BODIPY™ FL 马来酰亚胺(BODIPY™ FL N--(2-氨乙基))马来酰亚胺)
BODIPY&trade; FL 马来酰亚胺(BODIPY&trade; FL <i>N</i>--(2-氨乙基))马来酰亚胺)
Invitrogen™

BODIPY™ FL 马来酰亚胺(BODIPY™ FL N--(2-氨乙基))马来酰亚胺)

硫醇反应性 BODIPY™ FL 马来酰亚胺可产生电中性染料偶联物,该偶联物光谱与带负电荷的荧光素染料相似。该染料缺乏离子电荷,从而对与该荧光基团偶联的标准蛋白的等电点产生的影响极小。BODIPY™ FL 染料的小尺寸和相对较长的激发态寿命经证实有助于通过荧光偏振研究配体-受体相互作用。此外,BODIPY™ FL了解更多信息
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货号数量
B102505 mg
货号 B10250
价格(CNY)
5,270.00
Each
添加至购物车
数量:
5 mg
价格(CNY)
5,270.00
Each
添加至购物车
硫醇反应性 BODIPY™ FL 马来酰亚胺可产生电中性染料偶联物,该偶联物光谱与带负电荷的荧光素染料相似。该染料缺乏离子电荷,从而对与该荧光基团偶联的标准蛋白的等电点产生的影响极小。BODIPY™ FL 染料的小尺寸和相对较长的激发态寿命经证实有助于通过荧光偏振研究配体-受体相互作用。此外,BODIPY™ FL 染料与波长较长的染料(如四甲基罗丹明和 Texas Red™ 染料)几乎没有光谱重叠,从而可用作多色应用的绿色荧光基团。
仅供科研使用。不可用于诊断程序。
规格
化学反应性硫醇
标签或染料BODIPY™ FL
产品类型马来酰亚胺
数量5 mg
反应一部分马来酰亚胺
运输条件室温
标签类型BODIPY 染料
产品线BODIPY
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 (16)

引用和文献
Abstract
Small vertical movement of a K+ channel voltage sensor measured with luminescence energy transfer.
Authors:Posson DJ, Ge P, Miller C, Bezanilla F, Selvin PR
Journal:Nature
PubMed ID:16094368
'Voltage-gated ion channels open and close in response to voltage changes across electrically excitable cell membranes. Voltage-gated potassium (Kv) channels are homotetramers with each subunit constructed from six transmembrane segments, S1-S6 (ref. 2). The voltage-sensing domain (segments S1-S4) contains charged arginine residues on S4 that move across the membrane electric ... More
Quantitation of microparticles released from coated-platelets.
Authors:Dale GL, Remenyi G, Friese P,
Journal:J Thromb Haemost
PubMed ID:16102115
'Dual agonist stimulation of platelets with thrombin and convulxin results in generation of coated-platelets, a sub-population of cells known formerly as COAT-platelets (collagen and thrombin). Coated-platelets retain several procoagulant proteins on their surface and express phosphatidylserine (PS). In this report, we utilize a new methodology to demonstrate that coated-platelets also ... More
Evaluation of disulfide reduction during receptor-mediated endocytosis by using FRET imaging.
Authors:Yang J, Chen H, Vlahov IR, Cheng JX, Low PS
Journal:Proc Natl Acad Sci U S A
PubMed ID:16950881
'Despite functional evidence for disulfide bond-reducing activity in endosomal compartments, the mechanistic details pertaining to such process (e.g., kinetics and sites of disulfide reduction) remain largely controversial. To address these questions directly, we have synthesized a previously uncharacterized fluorescent folate conjugate, folate-(BODIPY FL)-SS-rhodamine (folate-FRET), that changes fluorescence from red to ... More
An in vitro fluorescence screen to identify antivirals that disrupt hepatitis B virus capsid assembly.
Authors:Stray SJ, Johnson JM, Kopek BG, Zlotnick A
Journal:Nat Biotechnol
PubMed ID:16474383
'Virus assembly has not been routinely targeted in the development of antiviral drugs, in part because of the lack of tractable methods for screening in vitro. We have developed an in vitro assay of hepatitis B virus (HBV) capsid assembly, based on fluorescence quenching of dye-labeled capsid protein, for testing ... More
The achondroplasia mutation does not alter the dimerization energetics of the fibroblast growth factor receptor 3 transmembrane domain.
Authors:You M, Li E, Hristova K
Journal:Biochemistry
PubMed ID:16634636
The Gly380 --> Arg mutation in the TM domain of fibroblast growth factor receptor 3 (FGFR3) of the RTK family is linked to achondroplasia, the most common form of human dwarfism. The molecular mechanism of pathology induction is under debate, and two different mechanisms have been proposed to contribute to ... More