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Key Documents

F4274

Sigma-Aldrich

Fluorescein isothiocyanate isomer I

≥97.5% purity (HPLC), powder

Synonym(s):

FITC, Fluorescein 5-isothiocyanate

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About This Item

Empirical Formula (Hill Notation):
C21H11NO5S
CAS Number:
Molecular Weight:
389.38
Beilstein:
1407295
EC Number:
MDL number:
UNSPSC Code:
12171500
PubChem Substance ID:
NACRES:
NA.47

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Product Name

Fluorescein isothiocyanate isomer I, ≥97.5% (HPLC)

Quality Level

Assay

≥97.5% (HPLC)

form

powder

technique(s)

titration: suitable

color

yellow to very dark yellow

mp

>360 °C (lit.)

solubility

acetone: soluble 10 mg/mL

fluorescence

λex 492 nm; λem 518 nm (green)

application(s)

diagnostic assay manufacturing
hematology
histology

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Show Differences

1 of 4

This Item
ZIQ7015T0CZIX7015P0CZIQ7005T0C
output

product water quality: type 1 water (18.2 MΩ·cm)

output

product water quality: type 1 water (18.2 MΩ·cm)
product water quality: type 2 water (> 5 MΩ·cm)

output

product water quality: type 2 water (> 5 MΩ·cm)

output

product water quality: type 2 water (> 5 MΩ·cm)
product water quality: type 1 water (18.2 MΩ·cm)

parameter

1.5 L/min flow rate, 9.1 kg operating weight (19.84 lb)

parameter

≤2 L/min distribution flow rate (Type I), 15 L/hr flow rate (Type II), 30 kg operating weight (66 lb), 300 L/day max. usage

parameter

15 L/hr flow rate, 30.0 kg operating weight (66 lb), 300 L/day max. usage, ~2 L/min distribution flow rate

parameter

≤2 L/min distribution flow rate (Type I), 100 L/day max. usage, 26.0 kg operating weight (57.3 lb), 5 L/hr flow rate (Type II)

input

feed water nature ultrapure water

input

feed water nature potable tap water

input

feed water nature potable tap water

input

feed water nature potable tap water

packaging

pkg of 1 unit

packaging

pkg of 1 unit

packaging

pkg of 1 unit (System + E-POD®)

packaging

pkg of 1 unit

conductivity

0.055 μS/cm (Ultrapure water)

conductivity

0.055 μS/cm at 25 °C (Ultrapure Water), <0.2 μS/cm at 25 °C (Pure Water)

conductivity

0.2 μS/cm at 25 °C (water output)

conductivity

0.055 μS/cm at 25 °C (Ultrapure Water), <0.2 μS/cm at 25 °C (Pure Water)

AC/DC input

100 V / 240 V, 50-60 Hz

AC/DC input

100 V / 230 V AC, 50-60 Hz

AC/DC input

100 V / 240 V, 50-60 Hz

AC/DC input

100 V / 230 V AC, 50-60 Hz

General description

Fluorescein isothiocyanate (FITC) is widely used to attach a fluorescent label to proteins via the amine group. The isothiocyanate group reacts with amino terminal and primary amines in proteins. It has been used for the labeling of proteins including antibodies and lectins.[1][2]

Application

Fluorescein isothiocyanate isomer I has been used for the staining of conidia.[3][4]
Reagent for the FITC labeling of proteins; Microsequencing of proteins and peptides (HPLC)

Packaging

Bottomless glass bottle. Contents are inside inserted fused cone.

related product

Product No.
Description
Pricing

Pictograms

Health hazard

Signal Word

Danger

Hazard Statements

Hazard Classifications

Resp. Sens. 1 - Skin Sens. 1

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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PU.1 serves a critical role in the innate defense against Aspergillus fumigatus via dendritic cell-associated C-type lectin receptor-1 and toll-like receptors-2 and 4 in THP-1-derived macrophages.
Liu C
Molecular Medicine Reports, 15, 4084-4084 (2017)
Binding of live conidia of Aspergillus fumigatus activates in vitro-generated human Langerhans cells via a lectin of galactomannan specificity.
Persat F
Clinical and Experimental Immunology, 133, 370-370 (2003)
Handbook of Affinity Chromatography (2005)
Ana Bratuša et al.
Colloids and surfaces. B, Biointerfaces, 181, 561-566 (2019-06-12)
This work describes the derivatization of dextran using N-(tert-butyloxycarbonyl)-S-(trityl)-L-cysteine in the presence of N,N'-carbonyldiimidazole (CDI) as a coupling agent. Homogeneous reactions in dimethyl sulfoxide allowed for an efficient coupling of the amino acid derivative to the polymer backbone. Derivatization was
Hermanson GT
Bioconjugate Techniques (2013)

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