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Read our guarantee »Products:Cell Biology >> Apoptosis >> Nucleus >> PARP
Anti-Cleaved PARP antibody [E51]
See all Cleaved PARP products (10) ...
Rabbit monoclonal [E51] to Cleaved PARP
This antibody is specific for the p25 cleaved form of human PARP.
WB, Flow Cyt, IHC-P, IP, ICCmore details
Reacts with
Mouse, Human
Predicted to work with
Chinese Hamster
Synthetic peptide corresponding to residues before the cleavage site of Human PARP.
Jurkat cells.
Liquid
Shipped at 4°C. Upon delivery aliquot and store at -20°C. Avoid freeze / thaw cycles.
Preservative: 0.01% Sodium Azide
Constituents: 40% Glycerol, 0.15M Sodium chloride, 50mM Tris glycine. pH 7.4
Concentration information loading...
Protein A purified
Monoclonal
E51
IgG
Epigenetics and Nuclear Signaling >> Chromatin Binding Proteins >> DNA / RNA binding
Epigenetics and Nuclear Signaling >> Cell cycle >> Apoptosis >> Nuclear
Epigenetics and Nuclear Signaling >> DNA / RNA >> DNA Damage & Repair >> DNA Damage Response >> Other
Epigenetics and Nuclear Signaling >> DNA / RNA >> DNA Damage & Repair >> DNA Damage Response >> DNA Damage Recognition
Epigenetics and Nuclear Signaling >> Chromatin Modifying Enzymes >> ADP-ribosylation
Cell Biology >> Apoptosis >> Nucleus >> PARP
Our Abpromise guarantee covers the use of ab32064 in the following tested applications.
The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.
WB: 1/100000Predicted molecular weight: 25 kDa.
Flow Cyt: 1/20 - 1/50.
IHC-P: 1/100
IP: 1/50
ICC: 1/250
Involved in the base excision repair (BER) pathway, by catalyzing the poly(ADP-ribosyl)ation of a limited number of acceptor proteins involved in chromatin architecture and in DNA metabolism. This modification follows DNA damages and appears as an obligatory step in a detection/signaling pathway leading to the reparation of DNA strand breaks. Mediates the poly(ADP-ribosyl)ation of APLF and CHFR. Positively regulates the transcription of MTUS1 and negatively regulates the transcription of MTUS2/TIP150.
Contains 1 BRCT domain.
Contains 1 PARP alpha-helical domain.
Contains 1 PARP catalytic domain.
Contains 2 PARP-type zinc fingers.
Phosphorylated by PRKDC. Phosphorylated upon DNA damage, probably by ATM or ATR.
Poly-ADP-ribosylated by PARP2. Poly-ADP-ribosylation mediates the recruitment of CHD1L to DNA damage sites.
S-nitrosylated, leading to inhibit transcription regulation activity.
Nucleus.
Target information above from: UniProt accessionP09874
The UniProt Consortium
The Universal Protein Resource (UniProt) in 2010
Nucleic Acids Res. 38:D142-D148 (2010).
Western blot - cleaved PARP antibody [E51] (ab32064)
![Western blot - cleaved PARP antibody [E51] (ab32064)](/ps/datasheet/Images/32/ab32064/ab32064_1.jpg)
All lanes : Anti-Cleaved PARP antibody [E51] (ab32064) at 1/1000000 dilution
Lane 1 : Jurkat cell lysate.
Untreated.
Lane 2 : Jurkat cell lysate.
Treated with Camptothecin.
Predicted band size : 25 kDa
Observed band size : 25 kDa
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - cleaved PARP antibody [E51] (ab32064)
![Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - cleaved PARP antibody [E51] (ab32064)](/ps/datasheet/Images/32/ab32064/ab32064_2.jpg)
ab32064 at a 1:100 dilution staining PARP cleaved p25 in human breast carcinoma tissue, using Immunohistochemistry, Paraffin Embedded Tissue.
Flow Cytometry-Cleaved PARP antibody [E51](ab32064)
](/ps/datasheet/images/32/ab32064/Cleaved-PARP-Primary-antibodies-ab32064-1.jpg)
Overlay histogram showing Jurkat cells stained with ab32064 (red line). The cells were fixed with methanol (5 min) and then permeabilized with 0.1% PBS-Tween for 20 min. The cells were then incubated in 1x PBS / 10% normal goat serum / 0.3M glycine to block non-specific protein-protein interactions followed by the antibody (ab32064, 1/20 dilution) for 30 min at 22°C. The secondary antibody used was DyLight® 488 goat anti-rabbit IgG (H+L) (ab96899) at 1/500 dilution for 30 min at 22°C. Isotype control antibody (black line) was rabbit monoclonal IgG (0.5µg/1x106 cells) used under the same conditions. Acquisition of >5,000 events was performed. This antibody gave a slightly decreased signal in Jurkat cells fixed with 4% paraformaldehyde (10 min)/permeabilized in 0.1% PBS-Tween used under the same conditions.
This product has been referenced in:
See all 3 publications for this product
Publishing research using ab32064? Please let us know so that we can cite the reference in this datasheet
Concentration of lot no. is
Concentration not available for this lot.
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![Western blot - cleaved PARP antibody [E51] (ab32064)](/ps/datasheet/Images/32/ab32064/ab32064_1.jpg)
All lanes : Anti-Cleaved PARP antibody [E51] (ab32064) at 1/1000000 dilution
Lane 1 : Jurkat cell lysate.
Untreated.
Lane 2 : Jurkat cell lysate.
Treated with Camptothecin.
Predicted band size : 25 kDa
Observed band size : 25 kDa
![Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - cleaved PARP antibody [E51] (ab32064)](/ps/datasheet/Images/32/ab32064/ab32064_2.jpg)
ab32064 at a 1:100 dilution staining PARP cleaved p25 in human breast carcinoma tissue, using Immunohistochemistry, Paraffin Embedded Tissue.
](/ps/datasheet/images/32/ab32064/Cleaved-PARP-Primary-antibodies-ab32064-1.jpg)
Overlay histogram showing Jurkat cells stained with ab32064 (red line). The cells were fixed with methanol (5 min) and then permeabilized with 0.1% PBS-Tween for 20 min. The cells were then incubated in 1x PBS / 10% normal goat serum / 0.3M glycine to block non-specific protein-protein interactions followed by the antibody (ab32064, 1/20 dilution) for 30 min at 22°C. The secondary antibody used was DyLight® 488 goat anti-rabbit IgG (H+L) (
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