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CACO-2 Cell Line human

86010202, human colon (Caucasian colon adenocarcinoma), Epithelial

Sinónimos:

Caco 2 Cells, Caco-II Cells, Caco2 Cells

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About This Item

UNSPSC Code:
41106514

product name

CACO-2 Cell Line human, from human colon(Caucasian colon adenocarcinoma), 86010202

biological source

human colon (Caucasian colon adenocarcinoma)

growth mode

Adherent

karyotype

Hypertetraploid, modal no. 96

morphology

Epithelial

products

Not specified

receptors

Not specified

technique(s)

cell culture | mammalian: suitable

relevant disease(s)

cancer

shipped in

dry ice

storage temp.

−196°C

General description

The CACO-2 cell line is a widely used in vitro model for mimicking the small intestine for drug transport studies. These cell lines form monolayers and are useful in intestinal permeation studies for screening excipients in drug formulations.

Cell Line Origin

Human Caucasian colon adenocarcinoma

Cell Line Description

Isolated from a primary colonic tumour in a 72-year-old Caucasian male using the explant culture technique. Forms moderately well differentiated adenocarcinomas consistent with colonic primary grade II, in nude mice.

Application

CACO-2 Cell Line human has been used:
  • to study if components of the sigma B regulon in Listeria monocytogenes contribute to cell invasion
  • for functional analysis of bacteriocin divercin AS7
  • to study the intracellular invasion by Listeria ivanovii
  • to study the effect of Maslinic acid, a pentacyclic triterpene, on colon cancer cell lines
  • in in vitro digestive enzymes toxicity studies
  • for Hazara virus infection and cultivation
  • to test the anti-cancer activity of the Curcuma longa and Origanum marjorana
  • in biocompatibility studies with the bark extracts of Salix spp.
  • to test the effect of N-3-oxo-dodecanoyl-homoserine (3O-C12-HSL) lactone from P.aeruginosa on the mitochondrial functionality
  • to test the effect of elastin-like recombinamer (ELR) based nanoparticle
  • as an in vitro epithelial cell model for studying the toxicity of zinc oxide nanoparticle
  • in the intestinal permeability assays with green rooibos extract
  • in toxicity studies with mycotoxin Deoxynivalenol (DON) cadmium (Cd)

DNA Profile

STR-PCR Data: Amelogenin: X
CSF1PO: 11
D13S317: 11,13,14
D16S539: 12,13
D5S818: 12,13
D7S820: 11,12
THO1: 6
TPOX: 9,11
vWA: 16,18

Culture Medium

EMEM (EBSS) + 2mM Glutamine + 1% Non Essential Amino Acids (NEAA) + 10% Foetal Bovine Serum FBS / FCS.

Subculture Routine

Split sub-confluent cultures (70-80%) 1:3 to 1:6 i.e. seeding at 2-4x10,000 cells/cm2 using 0.25% Trypsinor Trypsin/EDTA; 5% CO2; 37°C. NB: During routine subculture the cells should always be subcultured before they achieve confluence. Cells may show the appearance of circular vacuoles in the cytoplasm. These may increase in frequency as the culture density increases to confluence. To reduce their frequency, media change confluent cultures after 2-3 days if not subcultured. Cells can clump if not separated into a single cell suspension when split.

Other Notes

Additional freight & handling charges may be applicable for Asia-Pacific shipments. Please check with your local Customer Service representative for more information.
NaviCyte Scientific holds the exclusive commercial distribution rights to the CACO-2 cell line deposited by the Memorial Sloan-Kettering Cancer Center. Note: All uses of Catalogue Numbers 86010202 and 09042001, other than for research by a non-commercial or academic entity, require a license and use authorization from NaviCyte Scientific under its exclusive arrangement with Memorial Sloan-Kettering Cancer Center. For information on the licensing terms, please contact NaviCyte Scientific via contact@navicyte-scientific.com or (+1) 973-868-6100.

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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Artículos

DNA, RNA, cDNA derived from ECACC mammalian cell lines allow screening for genes or expression patterns to identify lines most suitable for specific research.

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