Products/Services Used | Details | Operation |
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Catalog Antibody> | The following antibodies at the indicated dilutions were employed for immunolocalization studies: rabbit polyclonal anti HA (SIGMA, 1:1000), rabbit polyclonal anti OLLAS (Genscript, 1:1500), rabbit polyclonal anti PAR (Trevigen, 1:1000), mouse monoclonal anti GFP (Roche, 1:500), guinea pig polyclonal anti HTP-3 (1:500) (Goodyer et al., 2008), guinea pig polyclonal anti HTP-3 (1:750) (Y. Kim lab), chicken polyclonal anti SYP-1 (1:500) (Silva et al., 2014), rabbit polyclonal anti HTP-1 (1:500) (Martinez-Perez et al., 2008), rabbit polyclonal anti RAD- 51 (Novus, 1:10,000), guinea pig polyclonal anti phospho-SUN-1S8 (1:750) (Woglar et al., 2013), rabbit polyclonal anti DSB-2 (1:5000) (Rosu et al., 2013), guinea pig polyclonal anti XND-1 (1:2500) (Wagner et al., 2010), mouse monoclonal anti H3K4me2 (Millipore, 1:250). All the secondary antibodies were Alexafluor-conjugated and used at 1:500 | Get A Quote |
Poly(ADP-ribosyl)ation is a reversible post-translational modification synthetized by ADP-ribose transferases and removed by poly(ADP-ribose) glycohydrolase (PARG), which plays important roles in DNA damage repair. While well-studied in somatic tissues, much less is known about poly(ADP-ribosyl)ation in the germline, where DNA double-strand breaks are introduced by a regulated program and repaired by crossover recombination to establish a tether between homologous chromosomes. The interaction between the parental chromosomes is facilitated by meiotic specific adaptation of the chromosome axes and cohesins, and reinforced by the synaptonemal complex. Here, we uncover an unexpected role for PARG in promoting the ... More