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Recombinant Human Myosin light chain 3 (MYL3)

ACP03496

Number
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High Purity LevelsPrecision and ReliabilityCustomization Options

Specifications


Cat.No ACP03496 Target NameMYL3
Target Synonymsalkali, alkali; myosin, B; Myosin light chain 3; Myosin, light chain 1, light chain 3, light polypeptide 3, skeletal, slow; myosin, slow; OTTHUMP00000165922; Slow skeletal ventricular myosin alkali light chain 3; slow-twitch muscle B/ventricular isoform; Ventricular/slow twitch myosin alkali light chain; VLC1, ventricular, ventricular; myosinFormLiquid or Lyophilized powder
Expression SystemE.coliExpression Range1-195aa
Mol Weight48.8kDaProtein LengthFull length
PurityGreater than 90% as determined by SDS-PAGE.Storage Buffer5%-50% glycerol. Lyophilized powder form: the buffer before lyophilization is Tris/PBS-based buffer, 6% Trehalose, Liquid form: default storage buffer is Tris/PBS-based buffer, pH 8.0.

Immunogen Information


Target SpeciesHumanUniprot IDP08590
Background Information
  • Uniprot Id

    P08590

  • Target Species

    Human

  • Target Name

    MYL3

  • Target Full Name

    Myosin light chain 3

  • Target Function

    Regulatory light chain of myosin. Does not bind calcium.

  • Target Involvement

    Cardiomyopathy, familial hypertrophic 8 (CMH8)

  • Target Synonyms

    Cardiac myosin light chain 1; CMH8 ; CMLC1; ELC of myosin; Essential light chain of myosin; MLC1SB; MLC1V; MYL3; MYL3_HUMAN; Myosin light chain 1; Myosin light chain 1 slow twitch muscle B/ventricular isoform; Myosin light chain 1 slow, B; Myosin light chain 3; Myosin, light chain 1, ventricular; myosin, light chain 3, alkali, ventricular, skeletal, slow; myosin, light polypeptide 3, alkali; myosin, light polypeptide 3, alkali, ventricular, skeletal, slow; OTTHUMP00000165922; Slow skeletal ventricular myosin alkali light chain 3; slow-twitch muscle B/ventricular isoform; Ventricular/slow twitch myosin alkali light chain; VLC1

  • Target Background

    MYL3 encodes myosin light chain 3, an alkali light chain also referred to in the literature as both the ventricular isoform and the slow skeletal muscle isoform. Mutations in MYL3 have been identified as a cause of mid-left ventricular chamber type hypertrophic cardiomyopathy.

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