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JM109 lysate Antibody is a Rabbit Polyclonal against JM109 lysate
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10561 1 Ig targets JM109 lysate in WB ELISA applications and shows reactivity with bacterial samples
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Image Search Results

Journal: Journal of Bacteriology
Article Title: Identification of a Reactivating Factor for Adenosylcobalamin-Dependent Ethanolamine Ammonia Lyase
doi: 10.1128/JB.186.20.6845-6854.2004
Figure Lengend Snippet: Time courses of in situ deamination of ethanolamine by permeabilized E. coli cells that were grown in medium containing ethanolamine and CN-Cbl. Toluene-treated cells of E. coli JM109 (7.2 × 10 6 cells) grown in the medium containing CN-Cbl at concentrations of 40 ng/ml (A) and 2 μg/ml (B) were incubated at 37°C for the indicated times in the following mixtures: 30 mM potassium phosphate buffer (pH 8.0), 50 mM KCl, 10 mM ethanolamine, with (circles) or without (triangles) 15 μM AdoCbl, in the presence (solid symbols) or absence (open symbols) of 3 mM ATP plus 3 mM MgCl 2 , in a total volume of 1.0 ml. The amount of acetaldehyde formed was determined as described in the text.
Article Snippet: To obtain direct evidence for the function of EutA as an EAL-reactivating factor, the EutA protein overexpressed in
Techniques: In Situ, Incubation

Journal: Journal of Bacteriology
Article Title: Identification of a Reactivating Factor for Adenosylcobalamin-Dependent Ethanolamine Ammonia Lyase
doi: 10.1128/JB.186.20.6845-6854.2004
Figure Lengend Snippet: Time courses of ethanolamine deamination by homogenates of E. coli cells that were grown in the medium containing ethanolamine and CN-Cbl. Homogenates of E. coli JM109 grown in the medium containing 40 ng of CN-Cbl/ml were incubated at 37°C for the indicated time in the following mixtures: 30 mM potassium phosphate buffer (pH 8.0), 50 mM KCl, 10 mM ethanolamine, 15 μM AdoCbl, in the presence (solid circles) or absence (open circles) of ATP plus MgCl 2 (3 mM each), in a total volume of 0.5 ml. The amount of acetaldehyde formed was determined as described in the text.
Article Snippet: To obtain direct evidence for the function of EutA as an EAL-reactivating factor, the EutA protein overexpressed in
Techniques: Incubation