![]() 双[2-(琥珀酰亚胺基氧羰基氧基)乙基]砜结构式
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常用名 | 双[2-(琥珀酰亚胺基氧羰基氧基)乙基]砜 | 英文名 | Carbonic acid,C,C'-(sulfonyldi-2,1-ethanediyl) C,C'-bis(2,5-dioxo-1-pyrrolidinyl) ester |
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CAS号 | 57683-72-4 | 分子量 | 436.34800 | |
密度 | 1.67 g/cm3 | 沸点 | 636ºC at 760 mmHg | |
分子式 | C14H16N2O12S | 熔点 | 169-173ºC | |
MSDS | 中文版 美版 | 闪点 | 338.4ºC |
Extensive cross-linking of calf brain plain synaptic vesicle proteins.
Eur. J. Biochem. 145(3) , 511-7, (1984) Calf brain plain synaptic vesicle proteins have been cross-linked with bis[2-(succinimidooxycarbonyloxy)ethyl] sulfone, a homobifunctional, cleavable reagent, as well as with N-hydroxysuccinimidyl 4-azidobenzoate, a photosensitive, heterobifunctional reagent.... |
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Quaternary structure of the calf testis follitropin receptor.
J. Biol. Chem. 261(21) , 9850-3, (1986) The quaternary structural relationships between subunits of the follitropin (FSH) receptor were determined through the use of the reversible, homobifunctional, chemical cross-linking reagent bis[2-(succinimidooxycarbonyloxy)ethyl]sulfone (BSOCOES) after forma... |
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Covalent labeling of opioid receptors with radioiodinated human beta-endorphin. Identification of binding site subunit.
J. Biol. Chem. 260 , 10833, (1985) 125I-beta-Endorphin (human) binds with high affinity, specificity, and saturability to rat brain and neuroblastoma X glioma hybrid cell (NG 108-15) membranes. Dissociation constants and binding capacities were obtained from Scatchard plots and are 2 nM and 0.... |
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Quantitative evaluation of the lengths of homobifunctional protein cross-linking reagents used as molecular rulers.
Protein Sci. 10 , 1293, (2001) Homobifunctional chemical cross-linking reagents are important tools for functional and structural characterization of proteins. Accurate measures of the lengths of these molecules currently are not available, despite their widespread use. Stochastic dynamics... |
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Purification and characterization of calcitonin receptors in rat kidney membranes by covalent cross-linking techniques.
Eur. J. Biochem. 155 , 141, (1986) We have characterized the binding parameters of renal receptors (Scatchard analysis revealed the presence of two binding sites: site I, Ka1 = 1.29 X 10(9) M-1, number of binding sites = 9.9 X 10(6)/micrograms protein; site II, Ka2 = 0.93 X 10(8) M-1, number o... |
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Mapping of lymphocyte surface polypeptide antigens by chemical cross-linking with BSOCOES.
J. Immunol. 124 , 913, (1980)
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Ligand-dependent responses of the silkworm prothoracicotropic hormone receptor, Torso, are maintained by unusual intermolecular disulfide bridges in the transmembrane region.
Sci. Rep. 6 , 22437, (2016) The insect membrane-protein, Torso, is a member of the receptor-tyrosine-kinase family, and is activated by its ligand, prothoracicotropic hormone (PTTH). Although PTTH is one of the most important regulators of insect development, the mechanism of Torso acti... |
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The quaternary geometry of transcription termination factor rho: assignment by chemical cross-linking.
J. Mol. Biol. 269(4) , 514-28, (1997) Transcription termination factor rho from Escherichia coli is a ring-shaped homohexamer of 419 amino acid subunits and catalyzes an ATP-dependent release of nascent RNA transcripts. Previous chemical cross-linking studies suggested that the rho hexamer might ... |
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Cross-linking of human T cell receptor proteins: association between the T cell idiotype beta subunit and the T3 glycoprotein heavy subunit.
Cell 40(1) , 183-90, (1985) Bifunctional cross-linking reagents DSP, DSS, and BSOCOES were used to cross-link 125I-surface-labeled viable T lymphocytes. The cross-linked cells were solubilized in Nonidet-P40, immunoprecipitated with anti-Ti (monoclonal antibody T40/25) or anti-T3 (monoc... |
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Molecular characterization of helodermin-preferring VIP receptors in SUP T1 lymphoma cells: evidence for receptor glycosylation.
J. Recept. Res. 11(5) , 831-48, (1991) Cross-linking of [125I]helodermin to human SUP-T1 lymphoblasts with bis[2-(succinimidooxycarbonyloxy)ethyl]sulfone (BSOCOES) revealed a 63 K binding protein. This cross-linking was inhibited by helodermin and VIP. In cells submitted for 3-4 days to 0.2 microg... |