Cat: IPD-X39821

Recombinant Human GATC Protein ,GST

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Analytical Data

  • Gene name

    GATC

  • Application

    SPRMSTBLIITCELISACELL ASSAYDRUG SCREENING

  • Alternative Names

    Protein 15E1.2

  • Species

    Human

  • Source

    E. coli

  • Tag

    N- GST

  • Purity

    Greater than 90% as determined by SDS-PAGE.

  • Uniprot

    O43716

  • Expression Region

    1-136aa

  • Molecular Weight

    42.1 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.

Quality inspection process

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Protein Description

GATC recombinants represent a significant advancement in the field of biochemistry and molecular biology, focusing on the intricate mechanisms of genetic recombination. The study of GATC sequences, specifically within bacterial genomes, has highlighted their role as crucial sites for DNA methylation and the regulation of gene expression. These adenine-methylated GATC sites are pivotal in maintaining genomic stability, influencing processes such as replication, repair, and horizontal gene transfer. Researchers have been keen to explore GATC recombination to understand better how these sites contribute to bacterial adaptability and antibiotic resistance. Furthermore, GATC sequences have become essential targets for genetic engineering applications, allowing for precise modifications in microbial systems. The development of GATC-based recombinant proteins has potential implications for biotechnology, pharmaceuticals, and synthetic biology. By harnessing the power of GATC recombination, scientists aim to create novel proteins with enhanced functionalities, paving the way for innovative therapeutic strategies and biotechnological advancements. Understanding the underlying mechanisms of GATC recombination is also vital for developing new tools for genome editing and synthetic biology applications, as researchers continue to explore the versatility of these sequences in diverse biological systems. Thus, the ongoing investigation into GATC recombination not only enriches our knowledge of bacterial genetics but also opens new avenues for research and application in various fields.

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