Cat: IPD-X37251

Recombinant Human ABL1 Protein,GST

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Analytical Data

  • Gene name

    ABL1

  • Application

    SPRMSTBLIITCELISACELL ASSAYDRUG SCREENING

  • Alternative Names

    Abelson murine leukemia viral oncogene homolog 1Abelson tyrosine-protein kinase 1;Proto-oncogene c-Ablp150

  • Species

    Human

  • Source

    E. coli

  • Tag

    N- GST

  • Purity

    Greater than 90% as determined by SDS-PAGE.

  • Uniprot

    P00519

  • Expression Region

    4-194aa

  • Molecular Weight

    48.1 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

ABL1, or Abelson murine leukemia virus gene 1, is a crucial proto-oncogene that encodes a non-receptor tyrosine kinase, playing a significant role in various cellular processes, including cell division, differentiation, and apoptosis. Its dysregulation is prominently associated with several types of cancers, particularly chronic myeloid leukemia (CML), where the BCR-ABL fusion protein acts as a constitutively active tyrosine kinase, driving malignant transformation. The development of BCR-ABL-targeted therapies, notably Imatinib (Gleevec), revolutionized CML treatment and highlighted the importance of ABL1 in cancer biology. Researchers have been focused on producing recombinant ABL1 proteins to better understand its biochemical properties, signaling pathways, and interactions with other molecules. This research aids in deciphering the mechanisms of BCR-ABL-associated oncogenesis and helps in identifying potential therapeutic targets. Additionally, the generation of ABL1 protein variants and their recombinant forms offers insights into drug resistance mechanisms and the development of second-generation tyrosine kinase inhibitors. As studies continue to explore the nuances of ABL1’s role in cancer, the insights gained from recombinant ABL1 protein research are crucial for advancing personalized medicine strategies and improving therapeutic outcomes for patients with ABL1-related malignancies.

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