Development of antibodies to human embryonic stem cell antigens

被引:15
作者
Cai, JL
Olson, JM
Rao, MS
Stanley, M
Taylor, E
Ni, HT
机构
[1] R&D Syst Inc, Stem Cell Dept, Minneapolis, MN 55413 USA
[2] NIA, Stem Cell Biol Unit, Neurosci Lab, Baltimore, MD 21224 USA
来源
BMC DEVELOPMENTAL BIOLOGY | 2005年 / 5卷
关键词
D O I
10.1186/1471-213X-5-26
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Background: Using antibodies to specific protein antigens is the method of choice to assign and identify cell lineage through simultaneous analysis of surface molecules and intracellular markers. Embryonic stem cell research can be benefited from using antibodies specific to transcriptional factors/markers that contribute to the "stemness" phenotype or critical for cell lineage. Results: In this report, we have developed and validated antibodies (either monoclonal or polyclonal) specific to human embryonic stem cell antigens and early differentiation transcriptional factors/markers that are critical for cell differentiation into definite lineage. Conclusion: These antibodies enable stem cell biologists to conveniently identify stem cell characteristics and to quantitatively assess differentiation.
引用
收藏
页数:7
相关论文
共 13 条
  • [1] Gene expression in human embryonic stem cell lines: unique molecular signature
    Bhattacharya, B
    Miura, T
    Brandenberger, R
    Mejido, J
    Luo, YQ
    Yang, AX
    Joshi, BH
    Ginis, I
    Thies, RS
    Amit, M
    Lyons, I
    Condie, BG
    Itskovitz-Eldor, J
    Rao, MS
    Puri, RK
    [J]. BLOOD, 2004, 103 (08) : 2956 - 2964
  • [2] Transcriptome characterization elucidates signaling networks that control human ES cell growth and differentiation
    Brandenberger, R
    Wei, H
    Zhang, S
    Lei, S
    Murage, J
    Fisk, GJ
    Li, Y
    Xu, CH
    Fang, R
    Guegler, K
    Rao, MS
    Mandalam, R
    Lebkowski, J
    Stanton, LW
    [J]. NATURE BIOTECHNOLOGY, 2004, 22 (06) : 707 - 716
  • [3] Nanog:: A new recruit to the embryonic stem cell orchestra
    Cavaleri, F
    Schöler, HR
    [J]. CELL, 2003, 113 (05) : 551 - 552
  • [4] Functional expression cloning of Nanog, a pluripotency sustaining factor in embryonic stem cells
    Chambers, I
    Colby, D
    Robertson, M
    Nichols, J
    Lee, S
    Tweedie, S
    Smith, A
    [J]. CELL, 2003, 113 (05) : 643 - 655
  • [5] ESTABLISHMENT IN CULTURE OF PLURIPOTENTIAL CELLS FROM MOUSE EMBRYOS
    EVANS, MJ
    KAUFMAN, MH
    [J]. NATURE, 1981, 292 (5819) : 154 - 156
  • [6] Differentiation of human embryonic stem cells into embryoid bodies comprising the three embryonic germ layers
    Itskovitz-Eldor, J
    Schuldiner, M
    Karsenti, D
    Eden, A
    Yanuka, O
    Amit, M
    Soreq, H
    Benvenisty, N
    [J]. MOLECULAR MEDICINE, 2000, 6 (02) : 88 - 95
  • [7] ISOLATION OF A PLURIPOTENT CELL-LINE FROM EARLY MOUSE EMBRYOS CULTURED IN MEDIUM CONDITIONED BY TERATOCARCINOMA STEM-CELLS
    MARTIN, GR
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1981, 78 (12): : 7634 - 7638
  • [8] The homeoprotein Nanog is required for maintenance of pluripotency in mouse epiblast and ES cells
    Mitsui, K
    Tokuzawa, Y
    Itoh, H
    Segawa, K
    Murakami, M
    Takahashi, K
    Maruyama, M
    Maeda, M
    Yamanaka, S
    [J]. CELL, 2003, 113 (05) : 631 - 642
  • [9] Quantitative expression of Oct-3/4 defines differentiation, dedifferentiation or self-renewal of ES cells
    Niwa, H
    Miyazaki, J
    Smith, AG
    [J]. NATURE GENETICS, 2000, 24 (04) : 372 - 376
  • [10] Pera MF, 2003, METHOD ENZYMOL, V365, P429