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Primordia resolution
Primordia resolution








primordia resolution
  1. PRIMORDIA RESOLUTION PDF
  2. PRIMORDIA RESOLUTION MANUAL
primordia resolution

PRIMORDIA RESOLUTION MANUAL

Semi-automated segmentation requiring user input and manual labelling can be error prone.

  • SMC contact: cells in contact with the SMC.
  • CC (Companion Cell): L2 cells in apical domain in contact with the SMC with an elongated shape (as judged in ovule longitudinal median section using the “clipping plane” IMARIS tool).
  • resolution images, samples were stained with 50 g/mL propidium. A basal domain appears only starting stage 0-III. Separation of the site of incipient primordium formation and the meristem was carried. At stages 0-I and 0-II only an apical domain is defined.
  • Basal domain: group of cells at the basis of the primordium below the apical domain and until, but not including cells of the placental surface.
  • Apical domain: group of cells at the apex of the primordium and encompassing the SMC and direct neighbor cells.
  • L2 and 元 were not distinguished originally.
  • L1 dome: most apical cells in contact with SMC.
  • At stage 0-I, as enlargement is not always detected visually, the most apical L2 cell was then selected as candidate SMC (cSMC).
  • SMC (Spore Mother Cell): most apical central enlarged L2 cell.
  • primordia resolution

    Each ovule was manually labelled in Imaris using customized Cell Labels for the different cell types and domains colored as shown in Figure 1. Cell-boundary based image segmentation was done using ImarisCell (Bitplane) as described in details previously ( Mendocilla-Sato, 2017). We described previously the manipulation, staining, mounting of the flower carpels and imaging procedures ( Mendocilla-Sato, 2017). Although the story takes place after the game.

    PRIMORDIA RESOLUTION PDF

    Imaging of ovule primordia stained in whole-mount for cell boundary was done as described ( Mendocilla-Sato, 2017) using a laser scanning confocal microscope Leica LCS SP8 equipped with a 63X glycerol immersion objective and HyD detectors.ģD imaging and image processing (segmentation and labeling).Įntire carpels were stained using the pseudo-Schiff propidium iodide (PS-PI) cell wall staining procedure providing excellent optical transparency for 3D imaging in depth in whole-mount. illustrated PDF (Deutsche bersetzung hier traduccin espaola aqu) or ePub (smaller resolution here).










    Primordia resolution