Cat: PA2000-2111

Recombinant Human MMUT Protein,His

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Analytical Data

  • Gene name

    MMUT

  • Application

    SPRMSTBLIITCELISACELL ASSAYDRUG SCREENING

  • Alternative Names

    MMUT;MUT;Methylmalonyl-CoA mutase. mitochondrial

  • Species

    Human

  • Source

    E. coli

  • Tag

    His tag N-Terminus

  • Purity

    Greater than 90% as determined by SDS-PAGE.

  • Uniprot

    P22033

  • Expression Region

    33-750aa

  • AA Sequence

    LHQQQPLHPEWAALAKKQLKGKNPEDLIWHTPEGISIKPLYSKRDTMDLPEELPGVKPFTRGPYPTMYTFRPWTIRQYAGFSTVEESNKFYKDNIKAGQQGLSVAFDLATHRGYDSDNPRVRGDVGMAGVAIDTVEDTKILFDGIPLEKMSVSMTMNGAVIPVLANFIVTGEEQGVPKEKLTGTIQNDILKEFMVRNTYIFPPEPSMKIIADIFEYTAKHMPKFNSISISGYHMQEAGADAILELAYTLADGLEYSRTGLQAGLTIDEFAPRLSFFWGIGMNFYMEIAKMRAGRRLWAHLIEKMFQPKNSKSLLLRAHCQTSGWSLTEQDPYNNIVRTAIEAMAAVFGGTQSLHTNSFDEALGLPTVKSARIARNTQIIIQEESGIPKVADPWGGSYMMECLTNDVYDAALKLINEIEEMGGMAKAVAEGIPKLRIEECAARRQARIDSGSEVIVGVNKYQLEKEDAVEVLAIDNTSVRNRQIEKLKKIKSSRDQALAERCLAALTECAASGDGNILALAVDASRARCTVGEITDALKKVFGEHKANDRMVSGAYRQEFGESKEITSAIKRVHKFMEREGRRPRLLVAKMGQDGHDRGAKVIATGFADLGFDVDIGPLFQTPREVAQQAVDADVHAVGISTLAAGHKTLVPELIKELNSLGRPDILVMCGGVIPPQDYEFLFEVGVSNVFGPGTRIPKAAVQVLDDIEKCLEKKQQSV

  • Molecular Weight

    84.8 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

MMUT (methylmalonyl-CoA mutase) is an essential enzyme involved in the catabolism of branched-chain amino acids and the metabolism of certain fatty acids. Deficiency in MMUT activity can lead to methylmalonic acidemia (MMA), a metabolic disorder characterized by the accumulation of toxic levels of methylmalonic acid in the body, resulting in significant health issues, including neurological impairment and metabolic crises. Research into recombinant MMUT proteins aims to understand the enzyme's structure-function relationship, gain insights into the molecular basis of MMUT-related disorders, and explore potential therapeutic interventions. The expression and purification of recombinant MMUT can provide ample quantities of the enzyme for biochemical studies, allowing researchers to investigate the effects of various mutations that lead to MMA. Furthermore, recombinant MMUT represents a promising avenue for developing enzyme replacement therapies, offering hope for affected individuals by restoring normal metabolic function. By leveraging advancements in recombinant DNA technology, researchers are focusing on characterizing the enzyme's kinetic properties, studying its interactions with substrates and cofactors, and exploring potential small-molecule chaperones that could enhance MMUT stability and function. Overall, the study of MMUT and its recombinant forms is a critical field of inquiry that holds promise not only for understanding the biochemistry underlying MMA but also for developing innovative strategies to treat this challenging metabolic disorder.

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