This video demonstrates an immunostaining technique to localize arabinogalactan proteins (AGPs) and pectins in plant tissues. Fixed and resin-embedded plant tissue sections are stained with AGP- and pectin-specific primary and fluorescent secondary antibodies and a cellulose-binding fluorescent dye to reveal their tissue-specific colocalization in the cell wall.
Protocol
1. Immunolocalization NOTE: The fluorescent immunolocalization procedure relies on sequential use of two antibodies. The primary antibody is raised against a specific target antigen. The secondary antibody is raised specifically against the primary antibody and for fluorescent techniques is conjugated to a fluorophore (FITC [fluorescein isothiocyanate] in this specific protocol). The primary antibody will be used to detect the target antigen in the sample, and t…
Representative Results
Figure 1. (A) Schematic representation of the block trimming sequence for preparing the sample (Yellow block) for sectioning with the ultramicrotome. Firstly, the gelatin capsule is removed (1). Then they are first trimmed at a 40° to 45° angle to the sides of the capsule tangentially to the sample (2), a second cut is made at 90° of the first (3) followed by a third (4) and fourth…
Divulgaciones
The authors have nothing to disclose.
Materials
8 wells Glass reaction slides
Marinfeld
MARI1216750
other brands may be used
Anti-Rat IgG (wole molecule)-FITC antibody produce in GOAT
Sigma-Aldrich
F6258
cover slips, 24 mm x 50 mm
Marinfeld
MARI0100222
The cover slip should cover all the wells. Other brands may be used
ddH2O
na
na
Ethanol absolute
na
na
Fluorescent brightner 28
Sigma-Aldrich
F-6259
Non fat dry milk
Nestlé
na
any non fat dry milk is adequate
Oven
na
na
generic laboratory oven
Rat generated Monoclonal Anti-Body
Plant probes
na
Several antibodies that recognize cell wall components are available at both the Complex Carbohydrate research center (CCRC, Georgia University USA) and Plant Probes (Paul Knox Cell Wall Lab, at Leeds University UK). A short list of some commonly used MABS and where they can be purchased is presented in Supplemental Table 1
upright epifluorescence microscope with UV and FITC fluorescence filters
Leica Mycrosistems
DMLb
vaccum chamber
na
na
vaccum pump
na
na
Vectashield
vecta Labs
T-1000
Other anti-fade may be used. Please do check for compatibility with FITC and the Fluorescente brightner 28. (Note: for a non-commercial alternative, (see Jonhson et al 198218) An antifade medium can be made by mixing 25 mg/mL of 1,4-Diazobicyclo-(2,2,2)octane (DABCO) in 9:1 (v/v) glycerol to 1xPBS. Adjust pH to 8.6 with diluted HCl.)