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model p97 stereomicroscope discovery v8 zeiss inverted microscope axioobserver d1 zeiss micromanipulators eppendorf nk2 thin wall capillary tubes  (Eppendorf AG)


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    Eppendorf AG model p97 stereomicroscope discovery v8 zeiss inverted microscope axioobserver d1 zeiss micromanipulators eppendorf nk2 thin wall capillary tubes
    Model P97 Stereomicroscope Discovery V8 Zeiss Inverted Microscope Axioobserver D1 Zeiss Micromanipulators Eppendorf Nk2 Thin Wall Capillary Tubes, supplied by Eppendorf AG, used in various techniques. Bioz Stars score: 99/100, based on 201118 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/axioobserver%2Ed1+microscope/Eppendorf/pm38625797-51-108-117
    Average 99 stars, based on 201118 article reviews
    model p97 stereomicroscope discovery v8 zeiss inverted microscope axioobserver d1 zeiss micromanipulators eppendorf nk2 thin wall capillary tubes - by Bioz Stars, 2026-10
    99/100 stars

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    Related Articles

    Gradient Centrifugation:

    Article Title: Ion channel/Stat6-driven nano-immune programming of tissue-resident macrophages by amide-functionalized nanocellulose
    Article Snippet: .. To purify macrophage cells, we next performed a density gradient centrifugation using OptiprepTM (Axis-Shield; 0%, 11.2%, 17.6%, and 24%) by centrifuging at 1400× g at room temperature for 20 min. After that, the fraction between 11.2 and 17.6% was gently collected using a transfer pipette (Eppendorf), washed 3 times with 1 × HBSS buffer, and resuspended in HBSS for FACS analysis. .. For cell sorting (FACS) analysis, the single-cell populations were incubated with a mouse Fc blocker (AAT Bioquest) for 20 min on ice, followed by staining with anti-CD45 (1:200, BD Biosciences).

    Transferring:

    Article Title: Ion channel/Stat6-driven nano-immune programming of tissue-resident macrophages by amide-functionalized nanocellulose
    Article Snippet: .. To purify macrophage cells, we next performed a density gradient centrifugation using OptiprepTM (Axis-Shield; 0%, 11.2%, 17.6%, and 24%) by centrifuging at 1400× g at room temperature for 20 min. After that, the fraction between 11.2 and 17.6% was gently collected using a transfer pipette (Eppendorf), washed 3 times with 1 × HBSS buffer, and resuspended in HBSS for FACS analysis. .. For cell sorting (FACS) analysis, the single-cell populations were incubated with a mouse Fc blocker (AAT Bioquest) for 20 min on ice, followed by staining with anti-CD45 (1:200, BD Biosciences).

    Article Title: Enzyme responsive antimicrobial hyaluronan-nanocellulose hybrid wound dressings for the treatment of infected wounds
    Article Snippet: .. Protocol b) involved mixing the supernatant by gentle pipetting, then transferring of 200 μL of supernatant to a new Eppendorf tube, which was subsequently centrifuged (10 min, 10,000 rpm). .. 100 μL of the supernatant were then extracted and measured, before being returned to the second Eppendorf tube, vortexed and transferred back to the dressing-containing tube.

    FACS:

    Article Title: Ion channel/Stat6-driven nano-immune programming of tissue-resident macrophages by amide-functionalized nanocellulose
    Article Snippet: .. To purify macrophage cells, we next performed a density gradient centrifugation using OptiprepTM (Axis-Shield; 0%, 11.2%, 17.6%, and 24%) by centrifuging at 1400× g at room temperature for 20 min. After that, the fraction between 11.2 and 17.6% was gently collected using a transfer pipette (Eppendorf), washed 3 times with 1 × HBSS buffer, and resuspended in HBSS for FACS analysis. .. For cell sorting (FACS) analysis, the single-cell populations were incubated with a mouse Fc blocker (AAT Bioquest) for 20 min on ice, followed by staining with anti-CD45 (1:200, BD Biosciences).

    Amplification:

    Article Title: Immune fitness and biomarkers of immune function: Relationships with the oral and gut microbiome composition
    Article Snippet: .. Amplicon libraries were pooled in equal volumes using an epMotion 5075 automated liquid handling system (Eppendorf, Hamburg, Germany). .. The pooled library was purified using AMPure XP magnetic beads (Beckman Coulter, cat. no. A63881) at a 0.6 × (vol/vol) bead-to-sample ratio to remove primer dimers and short nonspecific fragments.

    Gentle:

    Article Title: Enzyme responsive antimicrobial hyaluronan-nanocellulose hybrid wound dressings for the treatment of infected wounds
    Article Snippet: .. Protocol b) involved mixing the supernatant by gentle pipetting, then transferring of 200 μL of supernatant to a new Eppendorf tube, which was subsequently centrifuged (10 min, 10,000 rpm). .. 100 μL of the supernatant were then extracted and measured, before being returned to the second Eppendorf tube, vortexed and transferred back to the dressing-containing tube.



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    Schematic depiction of the CWLD system for high-speed ALEX and FWM optoacoustic microscopy. ( a ) The system equips three CWLDs, each of which was controlled by a custom-designed electrical circuit driver and received ultrashort trigger signals provided by arbitrary function generators. AL, achromatic doublet lens; AMP, low noise amplifier; AWG, arbitrary waveform function generator; CWLD, continuous wave laser diode; DAQ, data acquisition card; GM, galvanometric mirror scanner; GMC, GM controller; IM, inverted <t>microscope;</t> L, plano-convex lens; M, dielectric mirror; OL, microscope objective lens; PH, pinhole; S, high-precision motorized stage; UT, ultrasound transducer. ( b ) Principle of using the CWLD for alternating laser excitation (ALEX) or Frequency-Wavelength Multiplexed (FWM) optoacoustic microscopy. (Driver inset adapted from ).
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    Image Search Results


    Journal: STAR Protocols

    Article Title: Protocol for large DNA transgenesis in mice using the Cas9+Bxb1 toolbox

    doi: 10.1016/j.xpro.2024.103022

    Figure Lengend Snippet:

    Article Snippet: Inverted microscope AxioObserver.D1 , Zeiss , .

    Techniques: Recombinant, Sequencing, Staining, Embryo Culture, Sterility, Mutagenesis, Plasmid Preparation, DNA Extraction, Software, Imaging, Nucleic Acid Electrophoresis, Electrophoresis, Electroporation, Inverted Microscopy, Transferring

    Schematic depiction of the CWLD system for high-speed ALEX and FWM optoacoustic microscopy. ( a ) The system equips three CWLDs, each of which was controlled by a custom-designed electrical circuit driver and received ultrashort trigger signals provided by arbitrary function generators. AL, achromatic doublet lens; AMP, low noise amplifier; AWG, arbitrary waveform function generator; CWLD, continuous wave laser diode; DAQ, data acquisition card; GM, galvanometric mirror scanner; GMC, GM controller; IM, inverted microscope; L, plano-convex lens; M, dielectric mirror; OL, microscope objective lens; PH, pinhole; S, high-precision motorized stage; UT, ultrasound transducer. ( b ) Principle of using the CWLD for alternating laser excitation (ALEX) or Frequency-Wavelength Multiplexed (FWM) optoacoustic microscopy. (Driver inset adapted from ).

    Journal: Scientific Reports

    Article Title: Overdriven laser diode optoacoustic microscopy

    doi: 10.1038/s41598-023-46855-w

    Figure Lengend Snippet: Schematic depiction of the CWLD system for high-speed ALEX and FWM optoacoustic microscopy. ( a ) The system equips three CWLDs, each of which was controlled by a custom-designed electrical circuit driver and received ultrashort trigger signals provided by arbitrary function generators. AL, achromatic doublet lens; AMP, low noise amplifier; AWG, arbitrary waveform function generator; CWLD, continuous wave laser diode; DAQ, data acquisition card; GM, galvanometric mirror scanner; GMC, GM controller; IM, inverted microscope; L, plano-convex lens; M, dielectric mirror; OL, microscope objective lens; PH, pinhole; S, high-precision motorized stage; UT, ultrasound transducer. ( b ) Principle of using the CWLD for alternating laser excitation (ALEX) or Frequency-Wavelength Multiplexed (FWM) optoacoustic microscopy. (Driver inset adapted from ).

    Article Snippet: The merging of the beams was achieved by longpass dichroic mirrors (DMLP490R and DMLP550R, Thorlabs) before encountering a set of high-precision galvanometric (galvo) mirrors (6215H Galvanometer Scanners, Cambridge Technologies) in combination with an inverted microscope stand (AxioObserver.D1, Zeiss) for laser-scanning.

    Techniques: Microscopy, Inverted Microscopy