Validation Data Gallery
|Positive WB detected in||Jurkat cells, HeLa cells, Cobalt Chloride treated HeLa cells, C6 cells, Fas antibody treated HeLa cells|
|Positive IP detected in||K-562 cells|
|Positive IHC detected in||human liver cancer tissue, human breast cancer tissue|
Note: suggested antigen retrieval with TE buffer pH 9.0; (*) Alternatively, antigen retrieval may be performed with citrate buffer pH 6.0
|Positive IF detected in||Neuro-2a cells, mouse testis tissue|
|Positive FC detected in||K-562 cells|
|Western Blot (WB)||WB : 1:1000-1:8000|
|Immunoprecipitation (IP)||IP : 0.5-4.0 ug for IP and 1:500-1:1000 for WB|
|Immunohistochemistry (IHC)||IHC : 1:50-1:500|
|Immunofluorescence (IF)||IF : 1:50-1:500|
|Sample-dependent, check data in validation data gallery|
13371-1-AP targets PARP1 in WB, IP, IHC, IF, FC, CoIP, ELISA applications and shows reactivity with human, mouse, rat samples.
|Tested Reactivity||human, mouse, rat|
|Cited Reactivity||human, mouse, rat, Fungus, monkey, pig, sheep|
|Host / Isotype||Rabbit / IgG|
|Immunogen||PARP1 fusion protein Ag4193|
|Full Name||poly (ADP-ribose) polymerase 1|
|Calculated molecular weight||1014 aa, 113 kDa|
|Observed molecular weight||113-116 kDa, 89 kDa|
|GenBank accession number||BC037545|
|Gene ID (NCBI)||142|
|Purification Method||Antigen affinity purification|
|Storage Buffer||PBS with 0.02% sodium azide and 50% glycerol pH 7.3.|
|Storage Conditions||Store at -20°C. Stable for one year after shipment. Aliquoting is unnecessary for -20oC storage.|
PARP1 (poly(ADP-ribose) polymerase 1) is a nuclear enzyme catalyzing the poly(ADP-ribosyl)ation of many key proteins in vivo. The normal function of PARP1 is the routine repair of DNA damage. Activated by DNA strand breaks, the PARP1 is cleaved into an 85 to 89-kDa COOH-terminal fragment and a 24-kDa NH2-terminal peptide by caspases during the apoptotic process. The appearance of PARP fragments is commonly considered as an important biomarker of apoptosis. In addition to caspases, other proteases like calpains, cathepsins, granzymes and matrix metalloproteinases (MMPs) have also been reported to cleave PARP1 and gave rise to fragments ranging from 42-89-kDa. This antibody was generated against the C-terminal region of human PARP1 and it recognizes the full-length as well as the cleavage of the PARP1.
|Product Specific Protocols|
|WB protocol for PARP1 antibody 13371-1-AP||Download protocol|
|IHC protocol for PARP1 antibody 13371-1-AP||Download protocol|
|IF protocol for PARP1 antibody 13371-1-AP||Download protocol|
|IP protocol for PARP1 antibody 13371-1-AP||Download protocol|
|Click here to view our Standard Protocols|
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The reviews below have been submitted by verified Proteintech customers who received an incentive forproviding their feedback.
Marina (Verified Customer) (05-30-2022)
In the blot we could detect native PARP1 as well as its cleaved 89 kDa form after PARP inhibitor treatment
Huanzhou (Verified Customer) (04-08-2022)
This product works well for WB.
Azita (Verified Customer) (06-02-2021)
Western blot analysis using PARP1 polyclonal antibody in NSC34 cell line at dilution of 1:500.
Brandon (Verified Customer) (02-01-2019)
Detected Full-length and cleaved PARP-1. Also detected a smaller fragment in mouse mouse liver tissue.