BugDorm-2S400 Insect Rearing Cage

  • Model:BD2S400
 
Ordered Quantity (3) 1-2 3-5 6+
 Discount -0% -5% -10%
Price per Unit ($250.75 CAD) $263.95 CAD $250.75 CAD $237.56 CAD

Formerly BD2400

The tent-like BugDorm-2S400 insect cage provides a large space for potted plants.  The front and back panels of BugDorm-2S400 are of clear plastic for observation of insect activity; the two side panels are of Polyester netting (96 x 26 mesh) for ventilation.  The support poles of its base frame are of 4-mm diameter fiberglass.

There are three openings in the front panel of the BugDorm-2S400 insect rearing cage.  The zippered opening is large enough to insert potted plants.  The two smaller sleeve openings (18 cm diameter) o­n the zippered opening permit the addition or removal of insects and the replacement of food without letting insects escape.

BugDorm-2S400 insect cage is constructed so that support poles are outside the enclosure.  There are no places for insects to hide inside BugDorm-2S400.

Pack Contents
x1 Fabric Cage Body
x8 Fiberglass Rods (Ø4 mm, L37 cm)
x12 Fiberglass Rods (Ø4 mm, L55 cm, 2 spares)
x8 ABS Plastic Joints (2-Way)
x4 ABS Plastic Ridged Joints (2-Way)
x4 ABS Plastic Joints (3-Way)

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Collection of related articles from the last 10 years:
Silverleaf nightshade (Solanum elaeagnifolium), a reservoir host for ‘Candidatus Liberibacter solanacearum’, the putative causal agent of zebra chip disease of potato. Thinakaran et al. (2015). Plant Disease, 99(7), 910-915.
Tomato infection by whitefly-transmitted circulative and non-circulative viruses induce contrasting changes in plant volatiles and vector behaviour. Fereres et al. (2016). Viruses, 8(8), 225.
Oviposition preference and larval performance of Cnaphalocrocis medinalis (Lepidoptera: Pyralidae) on rice genotypes. Liao & Chen (2017). Journal of Economic Entomology, 110(3), 1291-1297.
The function of supplemental foods for improved crop establishment of generalist predators Orius insidiosus and Dicyphus hesperus. Labbé et al. (2018). Scientific Reports, 8(1), 1-12.
Plant-mediated indirect effects of two viruses with different transmission modes on Bemisia tabaci feeding behavior and fitness. Maluta et al. (2019). Journal of Pest Science, 92(2), 405-416.
About lipid metabolism in Hermetia illucens (L. 1758): on the origin of fatty acids in prepupae. Hoc et al. (2020). Scientific Reports, 10(1), 1-8.
Grapevine red blotch virus is transmitted by the three-cornered alfalfa hopper in a circulative, nonpropagative mode with unique attributes. Flasco et al. (2021). Phytopathology, 111(10).
Predator-prey interactions and life history of Orius laevigatus and O. majusculus feeding on flower and leaf-inhabiting thrips. Mouratidis et al. (2022). Biological Control, 172, 104954.
Pathogen-triggered metabolic adjustments to potato virus Y infection in potato. Manasseh et al. (2023). Frontiers in Plant Science, 13, 1031629.
Detecting sorghum aphid infestation in grain sorghum using leaf spectral response. Craigie et al. (2024). Scientific Reports, 14(1), 14053.