Development of a microchamber array for picoliter PCR

被引:124
作者
Nagai, H [1 ]
Murakami, Y [1 ]
Morita, Y [1 ]
Yokoyama, K [1 ]
Tamiya, E [1 ]
机构
[1] Japan Adv Inst Sci & Technol, Sch Mat Sci, Tatsunokuchi, Ishikawa 9231292, Japan
关键词
D O I
10.1021/ac000648u
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
A microchamber array for PCR was developed by semiconductor microfabrication technology. The microchambers were designed to be of picoliter quantity. To optimize fluid retention, the surface states of the substrate and the inner walls were examine for four different types of microchamber. The substrate was silicon, while silicon dioxide was selected for the inner walls. PCR was performed in the microchamber array, and the amplification of DNA was detected using a technique based on the energy transfer of fluorescent dyes. The lower volume limit for PCR was investigated using various sizes of microchambers. Microchambers with volume greater than 86 pL gave successful PCR. In addition, the system was improved in order to take up the PCR product, To prevent mixing of the samples, the samples were dried after PCR using a membrane that permeates only vapor.
引用
收藏
页码:1043 / 1047
页数:5
相关论文
共 24 条
  • [1] ANISOTROPIC ETCHING OF SILICON
    BEAN, KE
    [J]. IEEE TRANSACTIONS ON ELECTRON DEVICES, 1978, 25 (10) : 1185 - 1193
  • [2] The DNA sequence of human chromosome 22
    Dunham, I
    Shimizu, N
    Roe, BA
    Chissoe, S
    Dunham, I
    Hunt, AR
    Collins, JE
    Bruskiewich, R
    Beare, DM
    Clamp, M
    Smink, LJ
    Ainscough, R
    Almeida, JP
    Babbage, A
    Bagguley, C
    Balley, J
    Barlow, K
    Bates, KN
    Beasley, O
    Bird, CP
    Blakey, S
    Bridgeman, AM
    Buck, D
    Burgess, J
    Burrill, WD
    Burton, J
    Carder, C
    Carter, NP
    Chen, Y
    Clark, G
    Clegg, SM
    Cobley, V
    Cole, CG
    Collier, RE
    Connor, RE
    Conroy, D
    Corby, N
    Coville, GJ
    Cox, AV
    Davis, J
    Dawson, E
    Dhami, PD
    Dockree, C
    Dodsworth, SJ
    Durbin, RM
    Ellington, A
    Evans, KL
    Fey, JM
    Fleming, K
    French, L
    [J]. NATURE, 1999, 402 (6761) : 489 - 495
  • [3] Integrated microanalytical technology enabling rapid and automated protein identification
    Ekström, S
    Önnerfjord, P
    Nilsson, J
    Bengtsson, M
    Laurell, T
    Marko-Varga, G
    [J]. ANALYTICAL CHEMISTRY, 2000, 72 (02) : 286 - 293
  • [4] Hogan JC, 1996, NATURE, V384, P17
  • [5] DETECTION OF SPECIFIC POLYMERASE CHAIN-REACTION PRODUCT BY UTILIZING THE 5'-]3' EXONUCLEASE ACTIVITY OF THERMUS-AQUATICUS DNA-POLYMERASE
    HOLLAND, PM
    ABRAMSON, RD
    WATSON, R
    GELFAND, DH
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1991, 88 (16) : 7276 - 7280
  • [6] Fabricating large arrays of microwells with arbitrary dimensions and filling them using discontinuous dewetting
    Jackman, RJ
    Duffy, DC
    Ostuni, E
    Willmore, ND
    Whitesides, GM
    [J]. ANALYTICAL CHEMISTRY, 1998, 70 (11) : 2280 - 2287
  • [7] The ''one-bead-one-compound'' combinatorial library method
    Lam, KS
    Lebl, M
    Krchnak, V
    [J]. CHEMICAL REVIEWS, 1997, 97 (02) : 411 - 448
  • [8] Characterization of an inkjet chemical microdispenser for combinatorial library synthesis
    Lemmo, AV
    Fisher, JT
    Geysen, HM
    Rose, DJ
    [J]. ANALYTICAL CHEMISTRY, 1997, 69 (04) : 543 - 551
  • [9] LO DYM, 1998, CLIN APPL PCR
  • [10] Direct protein microarray fabrication using a hydrogel "stamper"
    Martin, BD
    Gaber, BP
    Patterson, CH
    Turner, DC
    [J]. LANGMUIR, 1998, 14 (15) : 3971 - 3975