Cat: PA2000-3289

Recombinant Human FMR1NB Protein,His

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Analytical Data

  • Gene name

    FMR1NB

  • Application

    SPRMSTBLIITCELISACELL ASSAYDRUG SCREENING

  • Alternative Names

    FMR1NB;FMR1 neighbor Protein

  • Species

    Human

  • Source

    E. coli

  • Tag

    His tag N-Terminus

  • Purity

    Greater than 90% as determined by SDS-PAGE.

  • Uniprot

    Q8N0W7

  • Expression Region

    90-183aa

  • AA Sequence

    LCSGSSYFVLANGHILPNSENAHGQSLEEDSALEALLNFFFPTTCNLRENQVAKPCNELQDLSESECLRHKCCFSSSGTTSFKCFAPFRDVPKQ

  • Molecular Weight

    15.4 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

FMR1NB (Fragile X Mental Retardation 1 Neighboring Gene) is a gene that has garnered attention in the realm of genetic research due to its potential role in neurodevelopmental disorders. Located adjacent to the FMR1 gene, which is famously associated with Fragile X syndrome, FMR1NB is believed to be involved in the regulation of various cellular processes and may impact neuronal function. Recent studies have suggested that FMR1NB could play a critical role in modulating synaptic plasticity, a key mechanism underlying learning and memory. The understanding of FMR1NB's function is still in its early stages, but it may also contribute to the broader spectrum of psychiatric and neurodevelopmental disorders beyond Fragile X syndrome itself. Researchers are investigating the mechanisms by which FMR1NB influences neuronal behavior, its interactions with other key proteins, and its expression patterns during brain development. The recombinant protein derived from FMR1NB is being studied for its potential applications in understanding the pathophysiology of related disorders and may lead to the identification of new therapeutic targets. As such, FMR1NB serves as a promising candidate for further exploration in the context of neurobiology, genetics, and therapeutic development. Understanding its role could provide deeper insights into the molecular underpinnings of critical neurodevelopmental processes and pave the way for interventions targeting related disorders.

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