Search
Citations & References (16)
Invitrogen™
Texas Red™ C2 Maleimide
チオール反応性のTexas Red™ C2マレイミドを使用すると、最大励起／最大発光波長が約595/615 nmの明るい赤色蛍光バイオコンジュゲートを作成できます。詳細を見る
| 製品番号（カタログ番号） | 数量 |
|---|---|
| T6008 または、製品番号T-6008 | 5 mg |
製品番号（カタログ番号） T6008
または、製品番号T-6008
価格（JPY）お問い合わせください ›
62,700
5 mg
数量:
5 mg
チオール反応性のTexas Red™ C2マレイミドを使用すると、最大励起／最大発光波長が約595/615 nmの明るい赤色蛍光バイオコンジュゲートを作成できます。
研究用にのみ使用できます。診断用には使用いただけません。
仕様
化学反応性チオール
発光615
励起595
標識または色素Texas Red™
製品タイプマレイミド
数量5 mg
反応性部分マレイミド
出荷条件室温
標識タイプ従来の色素
製品ラインTexas Red
Unit Size5 mg
組成および保存条件
フリーザー(-5∼-30度)に保存し、遮光してください。
引用および参考文献 (16)
引用および参考文献
Abstract
Sampling unfolding intermediates in calmodulin by single-molecule spectroscopy.
Journal:J Am Chem Soc
PubMed ID:16117552
'We used single-pair fluorescence resonance energy transfer (spFRET) measurements to characterize denatured and partially denatured states of the multidomain calcium signaling protein calmodulin (CaM) in both its apo and Ca(2+)-bound forms. The results demonstrate the existence of an unfolding intermediate. A CaM mutant (CaM-T34C-T110C) was doubly labeled with fluorescent probes
An allosteric mechanism controls antigen presentation by the H-2K(b) complex.
Journal:Biochemistry
PubMed ID:10508421
'The mechanism of assembly/dissociation of a recombinant water-soluble class I major histocompatibility complex (MHC) H-2Kb molecule was studied by a real-time fluorescence resonance energy transfer method. Like the H-2Kd ternary complex [Gakamsky et al. (1996) Biochemistry 35, 14841-14848], the interactions among the heavy chain, beta2-microglobulin (beta2m), and antigenic peptides were
High-throughput investigation of osteoblast response to polymer crystallinity: influence of nanometer-scale roughness on proliferation.
Journal:Biomaterials
PubMed ID:14643595
'A high-throughput method for analyzing cellular response to crystallinity in a polymer material is presented. Variations in crystallinity lead to changes in surface roughness on nanometer length scales, and it is shown that cells are exquisitely sensitive to these changes. Gradients of polymer crystallinity were fabricated on films of poly(L-lactic
Fluorescence labeling, purification, and immobilization of a double cysteine mutant calmodulin fusion protein for single-molecule experiments.
Journal:Anal Biochem
PubMed ID:14751262
'We present a method of labeling and immobilizing a low-molecular-weight protein, calmodulin (CaM), by fusion to a larger protein, maltose binding protein (MBP), for single-molecule fluorescence experiments. Immobilization in an agarose gel matrix eliminates potential interactions of the protein and the fluorophore(s) with a glass surface and allows prolonged monitoring
Influence of ADP on cross-bridge-dependent activation of myofibrillar thin filaments.
Journal:Biophys J
PubMed ID:10827987
'Contraction of skeletal muscle is regulated by calcium at the level of the thin filament via troponin and tropomyosin. Studies have indicated that strong cross-bridge binding is also involved in activation of the thin filament. To further test this, myofibrils were incubated with a wide range of fluorescent myosin subfragment