Culture Collections

General Cell Collection Detail

ECACC General Cell Collection: NTERA-2 clone D1

Supplied by: European Collection of Authenticated Cell Cultures (ECACC)
Culture Type: Cell line
Collection: ECACC General Collection
Catalogue No.: 01071221
Cell Line Name: NTERA-2 clone D1
Other Collection No.: ATCC CRL-1973
Citation Guidance: If use of this culture results in a scientific publication, it should be cited in the publication as: NTERA-2 clone D1 (ECACC 01071221)
Keywords: Human Caucasian pluripotent embryonal carcinoma
Cell Line Description: The pluripotent human embryonal carcinoma cell line NTERA-2 clone D1, also known as NT2/D1, is a subclone derived from the parent line NTERA-2. NTERA-2 cells were established from a nude mouse xenograft tumour of TERA-2 cells, which were originally isolated from a lung metastasis from a 22 year old patient with primary embryonal carcinoma of the testis. The subline NTERA-2 clone D1 differentiates into neuronal and other cell types in response to retinoic acid (RA) or hexamethylene bisacetamide (HMBA). Differentiated cells become permissive for human cytomegalovirus (HCMV) or human immunodeficiency virus (HIV). Differentiation with RA as inducer results in glycolipid changes, appearance of neurons and induction of Homeobox (HOX) gene clusters. When NTERA-2 clone D1 cells are passaged at high cell density EC-like cells predominate. However, when cultured at low density many large flat cells differing from typical EC cells are formed.
Species: Human
Tissue of Origin: Testis (lung metastasis)
CellType: Epithelial
Growth Mode: Adherent
DNA Profile: STR-PCR Data:

Amelogenin: X,Y
CSF1PO: 10,12
D13S317: 13
D16S539: 11,12,13
D5S818: 9,12
D7S820: 10,12
THO1: 9.3
vWA: 18,19

Karyotype: Aneuploid
Biosafety Information: Unless specified otherwise, at the European Collection of Authenticated Cell Cultures (ECACC) we routinely handle all of our cell lines at containment level 2 in accordance with the ACDP guidelines. ACDP = Advisory Committee on Dangerous Pathogens (UK)
All cell cultures have the potential to carry as yet unidentified adventitious agents. It is the responsibility of the end user to ensure that their facilities comply with biosafety regulations for their own country.

ACDP Guidance: Biological agents: Managing the risks in laboratories and healthcare premises.

Hyperlinks to MSDS documents:
Frozen cell cultures Material Safety Data Sheet
Growing cell cultures Material Safety Data Sheet
Nucleic acids derived from cell cultures Material Safety Data Sheet
Subculture Routine: Split confluent cultures (approximately 30 x 104 cells/ cm2) by gentle scraping to dislodge cells from the flask surface. Cell sheets/clumps can be dispersed by gently pipetting. Cultures should be maintained at high density by seeding new flasks at a density of at least 6 x 104 cells/ cm2. Medium should be renewed every 2-3 days and subcultured at approximately 5 days. As the embryonal cells tend to grow in large clumps and must be removed by gentle scraping , viable counts of only 40-50% are normal on resuscitation and when sub-culturing.
Culture Medium: DMEM containing 4.5 g/L glucose + 2mM Glutamine + 10% Foetal Bovine Serum (FBS). Cells should be cryopreserved in 95% FCS:5% DMSO
Depositor: Dr. M. Simpkins, Sir William Dunn School of Pathology, Oxford. Originator: Professor P W Andrews, Department Biomedical Science, University of Sheffield.
Originator: No
Country: UK
References: Andrews PW, Damjanov I, Simon D, Banting GS, Carlin C, Dracopoli NC, Fogh J. 1984 Pluripotent embryonal carcinoma clones derived from the human teratocarcinoma cell line Tera-2. Differentiation in vivo and in vitro. Lab Invest. 50(2):147-62. PMID: 6694356
Additional Bibliography: Andrews PW. 1984 Retinoic acid induces neuronal differentiation of a cloned human embryonal carcinoma cell line in vitro. Dev Biol. 103(2):285-93. PMID: 6144603. Mavilio F, Simeone A, Boncinelli E, Andrews PW. 1988 Activation of four homeobox gene clusters in human embryonal carcinoma cells induced to differentiate by retinoic acid. Differentiation. 37(1):73-9. PMID: 2898410. Andrews PW, Nudelman E, Hakomori S, Fenderson BA. 1990 Different patterns of glycolipid antigens are expressed following differentiation of TERA-2 human embryonal carcinoma cells induced by retinoic acid, hexamethylene bisacetamide (HMBA) or bromodeoxyuridine (BUdR). Differentiation.; 43(2):131-8. PMID: 2373286. Hirka G, Prakash K, Kawashima H, Plotkin SA, Andrews PW, Gonczol E. 1991 Differentiation of human embryonal carcinoma cells induces human immunodeficiency virus permissiveness which is stimulated by human cytomegalovirus coinfection. J Virol. 65(5):2732-5. PMID: 1850047
Patents: None specified by Depositor
Release Conditions: No

product imagesProduct Images

Note: Links open in a new window

The Culture Collections represent deposits of cultures from world-wide sources. While every effort is made to ensure details distributed by Culture Collections are accurate, Culture Collections cannot be held responsible for any inaccuracies in the data supplied. References where quoted are mainly attributed to the establishment of the cell culture and not for any specific property of the cell line, therefore further references should be obtained regarding cell culture characteristics. Passage numbers where given act only as a guide and Culture Collections does not guarantee the passage number stated will be the passage number received by the customer.

Cultures supplied by Culture Collections are for research purposes only. Enquiries regarding the commercial use of a cell line are referred to the depositor of the cell line. Some cell lines have additional special release conditions such as the requirement for a material transfer agreement to be completed by the potential recipient prior to the supply of the cell line. Please view the Terms & Conditions of Supply for more information.

Available Formats

DNA-5ug (100ng/ul)

Back to top
Copyright © Public Health England.

Please confirm your country of origin from the list below.