Cat: PA2000-8498

Recombinant Human INVS Protein,GST

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Analytical Data

  • Gene name

    INVS

  • Application

    SPRMSTBLIITCELISACELL ASSAYDRUG SCREENING

  • Alternative Names

    INVS; INV; NPHP2; Inversin; Inversion of embryo turning homolog; Nephrocystin-2

  • Species

    Human

  • Source

    E. coli

  • Tag

    GST-tag at N-terminal

  • Purity

    Greater than 90% as determined by SDS-PAGE.

  • Uniprot

    Q9Y283

  • Expression Region

    1-101aa

  • AA Sequence

    MNKSENLLFAGSSLASQVHAAAVNGDKGALQRLIVGNSALKDKEDQFGRTPLMYCVLADRLDCADALLKAGADVNKTDHSQRTALHLAAQKALRTISTGRI

  • Molecular Weight

    36.85 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

INVS (inversin) is a protein encoded by the INVS gene, primarily known for its role in normal kidney development and function, as well as its implications in polycystic kidney disease (PKD). Dysregulation or mutations in the INVS gene lead to severe developmental abnormalities, including disorders such as nephronophthisis and Bardet-Biedl syndrome. Researchers have increasingly focused on INVS due to its involvement in the planar cell polarity (PCP) signaling pathway, which is crucial for cellular organization and tissue morphogenesis. The study of INVS and its recombinant proteins offers insights into the molecular mechanisms that underlie kidney organogenesis and the pathophysiology of cystic kidney diseases. By producing INVS as a recombinant protein, scientists can investigate its functional properties, interaction with other cellular components, and potential therapeutic interventions for PKD. Additionally, understanding the structure and dynamics of INVS can aid in the development of targeted treatments that influence its activity and mitigate disease progression, thereby enhancing our ability to address the challenges posed by congenital kidney disorders.

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