Cat: PA1000-436DB

Recombinant Human CBFB Protein,His

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Analytical Data

  • Gene name

    CBFB

  • Application

    SPRMSTBLIITCELISACELL ASSAYDRUG SCREENING

  • Alternative Names

    CBFB;Nuclear transcription factor Y subunit alpha

  • Species

    Human

  • Source

    E. coli

  • Tag

    His tag N-Terminus

  • Purity

    Greater than 90% as determined by SDS-PAGE.

  • Uniprot

    Q13951

  • Expression Region

    1-182aa

  • AA Sequence

    MGSSHHHHHHSSGLVPRGSHMPRVVPDQRSKFENEEFFRKLSRECEIKYT GFRDRPHEERQARFQNACRDGRSEIAFVATGTNLSLQFFPASWQGEQRQT PSREYVDLEREAGKVYLKAPMILNGVCVIWKGWIDLQRLDGMGCLEFDEE RAQQEDALAQQAFEEARRRTREFEDRDRSHREEMEVRVSQLLAVTGKKTT RP

  • Molecular Weight

    24 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

CBFB, or core-binding factor beta, is a key regulatory protein that plays a crucial role in hematopoiesis and gene transcription through its interaction with the transcription factor RUNX. Abnormalities in the CBFB gene, such as mutations and translocations, have been linked to various hematological malignancies, including acute myeloid leukemia (AML) and myelodysplastic syndromes. These alterations can disrupt normal gene expression patterns, leading to hematopoietic dysregulation and the development of cancer. As a result, understanding the structure and function of the CBFB protein, as well as its interactions with RUNX and other proteins, is essential for elucidating the molecular mechanisms underlying these diseases. Research in this area has indicated that restoring normal CBFB function may have therapeutic potential in treating CBFB-related malignancies. Furthermore, the development of CBFB recombinant proteins for research purposes has emerged as a significant focus, allowing scientists to dissect its functional roles and explore potential interventions. This research not only contributes to the fundamental understanding of CBFB but also paves the way for innovative strategies in cancer therapy, highlighting the importance of targeted approaches in the treatment of hematological disorders.

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