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PARP2 | Poly [ADP-ribose] polymerase 2

AS16 3838 | Clonality: Polyclonal | Host: Rabbit | Reactivity: Arabidopsis thaliana

PARP2 | Poly [ADP-ribose] polymerase 2 in the group Plant/Algal Antibodies / DNA/RNA/Cell Cycle / Nuclear signaling at Agrisera AB (Antibodies for research) (AS16 3838)

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Background

PARP (EC=2.4.2.30) is a protein involved in the base excision repair pathway (BER) and is catalyzing the poly(ADP-ribosyl)ation of a limited number of acceptor proteins involved in chromatin architecture and in DNA metabolism. PARP is a marker of a single-strand breaks (SSBs), Rybaczek and Kowalewicz-Kulbat (2013).

Alternative names: ADPRT 2, NAD(+) ADP-ribosyltransferase 2, Poly[ADP-ribose] synthetase 2.

Immunogen

Recombinant Arabidopsis thaliana MBP-PARP2protein (AT2G31320)

Host Rabbit
Clonality Polyclonal
Clone
Purity Serum
Format Lyophilized
Quantity 50 µl
Reconstitution

For reconstitution add 50 µl of sterile water.

Storage

Store lyophilized/reconstituted at -20°C; once reconstituted make aliquots to avoid repeated freeze-thaw cycles. Please, remember to spin tubes briefly prior to opening them to avoid any losses that might occur from lyophilized material adhering to the cap or sides of the tubes.

Tested applications Western blot (WB)
Related products

Collection of antibodies for DNA/RNA metabolism and cell cycle

Plant protein extraction buffer

Secondary antibodies

Additional information
application information
Recommended dilution 1: 1000 (WB)
Expected | apparent MW

72.2 kDa

Confirmed reactivity Arabidopsis thaliana
Predicted reactivity
Not reactive in

No confirmed exceptions from predicted reactivity known in the moment

Additional information
Selected references To be added when available, antibody released in January 2018.

Application example

Western blot using anti-PARP2 antibodies
100 µg of total protein from 14 days old Arabidopsis thaliana seedlings extracted with extraction buffer (2% SDS, 50 mM Tris-HCl, pH 8.0, protease inhibitor cocktail (Sigma, P9599) 1:100) and denatured with Laemmli sample loading buffer at 70°C for 10 min were separated on 10 % SDS-PAGE and blotted 2h to PVDF using tank transfer. Blots were blocked with 5% milk for 1h at room temperature (RT) with agitation. Blot was incubated in the primary antibody at a dilution of 1: 1 000 in 1% milkTBS-T overnight with agitation at 4°C. The antibody solution was decanted and the blot was rinsed briefly twice, then washed once for 15 min and 3 times for 5 min in TBS-T at RT with agitation. Blot was incubated in secondary antibody (anti-rabbit IgG horse radish peroxidase conjugated) diluted to 1:10 000 in 1% milk TBS-T for 1h at RT with agitation. The blot was washed as above and developed for 5 min with ECL Prime (GE Healthcare). Exposure time was 2-5 min.

Courtesy of Dr Julia Vainonen, University of Helsinki, Finland

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