422-Asai-KinetochoreBeads/FigS3C_mitosis_10
Author reviewed
Z-series and time-lapse images of chromosomes and NDC80-NUF2 beads in embryo during the first mitosis
Dataset ID
FigS3C_mitosis_10
Title
Z-series and time-lapse images of chromosomes and NDC80-NUF2 beads in embryo during the first mitosis
Description
Z-series and time-lapse images of chromosomes and NDC80-NUF2 beads in embryo during the first mitosis. NDC80-NUF2 (NDC80-NUF2 heterodimer) beads were formed in the embryo as follows; The authors microinjected mRNAs encoding
C-terminally green fluorescent protein–tagged
NDC80 (NDC80-GFP) and NUF2, followed by
anti-GFP–conjugated microbeads into the cytoplasm. The mRNA for H2B-mCherry was also injected to visualize the chromosomes.
Folder Name
FigS3C_mitosis_10
Dimensions
512x512x25x4x210
Biosample
Description
Mouse embryo which was microinjected mRNAs encoding
C-terminally green fluorescent protein–tagged
NDC80 (NDC80-GFP) and NUF2, followed by
anti-GFP–conjugated microbeads (1.7 to 2.6 μm in diameter), into the cytoplasm
Extrinsic Variable
Mouse embryo was microinjected mRNAs encoding
C-terminally green fluorescent protein–tagged
NDC80 (NDC80-GFP) and NUF2, followed by
anti-GFP–conjugated microbeads (1.7 to 2.6 μm in diameter). The H2B-mCherry mRNA was also injexcted.
Ontology
Genetics
Protein / Probe
Kinetochore protein NDC80 homolog,
Kinetochore protein Nuf2
Method / Genotype
injection
Protein / Probe
Histone H2B type 1-J
Method / Genotype
injection
Treatments
Imaging Method
Visualization Method
Green fluorescent protein from Aequorea,
mCherry
Source of Contrast
distribution of a specific protein
Imaged Parameter
fluorescence emission
Sample Preparation Method
living tissue
Instrument
Objective
Zeiss 40×C-Apochromat 1.2NA