Cat: PAX2000-11650

Recombinant Human SPRYD5 Protein,His

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Analytical Data

  • Gene name

    SPRYD5

  • Application

    SPRMSTBLIITCELISACELL ASSAYDRUG SCREENING

  • Alternative Names

    MGC10977; SPRY domain containing 5; SPRY domain containing protein 5; SPRY domain-containing protein 5; SPRY5_HUMAN; SPRYD5; TRIM51; TRIM51A; Tripartite motif containing 51; Tripartite motif containing protein 51; Tripartite motif-containing protein 51

  • Species

    Human

  • Source

    E. coli

  • Tag

    His tag N-Terminus

  • Purity

    Greater than 90% as determined by SDS-PAGE.

  • Uniprot

    Q9BSJ1

  • Expression Region

    1-452aa

  • AA Sequence

    MNSGILQVFQ RALTCPICMN YFLDPVTIDC GHSFCRPCLY LNWQDTAVLA QCSECKKTTR QRNLNTDICL KNMAFIARKA SLRQFLSSEE QICGMHRETK KMFCEVDKSL LCLPCSNSQE HRNHIHCPIE WAAEERREEL LKKMQSLWEK ACENLRNLNM ETTRTRCWKD YVSLRIEAIR AEYQKMPAFL HEEEQHHLER LRKEGEDIFQ QLNESKARME HSRELLRGMY EDLKQMCHKA DVELLQAFGD ILHRYESLLL QVSEPVNPEL SAGPITGLLD SLSGFRVDFT LQPERANSHI FLCGDLRSMN VGCDPQDDPD ITGKSECFLV WGAQAFTSGK YYWEVHMGDS WNWAFGVCNN YWKEKRQNDK IDGEEGLFLL GCVKEDTHCS LFTTSPLVVQ YVPRPTSTVG LFLDCEGRTV SFVDVDQSSL IYTIPNCSFS PPLRPIFCCS HF

  • Molecular Weight

    52.2 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

SPRYD5, a member of the SPRY protein family known for its roles in cellular signaling and regulation, has garnered attention due to its potential implications in various biological processes and diseases. The SPRY domain is involved in modulating pathways such as RAS/MAPK signaling, which is crucial for cell proliferation, differentiation, and survival. Alterations in SPRYD5 expression or function have been implicated in cancer progression and other pathological conditions, making it a target of interest for therapeutic intervention. Recent studies have highlighted the importance of SPRYD5 in immune responses and its interaction with key signaling molecules, suggesting it may play a critical role in both innate and adaptive immunity. The development and characterization of recombinant SPRYD5 protein is essential for further investigating its biological functions, understanding its mechanisms of action, and exploring its potential as a biomarker or therapeutic target in disease contexts. By producing and studying this protein, researchers aim to elucidate the molecular pathways involving SPRYD5, potentially leading to novel strategies for disease treatment and prevention. The recombinant SPRYD5 serves as a valuable tool for examining its interactions, post-translational modifications, and the functional consequences of its activity in various cellular settings. As such, the study of SPRYD5 represents a promising frontier in biomedical research, with the potential for significant contributions to our understanding of cellular signaling and disease mechanisms.

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