DIRECT SEQUENCING OF DOUBLE-STRANDED DNA PCR PRODUCTS VIA REMOVING THE COMPLEMENTARY STRAND WITH SINGLE-STRANDED-DNA OF AN M13 CLONE

被引：7

作者：

GAL, S

HOHN, B

机构：

[1] Friedrich Miescher-Institute, CH-4002 Basel

来源：

NUCLEIC ACIDS RESEARCH | 1990年 / 18卷 / 04期

基金：

美国国家科学基金会;

关键词：

D O I：

10.1093/nar/18.4.1076

中图分类号：

Q5 [生物化学]; Q7 [分子生物学];

学科分类号：

071010 ; 081704 ;

摘要：

[No abstract available]

引用

收藏

页码：1076 / 1076

页数：1

相关论文

共 5 条

[1] GYLLENSTEN UB, 1989, BIOTECHNIQUES, V7, P700
[2] DIRECT SEQUENCING FROM LOW-MELT AGAROSE WITH SEQUENASE
KRETZ, KA
CARSON, GS
OBRIEN, JS
[J]. NUCLEIC ACIDS RESEARCH, 1989, 17 (14) : 5864 - 5864
[3] SEQUENCE-ANALYSIS OF MINUTE AMOUNTS OF VIROID RNA USING THE POLYMERASE CHAIN-REACTION (PCR)
PUCHTA, H
SANGER, HL
[J]. ARCHIVES OF VIROLOGY, 1989, 106 (3-4) : 335 - 340
[4] PRIMER-DIRECTED ENZYMATIC AMPLIFICATION OF DNA WITH A THERMOSTABLE DNA-POLYMERASE
SAIKI, RK
GELFAND, DH
STOFFEL, S
SCHARF, SJ
HIGUCHI, R
HORN, GT
MULLIS, KB
ERLICH, HA
[J]. SCIENCE, 1988, 239 (4839) : 487 - 491
[5] CHARACTERIZATION OF BETA-THALASSEMIA MUTATIONS USING DIRECT GENOMIC SEQUENCING OF AMPLIFIED SINGLE COPY DNA
WONG, C
DOWLING, CE
SAIKI, RK
HIGUCHI, RG
ERLICH, HA
KAZAZIAN, HH
[J]. NATURE, 1987, 330 (6146) : 384 - 386