Cat: PAX2000-10719

Recombinant Human RAD17 Protein,His

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Analytical Data

  • Gene name

    RAD17

  • Application

    SPRMSTBLIITCELISACELL ASSAYDRUG SCREENING

  • Alternative Names

    CCYC; Cell cycle checkpoint protein; Cell cycle checkpoint protein RAD17; FLJ41520; HRAD 17; hRad17; R24L; Rad 17; Rad 24; RAD1 (S. pombe) homolog; RAD1 homolog; RAD17; RAD17 homolog (S. pombe); RAD17 homolog; Rad17 like protein; RAD17; S. pombe; homolog of; RAD17_HUMAN; RAD17Sp; Rad24; Rad24; mouse; homolog of; Rad24; S. cerevisiae; homolog of; RF C activator 1 homolog; RF C/activator 1 homolog; RF-C/activator 1 homolog

  • Species

    Human

  • Source

    E. coli

  • Tag

    His tag N-Terminus

  • Purity

    Greater than 90% as determined by SDS-PAGE.

  • Uniprot

    O75943

  • Expression Region

    1-681 aa

  • AA Sequence

    MSKTFLRPKV SSTKVTDWVD PSFDDFLECS GVSTITATSL GVNNSSHRRK NGPSTLESSR FPARKRGNLS SLEQIYGLEN SKEYLSENEP WVDKYKPETQ HELAVHKKKI EEVETWLKAQ VLERQPKQGG SILLITGPPG CGKTTTLKIL SKEHGIQVQE WINPVLPDFQ KDDFKGMFNT ESSFHMFPYQ SQIAVFKEFL LRATKYNKLQ MLGDDLRTDK KIILVEDLPN QFYRDSHTLH EVLRKYVRIG RCPLIFIISD SLSGDNNQRL LFPKEIQEEC SISNISFNPV APTIMMKFLN RIVTIEANKN GGKITVPDKT SLELLCQGCS GDIRSAINSL QFSSSKGENN LRPRKKGMSL KSDAVLSKSK RRKKPDRVFE NQEVQAIGGK DVSLFLFRAL GKILYCKRAS LTELDSPRLP SHLSEYERDT LLVEPEEVVE MSHMPGDLFN LYLHQNYIDF FMEIDDIVRA SEFLSFADIL SGDWNTRSLL REYSTSIATR GVMHSNKARG YAHCQGGGSS FRPLHKPQWF LINKKYRENC LAAKALFPDF CLPALCLQTQ LLPYLALLTI PMRNQAQISF IQDIGRLPLK RHFGRLKMEA LTDREHGMID PDSGDEAQLN GGHSAEESLG EPTQATVPET WSLPLSQNSA SELPASQPQP FSAQGDMEEN IIIEDYESDG T

  • Molecular Weight

    77.0 kDa

  • Endotoxin

    < 1.0 EU per μg protein as determined by the LAL method.

  • Form

    Freeze-dried powder

  • Buffer formulation

    PBS, pH7.4, containing 0.01% SKL, 1mM DTT, 5% Trehalose and Proclin300.

  • Reconstitution

    Reconstitute in ddH2O to a concentration of 0.1-0.5 mg/mL. Do not vortex.

  • Customization

    Site-directed mutagenesis Custom tag design Custom buffer formulation Custom full-length protein production

  • Stability Test

    The thermal stability is described by the loss rate. The loss rate was determined by accelerated thermal degradation test, that is, incubate the protein at 37℃ for 48h, and no obvious degradation and precipitation were observed. The loss rate isless than 8% within the expiration date under appropriate storage condition.

  • Storage & Shelf Life

    Samples are stable for up to twelve months from date of receipt at -20℃ to -80℃. Store it under sterile conditions at -20℃ to -80℃. It is recommended that the protein be aliquoted for optimal storage. Avoid repeated freeze-thaw cycles.

  • Shipping

    In general, recombinant proteins are supplied as lyophilized powder and shipped at ambient temperature. For bulk packages, the proteins are provided as frozen liquid and shipped with blue ice, unless otherwise requested by the customer.

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Protein Description

RAD17 is a pivotal protein involved in the DNA damage response and cell cycle regulation. It is part of a larger complex responsible for sensing DNA lesions and facilitating the activation of the checkpoint pathways that ensure genomic integrity. Research on RAD17 has gained prominence due to its crucial role in the formation of the mediator complex that recruits repair proteins to sites of DNA damage, thus influencing the cellular response to genotoxic stress. Mutations or dysregulation of RAD17 have been implicated in various cancers, highlighting its potential as a biomarker for tumor progression and a target for therapeutic strategies. Moreover, studies have shown that RAD17 interacts with several other proteins, such as the Rad9-Rad1-Hus1 (9-1-1) complex, which further emphasizes its importance in the maintenance of genome stability. Understanding the molecular mechanisms of RAD17 function not only sheds light on the fundamental processes of DNA repair but also opens up avenues for developing novel cancer treatments that could exploit vulnerabilities in the DNA damage response pathways. Given its central role, RAD17 continues to be an area of active research, with ongoing studies aimed at elucidating its precise mechanisms of action and potential implications in oncology and therapeutic interventions.

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