Mouse Monoclonal FUT4 antibody. Suitable for IHC-FoFr, IHC-P, ICC, Flow Cyt and reacts with Human, Mouse samples. Cited in 62 publications.
Preservative: 0.02% Sodium azide
Constituents: 99% Tissue culture supernatant
IHC-FoFr | IHC-P | ICC | Flow Cyt | |
---|---|---|---|---|
Human | Expected | Tested | Expected | Expected |
Mouse | Predicted | Expected | Tested | Tested |
Species | Dilution info | Notes |
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Species Human | Dilution info Use at an assay dependent concentration. | Notes - |
Species | Dilution info | Notes |
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Species Mouse | Dilution info - | Notes - |
Species | Dilution info | Notes |
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Species Human | Dilution info 1/200 | Notes Perform heat-mediated antigen retrieval with citrate buffer pH 6 before commencing with IHC staining protocol. |
Species | Dilution info | Notes |
---|---|---|
Species Mouse | Dilution info Use at an assay dependent concentration. | Notes - |
Species | Dilution info | Notes |
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Species Mouse | Dilution info 1/1000 | Notes Fixation with 100% MeOH (5 min) or 4% PFA (10 min). |
Species | Dilution info | Notes |
---|---|---|
Species Human | Dilution info Use at an assay dependent concentration. | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Mouse | Dilution info - | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Human | Dilution info Use at an assay dependent concentration. | Notes - |
Catalyzes alpha(1->3) linkage of fucosyl moiety transferred from GDP-beta-L-fucose to N-acetyl glucosamine (GlcNAc) within type 2 lactosamine (LacNAc, Gal-beta(1->4)GlcNAc) glycan attached to N- or O-linked glycoproteins (PubMed:11485743). Robustly fucosylates nonsialylated distal LacNAc unit of the polylactosamine chain to form Lewis X antigen (CD15), a glycan determinant known to mediate important cellular functions in development and immunity. Fucosylates with lower efficiency sialylated LacNAc acceptors to form sialyl Lewis X and 6-sulfo sialyl Lewis X determinants that serve as recognition epitopes for C-type lectins (PubMed:11485743). Together with FUT7 contributes to SELE, SELL and SELP selectin ligand biosynthesis and selectin-dependent lymphocyte homing, leukocyte migration and blood leukocyte homeostasis (PubMed:11485743). In a cell type specific manner, may also fucosylate the internal LacNAc unit of the polylactosamine chain to form VIM-2 antigen that serves as recognition epitope for SELE (By similarity).
Elft, Fut4, 4-galactosyl-N-acetylglucosaminide 3-alpha-L-fucosyltransferase, Fucosyltransferase 4, Fucosyltransferase IV, Galactoside 3-L-fucosyltransferase, Fuc-TIV, FucT-IV
Mouse Monoclonal FUT4 antibody. Suitable for IHC-FoFr, IHC-P, ICC, Flow Cyt and reacts with Human, Mouse samples. Cited in 62 publications.
Preservative: 0.02% Sodium azide
Constituents: 99% Tissue culture supernatant
We guarantee IHC-P in Human only
Tissue culture supernatant was cross flow concentrated.
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Stage-specific embryonic antigen-1 (SSEA-1) also known as CD15 is a carbohydrate antigen often attached to glycoproteins or glycolipids. It has a molecular mass of approximately 480 Da. SSEA-1 is prominently expressed on the surface of murine embryonal carcinoma cells granulocytes and neural stem cells. It plays a role in cellular processes such as adhesion where it influences cell-to-cell and cell-to-extracellular matrix interactions.
SSEA-1 participates in the regulation of cell differentiation and migration. This carbohydrate antigen is particularly critical in developmental stages where it impacts cellular behaviors that are important for embryogenesis. It functions as an adhesion molecule playing a role in forming complexes with cell surface lectins. These complexes can influence how cells communicate and adhere to one another therefore affecting various aspects of cellular dynamics.
SSEA-1 is integral to the leukocyte extravasation signaling pathway which is significant for the immune system's operation. It interacts with proteins involved in the regulation of inflammation and immune response such as selectins. The antigen aids the tethering and rolling of leukocytes on endothelial surfaces a precursor step for their transmigration into tissues. SSEA-1's interaction with selectins is important in this process driving important cellular functions that enable immune surveillance and responses.
SSEA-1 is associated with certain cancers such as leukemia and neurological disorders. In leukemia SSEA-1 can act as a marker for cancer stem cells influencing tumor progression and resistance to chemotherapy. In the context of neurological disorders its altered expression is connected with the pathology of Alzheimer's disease where neural stem cell behavior may be affected. Other proteins like amyloid precursors potentially interact with SSEA-1 in Alzheimer's contributing to the disease's complexity.
We have tested this species and application combination and it works. It is covered by our product promise.
We have not tested this specific species and application combination in-house, but expect it will work. It is covered by our product promise.
This species and application combination has not been tested, but we predict it will work based on strong homology. However, this combination is not covered by our product promise.
We do not recommend this combination. It is not covered by our product promise.
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Full details and terms and conditions can be found here:
Terms & Conditions.
ab16285 staining SSEA1 in mES cells. The cells were fixed with 4% paraformaldehyde (10 min), permeabilized with 0.1% PBS-Tween for 5 minutes and then blocked with 1% BSA/10% normal goat serum/0.3M glycine in 0.1%PBS-Tween for 1h. The cells were then incubated overnight at 4°C with ab16285 at a 1/1000 dilution and Anti-beta Tubulin antibody - Loading Control ab6046, Rabbit polyclonal to beta Tubulin - Loading Control. Cells were then incubated with Goat Anti-Mouse IgM mu chain (Alexa Fluor® 488) ab150121, Goat polyclonal Secondary Antibody to Mouse IgM - mu chain (Alexa Fluor® 488) at 1/1000 dilution (shown in green) and Goat Anti-Rabbit IgG H&L (Alexa Fluor® 594) ab150080, Goat polyclonal Secondary Antibody to Rabbit IgG - H&L (Alexa Fluor® 594) at 1/1000 dilution (shown in pseudocolour red). Nuclear DNA was labelled with DAPI (shown in blue).
Also suitable in cells fixed with 100% methanol (5 min).
Image was acquired with a confocal microscope (Leica-Microsystems TCS SP8) and a single confocal section is shown.
Cell surface flow analysis of SSEA1 on D3 mouse ES cells using ab16285 at 1:100 dilution. Purple histogram represents negative control; green line represents anti-SSEA1 antibody (ab16285).
The image shows staining of the cell membranes of P19 mouse embryonic carcinoma cells using SSEA1-specific antibody, ab16285.
IHC image of SSEA1 staining in Human Hodgkin's Lymphoma formalin fixed paraffin embedded tissue section*. The section was pre-treated using pressure cooker heat mediated antigen retrieval with sodium citrate buffer (pH6.0). The section was incubated with ab16285, 1/200 dilution, overnight at 4°C. A Goat anti-Mouse (IgM) HRP conjugated secondary antibody (Goat Anti-Mouse IgM mu chain (HRP) ab97230 at 1/2000) was used to detect the primary and visualized using DAB as the chromogen. The section was counterstained with haematoxylin and mounted with DPX.
For other IHC staining systems (automated and non-automated) customers should optimize variable parameters such as antigen retrieval conditions, primary antibody concentration and antibody incubation times.
*Tissue obtained from the Human Research Tissue Bank, supported by the NIHR Cambridge Biomedical Research Centre
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