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Christensen, S., Cook, K., Cook, K. (2008.9.29). Isolation and characterization of Df(3L)BSC613. 
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From: 	Kevin Cook <kcook@XXXX>
To: 	FlyBase-Cambridge <flybase-cambridgeXXXX>, Kim Cook <ruacookXXXX>, Stacey Christensen <sjchristXXXX>, kaufmanXXXX
Subject: 	Isolation and characterization of Df(3L)BSC613
Date: 	Mon, 29 Sep 2008  15:37:48  -0400  ( 20:37  BST)
Isolation and characterization of Df(3L)BSC613
Stacey Christensen, Kim Cook and Kevin Cook
Bloomington Stock Center
Indiana University
Df(3L)BSC613 was isolated as a FLP recombinase-induced recombination 
event involving PBac{WH}CG10984[f05402] and P{XP}d03775. The deletion 
was isolated as a chromosome lacking miniwhite markers in progeny of 
w[1118]; P{hs-hid}3, Dr[1]/TM6C, Sb[1] females crossed to P{hsFLP}1, 
y[1] w[1118]; PBac{WH}CG10984[f05402]/P{XP}d03775 males. The males 
were heat shocked as larvae as described in Parks et al., Nature 
Genetics 36: 288-292, 2004 (FBrf0175003). This cross and crosses in 
preceding and succeeding generations maintained the original genetic 
background of the Exelixis insertion stocks (Thibault et al., Nature 
Genetics 36: 283-287, 2004; FBrf0175002). The recombination event 
generated the genetic element P+PBac{XP5.WH5}BSC613 from the segment 
of PBac{WH}CG10984[f05402] to the left of its FRT site and the 
segment of P{XP}d03775 to the right of its FRT site. Its presence was 
verified using the PCR methods and primers described in Parks et al. 
The cytological breakpoints of Df(3L)BSC613 predicted from the 
Release 5 genomic coordinates of the transposable element insertions 
sites are 69E1;69E6. Df(3L)BSC613 failed to complement Df(3L)BSC413 
and Atg1[00305].
Kevin Cook, Ph.D.               Bloomington Drosophila Stock Center
Department of Biology 
Jordan Hall 142
Indiana University              812-856-1213
1001 E. Third St.               812-855-2577 (fax)
Bloomington, IN  47405-7005     kcook@XXXX
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    Aberrations (2)
    Alleles (1)
    Genes (1)
    Insertions (3)
    Transgenic Constructs (1)