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Read our guarantee »Anti-PARG antibody
See all PARG products (3) ...
Mouse polyclonal to PARG
Reacts with
Fruit fly (Drosophila melanogaster)
Recombinant fusion protein: SYSRLIKEKS SKEPRENKAS KKKLYDFIKE ELKKVRDVPG EGASAEAGSS RVAGLGEGKS ETSAKSSPEL NKQPARPQIT ITQQSTDLLP AQLSQDNSNS , corresponding to amino acids 566-665 of Fruit fly (Drosophila melanogaster) PARG
SYSRLIKEKS SKEPRENKAS KKKLYDFIKE ELKKVRDVPG EGASAEAGSS RVAGLGEGKS ETSAKSSPEL NKQPARPQIT ITQQSTDLLP AQLSQDNSNS
Liquid
Shipped at 4°C. Upon delivery aliquot and store at -20°C. Avoid freeze / thaw cycles.
Preservative: None
Constituents: 50% Glycerol
Whole antiserum
This antibody was raised by a genetic immunization technique. Genetic immunization can be used to generate antibodies by directly delivering antigen-coding DNA into the animal, rather than injecting a protein or peptide (Tang et al. PubMed: 1545867; Chambers and Johnston PubMed 12910245; Barry and Johnston PubMed: 9234514). The animal's cells produce the protein, which stimulates the animal's immune system to produce antibodies against that particular protein. A vector coding for a partial fusion protein was used for genetic immunisation of a mouse and the resulting serum was tested in Western blot against an E.coli lysate containing that partial fusion protein. Genetic immunization offers enormous advantages over the traditional protein-based immunization method. DNA is faster, cheaper and easier to produce and can be produced by standard techniques readily amenable to automation. Furthermore, the antibodies generated by genetic immunization are usually of superior quality with regard to specificity, affinity and recognizing the native protein.
Polyclonal
IgG
Epigenetics and Nuclear Signaling >> Chromatin Modifying Enzymes >> ADP-ribosylation
Western blot - PARG antibody (ab43412)
(enlarge)
Our Abpromise guarantee covers the use of ab43412 in the following tested applications.
The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.
WB: 1/1000. Detects a band of approximately 38 kDa (predicted molecular weight: 111 kDa). This antibody has been tested in Western blot against an E.coli lysate containing the partial recombinant fusion protein used as an immunogen. We have no data on detection of endogenous protein
Not yet tested in other applications.
Optimal dilutions/concentrations should be determined by the end user.
Poly(ADP-ribose) synthesized after DNA damage is only present transiently and is rapidly degraded by poly(ADP-ribose) glycohydrolase. Poly(ADP-ribose) metabolism may be required for maintenance of the normal function of neuronal cells.
Ubiquitously expressed.
Belongs to the poly(ADP-ribose) glycohydrolase family.
Cytoplasm and Nucleus.
Target information above from: UniProt accessionQ86W56
The UniProt Consortium
The Universal Protein Resource (UniProt) in 2010
Nucleic Acids Res. 38:D142-D148 (2010).
Western blot - PARG antibody (ab43412)

All lanes : Anti-PARG antibody (ab43412) at 1/1000 dilution
Lane 1 : (Left) 50-100ng of tagged fusion protein of an irrelevant antigen
Lane 2 : (Right) 20ug of a total protein extract from E coli with ~50ng to 500ng of the antigen (tag-antigen fusion protein).
Secondary
Rabbit anti-mouse IgG + IgM, (H+L) horseradish peroxidase conjugated at 1/5000 dilution
Predicted band size : 111 kDa
ab43412 has not yet been referenced specifically in any publications.
Publishing research using ab43412? Please let us know so that we can cite the reference in this datasheet
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All lanes : Anti-PARG antibody (ab43412) at 1/1000 dilution
Lane 1 : (Left) 50-100ng of tagged fusion protein of an irrelevant antigen
Lane 2 : (Right) 20ug of a total protein extract from E coli with ~50ng to 500ng of the antigen (tag-antigen fusion protein).
Secondary
Rabbit anti-mouse IgG + IgM, (H+L) horseradish peroxidase conjugated at 1/5000 dilution
Predicted band size : 111 kDa
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