Product Details

Purity

Greater than 90% as determined by SDS-PAGE.

Target Names

RAD52

Uniprot No.

P06778

Research Area

Others

Alternative Names

RAD52; YML032C; DNA repair and recombination protein RAD52

Species

Saccharomyces cerevisiae (strain ATCC 204508 / S288c) (Baker's yeast)

Source

E.coli

Expression Region

60-282aa

Target Protein Sequence

IFGYNGWSTEVKSVVIDFLDERQGKFSIGCTAIVRVTLTSGTYREDIGYGTVENERRKPAAFERAKKSAVTDALKRSLRGFGNALGNCLYDKDFLAKIDKVKFDPPDFDENNLFRPTDEISESSRTNTLHENQEQQQYPNKRRQLTKVTNTNPDSTKNLVKIENTVSRGTPMMAAPAEANSKNSSNKDTDLKSLDASKQDQDDLLDDSLMFSDDFQDDDLINM
Note: The complete sequence may include tag sequence, target protein sequence, linker sequence and extra sequence that is translated with the protein sequence for the purpose(s) of secretion, stability, solubility, etc.
If the exact amino acid sequence of this recombinant protein is critical to your application, please explicitly request the full and complete sequence of this protein before ordering.

Mol. Weight

41.1kDa

Protein Length

Partial

Tag Info

N-terminal 6xHis-SUMO-tagged

Form

Liquid or Lyophilized powder
Note: We will preferentially ship the format that we have in stock, however, if you have any special requirement for the format, please remark your requirement when placing the order, we will prepare according to your demand.

Buffer

If the delivery form is liquid, the default storage buffer is Tris/PBS-based buffer, 5%-50% glycerol.
Note: If you have any special requirement for the glycerol content, please remark when you place the order.
If the delivery form is lyophilized powder, the buffer before lyophilization is Tris/PBS-based buffer, 6% Trehalose.

Reconstitution

We recommend that this vial be briefly centrifuged prior to opening to bring the contents to the bottom. Please reconstitute protein in deionized sterile water to a concentration of 0.1-1.0 mg/mL.We recommend to add 5-50% of glycerol (final concentration) and aliquot for long-term storage at -20°C/-80°C. Our default final concentration of glycerol is 50%. Customers could use it as reference.

Troubleshooting and FAQs

Protein FAQs

Storage Condition

Store at -20°C/-80°C upon receipt, aliquoting is necessary for mutiple use. Avoid repeated freeze-thaw cycles.

Shelf Life

The shelf life is related to many factors, storage state, buffer ingredients, storage temperature and the stability of the protein itself.
Generally, the shelf life of liquid form is 6 months at -20°C/-80°C. The shelf life of lyophilized form is 12 months at -20°C/-80°C.

Lead Time

3-7 business days

Notes

Repeated freezing and thawing is not recommended. Store working aliquots at 4°C for up to one week.

Datasheet & COA

Please contact us to get it.

Description

Delve into the fascinating world of DNA repair and recombination research with the Recombinant Saccharomyces cerevisiae RAD52. This product, derived from the well-established model organism Baker's yeast (Saccharomyces cerevisiae, strain ATCC 204508 / S288c), presents a remarkable tool for studying DNA damage response and its role in genetic stability. The protein encoded by the RAD52 gene plays a crucial part in homologous recombination repair, making it a subject of keen interest in genetics and molecular biology.

This recombinant RAD52 variant encompasses a partial sequence (60-282 amino acids), conserving essential functionalities to facilitate your research endeavors. The protein, expressed in E.coli, carries an N-terminal 6xHis-SUMO tag to facilitate its easy identification and purification. The SDS-PAGE analysis vouches for its high purity level, exceeding 90%. Choose between liquid or lyophilized powder form based on your lab's requirements. With the Recombinant Saccharomyces cerevisiae RAD52, you're not just purchasing a product; you're ensuring precise, high-quality, and reliable results for your research.

Target Background

Function

Involved in DNA double-strand break (DSB) repair and recombination. Promotes the annealing of complementary single-stranded DNA and by stimulation of the RAD51 recombinase.

Gene References into Functions

Global chromosome mobility is regulated by the Rad51 recombinase and its mediator, Rad52. PMID: 30181361
Rad52 inverse strand exchange plays an important role in RNA-templated double strand break repair in vivo. PMID: 28602639
The C-terminal region of yRad52, but not of hRAD52, is involved in ssDNA annealing. This suggests that the second DNA binding site is required for the efficient ssDNA annealing by yRad52. We propose an updated model of Rad52-mediated ssDNA annealing. PMID: 27362509
Rad52 is needed to repair telomere attrition-induced replication stress PMID: 27428329
investigated the contribution of the nuclear double-strand break repair (DSBR) proteins Rad51p, Rad52p and Rad59p in mtDNA repair PMID: 26540255
the homeologous pairing between the terminal TG1-3 repeats at VII-L and internal repeats on other chromosome ends was largely independent of Rad51, but instead it was facilitated by Rad59 that stimulates Rad52 strand annealing activity PMID: 25375789
It was found that, despite the absence of self-homology on the T-DNA, the homologous repair proteins Rad52 and Rad51 are involved in T-DNA circle formation. PMID: 24460832
The study suggested that phenylalanine-349 and tyrosine-409 are key residues in the C-terminal half of Rad52 and probably play an important role in the recombination mediator activity. PMID: 24163251
This conclusion is strengthened by the finding that Rad52 is often associated with complete Rad51 filaments in vitro PMID: 24130504
The Shu complex plays a central role in Rad52 rDNA localization as long as Rad52 can be sumoylated. PMID: 23790361
New scenario for homologous recombination where Rad52 and Rad51 are recruited to the fork to promote DNA damage tolerance by distinct and cell cycle-regulated replicative and repair functions. PMID: 23563117
Our results describe 8 new genes involved in SCR, including functions such as histone acetylation/deacetylation, SUMO-Ubiquitin metabolism, and stress response, as well as an allele of RAD52 PMID: 23357952
Ty1 sequence-specific gross chromosomal rearrangements are RAD52-dependent. PMID: 21637792
Rad52 within the complex associates with double-stranded DNA to assist Rad51-mediated homologous pairing. PMID: 21454474
results highlight the importance of Rad52 SUMOylation as part of a 'quality control' mechanism regulating the efficiency of recombination and DNA repair. PMID: 20371517
result suggests that spontaneous DNA lesions that require recombinational repair occur at the same frequency in wild-type and rad52-Y66A cells, but that the recombination process is slow in rad52-Y66A cells. PMID: 19892607
Results from chromatin immunoprecipitation experiments find that rad52-R70A associates with DNA double-strand breaks and promotes recruitment of Rad51 as efficiently as wild-type Rad52. PMID: 19812039
Increases in transposition activity in sir4 mutant strains at high temperature is dependent on the RAD52 gene. PMID: 15454529
These results imply that telomeres can use looped-out telomeric rings to promote telomere-telomere recombination through Rad52-, Rad50-, and polymerase delta in telomerase-deficient Saccharomyces cerevisiae. PMID: 15701795
examined the ssDNA annealing activity of Rad52 and Rad59 proteins and found significant differences in their biochemical properties PMID: 16565518
Multiple Rad52 protein species are due to promiscuous choice of start codons as well as post-translational modification. PMID: 16707661
The rearrangement frequency was found to increase with array size, and partial complementation of the rad27Delta mutation by hFEN1 demonstrated that the production of novel CEB1 alleles is Rad52 and Rad51 dependent. PMID: 16914748
S. cerevisiae Rad52 protein and its eukaryotic counterparts function by binding to single-stranded DNA formed as intermediates of recombination rather than by binding to the unprocessed DNA double-strand break. PMID: 17040915
Error-free RAD52 pathwaydetermines spontaneous mutagenesis in Saccharomyces cerevisiae PMID: 17396018
The contributions of the RAD51, RAD52, and RAD54 genes and of the RAD50 and XRS2 genes to the postreplicational repair of ultraviolet rays-damaged DNA, is examined. PMID: 17785441
These results provide a mechanistic framework for rationalizing the multi-faceted role of Rad52 in recombination and DNA repair. PMID: 18310075
Results show that Rad52 functions in temporally and biochemically distinct reactions and suggest a general annealing mechanism for reuniting DSB ends during recombination. PMID: 18313389
regulation of Rad52-mediated annealing suggests a control function for Rad51 in deciding the recombination path taken for a processed DNA break; the ssDNA can be directed to either Rad51-mediated DNA strand invasion or to Rad52-mediated DNA annealing PMID: 18337252
These findings indicate that nuclear localization of Rad52 is pre-requisite for its sumoylation. PMID: 18482582
support a role for Rad52-promoted annealing in the formation of Holliday junctions in double-stranded break repair PMID: 19204284
Rad52 interaction with replication protein-A (RPA) requires multiple molecules of RPA to be associated with ssDNA, suggesting that multiple contacts between the Rad52 ring and RPA-ssDNA filament are needed for stable binding. PMID: 19445949
condensin and Rad52 have opposing roles in the control of rDNA stability under nutrient starvation conditions PMID: 19520859
The structure and functions of Rad52 are briefly reviewed. The DNA annealing & mediator functions of Rad52 play a central role in homologous recombination-based DNA double-strand-break repair. Review. PMID: 19706272

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Subcellular Location

Nucleus.

Protein Families

RAD52 family

Database Links

KEGG: sce:YML032C

STRING: 4932.YML032C

Code	CSB-EP361943SVG
Abbreviation	Recombinant Saccharomyces cerevisiae RAD52 protein, partial
MSDS	MSDS Datasheet
Size	US$388
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Image	(Tris-Glycine gel) Discontinuous SDS-PAGE (reduced) with 5% enrichment gel and 15% separation gel.
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Recombinant Saccharomyces cerevisiae DNA repair and recombination protein RAD52 (RAD52), partial

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