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Merck

53048

Sigma-Aldrich

5-羧基-四甲基罗丹明-琥珀酰亚胺酯

BioReagent, suitable for fluorescence

别名:

" 4-羧基四甲基罗丹明-琥珀酰亚胺酯", 5-TAMRA

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About This Item

经验公式(希尔记法):
C29H25N3O7
分子量:
527.52
MDL號碼:
分類程式碼代碼:
12352116
PubChem物質ID:
NACRES:
NA.32

產品線

BioReagent

溶解度

DMF: soluble
acetonitrile: soluble

螢光

λex 543 nm; λem 578 nm in 0.1 M phosphate pH 7.0

適合性

suitable for fluorescence

儲存溫度

−20°C

SMILES 字串

CN(C)c1ccc2c(OC3=C\C(C=CC3=C2c4ccc(cc4C([O-])=O)C(=O)ON5C(=O)CCC5=O)=[N+](\C)C)c1

InChI

1S/C29H25N3O7/c1-30(2)17-6-9-20-23(14-17)38-24-15-18(31(3)4)7-10-21(24)27(20)19-8-5-16(13-22(19)28(35)36)29(37)39-32-25(33)11-12-26(32)34/h5-10,13-15H,11-12H2,1-4H3

InChI 密鑰

VWFRSNKRTNUMET-UHFFFAOYSA-N

相关类别

應用

5-羧基-四甲基罗丹明-琥珀酰亚胺酯(5-TAMRA)用作胺偶联剂,形成5-羧基-四甲基罗丹明(5-TAMRA)衍生化合物。5-TAMRA衍生化合物可用作酶底物、分子探针、分子信标和荧光共振能量转移(FRET)配体。

其他說明

脱氧核糖核酸和核糖核酸的荧光标记

相關產品

产品编号
说明
价格

儲存類別代碼

11 - Combustible Solids

水污染物質分類(WGK)

WGK 3

閃點(°F)

Not applicable

閃點(°C)

Not applicable

個人防護裝備

Eyeshields, Gloves, type N95 (US)


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Nucleic acids research, 48(2), 949-961 (2019-11-23)
RNA aptamers-artificially created RNAs with high affinity and selectivity for their target ligand generated from random sequence pools-are versatile tools in the fields of biotechnology and medicine. On a more fundamental level, they also further our general understanding of RNA-ligand
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The journal of physical chemistry. B, 114(22), 7602-7608 (2010-05-18)
Possible interaction mechanisms between oligonucleotide (DNA) of 14 base pairs with cetyl trimethyl ammonium bromide (CTAB) were postulated based on fluorescence and fluorescence resonance energy transfer (FRET) studies. Detailed FRET investigations were carried out by fluorometric titrations of the surfactant
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Nucleic acids research, 24(22), 4535-4542 (1996-11-15)
Several procedures have been described for fluorescent labeling of DNA and RNA. They are based on the introduction of aldehyde groups by partial depurination of DNA or oxidation of the 3'-terminal ribonucleoside in RNA by sodium periodate. Fluorescent labels with
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Fluorescence/luminescence-based techniques play an increasingly important role in the development of test systems for the characterization of future drug candidates, especially in terms of receptor binding in the field of G protein-coupled receptors (GPCRs). In this article, we present the

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