-
1
-
-
0027500002
-
A vector for facile PCR product cloning and modification generating any desired 4-base 5′ overhang: PRPM
-
Cease, K.B. and C.J. Lohff. 1993. A vector for facile PCR product cloning and modification generating any desired 4-base 5′ overhang: pRPM. BioTechniques 14:250-255.
-
(1993)
BioTechniques
, vol.14
, pp. 250-255
-
-
Cease, K.B.1
Lohff, C.J.2
-
2
-
-
0023734473
-
Novel non-templated nucleotide addition reactions catalyzed by procaryotic and eucaryotic DNA polymerases
-
Clark, J.M. 1988. Novel non-templated nucleotide addition reactions catalyzed by procaryotic and eucaryotic DNA polymerases. Nucleic Acids Res. 16:9677-9686.
-
(1988)
Nucleic Acids Res.
, vol.16
, pp. 9677-9686
-
-
Clark, J.M.1
-
3
-
-
0028240187
-
Polishing with T4 or Pfu polymerase increases the efficiency of cloning of PCR fragments
-
Costa, G.L. and M.P. Weiner. 1994. Polishing with T4 or Pfu polymerase increases the efficiency of cloning of PCR fragments. Nucleic Acids Res. 22:2423.
-
(1994)
Nucleic Acids Res.
, vol.22
, pp. 2423
-
-
Costa, G.L.1
Weiner, M.P.2
-
4
-
-
0028010854
-
Direct cloning of polymerase chain reaction products in an XcmI T-vector
-
Harrison, J., P.L. Molley and S.J. Clark. 1994. Direct cloning of polymerase chain reaction products in an XcmI T-vector. Anal. Biochem. 216:235-236.
-
(1994)
Anal. Biochem.
, vol.216
, pp. 235-236
-
-
Harrison, J.1
Molley, P.L.2
Clark, S.J.3
-
5
-
-
0028858881
-
Cloning PCR products using T-vectors
-
Hengen, P.N. 1995. Cloning PCR products using T-vectors. Trends Biotechnol. 20:85-86.
-
(1995)
Trends Biotechnol.
, vol.20
, pp. 85-86
-
-
Hengen, P.N.1
-
6
-
-
0027729359
-
DNA polymerase-catalyzed addition of non-template extra nucleotides to the 3′ end of a DNA fragment
-
Hu, G. 1993. DNA polymerase-catalyzed addition of non-template extra nucleotides to the 3′ end of a DNA fragment. DNA Cell Biol. 12:763-770.
-
(1993)
DNA Cell Biol.
, vol.12
, pp. 763-770
-
-
Hu, G.1
-
7
-
-
0029791306
-
A positive screen for cloning PCR products
-
Keese, P. and L. Graf. 1996. A positive screen for cloning PCR products. Nucleic Acids Res. 24:3474-3475.
-
(1996)
Nucleic Acids Res.
, vol.24
, pp. 3474-3475
-
-
Keese, P.1
Graf, L.2
-
8
-
-
0028363433
-
A simple ligation step improves the efficiency of T-overhang vectors
-
Khan, I.M., P.S. Zammit, M. Green and L. Buluwela. 1994. A simple ligation step improves the efficiency of T-overhang vectors. Trends Genet. 10:225-226.
-
(1994)
Trends Genet.
, vol.10
, pp. 225-226
-
-
Khan, I.M.1
Zammit, P.S.2
Green, M.3
Buluwela, L.4
-
9
-
-
0025982062
-
Construction of T-vectors, a rapid and general system for direct cloning of unmodified PCR products
-
Marchuk, D., M. Drumm, A. Saulino and F.S. Collins. 1991. Construction of T-vectors, a rapid and general system for direct cloning of unmodified PCR products. Nucleic Acids Res. 19:1154.
-
(1991)
Nucleic Acids Res.
, vol.19
, pp. 1154
-
-
Marchuk, D.1
Drumm, M.2
Saulino, A.3
Collins, F.S.4
-
10
-
-
0024892209
-
Transcription of infectious Yellow Fever RNA from full-length cDNA templates produced by in vitro ligation
-
Rice, C.M., A. Grakoui, R. Galler and T.J. Chambers. 1989. Transcription of infectious Yellow Fever RNA from full-length cDNA templates produced by in vitro ligation. New Biol. 1:285-296.
-
(1989)
New Biol.
, vol.1
, pp. 285-296
-
-
Rice, C.M.1
Grakoui, A.2
Galler, R.3
Chambers, T.J.4
-
11
-
-
0004136246
-
-
CSH Laboratory Press, Cold Spring Harbor, NY
-
Sambrook, J., E.F. Fritsch and T. Maniatis. 1989. Molecular Cloning: A Laboratory Manual, 2nd ed. CSH Laboratory Press, Cold Spring Harbor, NY.
-
(1989)
Molecular Cloning: A Laboratory Manual, 2nd Ed.
-
-
Sambrook, J.1
Fritsch, E.F.2
Maniatis, T.3
-
12
-
-
0031023680
-
Optimized conditions for cloning PCR products into an XcmI T-vector
-
Schutte, B.C., K. Ranade, J. Pruessner and N. Dracopoli. 1997. Optimized conditions for cloning PCR products into an XcmI T-vector. BioTechniques 22:40-44.
-
(1997)
BioTechniques
, vol.22
, pp. 40-44
-
-
Schutte, B.C.1
Ranade, K.2
Pruessner, J.3
Dracopoli, N.4
-
13
-
-
0028334173
-
Direct cloning of unmodified PCR products by exploiting an engineered restriction site
-
Testori, A., I. Listowsky and P. Sollitti. 1994. Direct cloning of unmodified PCR products by exploiting an engineered restriction site. Gene 143:151-152.
-
(1994)
Gene
, vol.143
, pp. 151-152
-
-
Testori, A.1
Listowsky, I.2
Sollitti, P.3
|