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Anti-APC antibody [CC-1]
See all APC products (11) ...
Mouse monoclonal [CC-1] to APC
This antibody has been shown to detect oligodendrocytes and astrocytes.
IHC-P, ICC/IF, IHC-Frmore details
Reacts with
Mouse, Rat, Human, Monkey
Immunogen used was a recombinant amino terminal fragment of APC
Epitope is within amino acid residues 1 - 226 of APC.
Liquid
Store at +4°C. Do not freeze.
Preservative: 0.1% Sodium Azide
Constituents: 0.2% Gelatin, 0.05M Sodium phosphate
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Immunogen affinity purified
APC is well suited for immunohistochemical and immunofluorescence studies of oligodendrocytes and optic nerves due to the antibody’s staining of the cell body as opposed to the myelinated processes.
Monoclonal
CC-1
IgG2b
Cardiovascular >> Heart >> Cardiogenesis >> Transcription factors/regulators
Cancer >> Oncoproteins/suppressors >> Tumor suppressors >> PTC & Wnt pathway
Cancer >> Cell cycle >> Cell division
Stem Cells >> Signaling Pathways >> Wnt >> Cytoplasmic
Epigenetics and Nuclear Signaling >> Transcription >> Cancer susceptibility >> Tumor Suppressors
Neuroscience >> Cell Type Marker >> Glia marker >> Oligodendrocyte marker
Cell Biology >> Cell Cycle >> Cell Division >> Spindle
Our Abpromise guarantee covers the use of ab16794 in the following tested applications.
The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.
IHC-P: Use a concentration of 5 µg/mlPerform heat mediated antigen retrieval via the pressure cooker method before commencing with IHC staining protocol.
ICC/IF: Use a concentration of 5 µg/ml
IHC-Fr: Use a concentration of 5 µg/ml
Adenomatous polyposis coli (APC) is a protein that plays a critical role in several cellular processes. APC is a tumor suppressor, regulates cell division, helps ensure that the number of chromosomes in a cell is correct following cell division and associates with other proteins involved in cell attachment and signaling. APC regulates ß-catenin levels through Wnt-signaling and is involved in actin cytoskeletal integrity, cell-cell adhesion and cell migration. Defects in this gene cause familial adenomatous polyposis (FAP), an autosomal dominant pre-malignant disease that usually progresses to malignancy. Disease-associated mutations tend to be clustered in a small region designated the mutation cluster region (MCR) and result in a truncated protein product.
Cell junction; adherens junction
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - APC antibody [CC-1] (ab16794)
![Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - APC antibody [CC-1] (ab16794)](/ps/datasheet/Images/16/ab16794/ab16794.jpg)
IHC-F formalin-fixed, paraffin embedded human cerebellum with ab16794.
Antibody was used at a concentration of 2.5 mg/ml and sections were pretreated with heat using a pressure cooker prior to staining. Detection with DAB and hematoxylin as a counterstain
Immunocytochemistry/ Immunofluorescence - APC antibody [CC-1] (ab16794)
![Immunocytochemistry/ Immunofluorescence - APC antibody [CC-1] (ab16794)](/ps/datasheet/images/16/ab16794/APC-Primary-antibodies-ab16794-1.jpg)
ICC/IF image of ab16794 stained HeLa cells. The cells were 4% PFA fixed (10 min) and then incubated in 1%BSA / 10% normal goat serum / 0.3M glycine in 0.1% PBS-Tween for 1h to permeabilise the cells and block non-specific protein-protein interactions. The cells were then incubated with the antibody (ab16794, 1µg/ml) overnight at +4°C. The secondary antibody (green) was Alexa Fluor® 488 goat anti-mouse IgG (H+L) used at a 1/1000 dilution for 1h. Alexa Fluor® 594 WGA was used to label plasma membranes (red) at a 1/200 dilution for 1h. DAPI was used to stain the cell nuclei (blue) at a concentration of 1.43µM.
This product has been referenced in:
See all 8 publications for this product
Publishing research using ab16794? Please let us know so that we can cite the reference in this datasheet
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![Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - APC antibody [CC-1] (ab16794)](/ps/datasheet/Images/16/ab16794/ab16794.jpg)
IHC-F formalin-fixed, paraffin embedded human cerebellum with ab16794.
Antibody was used at a concentration of 2.5 mg/ml and sections were pretreated with heat using a pressure cooker prior to staining. Detection with DAB and hematoxylin as a counterstain
![Immunocytochemistry/ Immunofluorescence - APC antibody [CC-1] (ab16794)](/ps/datasheet/images/16/ab16794/APC-Primary-antibodies-ab16794-1.jpg)
ICC/IF image of ab16794 stained HeLa cells. The cells were 4% PFA fixed (10 min) and then incubated in 1%BSA / 10% normal goat serum / 0.3M glycine in 0.1% PBS-Tween for 1h to permeabilise the cells and block non-specific protein-protein interactions. The cells were then incubated with the antibody (ab16794, 1µg/ml) overnight at +4°C. The secondary antibody (green) was Alexa Fluor® 488 goat anti-mouse IgG (H+L) used at a 1/1000 dilution for 1h. Alexa Fluor® 594 WGA was used to label plasma membranes (red) at a 1/200 dilution for 1h. DAPI was used to stain the cell nuclei (blue) at a concentration of 1.43µM.
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