Cat: PA2000-1539

Recombinant Human OPA1 Protein,His

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Analytical Data

  • Gene name

    OPA1

  • Application

    SPRMSTBLIITCELISACELL ASSAYDRUG SCREENING

  • Alternative Names

    OPA1;KIAA0567;Dynamin-like GTPase OPA1. mitochondrial

  • Species

    Human

  • Source

    E. coli

  • Tag

    His tag N-Terminus

  • Purity

    Greater than 90% as determined by SDS-PAGE.

  • Uniprot

    O60313

  • Expression Region

    1-960aa

  • AA Sequence

    MWRLRRAAVACEVCQSLVKHSSGIKGSLPLQKLHLVSRSIYHSHHPTLKL QRPQLRTSFQQFSSLTNLPLRKLKFSPIKYGYQPRRNFWPARLATRLLKL RYLILGSAVGGGYTAKKTFDQWKDMIPDLSEYKWIVPDIVWEIDEYIDFE KIRKALPSSEDLVKLAPDFDKIVESLSLLKDFFTSGSPEETAFRATDRGS ESDKHFRKVSDKEKIDQLQEELLHTQLKYQRILERLEKENKELRKLVLQK DDKGIHHRKLKKSLIDMYSEVLDVLSDYDASYNTQDHLPRVVVVGDQSAG KTSVLEMIAQARIFPRGSGEMMTRSPVKVTLSEGPHHVALFKDSSREFDL TKEEDLAALRHEIELRMRKNVKEGCTVSPETISLNVKGPGLQRMVLVDLP GVINTVTSGMAPDTKETIFSISKAYMQNPNAIILCIQDGSVDAERSIVTD LVSQMDPHGRRTIFVLTKVDLAEKNVASPSRIQQIIEGKLFPMKALGYFA VVTGKGNSSESIEAIREYEEEFFQNSKLLKTSMLKAHQVTTRNLSLAVSD CFWKMVRESVEQQADSFKATRFNLETEWKNNYPRLRELDRNELFEKAKNE ILDEVISLSQVTPKHWEEILQQSLWERVSTHVIENIYLPAAQTMNSGTFN TTVDIKLKQWTDKQLPNKAVEVAWETLQEEFSRFMTEPKGKEHDDIFDKL KEAVKEESIKRHKWNDFAEDSLRVIQHNALEDRSISDKQQWDAAIYFMEE ALQARLKDTENAIENMVGPDWKKRWLYWKNRTQEQCVHNETKNELEKMLK CNEEHPAYLASDEITTVRKNLESRGVEVDPSLIKDTWHQVYRRHFLKTAL NHCNLCRRGFYYYQRHFVDSELECNDVVLFWRIQRMLAITANTLRQQLTN TEVRRLEKNVKEVLEDFAEDGEKKIKLLTGKRVQLAEDLKKVREIQEKLD AFIEALHQEK

  • Molecular Weight

    138 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

OPA1 (Optic Atrophy 1) is a dynamin-related GTPase that plays a crucial role in mitochondrial dynamics, primarily in the regulation of mitochondrial fusion and maintenance of cristae structure. Mutations in the OPA1 gene are associated with dominant optic atrophy, a hereditary condition that leads to vision loss due to the degeneration of retinal ganglion cells. Research on OPA1 recombinant proteins has gained prominence as scientists seek to understand the molecular mechanisms underlying mitochondrial dysfunction in various diseases, including neurodegenerative disorders and metabolic syndromes. The study of OPA1 encompasses its interactions with other mitochondrial proteins, its role in apoptosis, and how it influences the overall mitochondrial morphology and bioenergetics. Additionally, exploring the potential for developing therapeutic interventions based on OPA1 modulation is of significant interest, as enhancing mitochondrial function may offer protective effects against cellular stress and degeneration. In this context, producing and characterizing OPA1 recombinant proteins can aid in elucidating its functional properties and interactions, providing valuable insights into its contribution to mitochondrial health and the pathophysiology of associated disorders.

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