bioimagesUnknownJulien EspeutThe Journal of Cell Biologyhttps://www.ebi.ac.uk/biostudies/studies/S-JCBD-201111107JCB

Timelapse sequence of one-cell C. elegans embryo expressing GFP::histone H2b and GFP::g-tubulin to mark chromosomes and spindle poles respectively, and KNL-1RR::mCherry 4A mutant (endogenous KNL-1 is depleted). 5 x 2 µm z-sections were acquired every 10s.

Timelapse sequence of one-cell C. elegans embryo expressing GFP::histone H2b and GFP::g-tubulin to mark chromosomes and spindle poles respectively, and KNL-1RR::mCherry wild-type (endogenous KNL-1 is depleted). This is the same image shown in Figure 2C for wild-type KLN-1. 5 x 2 µm z-sections were acquired every 10s.

Timelapse sequence of one-cell C. elegans embryo expressing GFP::histone H2b and GFP::g-tubulin to mark chromosomes and spindle poles respectively, and KNL-1RR::mCherry 4A-RRASA mutant (endogenous KNL-1 is depleted). 5 x 2 µm z-sections were acquired every 10s.

Timelapse sequence of one-cell C. elegans embryo expressing GFP::histone H2b and GFP::g-tubulin to mark chromosomes and spindle poles respectively, and KNL-1RR::mCherry wild-type (endogenous KNL-1 is depleted). This is the same image as shown in Figure 1J. 5 x 2 µm z-sections were acquired every 10s.

Timelapse sequence of one-cell C. elegans embryo expressing GFP::histone H2b and GFP::g-tubulin to mark chromosomes and spindle poles respectively, and KNL-1RR::mCherry RRASA mutant (endogenous KNL-1 is depleted). 5 x 2 µm z-sections were acquired every 10s.

bioimagesImage 132999 (Figure 2 - C)Image 133008 (Figure 2 - C)Figure 1 - JFigure 7 - BImage 133003 (Figure 7 - B)Figure 7Figure 6Image 132998 (Figure 2 - C)Figure 6 - CImage 132997 (Figure 1 - J)Figure 1Figure 2 - CImage 133000 (Figure 6 - C)Figure 2Dhanya K. CheerambathurArshad DesaiJulien EspeutLenno KrenningKaren OegemafalseMicrotubule binding by KNL-1 contributes to spindle checkpoint silencing at the kinetochore2012-02-13T11:22:42Z2018-11-29T11:22:42Z2018-11-29T11:22:42ZS-JCBD-20111110710.1083/jcb.201111107