C3669
Liquid chromatography columns
Luer Lock, Non-jacketed, bed volume 4 mL, I.D. × L 0.7 cm × 10 cm
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About This Item
UNSPSC Code:
12000000
eCl@ss:
32060201
NACRES:
SB.52
Recommended Products
grade
for chromatography
technique(s)
LPLC: suitable
I.D. × L
0.7 cm × 10 cm
bed volume
4 mL
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General description
All of the columns listed below are constructed of borosilicate glass and are rated at a maximum pressure of 15psi (1 bar). Five configurations are available:
A - Luer-Lock, Non Jacketed: Fixed polypropylene end caps, polyethylene bed supports, Luer-Lock inlet and outlet fittings.
B - Luer-Lock, Jacketed: Same as A (above), with a borosilicate glass jacket surrounding the column body for temperature control.
C - Open-ended: Fixed polypropylene ends (outside of tube only), without jacket or end fittings. Requires 2 flow adapters.
D - PTFE, non-jacketed: Threaded ends, removable PTFE fittings with shielded O-ring seals, 20 μm polyethylene bed supports, and 1/4-28 threaded tubing connections. Solvents contact only PTFE and borosilicate glass.
E - PTFE, jacketed: Same as D (above), with an acrylic jacket surrounding the column body for temperature control.
A - Luer-Lock, Non Jacketed: Fixed polypropylene end caps, polyethylene bed supports, Luer-Lock inlet and outlet fittings.
B - Luer-Lock, Jacketed: Same as A (above), with a borosilicate glass jacket surrounding the column body for temperature control.
C - Open-ended: Fixed polypropylene ends (outside of tube only), without jacket or end fittings. Requires 2 flow adapters.
D - PTFE, non-jacketed: Threaded ends, removable PTFE fittings with shielded O-ring seals, 20 μm polyethylene bed supports, and 1/4-28 threaded tubing connections. Solvents contact only PTFE and borosilicate glass.
E - PTFE, jacketed: Same as D (above), with an acrylic jacket surrounding the column body for temperature control.
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Peter Morris et al.
Journal of bacteriology, 190(6), 2172-2182 (2008-01-08)
A characteristic feature of bacteriophage genomes is that they are architecturally mosaic, with each individual genome representing a unique assemblage of individual exchangeable modules. Plausible mechanisms for generating mosaicism include homologous recombination at shared boundary sequences of module junctions, illegitimate
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