Abstract: A universal line components duct elbow (universal elbow) accommodates a variety of condensate tanks. The universal elbow includes an elbow base, an elbow cover, and an interface clip. The interface clip is releasably connected to the bottom wall and sidewalls of the elbow base and adapted for supporting a condensate tank within the universal elbow. In order to releasably connect the interface clip to the bottom wall of the elbow base, the bottom wall of the elbow base includes an elbow base/clip securing structure that engages a complementary clip/elbow base securing structure on one side of the interface clip. In order to secure the condensate tank within the universal elbow, the interface clip has a clip/tank securing structure on the opposite side that engages the structure of the condensate tank.

Abstract: A universal line components duct elbow (universal elbow) accommodates a variety of condensate tanks. The universal elbow includes an elbow base, an elbow cover, and an interface clip. The interface clip is releasably connected to the bottom wall and sidewalls of the elbow base and adapted for supporting a condensate tank within the universal elbow. In order to releasably connect the interface clip to the bottom wall of the elbow base, the bottom wall of the elbow base includes an elbow base/clip securing structure that engages a complementary clip/elbow base securing structure on one side of the interface clip. In order to secure the condensate tank within the universal elbow, the interface clip has a clip/tank securing structure on the opposite side that engages the structure of the condensate tank.

Abstract: Disclosed are methods, systems, and kits for screening a newborn infant for one or more gene variants comprising, obtaining a genomic DNA containing sample from the newborn infant; sequencing at least one target region of each of two or more genes selected from the group consisting of PCCA, PCCB, MUT, MMAA, MMAB, MMADHC, MCEE, IVD, ACAT1, ACADM, ACADVL, HADHA, ASL, BCKDHA, BCKDHB, DBT, DLD, CYP21A2, GALT, and ACAD8 in the genomic DNA; and screening for a gene variant from the sequenced target regions of each gene to identify gene variants present in the genomic DNA, wherein the sequencing does not include whole genome sequencing or whole exome sequencing.