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Read our guarantee »Products:Cell Biology >> Cell Cycle >> Cell differentiation
Anti-Bmi1 antibody [1.T.21] - ChIP Grade
See all Bmi1 products (10) ...
Mouse monoclonal [1.T.21] to Bmi1 - ChIP Grade
Recognizes mouse Bmi-1(triplet).
ICC/IF, Flow Cyt, ChIP, WB, ICC, IP, IHC-Fr, IHC-Pmore details
Reacts with
Mouse, Rat, Rabbit, Cat, Human, Zebrafish
Recombinant fragment, corresponding to amino acids 1-202 of Mouse Bmi1
U2OS whole cell lysate.
Liquid
Shipped at 4°C. Upon delivery aliquot and store at -20°C. Avoid freeze / thaw cycles.
Preservative: 0.05% Sodium Azide
Constituents: 30% Glycerol, 0.15M Sodium Chloride, 0.15M Tris-glycine. pH 7.4
Concentration information loading...
Protein G purified
Monoclonal
1.T.21
IgG1
Epigenetics and Nuclear Signaling >> ChIP'ing antibodies >> ChIP'ing antibodies
Cancer >> Oncoproteins/suppressors >> Oncoproteins >> Other
Cancer >> Cell cycle >> Cell differentiation
Stem Cells >> Hematopoietic Progenitors >> Intracellular Molecules
Epigenetics and Nuclear Signaling >> Transcription >> Cancer susceptibility >> Proto-oncogenes
Epigenetics and Nuclear Signaling >> Chromatin Remodeling >> Polycomb Silencing >> PRC2
Cell Biology >> Cell Cycle >> Cell differentiation
Our Abpromise guarantee covers the use of ab14389 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 0.65 µg/ml(PubMed: 19001505)
Flow Cyt: Use a concentration of 0.65 µg/ml(PubMed: 19001505)
ChIP: Use at an assay dependent dilution. (PubMed: 18332116)
WB: Use a concentration of 0.2 - 2.0 µg/ml.Predicted molecular weight: 37 kDa.(Detects Bmi-1 in RIPA lysates from U2OS cells. U2OS cell lysate was resolved by electrophoresis, transferred to nitrocellulose and probed with ab14389 0.2ug/ml. Proteins were visualized using a goat anti-mouse IgG labeled with HRP and a chemiluminescence detection system.)
ICC: Use at an assay dependent dilution.
IP: Use at an assay dependent dilution.
IHC-Fr: Use at an assay dependent dilution. (PubMed: 17210912)
IHC-P: 1/100
Component of the Polycomb group (PcG) multiprotein PRC1 complex, a complex required to maintain the transcriptionally repressive state of many genes, including Hox genes, throughout development. PcG PRC1 complex acts via chromatin remodeling and modification of histones; it mediates monoubiquitination of histone H2A 'Lys-119', rendering chromatin heritably changed in its expressibility. In the PRC1 complex, it is required to stimulate the E3 ubiquitin-protein ligase activity of RNF2/RING2.
Contains 1 RING-type zinc finger.
Monoubiquitinated (By similarity). May be polyubiquitinated; which does not lead to proteasomal degradation.
Nucleus. Cytoplasm.
Target information above from: UniProt accessionP35226
The UniProt Consortium
The Universal Protein Resource (UniProt) in 2010
Nucleic Acids Res. 38:D142-D148 (2010).
Immunocytochemistry - Bmi1 antibody [1.T.21] - Hematopoietic Stem Cell Marker (ab14389)
![Immunocytochemistry - Bmi1 antibody [1.T.21] - Hematopoietic Stem Cell Marker (ab14389)](/ps/datasheet/Images/14/ab14389/ab14389_1.jpg)
SK-N-SH cells were fixed in 4% paraformaldehyde, permeabilized in 0.55 Triton-X100 and incubated for 1 hour with ab14389 (1/200). The Bmi1 staining is shown in red. The cells were counterstained with DAPI (blue). 100x magnification.
Darin McDonald, Cross Cancer Institute
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Bmi1 antibody [1.T.21] - ChIP Grade (ab14389)
![Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Bmi1 antibody [1.T.21] - ChIP Grade (ab14389)](/ps/datasheet/images/14/ab14389/Bmi1-Primary-antibodies-ab14389-5.jpg)
ab14389 staining Bmi1 in human head and neck squamous cell cancers (HNSCC) by Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections).Sections were deparaffinized in xylene, dehydrated through graded alcohols, and placed in 0.1% hydrogen peroxide to quench any endogenous peroxidase activity. A 5 minute, 750 W microwave pretreatment in citrate buffer (pH 6.0) was repeated 4 times and followed by treatment with 10% normal rabbit serum for 30 minutes to block nonspecific antibody binding. The slides were then incubated with ab14389 at a 1/100. Primary antibody incubation was followed by three washes with PBST and incubation with fluorescently-labeled Cy2 (1/250) secondary antibody for 2 hours. Nuclei were counterstained with DAPI. Finally, sections were rinsed with PBST, dehydrated through sequential washes in 50%, 70%, 95%, and 100% ethanol and then cleared in xylene. Slides were mounted with DPX mounting media and allowed to dry overnight.
Image from Ganguli-Indra G et al, PLoS One. 2009;4(4):e5367. Epub 2009 Apr 28, Fig 2.
This product has been referenced in:
See all 16 publications for this product
Publishing research using ab14389? Please let us know so that we can cite the reference in this datasheet
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![Immunocytochemistry - Bmi1 antibody [1.T.21] - Hematopoietic Stem Cell Marker (ab14389)](/ps/datasheet/Images/14/ab14389/ab14389_1.jpg)
SK-N-SH cells were fixed in 4% paraformaldehyde, permeabilized in 0.55 Triton-X100 and incubated for 1 hour with ab14389 (1/200). The Bmi1 staining is shown in red. The cells were counterstained with DAPI (blue). 100x magnification.
Darin McDonald, Cross Cancer Institute
![Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Bmi1 antibody [1.T.21] - ChIP Grade (ab14389)](/ps/datasheet/images/14/ab14389/Bmi1-Primary-antibodies-ab14389-5.jpg)
ab14389 staining Bmi1 in human head and neck squamous cell cancers (HNSCC) by Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections).Sections were deparaffinized in xylene, dehydrated through graded alcohols, and placed in 0.1% hydrogen peroxide to quench any endogenous peroxidase activity. A 5 minute, 750 W microwave pretreatment in citrate buffer (pH 6.0) was repeated 4 times and followed by treatment with 10% normal rabbit serum for 30 minutes to block nonspecific antibody binding. The slides were then incubated with ab14389 at a 1/100. Primary antibody incubation was followed by three washes with PBST and incubation with fluorescently-labeled Cy2 (1/250) secondary antibody for 2 hours. Nuclei were counterstained with DAPI. Finally, sections were rinsed with PBST, dehydrated through sequential washes in 50%, 70%, 95%, and 100% ethanol and then cleared in xylene. Slides were mounted with DPX mounting media and allowed to dry overnight.
Image from Ganguli-Indra G et al, PLoS One. 2009;4(4):e5367. Epub 2009 Apr 28, Fig 2.
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