Resource data sheet
DNA Bank Top

Mouse E-cadherin full length cDNA (#RDB01184)

Mouse E-cadherin cDNA.


Drawn by SnapGene® software
Sequence information
(Assembled from experimentally sequenced data)		 GenBank Flat File Format open
SnapGene file download
Publication Nagafuchi, A., Nature, 329, 341-343 (1987). PMID 3498123. [PubMed] [Article] [RRC of NBRP]
Test sheet Data Sheet open 
 
Alternative name Mouse E-cadherin cDNA
Clone info. Mouse E-cadherin cDNA from F9 cells cDNA library.
Comment This clone contains a CDS fragment corresponding to the 69nt to 2723nt of X06115.1. Known differences (at least) : G to A substitution at 2714nt (Glu, synonym).
Vector backbone pBluescript (Plasmid)
Size of vector backbone 2.9 kb
Selectable markers Amp^r
Growth conditions 37 C, LB+Amp
Gene/insert name Mouse E-cadherin/Cdh1 cDNA
Reference of insert sequence X06115 (DDBJ accession number)
Depositor|Developer Takeichi, Masatoshi |

Distribution information

Please check terms and conditions set forth by the depositor, which are specified in the RIKEN BRC Catalog and/or Web Catalog.
Ordering forms
Order form [Credit Card Payment] [Bank Transfer Payment] [Example of order form ]
MTA, for use for not-for-profit academic purpose [Word] [Example of MTA ]
Approval form by depositor [Word]
Please visit Information of Request for Distribution.[link] For for-profit-research purpose, please contact us. 
Terms and conditions for distribution Distributed with written consent of Depositor.
Remarks ((Additional form)) Approval Form(FormD)
Please obtain written approval of the depositor.
提供案内 (日本国内) [open/close]

必要書類
提供依頼書  [依頼書の記入例 ]
提供同意書 (MTA, 非営利学術目的用)[Word] [MTAの記入例 ]
寄託者による提供承諾書 [Word]
手続きの概要は、「提供申込みについて[link]」をご覧ください。営利目的利用についてはお問い合わせください。
MTAに書く使用条件 寄託者に許可をとること。
備考 【追加提供依頼書】承諾書(FormD)
寄託者の書面による提供承諾が必要です。

Catalog # Resource name Shipping form Fee
RDB01184 Mouse E-cadherin full length cDNA DNA solution JPY 9,460 (not-for-profit academic purpose)
plus cost of shipping containers, dry ice (if required) and shipping charge

How to cite this biological resource

Materials & Methods section:

The Mouse E-cadherin full length cDNA was provided by the RIKEN BRC through the National BioResource Project of the MEXT, Japan (cat. RDB01184).

Reference section:

Nagafuchi, A., Shirayoshi, Y., Okazaki, K., Yasuda, K., Takeichi, M., Transformation of cell adhesion properties by exogenously introduced E-cadherin cDNA. Nature, 329, 341-343 (1987). PMID 3498123. [PubMed] [Article] [RRC of NBRP]

Further references such as user reports and related articles (go to bottom)

References

Original, user report and related articles

original Nagafuchi, A., Transformation of cell adhesion properties by exogenously introduced E-cadherin cDNA. Nature, 329, 341-343 (1987). PMID 3498123. [PubMed] [Article] [RRC of NBRP]
user_report Nag, K., E-Cadherin – Fc Chimeric Protein-Based Biomaterial: Breaking the Barriers in Stem Cell Technology and Regenerative Medicine. Advanced Materials Research, 810: 41-76 (2013). [Article] [RRC of NBRP]
user_report Jovic, D., Direct observation of cell cycle progression in living mouse embryonic stem cells on an extracellular matrix of E-cadherin. SpringerPlus, 2: 585 (2013). PMID 25674414. [PubMed] [Article] [RRC of NBRP]
user_report Meng, Q., The differentiation and isolation of mouse embryonic stem cells toward hepatocytes using galactose-carrying substrata. Biomaterials, 33 (5): 1414-1427 (2012). PMID 22118818. [PubMed] [Article] [RRC of NBRP]
user_report Jovic, D., Control of singular cell cycle synchronization of mouse ES cells for hepatocyte differentiation on E-cadherin substratum. J. Biotechnol. Biomaterial, 1: 6 (2011). [Article] [RRC of NBRP]
user_report Haque, A., The effect of recombinant E-cadherin substratum on the differentiation of endoderm-derived hepatocyte-like cells from embryonic stem cells. Biomaterials, 32, 2032-2042 (2011). PMID 21163520. [PubMed] [Article] [RRC of NBRP]
user_report Nagaoka M., Design of the artificial acellular feeder layer for the efficient propagation of mouse embryonic stem cells. J. Biol. Chem., 283, 26468-26476 (2008). PMID 18614540. [PubMed] [Article] [RRC of NBRP]
user_report Ito A., Enhancement of cell function through heterotypic cell-cell interactions using E-cadherin-expressing NIH3T3 cells. J. Biosci. Bioeng., 105, 679-682 (2008). PMID 18640611. [PubMed] [Article] [RRC of NBRP]
user_report Rosshart S., Interaction of KLRG1 with E-cadherin: new functional and structural insights. Eur. J. Immunol., 38, 3354-3364 (2008). PMID 19009530. [PubMed] [Article] [RRC of NBRP]
user_report Grundemann C., Cutting edge: identification of E-cadherin as a ligand for the murine killer cell lectin-like receptor G1. J. Immunol., 176, 1311-1315 (2006). PMID 16424155. [PubMed] [Article] [RRC of NBRP]
user_report Nagaoka M., E-cadherin-coated plates maintain pluripotent ES cells without colony formation. PLoS One, 1, (2006). PMID 17183641. [PubMed] [Article] [RRC of NBRP]
user_report Nagaoka M., Immobilized E-cadherin model can enhance cell attachment and differentiation of primary hepatocytes but not proliferation. Biotechnol. Lett., 24, 1857-1862 (2002). [Article] [RRC of NBRP]