Fucosylated xyloglucan | (CCRC-M1)

304 €

AS16 3136  | clonality: monoclonal  |  host: mouse  |  reactivity: Acer pseudoplatanus, Arabidopsis thaliana


1 st
Item No:
AS16 3136

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product information
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.

MeBSA-conjugated sycamore rhamnogalacturonan (non-covalent)

Host Mouse
Clonality Monoclonal
Clone IgG1, clone CCRC-M1
Format Cell culture supernatant, liquid
Quantity 5 ml

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)
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Plant and algal protein extraction buffer

Secondary antibodies

Additional information

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

application information
Recommended dilution

undiluted or at 1:10

Expected | apparent MW
Confirmed reactivity

Acer pseudoplatanus, Arabidopsis thaliana

Predicted reactivity dicots
Not reactive in

no confirmed exceptions from predicted reactivity are currently known

Additional information
Selected references

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

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