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引用和文献 (25)
Invitrogen™
俄勒冈绿™ 488 马来酰亚胺
硫醇反应性 Oregon Green™ 488 马来酰亚胺可用于生成绿色荧光生物偶联物，最大激发/发射波长 ∼496/524 nm。荧光素的该氟化类似物克服了荧光素的一些关键局限性，包括更强的光稳定性和更低的 pKa（pKa了解更多信息
| 货号 | 数量 |
|---|---|
| O6034 | 5 mg |
货号 O6034
价格（CNY)
5,504.00
Each
数量:
5 mg
价格（CNY)
5,504.00
Each
硫醇反应性 Oregon Green™ 488 马来酰亚胺可用于生成绿色荧光生物偶联物，最大激发/发射波长 ∼496/524 nm。
荧光素的该氟化类似物克服了荧光素的一些关键局限性，包括更强的光稳定性和更低的 pKa（pKa ∼4.7 vs 荧光素的 6.4），使其荧光在生理 pH 值范围内基本对 pH 值不敏感。
荧光素的该氟化类似物克服了荧光素的一些关键局限性，包括更强的光稳定性和更低的 pKa（pKa ∼4.7 vs 荧光素的 6.4），使其荧光在生理 pH 值范围内基本对 pH 值不敏感。
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524
激发496
标签或染料Oregon Green™ 488
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
标签类型经典染料
产品线Oregon Green
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 (25)
引用和文献
Abstract
Effect of the substitution of muscle actin-specific subdomain 1 and 2 residues in yeast actin on actin function.
Journal:J Biol Chem
PubMed ID:16882670
'Muscle and yeast actins display distinct behavioral characteristics. To better understand the allosteric interactions that regulate actin function, we created a muscle/yeast hybrid actin containing a muscle-specific outer domain (subdomains 1 and 2) and a yeast inner domain (subdomains 3 and 4). Actin with muscle subdomain 1 and the two
Activation of human acid sphingomyelinase through modification or deletion of C-terminal cysteine.
Journal:J Biol Chem
PubMed ID:12801930
'One form of Niemann-Pick disease is caused by a deficiency in the enzymatic activity of acid sphingomyelinase. During efforts to develop an enzyme replacement therapy based on a recombinant form of human acid sphingomyelinase (rhASM), purified preparations of the recombinant enzyme were found to have substantially increased specific activity if
A pathway of structural changes produced by monastrol binding to Eg5.
Journal:J Biol Chem
PubMed ID:16434397
'Monastrol is a small molecule inhibitor that is specific for Eg5, a member of the kinesin 5 family of mitotic motors. Crystallographic models of Eg5 in the presence and absence of monastrol revealed that drug binding produces a variety of structural changes in the motor, including in loop L5 and
A fluorescent glycolipid-binding peptide probe traces cholesterol dependent microdomain-derived trafficking pathways.
Journal:PLoS ONE
PubMed ID:18716682
'BACKGROUND: The uptake and intracellular trafficking of sphingolipids, which self-associate into plasma membrane microdomains, is associated with many pathological conditions, including viral and toxin infection, lipid storage disease, and neurodegenerative disease. However, the means available to label the trafficking pathways of sphingolipids in live cells are extremely limited. In order
Structure-function relationships in OxlT, the oxalate/formate transporter of Oxalobacter formigenes. Topological features of transmembrane helix 11 as visualized by site-directed fluorescent labeling.
Journal:J Biol Chem
PubMed ID:9651403
'Analysis of hydropathy suggests that in OxlT, the oxalate/formate antiporter of Oxalobacter formigenes, lysine 355 is within transmembrane helix no. 11. To test this idea, we used single-cysteine, histidine-tagged OxlT variants to study the organization of a 30-residue segment (residues 344-373) containing this region. Topology was examined by probing the