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Citations & References (11)
Invitrogen™
6-TAMRA (6-Carboxytetramethylrhodamine), single isomer
Tetramethylrhodamine (TMR, TRITC) has been a widely used fluorophore for preparing bioconjugates, especially fluorescent antibody and avidin derivatives used in immunochemistry.
| Catalog Number | Quantity |
|---|---|
| C6122 also known as C-6122 | 10 mg |
Catalog number C6122
also known as C-6122
Price (HKD)
-
Quantity:
10 mg
Tetramethylrhodamine (TMR, TRITC) has been a widely used fluorophore for preparing bioconjugates, especially fluorescent antibody and avidin derivatives used in immunochemistry. Under the name TAMRA, the carboxylic acid of 6-TAMRA has also achieved prominence as a dye for oligonucleotide labeling and automated DNA sequencing applications.
For Research Use Only. Not for use in diagnostic procedures.
Specifications
Chemical ReactivityAmine
Label or DyeTAMRA™ Isomers, TMR (Tetramethylrhodamine)
Product Type6-TAMRA
Quantity10 mg
Reactive MoietyCarboxylic Acid
Shipping ConditionRoom Temperature
Label TypeClassic Dyes
Unit Size10 mg
Contents & Storage
Store at room temperature and protect from light.
Citations & References (11)
Citations & References
Abstract
Inter- and intramolecular fluorescence quenching of organic dyes by tryptophan.
Journal:Bioconjug Chem
PubMed ID:14624626
'Steady-state and time-resolved fluorescence measurements were performed to elucidate the fluorescence quenching of oxazine, rhodamine, carbocyanine, and bora-diaza-indacene dyes by amino acids. Among the natural amino acids, tryptophan exhibits the most pronounced quenching efficiency. Especially, the red-absorbing dyes ATTO 655, ATTO 680, and the oxazine derivative MR 121 are strongly
Toxicity of organic fluorophores used in molecular imaging: literature review.
Journal:Mol Imaging
PubMed ID:20003892
'Fluorophores are potentially useful for in vivo cancer diagnosis. Using relatively inexpensive and portable equipment, optical imaging with fluorophores permits real-time detection of cancer. However, fluorophores can be toxic and must be investigated before they can be administered safely to patients. A review of published literature on the toxicity of
Synthesis and characterization of fluorescent ubiquitin derivatives as highly sensitive substrates for the deubiquitinating enzymes UCH-L3 and USP-2.
Journal:Anal Biochem
PubMed ID:15963938
'Deubiquitinating enzymes (DUBs) catalyze the removal of attached ubiquitin molecules from amino groups of target proteins. The large family of DUBs plays an important role in the regulation of the intracellular homeostasis of different proteins and influences therefore key events such as cell division, apoptosis, etc. The DUB family members
Extending the applicability of carboxyfluorescein in solid-phase synthesis.
Journal:Bioconjug Chem
PubMed ID:12757391
'Optimized coupling protocols are presented for the efficient and automated generation of carboxyfluorescein-labeled peptides. Side products, generated when applying earlier protocols for the in situ activation of carboxyfluorescein, were eliminated by a simple procedure, yielding highly pure fluorescent peptides and minimizing postsynthesis workup. For the cost-efficient labeling of large compound
Pathway for polyarginine entry into mammalian cells.
Journal:Biochemistry
PubMed ID:14992581
Cationic peptides known as protein transduction domains (PTDs) provide a means to deliver molecules into mammalian cells. Here, nonaarginine (R(9)), the most efficacious of known PTDs, is used to elucidate the pathway for PTD internalization. Although R(9) is found in the cytosol as well as the nucleolus when cells are