RuvA | Holliday junction ATP-dependent DNA helicase
AS21 4543 | Clonality: Polyclonal | Host: Rabbit | Reactivity: Escherichia coli

Data sheet | Product citations | Protocols | Add review |
Product Information
Immunogen
Purified, full length RuvA protein of Escherichia coli, UniProt: P0A809
Host
Rabbit
Clonality
Polyclonal
Purity
Serum. Contains 0.05 % sodium azide.
Format
Liquid
Quantity
100 ĩl
Storage
Store at 4°C for up to 6 monthss, for longer storage-80°C is recommended; once reconstituted make aliquots to avoid repeated freeze-thaw cycles. Please remember to spin the tubes briefly prior to opening them to avoid any losses that might occur from material adhering to the cap or sides of the tube.
Tested applications
ELISA (ELISA), Western blot (WB)
Recommended dilution
1 : 3000 (WB)
Expected | apparent MW
22 kDa
Reactivity
Confirmed reactivity
Escherichia coli
Application examples
Application examples

Samples: 0.8 ng of recombinant RuvA protein (1), E.coli AB1157 crude extract (2),E. coli AB1157 lexA mutant crude extract (3) were separated on SDS-PAGE and transferred to the membrane. Anti-RuvA antibody incubation was performed at 1: 3000 dilution. Following incubation with a secondary antibody HRP conjugated, visualization was done by chemiluminescence, following manufacture's recommendations.

Samples: 0.8 ng of recombinant RuvA protein (1), E.coli AB1157 crude extract (2),E. coli AB1157 lexA mutant crude extract (3) were separated on SDS-PAGE and transferred to the membrane. Anti-RuvA antibody incubation was performed at 1: 3000 dilution. Following incubation with a secondary antibody HRP conjugated, visualization was done by chemiluminescence, following manufacture's recommendations.
Additional information
Background
Background
RuvA protein of Escherichia coli binds specifically to the Holliday structure which is the intermediate of recombination at the late stage of homologous recombination and recombination repair, and forms a complex with RuvB motor protein, allowing the migration of Holliday junction using ATP hydrolysis energy and expands the heteroduplex region. In solution, it forms a tetramer and binds to the cross-like DNA of the Holliday junction from below and above, holding it in between
Product citations
Selected references
Shinagawa & Iwasaki (1996). Processing the holliday junction in homologous recombination. Trends Biochem Sci. 1996 Mar;21(3):107-11. PMID: 8882584.
Iwasaki et al. (1992) Escherichia coli RuvA and RuvB proteins specifically interact with Holliday junctions and promote branch migration. Genes Dev. 1992 Nov;6(11):2214-20. doi: 10.1101/gad.6.11.2214. PMID: 1427081.
Iwasaki et al. (1992) Escherichia coli RuvA and RuvB proteins specifically interact with Holliday junctions and promote branch migration. Genes Dev. 1992 Nov;6(11):2214-20. doi: 10.1101/gad.6.11.2214. PMID: 1427081.
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