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Read our guarantee »Products:Epigenetics and Nuclear Signaling >> Chromosome Structure >> Chromosome
Anti-INCENP antibody [58-217]
See all INCENP products (4) ...
Mouse monoclonal [58-217] to INCENP
ICC/IF, IHC-Pmore details
Reacts with
Human
Does not react with
Mouse, Rat
His-tagged human INCENP fragment aa231-298.
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: 0.02% Sodium Azide
Constituents: PBS, pH 7.4
Concentration information loading...
IgG fraction
Monoclonal
58-217
IgG1
Our Abpromise guarantee covers the use of ab23956 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 at a concentration of 1 µg/ml.
IHC-P: 1/200. Perform heat mediated antigen retrieval using citrate buffer pH 6.0 before commencing with IHC staining protocol.
Not yet tested in other applications.
Optimal dilutions/concentrations should be determined by the end user.
Component of the chromosomal passenger complex (CPC), a complex that acts as a key regulator of mitosis. The CPC complex has essential functions at the centromere in ensuring correct chromosome alignment and segregation and is required for chromatin-induced microtubule stabilization and spindle assembly. Probably acts through association with AURKB or AURKC. Seems to bind directly to microtubules. Controls the kinetochore localization of BUB1.
Belongs to the INCENP family.
Chromosome > centromere. Cytoplasm > cytoskeleton > spindle. Nucleus. Chromosome > centromere > kinetochore. Localizes to inner kinetochore. Localizes on chromosome arms and inner centromeres from prophase through metaphase and then transferring to the spindle midzone and midbody from anaphase through cytokinesis. Colocalizes with AURKB at mitotic chromosomes.
Target information above from: UniProt accessionQ9NQS7
The UniProt Consortium
The Universal Protein Resource (UniProt) in 2010
Nucleic Acids Res. 38:D142-D148 (2010).
Immunocytochemistry/ Immunofluorescence - INCENP antibody [58-217] (ab23956)
![Immunocytochemistry/ Immunofluorescence - INCENP antibody [58-217] (ab23956)](/ps/datasheet/Images/23/ab23956/ab23956-IF-Im1.jpg)
ICC/IF image of ab23956 stained human HeLa cells. The cells were methanol fixed (5 min) and incubated with the antibody (ab23956, 1µg/ml) for 1h at room temperature. The secondary antibody (green) was Alexa Fluor® 488 goat anti-mouse IgG (H+L) used at a 1/1000 dilution for 1h. Image-iTTM FX Signal Enhancer was used as the primary blocking agent, 5% BSA (in TBS-T) was used for all other blocking steps. DAPI was used to stain the cell nuclei (blue). Alexa Fluor® 594 WGA was used to label plasma membranes (red).
Immunofluorescence - INCENP antibody [58-217] (ab23956)
![Immunofluorescence - INCENP antibody [58-217] (ab23956)](/ps/datasheet/Images/23/ab23956/ab23956_3.jpg)
ab23956 staining INCENP in HeLa cells, by immunofluorescence.
optimal antibody dilution: 1mg/ml
optimal fixation protocol: PFA/Triton fixation: 10 min room temperature in 3,7 % PFA diluted in PHEM PEM buffer: 45 mM Hepes pH 6,9, 45 mM Pipes pH 6,9, 5mM MgCl2, 10 mM EGTA) containing 0 ,2% Triton X-100, followed by 3 washes in PBS. Also gives a good staining with PFA fixation: 10 min in 3,7 % PFA at room temperature, 5 min in PBS / 0,1%Triton X-100, then 3 washes in PBS.
IF staining was performed following a standard protocol: blocking: 30 min; primary antibody: 1 hr; secondary antibody: 45’. All incubations were at 37 °C in PBS/ 0,1% Tween containing 3% BSA.
This antibody was also tested using NIH-3T3 cells but it did not provide good results with these cells.
Image kindly submitted by Serena Orlando, Giulia Guarguaglini and Patrizia Lavia, from the University 'La Sapienza' CNR, Italy
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - INCENP antibody [58-217] (ab23956)
![Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - INCENP antibody [58-217] (ab23956)](/ps/datasheet/Images/23/ab23956/ab23956_4.jpg)
ab23956 staining human anal cancer tissue sections by IHC-P. Sections were formaldehyde fixed and subjected to heat mediated antigen retreival in citrate buffer (pH 6) prior to blocking in a commercially available blocking agent for 20 minutes at 20°C. The primary anibody was diluted 1/200 and incubated with the sample for 40 minutes at 20°C. A HRP-conjugated goat anti-mouse antibody was used as the secondary.
This image is courtesy of an Abreview submitted by Antibody Solutions Ltd.
Immunocytochemistry/ Immunofluorescence - INCENP antibody [58-217] (ab23956)
![Immunocytochemistry/ Immunofluorescence - INCENP antibody [58-217] (ab23956)](/ps/datasheet/images/23/ab23956/INCENP-Primary-antibodies-ab23956-1.jpg)
ab23956 staining INCENP in siRNA-treated HeLa cells by Immunocytochemistry/ Immunofluorescence.
Image from Mackay DR et al, J Cell Biol. 2010 Nov 29;191(5):923-31. Epub 2010 Nov 22, Fig 3. DOI 10.1083/jcb.201007124
This product has been referenced in:
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![Immunocytochemistry/ Immunofluorescence - INCENP antibody [58-217] (ab23956)](/ps/datasheet/Images/23/ab23956/ab23956-IF-Im1.jpg)
ICC/IF image of ab23956 stained human HeLa cells. The cells were methanol fixed (5 min) and incubated with the antibody (ab23956, 1µg/ml) for 1h at room temperature. The secondary antibody (green) was Alexa Fluor® 488 goat anti-mouse IgG (H+L) used at a 1/1000 dilution for 1h. Image-iTTM FX Signal Enhancer was used as the primary blocking agent, 5% BSA (in TBS-T) was used for all other blocking steps. DAPI was used to stain the cell nuclei (blue). Alexa Fluor® 594 WGA was used to label plasma membranes (red).
![Immunofluorescence - INCENP antibody [58-217] (ab23956)](/ps/datasheet/Images/23/ab23956/ab23956_3.jpg)
ab23956 staining INCENP in HeLa cells, by immunofluorescence.
optimal antibody dilution: 1mg/ml
optimal fixation protocol: PFA/Triton fixation: 10 min room temperature in 3,7 % PFA diluted in PHEM PEM buffer: 45 mM Hepes pH 6,9, 45 mM Pipes pH 6,9, 5mM MgCl2, 10 mM EGTA) containing 0 ,2% Triton X-100, followed by 3 washes in PBS. Also gives a good staining with PFA fixation: 10 min in 3,7 % PFA at room temperature, 5 min in PBS / 0,1%Triton X-100, then 3 washes in PBS.
IF staining was performed following a standard protocol: blocking: 30 min; primary antibody: 1 hr; secondary antibody: 45’. All incubations were at 37 °C in PBS/ 0,1% Tween containing 3% BSA.
This antibody was also tested using NIH-3T3 cells but it did not provide good results with these cells.
Image kindly submitted by Serena Orlando, Giulia Guarguaglini and Patrizia Lavia, from the University 'La Sapienza' CNR, Italy
![Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - INCENP antibody [58-217] (ab23956)](/ps/datasheet/Images/23/ab23956/ab23956_4.jpg)
ab23956 staining human anal cancer tissue sections by IHC-P. Sections were formaldehyde fixed and subjected to heat mediated antigen retreival in citrate buffer (pH 6) prior to blocking in a commercially available blocking agent for 20 minutes at 20°C. The primary anibody was diluted 1/200 and incubated with the sample for 40 minutes at 20°C. A HRP-conjugated goat anti-mouse antibody was used as the secondary.
This image is courtesy of an Abreview submitted by Antibody Solutions Ltd.
![Immunocytochemistry/ Immunofluorescence - INCENP antibody [58-217] (ab23956)](/ps/datasheet/images/23/ab23956/INCENP-Primary-antibodies-ab23956-1.jpg)
ab23956 staining INCENP in siRNA-treated HeLa cells by Immunocytochemistry/ Immunofluorescence.
Image from Mackay DR et al, J Cell Biol. 2010 Nov 29;191(5):923-31. Epub 2010 Nov 22, Fig 3. DOI 10.1083/jcb.201007124
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