Cat: IPD-X39156

Recombinant Human CLSTN2 Protein,His

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Analytical Data

  • Gene name

    CLSTN2

  • Application

    SPRMSTBLIITCELISACELL ASSAYDRUG SCREENING

  • Alternative Names

    CSTN2; CS2; CDHR13; Cadherin-Related Family Member 13; Alcadein-gamma

  • Species

    Human

  • Source

    E. coli

  • Tag

    N-His

  • Purity

    Greater than 90% as determined by SDS-PAGE.

  • Uniprot

    Q9H4D0

  • Expression Region

    Arg31~Gln271

  • Molecular Weight

    36kDa

  • 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

CLSTN2, or calsyntenin-2, is a member of the calsyntenin family of proteins, which are implicated in various neurobiological processes, including synaptic transmission and neuronal differentiation. The interest in CLSTN2 has grown due to its potential role in neurodevelopmental disorders and neurodegenerative diseases. Research has suggested that CLSTN2 interacts with other key proteins involved in synapse formation and maintenance, thus influencing neuronal communication and plasticity. Additionally, variations in the CLSTN2 gene have been associated with conditions such as autism spectrum disorder, drawing attention to its significance in understanding the molecular underpinnings of these disorders. The development of recombinant CLSTN2 protein allows for the exploration of its structure-function relationships, facilitating studies on its biochemical properties and interactions within neuronal contexts. Overall, investigating CLSTN2 and its recombinant forms offers valuable insights into both its physiological roles in the nervous system and its potential implications in pathology, with prospects for therapeutic interventions in related disorders.

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