Cat: PA1000-9225

Recombinant Human XPO1 Protein,His

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Analytical Data

  • Gene name

    XPO1

  • Application

    SPRMSTBLIITCELISACELL ASSAYDRUG SCREENING

  • Alternative Names

    XPO1;CRM1;Exportin-1

  • Species

    Human

  • Source

    E. coli

  • Tag

    His tag N-Terminus

  • Purity

    Greater than 90% as determined by SDS-PAGE.

  • Uniprot

    O14980

  • Expression Region

    1-1071aa

  • AA Sequence

    MPAIMTMLADHAARQLLDFSQKLDINLLDNVVNCLYHGEGAQQRMAQEVL THLKEHPDAWTRVDTILEFSQNMNTKYYGLQILENVIKTRWKILPRNQCE GIKKYVVGLIIKTSSDPTCVEKEKVYIGKLNMVLVQILKQEWPKHWPTFI SDIVGASRTSESPCQNNMVILKLLSEEVFDFSSGQITQVKSKHLKDSMCN EFSQIFQLCQFVMENSQNAPLVHATLETLLRFLNWIPLGYIFETKLISTL IYKFLNVPMFRNVSLKCLTEIAGVSVSQYEEQFVTLFTLTMMQLKQMLPL NTNIRLAYSNGKDDEQNFIQNLSLFLCTFLKEHDQLIEKRLNLRETLMEA LHYMLLVSEVEETEIFKICLEYWNHLAAELYRESPFSTSASPLLSGSQHF DVPPRRQLYLPMLFKVRLLMVSRMAKPEEVLVVENDQGEVVREFMKDTDS INLYKNMRETLVYLTHLDYVDTERIMTEKLHNQVNGTEWSWKNLNTLCWA IGSISGAMHEEDEKRFLVTVIKDLLGLCEQKRGKDNKAIIASNIMYIVGQ YPRFLRAHWKFLKTVVNKLFEFMHETHDGVQDMACDTFIKIAQKCRRHFV QVQVGEVMPFIDEILNNINTIICDLQPQQVHTFYEAVGYMIGAQTDQTVQ EHLIEKYMLLPNQVWDSIIQQATKNVDILKDPETVKQLGSILKTNVRACK AVGHPFVIQLGRIYLDMLNVYKCLSENISAAIQANGEMVTKQPLIRSMRT VKRETLKLISGWVSRSNDPQMVAENFVPPLLDAVLIDYQRNVPAAREPEV LSTMAIIVNKLGGHITAEIPQIFDAVFECTLNMINKDFEEYPEHRTNFFL LLQAVNSHCFPAFLAIPPTQFKLVLDSIIWAFKHTMRNVADTGLQILFTL LQNVAQEEAAAQSFYQTYFCDILQHIFSVVTDTSHTAGLTMHASILAYMF NLVEEGKISTSLNPGNPVNNQIFLQEYVANLLKSAFPHLQDAQVKLFVTG LFSLNQDIPAFKEHLRDFLVQIKEFAGEDTSDLFLEEREIALRQADEEKH KRQMSVPGIFNPHEIPEEMCD

  • Molecular Weight

    144 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

XPO1 (Exportin 1), also known as CRM1 (Chromosomal Maintenance 1), is a pivotal nuclear export receptor that facilitates the transport of various proteins and RNA molecules from the nucleus to the cytoplasm. Its role is crucial for maintaining cellular homeostasis and regulating numerous biological processes, including cell cycle progression, apoptosis, and gene expression. Given its involvement in these fundamental processes, dysregulation of XPO1 is linked to various diseases, particularly cancer. Overexpression of XPO1 has been associated with the progression of several malignancies, making it a promising target for therapeutic interventions. Researchers have been increasingly focused on understanding the structure-function relationship of XPO1, leading to the development of small molecule inhibitors that can block its activity. The study of XPO1 recombinant proteins has facilitated detailed investigations into its functional mechanisms and interactions with substrate proteins. This research is instrumental in elucidating the nuances of XPO1-mediated transport and identifying potential biomarkers for disease prognosis and treatment response. Furthermore, as XPO1 and its inhibitors advance into clinical trials, the exploration of its biological implications continues to be a major focus in oncology and cellular biology, contributing to the broader understanding of nuclear-cytoplasmic transport processes.

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