DSPE-PEG2000-FITC

Cat. No.: HY-W440915 Pureza: 99.76%: Ficha de datos
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DSPE-PEG2000-FITC is a PEG lipid conjugated with fluorescein. FITC is a green dye with a peak absorption at 494 nm and a maximum emission at 520 nm, which is used for staining biological samples or nanoparticles. DSPE-PEG2000-FITC spontaneously forms lipid bilayers or micelles in water and can be used to prepare liposomes for delivering substances such as mRNA vaccines.

Para uso exclusivo en investigación. No vendemos a pacientes.

DSPE-PEG2000-FITC Estructura química

No. CAS : 1000788-53-3

Tamaño	Stock	Cantidad
1 mg	En stock	Estimated Time of Arrival: December 31
5 mg	En stock	Estimated Time of Arrival: December 31
10 mg	En stock	Estimated Time of Arrival: December 31
25 mg	En stock	Estimated Time of Arrival: December 31
50 mg	Obtener un presupuesto
100 mg	Obtener un presupuesto

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Other Forms of DSPE-PEG2000-FITC:

DSPE-PEG1000-FITC In-stock
DSPE-PEG10000-FITC In-stock
DSPE-PEG600-FITC In-stock
DSPE-PEG5000-FITC In-stock
DSPE-PEG400-FITC Obtener un presupuesto

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Actividad biológica
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Descripciòn

In Vitro

DSPE-PEG-FITC (MW 2000) spontaneously forms lipid bilayers or micelles in water, and can be used to prepare liposomes for delivering nutrients such as mRNA vaccines.

MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.

Peso molecular

2000 (Average)

No. CAS

1000788-53-3

Appearance

Solid

Color

Light yellow to yellow

SMILES

O=C(CCCCCCCCCCCCCCCCCCC)OC[C@](OC(CCCCCCCCCCCCCCCCCCC)=O)([H])COP(O)(OCCNC(OCCNC(NC1=CC(C2(C(C=CC(O)=C3)=C3OC4=C2C=CC(O)=C4)OC5=O)=C5C=C1)=S)=O)=O.[n]

Envío

Room temperature in continental US; may vary elsewhere.

Almacenamiento

Powder	-20°C	3 years
In solvent	-80°C	6 months
	-20°C	1 month

Solvente y solubilidad

In Vitro:

DMSO : 50 mg/mL (Need ultrasonic; Hygroscopic DMSO has a significant impact on the solubility of product, please use newly opened DMSO)

Calculadora de molaridad
Calculadora de dilución

Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)

Concentration _(start) × Volume _(start) = Concentration _(final) × Volume _(final)

This equation is commonly abbreviated as: C₁V₁ = C₂V₂

Concentration _(start)

Volume _(start)

Concentration _(final)

Volume _(final)

In Vivo Dissolution Calculator

Please enter the basic information of animal experiments:

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Recommended: Prepare an additional quantity of animals to account for potential losses during experiments.

Calculation results:

Working solution concentration: mg/mL

Pureza y Documentación

Purity: 99.76%

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Ficha de datos (265 KB) SDS (393 KB)

COA (241 KB) HNMR (326 KB) RP-HPLC (236 KB)

Instrucciones de manejo (2659 KB)

Referencias

[1]. Saucier-Sawyer JK, et al. Systemic delivery of blood-brain barrier-targeted polymeric nanoparticles enhances delivery to brain tissue. J Drug Target. 2015;23(7-8):736-749. [Content Brief]

[2]. Lufeng Shi, et al. Extracellular Vesicle Crosslinkers Constructing Hydrogels with Stress-Relaxation and Bioactive Protein Modification. Adv. Mater. Interfaces 2025, 12, 2400885.