Rat Monoclonal xyloglucan antibody. Suitable for ICC/IF and reacts with Tobacco, Plants samples. Cited in 3 publications.
pH: 7.4
Preservative: 0.02% Sodium azide
Constituents: PBS, 6.97% L-Arginine
ICC/IF | |
---|---|
Arabidopsis suecica | Predicted |
Arabidopsis thaliana | Predicted |
Arachis hypogaea | Predicted |
Plants | Expected |
Tobacco | Tested |
Species | Dilution info | Notes |
---|---|---|
Species Tobacco | Dilution info 3 µg/mL | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Plants | Dilution info 3 µg/mL | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Arabidopsis thaliana, Arabidopsis suecica, Arachis hypogaea | Dilution info - | Notes - |
Rat Monoclonal xyloglucan antibody. Suitable for ICC/IF and reacts with Tobacco, Plants samples. Cited in 3 publications.
pH: 7.4
Preservative: 0.02% Sodium azide
Constituents: PBS, 6.97% L-Arginine
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ab190146 staining Xyloglucan in 10μm thick tobacco plant stem internode sections, after 6 weeks of growth, fixed in 4% formaldehyde.
Sections were treated with and without pectate lysate (to remove pectic homogalacturonan and further expose the LM15 epitope). Non-specific protein-protein interactions were blocked in 3% BSA/0.3M glycine in 0.1%PBS-Tween for 1h. The sections were then incubated with ab190146 at 3μg/ml, for 2h at room temperature. Goat Anti-Rat IgG H&L (Alexa Fluor® 488) preadsorbed ab150165, Goat Anti-Rat IgG H&L (Alexa Fluor® 488) preadsorbed, was used as the secondary antibody at 2μg/ml, for 1h at room temperature (shown in green) As expected, the staining is stronger in pectate lysate treated sections than in untreated.
Also included are negative control images (secondary antibody only) for both treatments, demonstrating antibody specificity and low levels of auto-fluorescence.
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