8-AHA-CAMP
8-AHA-CAMP structure
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Common Name | 8-AHA-CAMP | ||
|---|---|---|---|---|
| CAS Number | 39824-30-1 | Molecular Weight | 443.39500 | |
| Density | 1.87 g/cm3 | Boiling Point | 757.6ºC at 760 mmHg | |
| Molecular Formula | C16H26N7O6P | Melting Point | N/A | |
| MSDS | USA | Flash Point | 412ºC | |
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Analysis of epithelial cell shedding and gaps in the intestinal epithelium.
Methods Mol. Biol. 763 , 105-14, (2011) The intestinal barrier is formed by a monolayer of columnar epithelial cells. This barrier is effectively maintained despite the high turnover of epithelial cells in the gut. Defects in the mechanism by which barrier function is maintained are believed to pla... |
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4D super-resolution microscopy with conventional fluorophores and single wavelength excitation in optically thick cells and tissues.
PLoS ONE 6(5) , e20645, (2011) Optical super-resolution imaging of fluorescently stained biological samples is rapidly becoming an important tool to investigate protein distribution at the molecular scale. It is therefore important to develop practical super-resolution methods that allow c... |
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Dual-view imaging system using a wide-range dichroic mirror for simultaneous four-color single-molecule detection.
Anal. Chem. 83(18) , 6948-55, (2011) A dual-view imaging system for simultaneous four-color single-molecule (SM) detection was developed. As for the detection procedure, four species of SM fluorophores, namely, Alexa 488, 555, 647, and 680, are immobilized on different slides and excited by evan... |
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Orientation of GST-tagged lectins via in situ surface modification to create an expanded lectin microarray for glycomic analysis.
Mol. Biosyst. 7(7) , 2114-7, (2011) Herein we describe the orientation of GST-tagged lectins on NHS-activated slides via a one-step deposition of the protein and a glutathione (GSH) scaffold. This technology overcomes the need for a premade GSH-surface to orient GST-tagged proteins, enabling us... |
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In situ roughening of polymeric microstructures.
ACS Appl. Mater. Interfaces 2(4) , 1086-93, (2010) A method to perform in situ roughening of arrays of microstructures weakly adherent to an underlying substrate was presented. SU8, 1002F, and polydimethylsiloxane (PDMS) microstructures were roughened by polishing with a particle slurry. The roughness and the... |
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Differential regulation of macropinocytosis by Abi1/Hssh3bp1 isoforms.
PLoS ONE 5(5) , e10430, (2010) Macropinocytosis, which is a constitutive cellular process of fluid and macromolecule uptake, is regulated by actin cytoskeleton rearrangements near the plasma membrane. Activation of Rac1, which is proposed to act upstream of the actin polymerization regulat... |
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FSH modulates PKAI and GPR3 activities in mouse oocyte of COC in a gap junctional communication (GJC)-dependent manner to initiate meiotic resumption.
PLoS ONE 7(9) , e37835, (2012) Many studies have shown that cyclic adenosine-5'-monophosphate (cAMP)-dependent protein kinase A (PKA) and G-protein-coupled receptor 3 (GPR3) are crucial for controlling meiotic arrest in oocytes. However, it is unclear how gonadotropins modulate these facto... |
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Identification and sequence composition characterization of chondroitin sulfate-binding peptides through peptide array screening.
Biochemistry 49(7) , 1549-55, (2010) Chondroitin sulfate (CS) is an important glycosaminoglycan that has been implicated in several disease processes, such as cancer and spinal cord injury. However, few studies have characterized CS-binding protein and peptide sequences for diagnostic and therap... |
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The third dimension of ELISPOTs: quantifying antibody secretion from individual plasma cells.
J. Immunol. Methods 346(1-2) , 75-9, (2009) The enzyme-linked immunospot assay (ELISPOT) is a technique widely used to enumerate the number of immune cells secreting a specific protein, such as antibodies or cytokines. A limitation with the ELISPOT assay is that it can only be used to detect a single p... |
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Characterization of peripheral blood acetylcholine receptor-binding B cells in experimental myasthenia gravis.
Cell. Immunol. 271(2) , 292-8, (2011) In myasthenia gravis (MG), the neuromuscular transmission is impaired by antibodies (Abs) specific for muscle acetylcholine receptor (AChR). Anti-AChR Abs can be detected in the serum of MG patients, although their levels do not correlate with disease severit... |