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Read our guarantee »Products:Immunology >> Adaptive Immunity >> B Cells >> Non-CD
Anti-Bcl3 antibody [1E8]
See all Bcl3 products (5) ...
Mouse monoclonal [1E8] to Bcl3
ICC/IF, IHC-P, IHC-Frmore details
Reacts with
Human
Recombinant protein corresponding to a 200 amino acid N terminal truncate of the Bcl-3 molecule.
Immunohistochemistry: Tonsil.
Liquid
Store at +4°C short term (1-2 weeks). Aliquot and store at -20°C or -80°C. Avoid repeated freeze / thaw cycles.
Preservative: 15mM Sodium Azide
Constituents: Tissue culture supernatant
Tissue culture supernatant
Monoclonal
1E8
P3-NS1/1-Ag4-1
IgG2a
kappa
Our Abpromise guarantee covers the use of ab49470 in the following tested applications.
The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.
ICC/IF: Use a concentration of 5 µg/ml
IHC-P: 1/25 - 1/50.
IHC-Fr: 1/100(Acetone fixation is recommended.)
Is unsuitable for or WB.
Contributes to the regulation of transcriptional activation of NF-kappa-B target genes. In the cytoplasm, inhibits the nuclear translocation of the NF-kappa-B p50 subunit. In the nucleus, acts as transcriptional activator that promotes transcription of NF-kappa-B target genes. Contributes to the regulation of cell proliferation.
Note=A chromosomal aberration involving BCL3 may be a cause of B-cell chronic lymphocytic leukemia (B-CLL). Translocation t(14;19)(q32;q13.1) with immunoglobulin gene regions.
Contains 7 ANK repeats.
Polyubiquitinated. Ubiquitination via 'Lys-63'-linked ubiquitin chains is required for nuclear accumulation. Deubiquitinated by CYLD, which acts on 'Lys-63'-linked ubiquitin chains. Deubiquitination by CYLD prevents nuclear accumulation.
Activated by phosphorylation.
Nucleus. Cytoplasm. Cytoplasm > perinuclear region. Ubiquitination via 'Lys-63'-linked ubiquitin chains is required for nuclear accumulation.
Target information above from: UniProt accessionP20749
The UniProt Consortium
The Universal Protein Resource (UniProt) in 2010
Nucleic Acids Res. 38:D142-D148 (2010).
Immunohistochemistry (Paraffin-embedded sections) - Bcl3 antibody [1E8] (ab49470)
![Immunohistochemistry (Paraffin-embedded sections) - Bcl3 antibody [1E8] (ab49470)](/ps/datasheet/Images/49/ab49470/ab49470_1.jpg)
ab49470, at a dilution of 1/25, staining Bcl3 oncoprotein in paraffin sections of normal human tonsil by immunohistochemistry. Note nuclear staining of a proportion of follicular cells, parafollicular cells and mucosa.
Immunocytochemistry/ Immunofluorescence-Bcl3 antibody [1E8](ab49470)
](/ps/datasheet/images/49/ab49470/Bcl3-Primary-antibodies-ab49470-1.jpg)
ICC/IF image of ab49470 stained MCF7 cells. The cells were 4% formaldehyde 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 (ab49470, 5µg/ml) overnight at +4°C. The secondary antibody (green) was ab96879, DyLight® 488 goat anti-mouse IgG (H+L) used at a 1/250 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.
ab49470 has not yet been referenced specifically in any publications.
Publishing research using ab49470? Please let us know so that we can cite the reference in this datasheet
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![Immunohistochemistry (Paraffin-embedded sections) - Bcl3 antibody [1E8] (ab49470)](/ps/datasheet/Images/49/ab49470/ab49470_1.jpg)
ab49470, at a dilution of 1/25, staining Bcl3 oncoprotein in paraffin sections of normal human tonsil by immunohistochemistry. Note nuclear staining of a proportion of follicular cells, parafollicular cells and mucosa.
](/ps/datasheet/images/49/ab49470/Bcl3-Primary-antibodies-ab49470-1.jpg)
ICC/IF image of ab49470 stained MCF7 cells. The cells were 4% formaldehyde 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 (ab49470, 5µg/ml) overnight at +4°C. The secondary antibody (green) was ab96879, DyLight® 488 goat anti-mouse IgG (H+L) used at a 1/250 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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