Cat: PA2000-5722

Recombinant Human ATXN7L4 Protein,GST

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Analytical Data

  • Gene name

    ATXN7L4

  • Application

    SPRMSTBLIITCELISACELL ASSAYDRUG SCREENING

  • Alternative Names

    AT7L1_HUMAN; Ataxin 7 like 4; Ataxin 7 like Protein 1; ataxin 7-like 1; Ataxin-7-like Protein 1

  • Species

    Human

  • Source

    E. coli

  • Tag

    GST-tag at N-terminal

  • Purity

    Greater than 90% as determined by SDS-PAGE.

  • Uniprot

    Q9ULK2

  • Expression Region

    1-146aa

  • AA Sequence

    MTSERSRIPCLSAAAAEGTGKKQQEGRAMATLDRKVPSPEAFLGKPWSSWIDAAKLHCSDNVDLEEAGKEGGKSREVMRLNKEDMHLFGHYPAHDDFYLVVCSACNQVVKPQVFQSHCGRKQDNRRNEGISRSGPESSQAIEKHQV

  • Molecular Weight

    42.6 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

ATXN7L4, a member of the Ataxin-7-like family, plays a significant role in various cellular processes, including transcription regulation and RNA processing. The gene encoding ATXN7L4 is thought to be involved in neurodegenerative diseases, particularly due to its homology with ATXN7, which is linked to spinocerebellar ataxia type 7 (SCA7). Research into ATXN7L4 has gained traction as scientists seek to understand its structure and function in both normal physiology and disease states. The production of recombinant ATXN7L4 protein allows for detailed investigation into its molecular mechanisms, interactions with other proteins, and potential implications in cellular signaling pathways. Techniques such as recombinant DNA technology facilitate the expression and purification of this protein, which is crucial for functional assays and structural studies. By elucidating the role of ATXN7L4, researchers aim to uncover its potential as a biomarker or therapeutic target in neurodegenerative conditions, contributing to the broader understanding of related pathologies and the development of targeted interventions. Overall, the study of ATXN7L4 serves as an important avenue for exploring the complexities of gene function and its impact on human health.

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