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引用和文献 (151)
Invitrogen™
CPM（7-二乙氨基-3-(4'-马来酰亚胺苯基)-4-甲基香豆素）
硫醇反应性香豆素 CPM 的荧光非常弱，直至与硫醇反应产生偶联物，最大激发/发射波长为 ∼384/470 nm。了解更多信息
| 货号 | 数量 |
|---|---|
| D346 | 25 mg |
货号 D346
价格（CNY)
7,694.00
Each
数量:
25 mg
价格（CNY)
7,694.00
Each
硫醇反应性香豆素 CPM 的荧光非常弱，直至与硫醇反应产生偶联物，最大激发/发射波长为 ∼384/470 nm。
仅供科研使用。不可用于诊断程序。
规格
化学反应性硫醇
发射470 nm
激发384 nm
标签或染料甲基香豆素
产品类型CPM
数量25 mg
反应一部分马来酰亚胺
运输条件室温
标签类型经典染料
Unit SizeEach
内容与储存
储存在冰箱（-5 至 -30°C）中并避光。
引用和文献 (151)
引用和文献
Abstract
Fluorescence resonance energy transfer mapping of the fourth of six nucleotide-binding sites of chloroplast coupling factor 1.
Journal:J Biol Chem
PubMed ID:1832671
Equilibrium dialysis measurements of adenine nucleotide binding to chloroplast coupling factor 1 suggest that the enzyme has six binding sites for ADP, adenylyl-beta,gamma-imidodiphosphate (AMP-PNP), and 2'(3')-O-2,4,6-trinitrophenyl-ATP (TNP-ATP). High affinity binding at all six sites requires the divalent cation, Mg2+. Three of the nucleotide-binding sites, sites 1, 2, and 3, have
Arrangement of the COOH-terminal and NH2-terminal domains of caldesmon bound to actin.
Journal:Biochemistry
PubMed ID:9092808
'Smooth muscle caldesmon is a single polypeptide chain with its NH2- and COOH-terminal domains separated by a long alpha-helix. Caldesmon was labeled at either Cys-153 in the NH2 domain or Cys-580 in the COOH domain with a variety of fluorescence probes. Fluorescence intensity, peak position, and polarization of probes on
The pleckstrin homology domain of phospholipase Cbeta transmits enzymatic activation through modulation of the membrane-domain orientation.
Journal:Biochemistry
PubMed ID:16669615
'Phospholipase Cbeta (PLCbeta) enzymes are activated by Galpha q and Gbetagamma subunits and catalyze the hydrolysis of the minor membrane lipid phosphatidylinositol 4,5-bisphosphate [PI(4,5)P2]. Activation of PLCbeta2 by Gbetagamma subunits has been shown to be conferred through its N-terminal pleckstrin homology (PH) domain, although the underlying mechanism is unclear. Also
Structural organization of chloroplast coupling factor.
Journal:Biochemistry
PubMed ID:2859887
'Fluorescence resonance energy transfer measurements have been used to construct spatial maps for the accessible sulfhydryl of the gamma subunit (dark site) and the essential tyrosine residue of the beta subunits relative to previously mapped sites on the H+-ATPase from chloroplasts. The extent of energy transfer was measured between a
Signaling through a G Protein-coupled receptor and its corresponding G protein follows a stoichiometrically limited model.
Journal:J Biol Chem
PubMed ID:17420253
'The bradykinin receptor is a G protein-coupled receptor (GPCR) that is coupled to the Galpha(q) family of heterotrimeric G proteins. In general, a GPCR can exert intracellular signals either by transiently associating with multiple diffusing G protein subunits or by activating a G protein that is stably bound to the