Cost-effective method to synthesize fluorescently labeled DNA size standards using cloned AFLP fragments

被引：3

作者：

Ueno, S

Tsumura, Y

Washitani, I

机构：

[1] Forestry & Forest Prod Res Inst, Dept Forest Genet, Genome Anal Lab, Tsukuba, Ibaraki 3058687, Japan

[2] Japan Wildlife Res Ctr, Tokyo, Japan

[3] Univ Tokyo, Tokyo, Japan

来源：

BIOTECHNIQUES | 2003年 / 34卷 / 06期

关键词：

D O I：

10.2144/03346bm05

中图分类号：

Q5 [生物化学];

学科分类号：

071010 ; 081704 ;

摘要：

[No abstract available]

引用

页码：1146 / +

页数：2

共 5 条

[1]

Brondani RPV, 2001, BIOTECHNIQUES, V31, P793

[2] Substrate nucleotide-determined non-templated addition of adenine by Taq DNA polymerase: Implications for PCR-based genotyping and cloning [J].

Magnuson, VL ;

Ally, DS ;

Nylund, SJ ;

Karanjawala, ZE ;

Rayman, JB ;

Knapp, JI ;

Lowe, AL ;

Ghosh, S ;

Collins, FS .

BIOTECHNIQUES, 1996, 21 (04) :700-709

[3] MEASUREMENT OF DNA LENGTH BY GEL-ELECTROPHORESIS [J].

SOUTHERN, EM .

ANALYTICAL BIOCHEMISTRY, 1979, 100 (02) :319-323

[4]

UENO S, IN PRESS CONSERV GEN

[5] AFLP - A NEW TECHNIQUE FOR DNA-FINGERPRINTING [J].

VOS, P ;

HOGERS, R ;

BLEEKER, M ;

REIJANS, M ;

VANDELEE, T ;

HORNES, M ;

FRIJTERS, A ;

POT, J ;

PELEMAN, J ;

KUIPER, M ;

ZABEAU, M .

NUCLEIC ACIDS RESEARCH, 1995, 23 (21) :4407-4414

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