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AB63827

Recombinant E. coli RuvB protein (Active)

Recombinant E. coli RuvB protein (Active)

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Recombinant E. coli RuvB protein (Active) is a Escherichia coli K-12 Full Length protein, expressed in Escherichia coli, with >90%, suitable for SDS-PAGE, ELISA, WB, FuncS.

別名を表示する

b1860, JW1849, ruvB, Holliday junction branch migration complex subunit RuvB, Holliday junction helicase subunit A, RUVB (recombination protein) homolog, Holliday junction ATP dependent DNA helicase ruvB, ATP dependent DNA helicase, component of RuvABC resolvasome

2 Images
SDS-PAGE - Recombinant E. coli RuvB protein (Active) (AB63827)
  • SDS-PAGE

Supplier Data

SDS-PAGE - Recombinant E. coli RuvB protein (Active) (AB63827)

SDS-PAGE analysis of Recombinant E. coli RuvB protein (ab63827).

SDS-PAGE - Recombinant E. coli RuvB protein (Active) (AB63827)
  • SDS-PAGE

Unknown

SDS-PAGE - Recombinant E. coli RuvB protein (Active) (AB63827)

SDS Page analysis of ab63827

Key facts

精製度

>90% SDS-PAGE

purified by methods such as chromatography

発現系

Escherichia coli

タグ

Tag free

アプリケーション

FuncS, ELISA, SDS-PAGE, WB

applications

生物活性

No

アクセッション番号

P0A812

アニマルフリー

No

キャリアフリー

No

種

Escherichia coli K-12

バッファー組成

pH: 6 - 8.5 Constituents: 50% Glycerol (glycerin, glycerine), 0.58% Sodium chloride, 0.158% Tris HCl, 0.0584% EDTA, 0.039% 2-Mercaptoethanol

storage-buffer

Reactivity data

{ "title": "Reactivity Data", "filters": { "stats": ["", "Reactivity", "Dilution Info", "Notes"] }, "values": { "SDS-PAGE": { "reactivity":"TESTED_AND_REACTS", "dilution-info":"", "notes":"<p></p>" }, "ELISA": { "reactivity":"TESTED_AND_REACTS", "dilution-info":"", "notes":"<p></p>" }, "WB": { "reactivity":"TESTED_AND_REACTS", "dilution-info":"", "notes":"<p></p>" }, "FuncS": { "reactivity":"TESTED_AND_REACTS", "dilution-info":"", "notes":"<p>Functional studies in vitro; RuvA and RuvB form a complex that promotes Holidayjunction (a recombination intermediate) branch-migration by using ATP hydrolysis energy. RuvB also has ATPase activity which is stimulated by RuvA and DNA.</p>" } } }

製品の詳細

This protein can be used for:- 1) Studies on homologous recombination mechanism. 2) To make use of the motor protein function that specifically migrates the Holliday junction by forming a complex with RuvA (branch-migration protein).

配列情報

[{"linker":null,"sequence":"","proteinLength":"Full Length","predictedMolecularWeight":null,"actualMolecularWeight":null,"aminoAcidEnd":0,"aminoAcidStart":0,"nature":"Recombinant","expressionSystem":null,"accessionNumber":"P0A812","tags":[]}]

出荷温度及び保存条件

製品の状態
Liquid
出荷温度
Blue Ice
短期保存温度
-20°C
長期保存温度
-20°C
分注に関する情報
Upon delivery aliquot
保管に関する情報
Avoid freeze / thaw cycle
False

補足情報

This supplementary information is collated from multiple sources and compiled automatically.

RuvB also known as RuvB-like 1 and 2 (RUVBL1/RUVBL2) is a highly conserved ATP-dependent helicase with a molecular mass of roughly 51 kDa. This protein can unwind DNA a function that plays an essential role in DNA repair and recombination. It is expressed in various tissues across different species with high expression in rapidly dividing cells and tissues undergoing repair. RuvB forms hexameric or dodecameric rings which allow it to interact with other protein complexes and nucleic acids.
Biological function summary

The RuvB proteins participate in the regulation of essential cellular events. They integrate into larger multi-protein complexes such as the chromatin remodeling complex INO80 and the TIP60 complex which are involved in modulating nucleosome structure. In the context of chromatin remodeling RuvB helps regulate access to the DNA by other proteins and enzymes affecting transcription DNA repair and replication. These activities underline RuvB's role in maintaining genomic stability.

Pathways

The participation of RuvB in key regulatory pathways includes DNA damage response and transcription regulation. In the DNA damage repair pathway it collaborates with proteins like RAD51 and BRCA1 to resolve DNA breaks. Additionally in the transcriptional regulation pathway RuvB interacts with RNA Polymerase complexes and is implicated in the regulation of gene expression. These interactions illustrate how RuvB is important for cellular responses to various stimuli that require rapid changes in gene transcription profiles and maintenance of DNA integrity.

Mutations or dysregulation of RuvB can contribute to the development of cancer and neurological disorders. Cancer often involves RuvB in its chromatin remodeling role where altered RuvB function can lead to unchecked cell proliferation due to improper DNA repair and transcription. Furthermore in some neurological disorders abnormal interaction between RuvB and proteins like Huntingtin has been observed suggesting a link between RuvB function and the pathogenic mechanisms in Huntington’s disease. These associations highlight RuvB as a significant target for therapeutic research in oncology and neurobiology.

一般的な情報

機能

The RuvABC complex is involved in recombinational repair of UV or chemically damaged DNA (PubMed : 6374379). The complex also plays an important role in the rescue of blocked DNA replication forks via replication fork reversal (RFR); RFR and homologous recombination required for UV light survival can be separated (PubMed : 16424908, PubMed : 18942176, PubMed : 9814711). This subunit has a weak ATPase activity that is inhibited by its ADP product; binds ADP better than ATP (PubMed : 2529252). Promotes Holliday junction (HJ) branch migration in conjunction with RuvA. Binds to HJ cruciform DNA; in the presence of RuvA, ATP and Mg(2+) the junction is dissociated. Hydrolyzable (d)NTPs can replace ATP but other analogs cannot (PubMed : 1608954, PubMed : 1617728, PubMed : 6374379, PubMed : 8393934). The RuvB hexamer acts as a pump, pulling DNA into and through the RuvAB complex (PubMed : 9078376). Can bypass UV-induced lesions (PubMed : 1617728) and physically cross-linked DNA strands (PubMed : 10662672), suggesting RuvB does not unwind large sections of DNA. RuvA gives specificity by binding to cruciform junctions, while the RuvB ATPase provides the motor force for branch migration; excess RuvB can promote branch migration in the absence of RuvA (PubMed : 10662672, PubMed : 1617728). In vitro the RuvA-RuvB complex has 5'-3' helicase activity that is ATP-dependent and works best on short dsDNA hybrids; 52 and 66-nucleotide (nt) pairs are easily displaced, hybrids greater than 140-nts are not (PubMed : 8433990). RuvA stimulates the weak ATPase activity of RuvB in the presence of DNA; HJ DNA stimulates ATPase about 10-fold (PubMed : 1435721, PubMed : 1833759, PubMed : 8393934).. An in vitro resolvase system that forms and processes HJ has been reconstituted with DNA substrates, RuvA, RuvB and RuvC. RuvA-RuvB increases the rate of strand exchange (branch migration), dissociates the RecA filament and allows RuvC to cleave in both orientations at the cruciform junction (PubMed : 10421637, PubMed : 9160752). HJ-RuvA-RuvB-RuvC complexes resolve Holliday junctions and also undergo branch migration, providing evidence for a coupled branch migration/HJ resolution reaction (PubMed : 10421637).

配列の類似性

Belongs to the RuvB family.

製品プロトコール

ターゲットの情報

The RuvABC complex is involved in recombinational repair of UV or chemically damaged DNA (PubMed : 6374379). The complex also plays an important role in the rescue of blocked DNA replication forks via replication fork reversal (RFR); RFR and homologous recombination required for UV light survival can be separated (PubMed : 16424908, PubMed : 18942176, PubMed : 9814711). This subunit has a weak ATPase activity that is inhibited by its ADP product; binds ADP better than ATP (PubMed : 2529252). Promotes Holliday junction (HJ) branch migration in conjunction with RuvA. Binds to HJ cruciform DNA; in the presence of RuvA, ATP and Mg(2+) the junction is dissociated. Hydrolyzable (d)NTPs can replace ATP but other analogs cannot (PubMed : 1608954, PubMed : 1617728, PubMed : 6374379, PubMed : 8393934). The RuvB hexamer acts as a pump, pulling DNA into and through the RuvAB complex (PubMed : 9078376). Can bypass UV-induced lesions (PubMed : 1617728) and physically cross-linked DNA strands (PubMed : 10662672), suggesting RuvB does not unwind large sections of DNA. RuvA gives specificity by binding to cruciform junctions, while the RuvB ATPase provides the motor force for branch migration; excess RuvB can promote branch migration in the absence of RuvA (PubMed : 10662672, PubMed : 1617728). In vitro the RuvA-RuvB complex has 5'-3' helicase activity that is ATP-dependent and works best on short dsDNA hybrids; 52 and 66-nucleotide (nt) pairs are easily displaced, hybrids greater than 140-nts are not (PubMed : 8433990). RuvA stimulates the weak ATPase activity of RuvB in the presence of DNA; HJ DNA stimulates ATPase about 10-fold (PubMed : 1435721, PubMed : 1833759, PubMed : 8393934).. An in vitro resolvase system that forms and processes HJ has been reconstituted with DNA substrates, RuvA, RuvB and RuvC. RuvA-RuvB increases the rate of strand exchange (branch migration), dissociates the RecA filament and allows RuvC to cleave in both orientations at the cruciform junction (PubMed : 10421637, PubMed : 9160752). HJ-RuvA-RuvB-RuvC complexes resolve Holliday junctions and also undergo branch migration, providing evidence for a coupled branch migration/HJ resolution reaction (PubMed : 10421637).
See full target information ruvB

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