Comparison of Matrigel and type-I-collagen matrix architecture.

Slides:



Advertisements
Similar presentations
From: Artificial Polymeric Scaffolds as Extracellular Matrix Substitutes for Autologous Conjunctival Goblet Cell Expansion Invest. Ophthalmol. Vis. Sci..
Advertisements

Sec1p requires Boi1/2p for proper localization.
Scanning electron microscopy analysis of EGK-I to -V chick embryos.
ΔsimA yeast cells appear degraded in vivo.
Fig. 2 In vitro assessment of hESC-RPE cell sheets.
Cell wall structure. Cell wall structure. (A) Transmission electron micrograph of a section of a C. albicans cell prepared by freeze-substitution, showing.
Comparison of electron microscopy findings in paraproteins with organized fibrillar deposits. Comparison of electron microscopy findings in paraproteins.
Fig. 8 Analysis of bone structure within the soft and stiff scaffold.
Evaluation of LC3 and ATG13 dynamics in AS-stimulated microglial cells using live-imaging. Evaluation of LC3 and ATG13 dynamics in AS-stimulated microglial.
Fig. 1 Device structure, typical output performance, and cytocompatibility of BD-TENG. Device structure, typical output performance, and cytocompatibility.
Fig. 6. Ultrastructural changes in the glycocalyx of N
Fig. 1. Representative images of the four cell lines using fluorescence microscopy. Representative images of the four cell lines using fluorescence microscopy.
Fig. 2. Morphological changes of cultured adherent fibroblastic cells after OA treatment related to actin microfilament reorganization.(A) Cells observed.
A highly conserved six-amino-acid region in the C-terminal CT domain of MARCH8 is responsible for its ability to downregulate TfR. A highly conserved six-amino-acid.
Subcellular distribution of TACE-eGFP changes with the coexpression of active ERK2. Subcellular distribution of TACE-eGFP changes with the coexpression.
PARP cleavage is detected in TA cells, but not in KSC
Indirect fluorescence assay of N. gruberi cells.
IQGAPs localize at the tips of axons in hippocampal neurons.
Fig. 1. Morphological and growth characterization of hBMCs and hPDCs
Fig. 2. Transfection and clonal selection of rat pluripotent stem cells to generate stable transgenic lines. Transfection and clonal selection of rat pluripotent.
The bioactive compounds restored α-syn membrane localization, ER-to-Golgi trafficking and mitochondrial morphology. The bioactive compounds restored α-syn.
Scanning EM shows cilia abnormalities in the neural tube.
PfSec13 does not co-localize with P. falciparum heterochromatin.
Fig. 2. DDR1 over-expression enhances collagen fibril reorganization
Kinetics of induced and non-induced AR, and its relationship to cell death and motility. Kinetics of induced and non-induced AR, and its relationship to.
Severing of trailing arms during meiosis II also resulted in backward movement of acentric fragments. Severing of trailing arms during meiosis II also.
(A) Faucher and Pliska hydrophobicity plot of D2SV protein sequence.
Caspases are activated earlier in young TA (yTA) than in KSC
Fig. 6. Comparison of Plk4 with Sas-6 localization
The expression of histone H1. X::GFP in C
Acridine orange (red)- and DAPI (yellow)-stained nematocysts in tentacles of Hydra. Acridine orange (red)- and DAPI (yellow)-stained nematocysts in tentacles.
Actin network polarisation.
ArfGAP1 expression alters GBF1 recruitment to Golgi membranes.
Injection volume influences tumor architecture and desmoplastic response. Injection volume influences tumor architecture and desmoplastic response. (A)
Expression analysis of periostin in DRG
Characterization of anti-N-mPres.
N-cadherin deficient cells do not adhere or migrate.
Facilitated migration of implanted Schwann cells infected with Ad-Cdc2 viral vectors in the injured sciatic nerve. Facilitated migration of implanted Schwann.
V-ATPase and proteins involved in late endosomal protein sorting are required for efficient utilization of LDs during growth resumption. V-ATPase and proteins.
Prophase nuclear movements in wild-type, rec8 and rec7 mutant cells.
Cdc2 expression in cultured Schwann cells.
IGF1R is present in endometrial luminal epithelium at the receptive phase. IGF1R is present in endometrial luminal epithelium at the receptive phase. Endometrial.
Characterization of BMSSCs in vivo.
Defective MEK-Erk1/2 kinase activation in RIAM-depleted cells accounts for their impaired FA disassembly. Defective MEK-Erk1/2 kinase activation in RIAM-depleted.
Expression of active Rho partially rescues Erk1/2 activation and peripheral FA phenotype in RIAM-knockdown cells. Expression of active Rho partially rescues.
c-Met overexpression promotes cell rounding.
Wrch-1 localizes to focal adhesions.
CENP-F staining in prometaphase and metaphase spermatocytes from B6 and Rb/+ mice. CENP-F staining in prometaphase and metaphase spermatocytes from B6.
Downregulation of caveolin-1 by si-RNA in NIH3T3 cells increased survivin expression. Downregulation of caveolin-1 by si-RNA in NIH3T3 cells increased.
Proliferation on soft matrices is decoupled from myosin light chain phosphorylation, cell tractions, and focal adhesions. Proliferation on soft matrices.
Clustering of CD14 in the plane of the plasma membrane of LPS-stimulated cells. Clustering of CD14 in the plane of the plasma membrane of LPS-stimulated.
Depletion of COPI protein inhibits cis to trans cisternal maturation.
PtdIns(4,5)P2 dependence of TbEpsinR and TbCALM membrane targeting.
Sensory neurons grow and downregulate UCHL1 expression levels during postnatal maturation. Sensory neurons grow and downregulate UCHL1 expression levels.
Fig. 7. Analysis of dFMRP kinetics in dFMRP granules by FRAP
Role of Src and PTP-PEST in upregulation of tyrosine phosphorylation of paxillin and FAK. (A) Mock and D11 cells were pre-incubated with PP2 or PP3 (10 µM,
Generation of an inducible form of FOXN1.
Tsg protein stimulates endothelial cell migration, proliferation and collagen gel spheroid sprouting. Tsg protein stimulates endothelial cell migration,
Fig. 1 Device structure, typical output performance, and cytocompatibility of BD-TENG. Device structure, typical output performance, and cytocompatibility.
Phenotype of S. pombe cells in the presence of B21P2 or LMB
Detection and classification of dendritic spines in transfected hippocampal neurons. Detection and classification of dendritic spines in transfected hippocampal.
Recruitment of epiplakin to keratin filaments and aggregates after application of various types of stress. Recruitment of epiplakin to keratin filaments.
Ca2+-mediated differentiation of primary mouse keratinocytes is independent of epiplakin. Ca2+-mediated differentiation of primary mouse keratinocytes.
Nuclear invaginations observed in thin sections are 3D tunnels and crevices, as shown by FIB-SEM and STORM. (A) In thin section TEM, large nuclear invaginations.
Electron microscopy of SorLA intracellular localization.
Effect of myosin Vb shRNA on ezrin phosphorylation and microvilli organization in Caco-2 cells. Effect of myosin Vb shRNA on ezrin phosphorylation and.
APLF regulates genes implicated in MET during the generation of iPSCs from fibroblasts. APLF regulates genes implicated in MET during the generation of.
Disruption of Autophagy Blocks Autophagic Degradation of LDs
Fig. 4 Comparison of different catalyst loading methods and substrates in the cathode of a PEMEC (one is on the membrane and the other one is on the LGDL).
Microscopic imaging of different C
Presentation transcript:

Comparison of Matrigel and type-I-collagen matrix architecture. Comparison of Matrigel and type-I-collagen matrix architecture. Matrigel (10 mg/ml, BD Biosciences) and acid-solubilized type-I collagen (3 mg/ml, Koken, Tokyo, Japan) matrices were prepared as described for ultrastructural analysis by scanning electron microscopy (Lizarraga et al., 2009; Steffen et al., 2008). (A) Matrigel, which is commonly used as a model of the BM, forms a dense gel with small pores compared with the dimensions of a cell. (B) By contrast, type-I collagen, which is often used as a model of the interstitial matrix, forms a typical fibrillar meshwork with large pores. Scale bars: 1 μm. Renaud Poincloux et al. J Cell Sci 2009;122:3015-3024 © The Company of Biologists Limited 2009