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The camera's unwavering stare implies that something about the original identity of the structures will be revealed.
Subsequent publications saw some of the team members disagreeing over the identity of the structures.
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In this transitional vertebra, it is difficult to determine the identity of the structure separating it from the larger spinodiapophyseal fossa on the lateral aspect of the neural spine, which could be either the eprl or the spdl.
To confirm the identity of these structures, we determined their expression of the adhesion molecule, PECAM-1 (platelet endothelial cell adhesion molecule) or CD31, known to be strongly expressed on endothelial cells lining blood vessels.
These structures also accumulated the endocytic tracer dextran (Fig. 6H″), which is taken up from the extracellular space via endocytosis and subsequently trafficked through the endocytic pathway, thus confirming the identity of these structures as endosomes.
Therefore, it is for the moment hard to conclude on the identity of these structures.
Further work is necessary to define the identity of these structures.
To verify the identity of these structures, GFP-AtRabD2b and GFP-AtRabD2c were co-transfected into Arabidopsis leaf protoplasts with the trans-Golgi marker ST-YFP [ 15], and YFP and GFP signals were observed.
The anatomical identity of these structures remains to be established, but similar to what was reported for the Euphorbia root cells, the ontogenesis of larger anthocyanin-containing vacuoles from smaller ones is reminiscent of vacuolar fusion and/or autophagy.
The vascular identity of these structures was verified by staining with PE-anti-CD31.
The identification of the podosome regulatory protein Tks5 [41], [41] as binding partner for β-dystroglycan and the demonstration that the two proteins were co-localised in podosome like structures but not in focal adhesions, further substantiates the identity of the adhesion structures in myoblasts as podosomes.
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