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RuvB

AS21 4544   | Clonality: Polyclonal  |  Host: Rabbit  | Reactivity: Escherichia coli

RuvB  in the group Antibodies Other Species / Bacteria at Agrisera AB (Antibodies for research) (AS21 4544)



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Product Information

Immunogen Purified, full length, recombinant RuvB protein from E.coli, UniProt: P0A812
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, afterwards at -20°C; 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 Western blot (WB)
Recommended dilution 1 : 3000 (WB)
Expected | apparent MW 37 | 39 kDa

Reactivity

Confirmed reactivity Escherichia coli

Application examples

Application examples Western blot using anti-RuvB antibodies (E.coli)

Samples: 5 ng of recombinant RuvB protein (1)E. coli AB1157 crude extract (2); E. coli AB1157 lexA mutant crude extract (3) were separated on SDS-PAGE and transferred to a membrane, followed by incubation with a primary antibodies at 1: 3000 dilution, washes and incubation with secondary antibodies HRP conjugated. Reaction was visualized by chemiluminescnce following manufacture's recommendations.

Expression of RuvB is enhanced by lexA mutation.

Additional information

Related products

Background

Background RuvB protein of Escherichia coli forms a complex with RuvA protein and the complex promotes branch migration of Holliday junction at the late stage of homologous recombination and recombination repair. RuvB is a DNA motor protein which possesses the ATPase activity, activated by DNA and RuvA protein. RuvB in the absence of ATP, it predominantly occurs in a monomer form. In the presence of ATP, it forms dimer and hexamer depending upon the concentration. With RuvA and Holliday junction., it forms a double hexamer.

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.
immunogen: Purified, full length, recombinant RuvB protein from E.coli, UniProt: P0A812
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, afterwards at -20°C; 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: Western blot (WB)
recommended dilution: 1 : 3000 (WB)
calculated | apparent molecular mass [kDa]: 37 | 39 kDa
Confirmed reactivity: Escherichia coli
Picture (footer): Western blot using anti-RuvB antibodies (E.coli)

Samples: 5 ng of recombinant RuvB protein (1)E. coli AB1157 crude extract (2); E. coli AB1157 lexA mutant crude extract (3) were separated on SDS-PAGE and transferred to a membrane, followed by incubation with a primary antibodies at 1: 3000 dilution, washes and incubation with secondary antibodies HRP conjugated. Reaction was visualized by chemiluminescnce following manufacture's recommendations.

Expression of RuvB is enhanced by lexA mutation.

background: RuvB protein of Escherichia coli forms a complex with RuvA protein and the complex promotes branch migration of Holliday junction at the late stage of homologous recombination and recombination repair. RuvB is a DNA motor protein which possesses the ATPase activity, activated by DNA and RuvA protein. RuvB in the absence of ATP, it predominantly occurs in a monomer form. In the presence of ATP, it forms dimer and hexamer depending upon the concentration. With RuvA and Holliday junction., it forms a double hexamer.
All 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.

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