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PARP1 Monoclonal antibody
PARP1 Monoclonal Antibody for FC, IF, IHC, IP, WB, ELISA
Cat no : 66520-1-Ig
Validation Data Gallery
|Positive WB detected in||Jurkat cells, RAW 264.7 cells, HeLa cells, HSC-T6 cells, ROS1728 cells, NIH/3T3 cells|
|Positive IP detected in||K-562 cells|
|Positive IHC detected in||human lung 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, HeLa cells|
|Positive FC detected in||HeLa cells|
|Western Blot (WB)||WB : 1:5000-1:50000|
|Immunoprecipitation (IP)||IP : 0.5-4.0 ug for IP and 1:5000-1:50000 for WB|
|Immunohistochemistry (IHC)||IHC : 1:100-1:1200|
|Immunofluorescence (IF)||IF : 1:2000-1:8000|
|Sample-dependent, check data in validation data gallery|
66520-1-Ig targets PARP1 in WB, IP, IHC, IF, FC, ELISA applications and shows reactivity with Human, mouse, rat samples.
|Tested Reactivity||Human, mouse, rat|
|Cited Reactivity||human, mouse, rat, chicken, zebrafish|
|Host / Isotype||Mouse / IgG1|
|Immunogen||PARP1 fusion protein Ag19173|
|Full Name||poly (ADP-ribose) polymerase 1|
|Calculated molecular weight||1014 aa, 113 kDa|
|Observed molecular weight||113-116 kDa, 85-89 kDa|
|GenBank accession number||BC037545|
|Gene ID (NCBI)||142|
|Purification Method||Protein G 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 N-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 66520-1-Ig||Download protocol|
|IHC protocol for PARP1 antibody 66520-1-Ig||Download protocol|
|IF protocol for PARP1 antibody 66520-1-Ig||Download protocol|
|IP protocol for PARP1 antibody 66520-1-Ig||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.
Carly (Verified Customer) (11-17-2020)
Tested using EDTA plasma on an antibody microarray
MANOHAR (Verified Customer) (12-11-2019)
No nonspecific binding