DrosDel Immunity Panel

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Name VDRC Id Library Sub-Category Genotype Comment Construct Id Publication Provider Scientist Provider Organization Gene Symbol FlyBase gene number Synonyms Sequence RRID Comment Gene Name Keywords Price (net) Add to Cart
349900
349900
DD-Im
mutants
w[1118]; ; Rel[E20]
BL1. A deletion of Relish (which also affects a nearby gene). The ebony marker of the original stock (Dan Hultmark‘s lab) was removed  by recombination with an Oregon stock. The Rel[E20] mutation was then introgressed in the w[1118] DrosDel genetic background. Rel[E20] lack a functional Imd pathway and are susceptible to Gram negative bacterial infection. The transcription factor Relish may also be involved in the immune defence against viruses downstream of cGas-like, Sting and IKK (Cai et al., Curr Opin Immumol (2022)).
349900
Bruno Lemaitre with the help of Mark Hanson
EPFL
Rel
DrosDel Immunity panel
NF-KB
NF-kappaB
NF-κB
NFkappaB
NFκB
Nuclear Factor-kappa-B p110
Nuclear factor NF-kappa-B p110 subunit
REL
RELI
RELISH
Rel
Rel-p110
Rel/NF-kappaB
Rel/NF-κB
Rel1
Rel49
RelA
Relish
BL1. A deletion of Relish (which also affects a nearby gene). The ebony marker of the original stock (Dan Hultmark‘s lab) was removed  by recombination with an Oregon stock. The Rel[E20] mutation was then introgressed in the w[1118] DrosDel genetic background. Rel[E20] lack a functional Imd pathway and are susceptible to Gram negative bacterial infection. The transcription factor Relish may also be involved in the immune defence against viruses downstream of cGas-like, Sting and IKK (Cai et al., Curr Opin Immumol (2022)).
Relish
DrosDel Immunity panel
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349901
349901
DD-Im
mutants
w[1118]; ; spz[rm7]/TM6C, Sb[1]
BL2. spz[rm7] or spz[4] is a genetically null mutation in spz (generated by EMS during Nusslein-Volhard and Wieschaus screen). Several markers of the original stock (M317 Tubingen stock center) including ebony were removed by recombination (Lemaitre et al., Cell 1996). spz[rm7] are homozygous viable, female sterile. This mutation blocks the activation of the Toll pathway. Note that the Toll pathway might be activated independently of spz by spz[5] (Nonaka et al., Biochem Biophys Res Comm 2018)). 
349901
Bruno Lemaitre with the help of Mark Hanson
EPFL
spz
CT19282
DrosDel Immunity panel
Protein spaetzle precursor
SPZ
Spaetzle
Spatzle
Spatzle-1
Spz
Spz-1
Spz1
mel(3)7
spaetzle
spatzle
spazle
spaztle
spz
BL2. spz[rm7] or spz[4] is a genetically null mutation in spz (generated by EMS during Nusslein-Volhard and Wieschaus screen). Several markers of the original stock (M317 Tubingen stock center) including ebony were removed by recombination (Lemaitre et al., Cell 1996). spz[rm7] are homozygous viable, female sterile. This mutation blocks the activation of the Toll pathway. Note that the Toll pathway might be activated independently of spz by spz[5] (Nonaka et al., Biochem Biophys Res Comm 2018)). 
spatzle
DrosDel Immunity panel
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349907
349907
DD-Im
mutants
w[1118]; ; Sp7[SK6]
BL8. Null mutation affecting the Sp7/MP2 serine protease that regulates melanization in Drosophila, isogenized in the w[1118] DrosDel genetic background. Sp7 strongly blocks the blackening reaction at the injury site of larvae but has less effect in adults (Dudzic et al., 2015).
349907
Bruno Lemaitre with the help of Mark Hanson
EPFL
Sp7
DrosDel Immunity panel
MP1
MP2
MP2/sp7/PAE1
Melanization Protease 2
PAE
PAE1
SP13
SP7
Serine protease 7
Serine protease-7
Sp 7
Sp7
anon-Ryu
cSP7
proPO-AE
prophenoloxidase-activating enzyme
prophenoloxidas
BL8. Null mutation affecting the Sp7/MP2 serine protease that regulates melanization in Drosophila, isogenized in the w[1118] DrosDel genetic background. Sp7 strongly blocks the blackening reaction at the injury site of larvae but has less effect in adults (Dudzic et al., 2015).
Serine protease 7
DrosDel Immunity panel
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349909
349909
DD-Im
mutants
w[1118]; ; PGRP-SD[SK1]
BL10. Null mutation affecting the secreted pattern recognition receptor PGRP-SD that promotes the activation of the Imd pathway upstream of PGRP-LC, isogenized in the w[1118] DrosDel genetic background.
349909
Bruno Lemaitre with the help of Mark Hanson
EPFL
PGRP-SD
Dm PGRP-SD
DrosDel Immunity panel
PGRP-SD
Peptidoglycan recognition protein SD
Peptidoglycan-recognition protein-SD precursor
pgrp-sd
BL10. Null mutation affecting the secreted pattern recognition receptor PGRP-SD that promotes the activation of the Imd pathway upstream of PGRP-LC, isogenized in the w[1118] DrosDel genetic background.
Peptidoglycan recognition protein SD
DrosDel Immunity panel
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349910
349910
DD-Im
mutants
w[1118]; ; PGRP-LB[Delta]
BL11. Null mutation affecting PGRP-LB (created by homologous replacement of PGRP-LB sequences with w[+]), which encodes a secreted negative regulator of the Imd pathway upstream of PGRP-LC, isogenized in the w[1118] DrosDel genetic background.
349910
Bruno Lemaitre with the help of Mark Hanson
EPFL
PGRP-LD
CG32912
CG5523
DrosDel Immunity panel
PGRP-LD
Peptidoglycan recognition protein LD
Peptidoglycan recognition protein-LD
BL11. Null mutation affecting PGRP-LB (created by homologous replacement of PGRP-LB sequences with w[+]), which encodes a secreted negative regulator of the Imd pathway upstream of PGRP-LC, isogenized in the w[1118] DrosDel genetic background.
Peptidoglycan recognition protein LD
DrosDel Immunity panel
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349916
349916
DD-Im
mutants
w[1118]; ; Df(3R)CecA-C[Delta]
BL17. A deletion removing the Cecropin Locus (4 genes), all isogenized in the w[1118] DrosDel genetic background. 
349916
Bruno Lemaitre with the help of Mark Hanson
EPFL
CecA1
CEC
CG4740
Cec
Cec A1
CecA
CecA-C
CecA1
CecA2
CecB
CecC
Cecropin
Cecropin A
Cecropin A1
Cecropin-A
Cecropin-A1
Cecropin-A1/A2 precursor
CecropinA
CecropinA1
DrosDel Immunity panel
cec
cecA
cec
BL17. A deletion removing the Cecropin Locus (4 genes), all isogenized in the w[1118] DrosDel genetic background. 
Cecropin A1
DrosDel Immunity panel
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349917
349917
DD-Im
mutants
w[1118]; ; AttD[SK1]
BL18. A mutation affecting Attacin D, isogenized in the w[1118] DrosDel genetic background. 
349917
Bruno Lemaitre with the help of Mark Hanson
EPFL
AttD
Att
AttD
Attacin
Attacin D
Attacin-D
AttacinD
Attackin
DrosDel Immunity panel
att
att D
attD
attacin
attacin D
BL18. A mutation affecting Attacin D, isogenized in the w[1118] DrosDel genetic background. 
Attacin-D
DrosDel Immunity panel
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349924
349924
DD-Im
mutants
w[1118]; ; Drs[R1]
BL25. A deletion removing the Drs locus (generated by homologous recombination, contains a w+ gene), isogenized in the w[1118] DrosDel genetic background
349924
Bruno Lemaitre with the help of Mark Hanson
EPFL
Drs
BcDNA:LP03851
Crp
Cysteine-rich-protein
DIM 19
DIM 21
DRO
DROM
DROS
DRS
Drm
Drom
Dros
DrosDel Immunity panel
Droso
Drosomcycin
Drosomycin
Drosomycin precursor
Drosomycin-B
Drosomycine
Drosomyocin
BL25. A deletion removing the Drs locus (generated by homologous recombination, contains a w+ gene), isogenized in the w[1118] DrosDel genetic background
Drosomycin
DrosDel Immunity panel
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349930
349930
DD-Im
mutants
w[1118]; ; Df(3L)LysB-P[Delta]
BL31. An  11.5-kb deletion, removing LysC (a putative pseudogene) and the 4 lysozyme genes (i.e., Lys B, LysD, LysE, and Lys P) that are known to be strongly induced in the gut; isogenized in the w[1118] DrosDel genetic background.
349930
Bruno Lemaitre with the help of Mark Hanson
EPFL
LysB
DrosDel Immunity panel
Lys B
Lys P
LysB
LysC
LysD
LysE
Lysozyme B
Lyzozyme B
lysB
BL31. An  11.5-kb deletion, removing LysC (a putative pseudogene) and the 4 lysozyme genes (i.e., Lys B, LysD, LysE, and Lys P) that are known to be strongly induced in the gut; isogenized in the w[1118] DrosDel genetic background.
Lysozyme B
DrosDel Immunity panel
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349934
349934
DD-Im
mutants
w[1118]; ; TotAZ[SK6]
BL35. A fly line, called TotAZ, with a deletion removing the TotA, TotB, TotC and TotZ genes, isogenized in the w[1118] DrosDel genetic background.
349934
Bruno Lemaitre with the help of Mark Hanson
EPFL
TotA
DrosDel Immunity panel
Stress-inducible humoral factor Turandot A
Tot
Tot A
Tot-A
TotA
TotAZ
TotB
TotC
TotZ
Turandot
Turandot A
Turt
tot
totA
turandot A
BL35. A fly line, called TotAZ, with a deletion removing the TotA, TotB, TotC and TotZ genes, isogenized in the w[1118] DrosDel genetic background.
Turandot A
DrosDel Immunity panel
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