclipse body, Yokogawa CSU-X1 spinning disc head and a Photometrics Evolve 512 camera.

    Article Title: Hydrogen-rich electrolyzed warm water represses wrinkle formation against UVA ray together with type-I collagen production and oxidative-stress diminishment in fibroblasts and cell-injury prevention in keratinocytes.
    Article Snippet: Hydrogen-rich electrolyzed warm water (HW) was prepared at 41 C and exhibited dissolved hydrogen (DH) of 1.13 ppm and an oxidation–reduction potential (ORP) of 741 mV in contrast to below 0.01 ppm and +184 mV for regular warm water (RW).. Fibroblasts OUMS-36 and keratinocytes HaCaT were used to examine effects of HW against UVA-ray irradiation.. Type-I collagen was synthesized 1.85to 2.03-fold more abundantly by HW application for 3–5 days than RW in OUMS-36 fibroblasts, and localized preferentially around the nuclei as shown by immunostain.

    Article Title: Arabidopsis NPCC6/NaKR1 Is a Phloem Mobile Metal Binding Protein Necessary for Phloem Function and Root Meristem Maintenance
    Article Snippet: .. GUS expression images were collected using the MZFLIII dissection microscope (Leica), Hoffman modulation contrast microscope (Nikon), and Qcapture acquisition software. .. Differential interference contrast images of root meristems and starch accumulation in root columella cells and epifluorescence images of GFP and aniline blue staining were captured using a DM5000B microscope (Leica) and Leica Applicaion Suite software (version 2.4.0 R1).

    Software:

    Article Title: Phytophthora infestans RXLR effector AVR1 disturbs the growth of Physcomitrium patens without affecting Sec5 localization
    Article Snippet: .. Phenotyping was performed using a Nikon Hoffman modulation contrast microscope equipped with an Axiocam MRc5 with Axiovision software and 4 x (Leitz Wetzlar, NA 0.12) or 20 x (Nikon MC2, NA 0.4) objectives. .. Fluorescent live-cell imaging was performed on a Roper spinning disk microscope system composed of a Nikon Ti eclipse body, Yokogawa CSU-X1 spinning disc head and a Photometrics Evolve 512 camera.

    Article Title: Arabidopsis NPCC6/NaKR1 Is a Phloem Mobile Metal Binding Protein Necessary for Phloem Function and Root Meristem Maintenance
    Article Snippet: .. GUS expression images were collected using the MZFLIII dissection microscope (Leica), Hoffman modulation contrast microscope (Nikon), and Qcapture acquisition software. .. Differential interference contrast images of root meristems and starch accumulation in root columella cells and epifluorescence images of GFP and aniline blue staining were captured using a DM5000B microscope (Leica) and Leica Applicaion Suite software (version 2.4.0 R1).

    Expressing:

    Article Title: Arabidopsis NPCC6/NaKR1 Is a Phloem Mobile Metal Binding Protein Necessary for Phloem Function and Root Meristem Maintenance
    Article Snippet: .. GUS expression images were collected using the MZFLIII dissection microscope (Leica), Hoffman modulation contrast microscope (Nikon), and Qcapture acquisition software. .. Differential interference contrast images of root meristems and starch accumulation in root columella cells and epifluorescence images of GFP and aniline blue staining were captured using a DM5000B microscope (Leica) and Leica Applicaion Suite software (version 2.4.0 R1).

    Dissection:

    Article Title: Arabidopsis NPCC6/NaKR1 Is a Phloem Mobile Metal Binding Protein Necessary for Phloem Function and Root Meristem Maintenance
    Article Snippet: .. GUS expression images were collected using the MZFLIII dissection microscope (Leica), Hoffman modulation contrast microscope (Nikon), and Qcapture acquisition software. .. Differential interference contrast images of root meristems and starch accumulation in root columella cells and epifluorescence images of GFP and aniline blue staining were captured using a DM5000B microscope (Leica) and Leica Applicaion Suite software (version 2.4.0 R1).



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    Knockdown of LEDGF/p75, JPO2, menin, or HRP2 impairs tumorsphere formation in PC3-DR and DU145-DR cells. siRNA-mediated knockdowns of LEDGF/p75 ( A ), JPO2 ( B ), menin ( C ), and HRP2 ( D ) were confirmed by immunoblotting in PC3-DR and DU145-DR cells transfected with specific siRNAs (KD) compared to cells transfected with SD control oligos. Representative images of tumorsphere formation assays showing a decrease in spheroid size in PC3-DR and DU145-DR cells after individual siRNA-mediated depletion of LEDGF/p75, JPO2, menin, or HRP2 compared to SD control spheres. Tumorspheres were visualized using phase contrast or <t>Hoffman</t> <t>Modulation</t> Contrast microscopy. Tumorsphere area was quantified (bottom graphs) from triplicate images per experiment using ImageJ software. Data are from at least 3 independent experiments and are represented as mean SEM. * p < 0.05, ** p < 0.01, **** p < 0.0001.
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    Image Search Results


    Knockdown of LEDGF/p75, JPO2, menin, or HRP2 impairs tumorsphere formation in PC3-DR and DU145-DR cells. siRNA-mediated knockdowns of LEDGF/p75 ( A ), JPO2 ( B ), menin ( C ), and HRP2 ( D ) were confirmed by immunoblotting in PC3-DR and DU145-DR cells transfected with specific siRNAs (KD) compared to cells transfected with SD control oligos. Representative images of tumorsphere formation assays showing a decrease in spheroid size in PC3-DR and DU145-DR cells after individual siRNA-mediated depletion of LEDGF/p75, JPO2, menin, or HRP2 compared to SD control spheres. Tumorspheres were visualized using phase contrast or Hoffman Modulation Contrast microscopy. Tumorsphere area was quantified (bottom graphs) from triplicate images per experiment using ImageJ software. Data are from at least 3 independent experiments and are represented as mean SEM. * p < 0.05, ** p < 0.01, **** p < 0.0001.

    Journal: Cells

    Article Title: The LEDGF/p75 Integrase Binding Domain Interactome Contributes to the Survival, Clonogenicity, and Tumorsphere Formation of Docetaxel-Resistant Prostate Cancer Cells

    doi: 10.3390/cells10102723

    Figure Lengend Snippet: Knockdown of LEDGF/p75, JPO2, menin, or HRP2 impairs tumorsphere formation in PC3-DR and DU145-DR cells. siRNA-mediated knockdowns of LEDGF/p75 ( A ), JPO2 ( B ), menin ( C ), and HRP2 ( D ) were confirmed by immunoblotting in PC3-DR and DU145-DR cells transfected with specific siRNAs (KD) compared to cells transfected with SD control oligos. Representative images of tumorsphere formation assays showing a decrease in spheroid size in PC3-DR and DU145-DR cells after individual siRNA-mediated depletion of LEDGF/p75, JPO2, menin, or HRP2 compared to SD control spheres. Tumorspheres were visualized using phase contrast or Hoffman Modulation Contrast microscopy. Tumorsphere area was quantified (bottom graphs) from triplicate images per experiment using ImageJ software. Data are from at least 3 independent experiments and are represented as mean SEM. * p < 0.05, ** p < 0.01, **** p < 0.0001.

    Article Snippet: Tumorspheres were grown for 4 days at 37 °C/5% CO 2 and visualized in an Olympus IX70 microscope equipped with Phase Contrast and Hoffman Modulation Contrast, and a SPOT imaging system.

    Techniques: Western Blot, Transfection, Microscopy, Software