Literature DB >> 19143759

Capacity of robot handling for Epstein-Barr virus transformation.

I-C Chang1, H-W Ko, S-M Hwang.   

Abstract

OBJECTIVES: Epstein-Barr virus (EBV) transformation has been described as a routine method to establish human B lymphoblastoid cell lines. Each established lymphoblastoid cell line represents one unique genetic information carrier and can produce unlimited quantities of DNA materials available for downstream applications and research. Undoubtedly, it is of great value to human clinical and experimental genetic studies. However, the current process of EBV transformation requires much manpower in the routine renewal of medium, which is time-consuming. This situation can become a serious problem especially when establishing a human B lymphoblastoid cell bank. A modified and cost-effective protocol for EBV transformation should be considered.
MATERIALS AND METHODS: In the present study, process in EBV transformation was modified to fit the requirements of robot handling.
RESULTS: 1 mL of whole blood was demonstrated to be sufficient to perform EBV transformation. Additionally, EBV transformation can performed in 96-deep-well plates that are directly and widely used with automatic work platforms.
CONCLUSIONS: Based on these facts, a process of EBV transformation can be modified to fit the requirements of robot handling.

Entities:  

Mesh:

Year:  2009        PMID: 19143759      PMCID: PMC6495527          DOI: 10.1111/j.1365-2184.2008.00568.x

Source DB:  PubMed          Journal:  Cell Prolif        ISSN: 0960-7722            Impact factor:   6.831


  8 in total

1.  Successful transformation of cryopreserved lymphocytes: a resource for epidemiological studies.

Authors:  J C Beck; C M Beiswanger; E M John; E Satariano; D West
Journal:  Cancer Epidemiol Biomarkers Prev       Date:  2001-05       Impact factor: 4.254

2.  Whole blood cryopreservation in epidemiological studies.

Authors:  Richard B Hayes; Craig O Smith; Wen-Yi Huang; Yvonne Read; William C Kopp
Journal:  Cancer Epidemiol Biomarkers Prev       Date:  2002-11       Impact factor: 4.254

3.  High-potentiality preliminary selection criteria and transformation time-dependent factors analysis for establishing Epstein-Barr virus transformed human lymphoblastoid cell lines.

Authors:  I-C Chang; J-Y Wu; H-I Lu; H-W Ko; J-L Kuo; C-Y Wang; P-S Shen; S-M Hwang
Journal:  Cell Prolif       Date:  2006-12       Impact factor: 6.831

4.  Successful use of long-term frozen lymphocytes for the establishment of lymphoblastoid cell lines.

Authors:  S Tremblay; E W Khandjian
Journal:  Clin Biochem       Date:  1998-10       Impact factor: 3.281

5.  A routine method for the establishment of permanent growing lymphoblastoid cell lines.

Authors:  H Neitzel
Journal:  Hum Genet       Date:  1986-08       Impact factor: 4.132

6.  Epstein-Barr virus-mediated B-cell proliferation is dependent upon latent membrane protein 1, which simulates an activated CD40 receptor.

Authors:  E Kilger; A Kieser; M Baumann; W Hammerschmidt
Journal:  EMBO J       Date:  1998-03-16       Impact factor: 11.598

7.  Epstein-Barr Virus nuclear protein EBNA3A is critical for maintaining lymphoblastoid cell line growth.

Authors:  Seiji Maruo; Eric Johannsen; Diego Illanes; Andrew Cooper; Elliott Kieff
Journal:  J Virol       Date:  2003-10       Impact factor: 5.103

8.  An efficient method for the rapid establishment of Epstein-Barr virus immortalization of human B lymphocytes.

Authors:  H-M Oh; J-M Oh; S-C Choi; S-W Kim; W-C Han; T-H Kim; D-S Park; C-D Jun
Journal:  Cell Prolif       Date:  2003-08       Impact factor: 6.831

  8 in total
  1 in total

1.  Efficient and reliable establishment of lymphoblastoid cell lines by Epstein-Barr virus transformation from a limited amount of peripheral blood.

Authors:  Natsue Omi; Yuichi Tokuda; Yoko Ikeda; Morio Ueno; Kazuhiko Mori; Chie Sotozono; Shigeru Kinoshita; Masakazu Nakano; Kei Tashiro
Journal:  Sci Rep       Date:  2017-03-08       Impact factor: 4.379

  1 in total

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