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MTOX1006P24

Sigma-Aldrich

BCRP/MRP2 Double Knockout Caco-2 Cells

human cervix, Epithelial

Sinónimos:

BCRP/MRP2 Double Knockout C2BBe1 Cells

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About This Item

UNSPSC Code:
41106514
NACRES:
NA.81

product name

BCRP/MRP2 Double Knockout Caco-2 Cells, one assay ready, 24 well plate

biological source

human colon

form

solid

morphology

Epthelial

technique(s)

drug transporter assay: suitable
permeability assay: suitable

application(s)

ADME/TOX

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General description

The C2BBe1 cells, a subclone of Caco-2 cells, correspond to ATCC CRL-2102. The BCRP/MRP2 double knockout C2BBe1 cells are adenocarcinoma, epithelial cells from a human caucasian male (aged 72 years) with functional knockout of the BCRP and MRP2 efflux transporters.

The three week production lead time begins on the Monday following a purchase, in the third week the plates are shipped on Tuesday for receipt on Wednesday or Thursday. As a biologic product that′s shipped at room temperature the cells must be processed immediately upon receipt.

Application

The following posters and articles demonstrate how Caco-2 cells can be used for cell based assays:

Transporter Function in Caco-2 Cells with Targeted P-Glycoprotein, MRP2 and BCRP Gene Knockout Using Zinc Finger Nucleases

Comparison of Function and Relative Transporter Protein Concentrations in Caco-2 Cells with Single and Double Knockouts of the ABCB1, ABCG2, and ABCC2 Genes

Caco-2 Transporter Knockout Cell Based Assays

Features and Benefits

The Caco-2 subclone, C2BBe1 cells, are ideal for transporter analysis as they express multiple transporters, are human derived and grow in a homogenous monolayer that forms tight juntions which is necessary for efflux ratio analysis. Other benefits include:

  • Functional knockout of the BCRP and MRP2 genes eliminates the reliance on chemical inhibitors to determine if a compound is a BCRP or MRP2 substrate
  • The 24 well Transwell format enables the BCRP and MRP2 knockout cells to be included in standard drug transporter protocols
  • Human assay with no interference from animal inhibitors
  • Overcome the limitations of RNAi and knockdown cell lines that arise from remaining transporter functionality

Related product

Referencia del producto
Descripción
Precios

MTOX1001P24

MDR1 Knockout Caco-2 Cells, one assay ready, 24 well plate

MTOX1002P24

BCRP Knockout Caco-2 Cells, one assay ready, 24 well plate

MTOX1003P24

MRP2 Knockout Caco-2 Cells, one assay ready, 24 well plate

MTOX1004P24

MDR1/BCRP Double Knockout Caco-2 Cells, one assay ready, 24 well plate

MTOX1005P24

MDR1/MRP2 Double Knockout Caco-2 Cells, one assay ready, 24 well plate

MTOX1092P24

MRP1 Knockout Caco-2 Cells, one assay ready, 24 well plate

MTOX1094P24

MRP4 Knockout Caco-2 Cells, one assay ready, 24 well plate

MTOX1097P24

MRP7 Knockout Caco-2 Cells, one assay ready, 24 well plate

Storage Class

13 - Non Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

Certificados de análisis (COA)

Busque Certificados de análisis (COA) introduciendo el número de lote del producto. Los números de lote se encuentran en la etiqueta del producto después de las palabras «Lot» o «Batch»

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P Artursson
Journal of pharmaceutical sciences, 79(6), 476-482 (1990-06-01)
A human intestinal cell line, Caco-2, was used as a model to study the passive diffusion of drugs across intestinal epithelium. The cells formed continuous monolayers when grown on permeable filters of polycarbonate. After 10 days in culture, the monolayers
Mark I Kaldas et al.
The Journal of pharmacy and pharmacology, 55(3), 307-312 (2003-05-02)
Resveratrol is a dietary constituent suggested to have protective effects against cancer as well as cardiovascular disease. The purpose of the study was to learn whether this agent could be absorbed in man and enter the systemic circulation. This was
S Yee
Pharmaceutical research, 14(6), 763-766 (1997-06-01)
To evaluate and optimize the use of Caco-2 cell monolayers to predict the in vivo absorption of a broad range of compounds in man. Caco-2 cells are derived from human adenocarcinoma colon cells and spontaneously differentiate when grown on porous
X Wu et al.
Pharmaceutical research, 17(2), 209-215 (2000-04-06)
The purpose of this study was to elucidate the mechanisms by which an HMG-CoA reductase inhibitor, atorvastatin (an organic acid with a pKa of 4.46), was transported in the secretory and absorptive directions across Caco-2 cell monolayers. Caco-2 cells were
V Pade et al.
Journal of pharmaceutical sciences, 87(12), 1604-1607 (1999-04-03)
The objective of this investigation was to establish a relationship between drug permeability and solubility in vitro and the extent of drug absorption in humans. We selected drugs with varying permeabilities and solubilities with the aim of establishing a relationship
Ver todos los artículos relacionados

Artículos

Drug transport assays in a 96-well system: reproducibility and correlation to human absorption

Application note on Drug transport assays in a 96-well system using Millicell-96 System from Millipore.

Caco-2 Intestinal Drug Transporter Models for More Predictive Drug Absorption

Utilize these Caco-2 cell based assay tools for screening small molecule drug compounds prior to clinical studies and submission to regulatory agencies.

Caco-2 Intestinal Drug Transporter Models for More Predictive Drug Absorption

Utilize these Caco-2 cell based assay tools for screening small molecule drug compounds prior to clinical studies and submission to regulatory agencies.

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El cribado satisfactorio para el descubrimiento de compuestos candidatos y dianas farmacológicas requiere reactivos y suministros de gran rendimiento, probados y adecuados para el proceso. Encuentre las herramientas adecuadas para sus procesos de CRO, farmacéuticos o biotecnológicos destinadas al cribado de moléculas pequeñas y productos biológicos, así como para sólidos análisis de inmunogenicidad destinados a garantizar la seguridad terapéutica.

Elementos esenciales para el cribado de la seguridad, los compuestos candidatos y las dianas en el descubrimiento de medicamentos

El cribado satisfactorio para el descubrimiento de compuestos candidatos y dianas farmacológicas requiere reactivos y suministros de gran rendimiento, probados y adecuados para el proceso. Encuentre las herramientas adecuadas para sus procesos de CRO, farmacéuticos o biotecnológicos destinadas al cribado de moléculas pequeñas y productos biológicos, así como para sólidos análisis de inmunogenicidad destinados a garantizar la seguridad terapéutica.

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