Usage of the IT libraries

(for the first hundred of analyzed screenings)

1. Libraries listed in Current Protocols

were used in 79 screenings

# Source of RNA/DNA; link to request: Indepen-
dent Clones
Insert Size (Avg.) Usage/success

(+, -, under investigation)

Constructed by/ link to the original article
1 HeLa cells (human cervical carcinoma), exponentially growing, cDNA
        6
9.6x10
0.5-2.0 kb (1.0 kb) IIIIIIIIIIIIIIIIII
IIIIIIIIII
IIIIIII
total 35; 18+, 7 -, 10?
J. Gyuris
2 WI-38 cells (human lung fibroblasts), serum starved, cDNA
        6
5.7x10
0.3-3.2 kb (1.4 kb) II
II
total 3: 2+, 1?
C. Sardet and J. Gyuris
3 Jurkat cells (human T cell leukemia), exponentially growing, cDNA
       6
4.0x10
0.7-2.8 kb (1.5 kb) I
II
total 2: 1+, 1?
W. Kolanus, J. Gyuris, B.Seed
4 fetal brain, 22 weeks, human, cDNA
        6
3.5x10
(1.5 kb) IIIIIIIIIIIII
III
I
total 17: 13+; 1-, 3?
D. Krainc
5 liver, human, cDNA
     6
> 10
0.6-4.0 kb (>1 kb) ? J. Pugh
6 CD4+ T cell, murine, cDNA
     6
> 10
0.3-2.5 kb (>0.5 kb) II

total 2; 2+
V. Prasad
7 CHO cells (Chinese Hamster Ovary), exponentially growing, cDNA
        6
1.5x10
0.3-3.5 kb (1 kb) ? V. Prasad
8 Drosophila melanogaster, 0-12 hour embryos, cDNA
       6
4.2x10
0.5-2.5 kb (1.0 kb) I
II
I
total 4; 1+, 1-, 2?
R. Finley
9 Drosophila melanogaster, ovary, cDNA
        6
3.2x10
0.3-1.5 kb (800 bp) IIII
I
I

total 6; 4+, 1-, 1?
R. Finley
10 Drosophila melanogaster, disc, cDNA
       6
4.0x10
0.3-2.1 kb (900 bp) I
III
total 4; 1+, 3?
R. Finley
11 S. cerevisiae, S288C, genomic
         6
> 3 x10
0.8-4.0 kb IIII
I
I

6:total 4+, 1-, 1?
P. Watt
Color code: red: success; blue: failure ; green: ongoing



2. Recently constructed libraries

were used in 22 screenings

# Source of RNA/DNA Indepen- dent Clones Insert Size (Avg.) Usage/success Constructed by/ contact to:
1 day 18 rat brain cDNA library . . II
I

total 3; 2+, 1-
.
2 HeLa adenovirus infected . . I
total 1; 1+
.
3 human 293 adenovirus infected (early and late stages) . . I
total 1; 1+
.
4 mouse embrio . . I
II

total 3; 1+, 2?
.
5 mouse pachyten spermatocytes . . II
total 2; 2?
.
6 G0 fibroblast . . I
total 1; 1+
.
7 MDCK polyA+ . . I
total 1; 1+
.
8 HepG2 cell line cDNA . . I
total 1; 1+
.
9 Trypanosoma brucei . . I
total 1; 1+
.
10 Agrobacterium tumefaciens . . I
total 1; 1?
.
11 Drosophila melanogaster, head . . I
I

total 2; 1+, 1?
.
12 Arabidopsis thaliana, 7 day old seedlings . . I
I

total 2; 1+, 1-
.
13 tomato/P.syringae 8 x 106 . II
I

total 3; 2+, 1?
G.Martin

2 colleagues did not give the names of the RFLY libraries they used; finally, some investigators used the libraries designed for the other systems and selected the interators using only lacZ screen.

http://www.clontech.com/clontech/JUL96UPD/JUL96MMLibraries.html


Back to the introduction page

Click here to see the table of analyzed library screenings

See alist of articles using any kind of two-hybrid system (published till October 1995)

Go to the Table summarizing some of the two-hybrid system usage


Request the appropiate strains and plasmids in the Roger Brent lab. or fill our questionnaire.