Fucosylated xyloglucan (clone CCRC-M1)

AS16 3136-1ml  | Clonality: monoclonal  |  Host: Mouse  |  Reactivity: Acer pseudoplatanus, Arabidopsis thaliana

From the laboratory of Michael G. Hahn, PhD, University of Georgia

Fucosylated xyloglucan (clone CCRC-M1) in the group Antibodies for Plant/Algal  / Cell Wall / Dr. Hahn collection, University of Georgia at Agrisera AB (Antibodies for research) (AS16 3136-1ml)


How to cite this product:
Product name, number (Agrisera, Sweden)

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Product Information


MeBSA-conjugated sycamore rhamnogalacturonan (non-covalent)

Host Mouse
Clonality Monoclonal
Subclass/isotype IgG1
Format Cell culture supernatant, liquid
Quantity 1ml

Antibody can be stored up to 1 month at 4°C, and at -80°C for up to 1 year.

Make aliquots to avoid repeated freeze-thaw cycles. Please, remember to spin tubes briefly prior to opening them to avoid any losses that might occur from liquid material adhering to the cap or sides of the tubes.

Tested applications ELISA (ELISA), Immunohistochemistry (IHC), Immunofluorescence (IF)
Recommended dilution 1 : 10 or nondiluted (ELISA, (IF), (IHC)


Confirmed reactivity Acer pseudoplatanus, Arabidopsis thaliana
Predicted reactivity Dicots
Species of your interest not listed? Contact us
Not reactive in No confirmed exceptions from predicted reactivity are currently known.

Application examples

Application examples Application example

Immunofluorescence detection using Anti-Fucosylated xyloglucan monoclonal antibodies| (CCRC-M1)

Localization of fucosylated xyloglucan (red) in Arabidopsis thaliana hypocotyl, Calcufluor White counterstain (blue) and cell wall autofluorescence (yellow).

The 31 days-old hypocotyls were immersed in 150 μL PME fixation buffer (25 mM PIPES, 1 mM MgSO4, 1 mM EGTA) and then subjected to three consecutive cycles of 5 min-long vacuum infiltration (21°C, 68 kPa). Afterwards they were washed three times in PME (21°C, 68 kPa) prior to storage at 4°C in PME. Hypocotyls were encased in 1 cm3 blocks of 5% agar at 65°C, and stored at 4°C to set. Transverse 40 μm thick sections were cut from segments using a VT100S vibrating microtome (Leica) and blocked for at least 1 h in 5% bovine serum albumin in TBST. Blocking solution was discarded and sections were incubated at 4°C for 16 h with 5 μl of the anti-Fucosylated xyloglucan antibody, followed by 2 washes in 100 μL TBST. Sections were then incubated for 1 h at 21°C in the dark in 10 μl of 2 μg/μl Alexa FluorTM 568 donkey anti-mouse IgG (H+L; 1:36). Sections were again washed twice in 40 μL TBST prior to counter-staining with 0.015% Calcofluor White (Sigma-Aldrich). Sections were again washed twice in 100 μL TBST to remove excess counter-stain and unbound secondary antibody. Immunofluorescence of AlexaFluor 568 was excited with a 561 nm laser, and emitted light filtered at 575–600 nm, while Calcufluor White was subsequently scanned on an independent channel with a 405 nm laser and emission observed at 420–430 nm using laser scanning microscope Zeiss LSM780 point-scan system at 1024 × 1024 pixels (pixel size, 0.6–0.83 μm) with a 10X objective.

Courtesy Dr. Urs Fisher, Umeå Plant Science Centre, Sweden

Additional information

Additional information

Exact working dilution needs to be determined by end user. Epitope structure for carbohydrate antigen is: alpha-Fuc-(1,2)-beta-Gal.

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Plant and algal protein extraction buffer

Secondary antibodies


Background Xyloglucans are polysaccharides commonly referred to as hemicelluloses found in the primary cell walls of vascular plants. This antibody binds to α-Fuc-(1,2)-β-Gal glacan epitope of fucosylated xyloglucan.

Product citations

Selected references Pattathil et al. (2012). Immunological approaches to plant cell wall and biomass characterization: Glycome Profiling. Methods Mol Biol. 2012;908:61-72.doi: 0.1007/978-1-61779-956-3_6.
Patathil et al. (2010). A comprehensive toolkit of plant cell wall glycan-directed monoclonal antibodies. Plant Physiol. 2010 Jun;153(2):514-25.doi: 10.1104/pp.109.151985.

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