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21953

5(6)-Carboxytetramethylrhodamin

BioReagent, suitable for fluorescence, ≥85% (sum of isomers, HPCE)

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100 MG

€ 317,00

500 MG

€ 1.160,00

€ 317,00

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Über diesen Artikel

Empirische Formel (Hill-System):
C25H22N2O5
CAS-Nummer:
98181-63-6
Molekulargewicht:
430.45
NACRES:
NA.32
PubChem Substance ID:
329752227
UNSPSC Code:
12352116
MDL number:
MFCD16661194

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InChI

1S/2C25H22N2O5/c1-26(2)15-6-9-19-21(12-15)31-22-13-16(27(3)4)7-10-20(22)25(19)18-8-5-14(23(28)29)11-17(18)24(30)32-25;1-26(2)15-6-9-18-21(12-15)31-22-13-16(27(3)4)7-10-19(22)25(18)20-11-14(23(28)29)5-8-17(20)24(30)32-25/h2*5-13H,1-4H3,(H,28,29)

SMILES string

CN(C)c1ccc2c(Oc3cc(ccc3C24OC(=O)c5cc(ccc45)C(O)=O)N(C)C)c1.CN(C)c6ccc7c(Oc8cc(ccc8C79OC(=O)c%10ccc(cc9%10)C(O)=O)N(C)C)c6

InChI key

LBUFYZITRTUEFI-UHFFFAOYSA-N

product line

BioReagent

assay

≥85% (sum of isomers, HPCE)

form

solid

mp

≥300 °C (lit.)

solubility

DMF: soluble, DMSO: soluble

fluorescence

λex 543 nm; λem 572 nm in methanol

suitability

suitable for fluorescence

Quality Level

100

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Dieser Artikel
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5(6)-Carboxytetramethylrhodamine BioReagent, suitable for fluorescence, ≥85% (sum of isomers, HPCE)

Sigma-Aldrich

21953

5(6)-Carboxytetramethylrhodamine

Tetramethylrhodamine-5-maleimide suitable for fluorescence, ≥85% (HPLC)

Sigma-Aldrich

94506

Tetramethylrhodamine-5-maleimide

6-[Fluorescein-5(6)-carboxamido]hexanoic acid suitable for fluorescence, ≥90% (HPCE)

Sigma-Aldrich

46935

6-[Fluorescein-5(6)-carboxamido]hexanoic acid

5(6)-Carboxy-2′,7′-dichlorofluorescein BioReagent, suitable for fluorescence, ≥95% (TLC)

Sigma-Aldrich

21882

5(6)-Carboxy-2′,7′-dichlorofluorescein

suitability

suitable for fluorescence

suitability

suitable for fluorescence

suitability

suitable for fluorescence

suitability

suitable for fluorescence

fluorescence

λex 543 nm; λem 572 nm in methanol

fluorescence

λex 543 nm; λem 575 nm in 0.1 M phosphate pH 7.0

fluorescence

λex 491 nm; λem 515 nm in 0.1 M Tris pH 9.0

fluorescence

λex 504 nm; λem 529 nm in 0.1 M Tris pH 8.0

form

solid

form

powder

form

solid

form

solid

solubility

DMF: soluble, DMSO: soluble

solubility

DMSO: soluble, methanol: soluble

solubility

DMF: soluble, DMSO: soluble

solubility

DMF: soluble, DMSO: soluble, H2O: soluble (pH ≥ 5)

assay

≥85% (sum of isomers, HPCE)

assay

≥85% (HPLC)

assay

≥90% (HPCE)

assay

≥95% (TLC)

product line

BioReagent

product line

-

product line

-

product line

BioReagent

Application

Reagiert mit primären und sekundären Aminogruppen von Proteinen, Nukleinsäuren und anderen Biomolekülen.
5(6)-Carboxytetramethylrhodamine (TAMRA, TMR) may be used as a fluorescence probe to study the distribution of molecules such as cell-penetrating peptides (CPPs) and as fluorescence partner in applications such as two-dimensional fluorescence intensity distribution analysis (2D-FIDA), luminescence resonance energy transfer (LRET) and fluorescence resonance energy transfer (FRET).

Packaging

Bottomless glass bottle. Contents are inside inserted fused cone.

Lagerklasse

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

Hier finden Sie alle aktuellen Versionen:

Analysenzertifikate (COA)

Lot/Batch Number
BCCG9050
BCBX0355
BCBS8714V
BCBQ5140V
BCBM6735V

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Die Dokumentenbibliothek aufrufen

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Dongyun Liu et al.
The AAPS journal, 15(1), 288-298 (2012-12-01)
Peptide and protein drugs have become the new generation of therapeutics, yet most of them are only available as injections, and reports on oral local intestinal delivery of peptides and proteins are quite limited. The aim of this work was
P Kask et al.
Biophysical journal, 78(4), 1703-1713 (2000-03-29)
A method of sample analysis is presented which is based on fitting a joint distribution of photon count numbers. In experiments, fluorescence from a microscopic volume containing a fluctuating number of molecules is monitored by two detectors, using a confocal
Daniel Renčiuk et al.
Methods (San Diego, Calif.), 57(1), 122-128 (2012-04-03)
Some of the most serious diseases are characterized by the presence of a specific secondary structure within DNA or RNA, often in the promoter or the coding region of the responsible gene, that enhances or disrupts expression of the protein.
Yoshiaki Yano et al.
Biochemistry, 41(9), 3073-3080 (2002-02-28)
Investigation of interactions between hydrophobic model peptides and lipid bilayers is perhaps the only way to elucidate the principles of the folding and stability of membrane proteins (White, S. H., and Wimley, W. C. (1998) Biochim. Biophys. Acta 1367, 339-352).
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