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confocor 3 fcs unit  (Carl Zeiss)


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    Structured Review

    Carl Zeiss confocor 3 fcs unit
    Confocor 3 Fcs Unit, 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/fcs/confocor3+fcs+unit/pmc03733713-97-24-28
    Average 90 stars, based on 1 article reviews
    confocor 3 fcs unit - by Bioz Stars, 2026-11
    90/100 stars

    Images

    Related Articles

    Laser-Scanning Microscopy:

    Article Title: Downscaling the Analysis of Complex Transmembrane Signaling Cascades to Closed Attoliter Volumes
    Article Snippet: The vesicles were imaged with a LSM510 confocal microscope equipped with a C-Apochromat 63×/1.2NA water immersion objective (Zeiss). .. FCS measurements were performed using a LSM 510 Meta laser scanning microscope based on an Axiovert 200 M microscope stand and equipped with a ConfoCor 3 FCS unit (Zeiss). ..

    Microscopy:

    Article Title: Downscaling the Analysis of Complex Transmembrane Signaling Cascades to Closed Attoliter Volumes
    Article Snippet: The vesicles were imaged with a LSM510 confocal microscope equipped with a C-Apochromat 63×/1.2NA water immersion objective (Zeiss). .. FCS measurements were performed using a LSM 510 Meta laser scanning microscope based on an Axiovert 200 M microscope stand and equipped with a ConfoCor 3 FCS unit (Zeiss). ..

    other:

    Article Title: F2Cor: fast 2-stage correlation algorithm for FCS and DLS
    Article Snippet: Several FCS systems based on software correlators are available on the market (Confocor3 from Zeiss, TCSPC cards from Becker & Hickl and Picoquand, M9003 counting board and C9413 FCS Unit from Hamamtsu, Alba FCS system from ISS), which means that many labs are already equipped with such devices.

    Article Title: Trapped Pore Waters in the Open Proton Channel H V 1.
    Article Snippet: [49] In brief, the FCS unit (Confocor3, Carl Zeiss, Jena, Germany) of a commercial laser scanning microscope (LSM 510) measured the temporal fluctuations of the fluorescence intensity I in the focal volume of a C-Apochromat 40x/1.2 W objective.

    Article Title: The Sodium Glucose Cotransporter SGLT1 Is an Extremely Efficient Facilitator of Passive Water Transport
    Article Snippet: In brief, temporal fluctuations of the fluorescence intensity ( I ) were measured in the focal volume of a commercial laser scanning microscope (LSM 510) that was equipped with FCS unit (Confocor3; Carl Zeiss, Jena, Germany).

    Inverted Microscopy:

    Article Title: Biocompatible fluorescent silicon nanocrystals for single-molecule tracking and fluorescence imaging
    Article Snippet: .. The FCS system (ConfoCor 3; Carl Zeiss) consisted of an inverted microscope equipped with a water immersion objective lens (40×, 1.2 NA; Carl Zeiss), an Ar + laser, an avalanche photodiode, and a digital correlator. .. All samples were placed in chambered 140-μm-thick cover glasses (Lab-Tek; Thermo Fisher Scientific) and were measured at 25°C.



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    Image Search Results


    A cluster of rRNA modifications in h44 surrounds the ribosome decoding center on the 30S subunit. ( A ) Structure of the Escherichia coli 30S subunit (PDB 8FTO) with a zoomed-in view of the top of h44 and the neighboring 16S rRNA helices that form the A and P sites. ( B ) Detailed views of the structural context of each h44 methylated nucleotide m 3 U1498 (left), m 4 Cm1402 (center), and m 5 C1407 (right). The h44 methyl groups are shown as colored-coded spheres in panels A and B. ( C ) Workflow for generation of double, triple, and quadruple Rsm deletion strains. Solid line arrows denote connections from recipient strain to new deletion, and dashed line arrows indicate the DNA source for P1 phage transduction.

    Journal: Nucleic Acids Research

    Article Title: E. coli RsmF activity depends on prior modification of 16S rRNA helix 44

    doi: 10.1093/nar/gkag1005

    Figure Lengend Snippet: A cluster of rRNA modifications in h44 surrounds the ribosome decoding center on the 30S subunit. ( A ) Structure of the Escherichia coli 30S subunit (PDB 8FTO) with a zoomed-in view of the top of h44 and the neighboring 16S rRNA helices that form the A and P sites. ( B ) Detailed views of the structural context of each h44 methylated nucleotide m 3 U1498 (left), m 4 Cm1402 (center), and m 5 C1407 (right). The h44 methyl groups are shown as colored-coded spheres in panels A and B. ( C ) Workflow for generation of double, triple, and quadruple Rsm deletion strains. Solid line arrows denote connections from recipient strain to new deletion, and dashed line arrows indicate the DNA source for P1 phage transduction.

    Article Snippet: Libraries were then constructed with the Nextera XT DNA library Preparation Kit (Illumina, FC-131-1096) and Illumina DNA/RNA UD indexes at the Emory NPRC Genomics Core.

    Techniques: Methylation, Transduction