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Cytoplasmic and surface CXCR4 staining of fibrillary astrocytes, stimulated by TNF-a, with the monoclonal antibody 12G5. Note cluster of fetal neurons, center of field, that are also positive for CXCR4.

Cytoplasmic drug delivery using lysosomal-pH-responsive fast-release nanoparticles

Cytoplasmic inclusion bodies in cells infected with Orthopoxviruses, This section of the skin of a patient with hemorrhagic-type smallpox shows Guarnieri bodies and free erythrocytes below an early vesicle. Hematoxylin-eosin stain. Photographs

Cytoprotective action of adenosine in a quantitative model of mouse hindlimb ischemia and reperfusion

Cytoprotective activities of EUK-8 and EUK-134. Cytoprotection assays were conducted as described previously . Other additions

Cytoprotective cyclopeptides

Cytoprotective functions of plant phenolic compounds

CYTOS benchtop continuous microreactor system.

Cytoscribing as a method for high-precision micropositioning of cell populations. A plastic surface was cytoscribed with fibronectin by application of the cell adhesion protein by an ink jet printer. Cells attach to those areas of the plastic to which fibronectin had been applied.

Cytoscribing as a method for high-precision micropositioning of cell populations. Cytoscribing was carried out by photopolymerizing a polymer over a nonadhesive agar substratum. Cells attach selectively to the photoengraved region of the substratum.

Cytosegresomes in an alveolar macrophage . Postfixation with 1 osmium te-troxide in sodium cacodylate buffer. Embedded in Epon 812 and sectioned at 50 nm. Lead citrate and uranyl acetate. Plates 4199 and 4200

Cytosine arabinoside

Cytosine bases are susceptible to bromination at the C-5 double bond position, resulting in active intermediates capable of reacting with amine nucleophiles.

Cytosine HC1 i, inversion center

Cytosine reacts with water to form uracil. The reverse reaction occurs when uracil reacts with ammonia

Cytosine-sapphyrin conjugate attached to silica gel.

Cytoskeletal proteins are found in COPI vesicle-enriched fractions. Shown are Western blots of Golgi-budding assays. of the gradient. COPI vesicles fractionate in the middle of the gradient. Note that the presence of active Cdc42 decreased the amount of the motor protein, dynein, present in the middle vesicle fraction.

Cytoskeletal proteins in nucleus. HeLa cells were immunostained with anti-keratin 8 or anti-keratin 18 antibodies, Cells treated with detergent before the fixation. Scale bars

Cytosolic ATP measurement of HeLa cells during apoptosis by luminometer .

Cytosolic Ca increase induced by cAMP in electroporated cells loaded with fura-2-dextran at 4 h development. Mean R340 380 SEM of nine cells tested at 6.5 h is plotted versus time R340 380 was taken as a measure for Ca J.. The time of addition of cAMP .

Cytosolic Ca waves in hepatocytes is indicated for successive snapshots of the intracellular spatial Ca distribution.

Cytosolic responses recorded in wild-type cells in response to 1 pM cAMP . The chemoattractants were delivered within 1 s of the onset of recording as indicated by the arrows. Both folate- and cAMP-induced Ca responses are developmentally regulated and exhibit similar kinetics. They are dependent on the relative rather than the absolute magnitude of increases in attractant concentration. Responses began after a short delay of 5-10 s. The Ca J reaches a maximum after 25 s and then returns to basal level within 60 s after stimulation.

Cytosolic synthesis of fatty acids.

Cytotoxic activity of CI against B16 melanoina

Cytotoxic activity of compound 73



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