Mouse Anti-FUT4 Recombinant Antibody (10) (CBMAB-Z0149-LY)
decrease/loss of Western blot signal on defined conjugated Lewis epitopes presented by the recombinant glyco-engineered P-selectin
glycoprotein ligand-1 (PSGL1) from engineered CHO cells. Each enzyme (2 µM) wasincubated with beads carrying PSGL-1 glycoprotein (displaying
a specific Le antigens) in 20 mM HEPES buffer 150 mM NaCl pH 6.8 at 37 °C for 3 h in 50 µl. The beads were boiled in presence of SDS-loading
buffer containing 25 mM DTT for 10 min at 95°C and western blot analysis was performed (see materials and methods). For simplicity, only the
defined Lewis epitopes of the native protein O-glycome are shown. The enzymatic activity is monitored by the loss of Western blot signal
originating from specific Le-epitope antibodies after enzyme incubation. The cleavage of a fucosyl would be observed as a loss/decrease of signal
due to the large decrease/abolished binding of the antibody. Inactive enzymes serve also as negative controls as they show independently the
full-signal, whereas the active enzymes serve as positive controls, showing signal level when the motif is depleted. The data are from a single
(n=1) experiment. Source data are provided as a Source Data file labelled with the corresponding figure number and panel definition. ...View More
Robust anti-CD15 (red) and anti-AQP9 co-labeling was observed in myelomonocytic cells (asterisk). In 4 patient-biopsies weaker CD15 immunolabeling was also observed in a number of larger cells, likely identifying these cells as BTSCs (examples marked by arrowheads). Non-myelomonocytic AQP9 positive cells (examples marked by arrows) were located near putative BTSCs, but no clear examples of AQP9 and CD15 co-expression were observed in these cells. Two areas are shown as overlay images (left), green channel (center) and red channel (right). Nuclei (blue). Scale bar = 20 µm. ...View More
Basic Information
| Application | Note |
| WB | 1:100-1:1,000 |
| IP | 1-2 µg per 100-500 µg of total protein (1 ml of cell lysate) |
| IF(ICC) | 1:50-1:500 |
| IHC-P | 1:50-1:500 |
Formulations & Storage [For reference only, actual COA shall prevail!]
Target
Fucosylation Source: GO_Central
L-fucose catabolic process Source: UniProtKB
Oligosaccharide biosynthetic process Source: Reactome
Oligosaccharide metabolic process Source: UniProtKB
Positive regulation of leukocyte tethering or rolling Source: UniProtKB
Protein glycosylation Source: UniProtKB
Regulation of leukocyte cell-cell adhesion Source: UniProtKB
Helical: 148-172
Lumenal: 173-530
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Please try the standard protocols which include: protocols, troubleshooting and guide.
Enzyme-linked Immunosorbent Assay (ELISA)
Flow Cytometry
Immunofluorescence (IF)
Immunohistochemistry (IHC)
Immunoprecipitation (IP)
Western Blot (WB)
Enzyme Linked Immunospot (ELISpot)
Proteogenomic
Other Protocols
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Custom Antibody Labeling
We also offer labeled antibodies developed using our catalog antibody products and nonfluorescent conjugates (HRP, AP, Biotin, etc.) or fluorescent conjugates (Alexa Fluor, FITC, TRITC, Rhodamine, Texas Red, R-PE, APC, Qdot Probes, Pacific Dyes, etc.).
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