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双[2-(琥珀酰亚胺基氧羰基氧基)乙基]砜

双[2-(琥珀酰亚胺基氧羰基氧基)乙基]砜结构式
双[2-(琥珀酰亚胺基氧羰基氧基)乙基]砜结构式
品牌特惠专场
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
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....

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...

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....

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...

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...

Mapping of lymphocyte surface polypeptide antigens by chemical cross-linking with BSOCOES.

J. Immunol. 124 , 913, (1980)

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...

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 ...

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...

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...