Cat: IPD-X41664

Recombinant Human CHRM5 Protein ,His

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Analytical Data

  • Gene name

    CHRM5

  • Application

    SPRMSTBLIITCELISACELL ASSAYDRUG SCREENING

  • Species

    Human

  • Source

    E. coli

  • Tag

    N- His

  • Purity

    Greater than 90% as determined by SDS-PAGE.

  • Uniprot

    P08912

  • Expression Region

    215-443aa

  • Molecular Weight

    31.5 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

CHRM5, or Cholinergic Receptor Muscarinic 5, is a member of the muscarinic acetylcholine receptor family, which are G protein-coupled receptors critically involved in various physiological processes, including neurotransmission, memory, and cognition. Research has indicated that CHRM5 plays a significant role in the central nervous system and is implicated in neurodegenerative diseases such as Alzheimer’s disease and schizophrenia, where its dysregulation may contribute to cognitive deficits and altered mood states. Given its potential as a therapeutic target, the expression and characterization of recombinant CHRM5 protein are essential for understanding its structure-function relationship and pharmacological properties. By utilizing recombinant DNA technology, researchers can produce CHRM5 in suitable expression systems, enabling comprehensive studies of its interaction with ligands and signaling pathways. Furthermore, the availability of purified CHRM5 protein is crucial for the development of novel drugs aimed at modulating its activity, which might lead to new treatment strategies for cognitive impairments associated with various neurological disorders. Overall, the study of CHRM5 recombinant protein not only enhances the understanding of cholinergic signaling but also holds promise for advancing therapeutic approaches in neuropharmacology.

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