M041080

Fluorescein Phosphoramidite

Name: Fluorescein Phosphoramidite
Brand: SIGMA
Price: 139 USD

configured for PerkinElmer, configured for Polygen

Synonym(s):

Fluorescein amidite

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0.1 G

$139.00

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About This Item

Empirical Formula (Hill Notation):

C₄₆H₅₈N₃O₁₀P

Molecular Weight:

843.94

NACRES:

NA.21

PubChem Substance ID:

329817775

UNSPSC Code:

41116105

MDL number:

MFCD08062008

Key Documents

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Product Name

Fluorescein Phosphoramidite, configured for PerkinElmer, configured for Polygen

InChI

1S/C46H58N3O10P/c1-29(2)49(30(3)4)60(55-25-15-22-47)54-24-14-12-11-13-23-48-40(50)31-16-19-35-34(26-31)41(51)59-46(35)36-20-17-32(56-42(52)44(5,6)7)27-38(36)58-39-28-33(18-21-37(39)46)57-43(53)45(8,9)10/h16-21,26-30H,11-15,23-25H2,1-10H3,(H,48,50)

SMILES string

CC(C)N(C(C)C)P(OCCCCCCNC(=O)c1ccc2c(c1)C(=O)OC23c4ccc(OC(=O)C(C)(C)C)cc4Oc5cc(OC(=O)C(C)(C)C)ccc35)OCCC#N

InChI key

XUQUNBOKLNVMMK-UHFFFAOYSA-N

type

for DNA synthesis

product line

Proligo Reagents

assay

≥95% (³¹P-NMR)

suitability

conforms to structure for H-NMR

compatibility

configured for PerkinElmer
configured for Polygen

storage temp.

−20°C

Quality Level

200

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This Item	M041180	M043100	M045000
Sigma-Aldrich M041080 Fluorescein Phosphoramidite	Sigma-Aldrich M041180 6-Fluorescein Phosphoramidite	Sigma-Aldrich M043100 6-Hexachloro-Fluorescein Phosphoramidite	Sigma-Aldrich M045000 6-Tetrachloro-Fluorescein Phosphoramidite
suitability conforms to structure for H-NMR	suitability conforms to structure for H-NMR	suitability conforms to structure for H-NMR	suitability conforms to structure for H-NMR
storage temp. −20°C	storage temp. −20°C	storage temp. −20°C	storage temp. −70°C
Quality Level 200	Quality Level 200	Quality Level 200	Quality Level 200
assay ≥95% (³¹P-NMR)	assay ≥97% (³¹P-NMR), ≥97.0% (reversed phase HPLC)	assay ≥97% (³¹P-NMR), ≥97.0% (reversed phase HPLC)	assay ≥97% (³¹P-NMR), ≥97.0% (reversed phase HPLC)
product line Proligo Reagents	product line Proligo Reagents	product line -	product line -
type for DNA synthesis	type for DNA synthesis	type -	type -

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

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Evaluation of clinical criteria for the identification of Lynch syndrome among unselected patients with endometrial cancer.

Amanda S Bruegl et al.

Cancer prevention research (Philadelphia, Pa.), 7(7), 686-697 (2014-04-29)

Clinical criteria, primarily young age of cancer onset and family history of signature cancers, have been developed to identify individuals at elevated risk for Lynch syndrome with the goals of early identification and cancer prevention. In 2007, the Society of

Somatic loss of function mutations in neurofibromin 1 and MYC associated factor X genes identified by exome-wide sequencing in a wild-type GIST case.

Martin G Belinsky et al.

BMC cancer, 15, 887-887 (2015-11-12)

Approximately 10-15 % of gastrointestinal stromal tumors (GISTs) lack gain of function mutations in the KIT and platelet-derived growth factor receptor alpha (PDGFRA) genes. An alternate mechanism of oncogenesis through loss of function of the succinate-dehydrogenase (SDH) enzyme complex has

Detection of Anaplasma phagocytophilum in Ixodes ricinus ticks from Norway using a realtime PCR assay targeting the Anaplasma citrate synthase gene gltA.

Anna J Henningsson et al.

BMC microbiology, 15, 153-153 (2015-08-02)

A TaqMan real-time PCR assay targeting the Anaplasma citrate synthase gene, gltA, was developed and used for detection of Anaplasma phagocytophilum in 765 Ixodes ricinus ticks collected from dogs and cats in northern Norway (n = 669) and Telemark county in southern

Rapid single nucleotide polymorphism based method for hematopoietic chimerism analysis and monitoring using high-speed droplet allele-specific PCR and allele-specific quantitative PCR.

Chiaki Taira et al.

Clinica chimica acta; international journal of clinical chemistry, 445, 101-106 (2015-03-24)

Chimerism analysis is important for the evaluation of engraftment and predicting relapse following hematopoietic stem cell transplantation (HSCT). We developed a chimerism analysis for single nucleotide polymorphisms (SNPs), including rapid screening of the discriminable donor/recipient alleles using droplet allele-specific PCR

On-chip quantitative detection of pathogen genes by autonomous microfluidic PCR platform.

Hiroaki Tachibana et al.

Biosensors & bioelectronics, 74, 725-730 (2015-07-27)

Polymerase chain reaction (PCR)-based genetic testing has become a routine part of clinical diagnoses and food testing. In these fields, rapid, easy-to-use, and cost-efficient PCR chips are expected to be appeared for providing such testing on-site. In this study, a

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Fluorescein Phosphoramidite