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Recombinant Human Ceroid-lipofuscinosis neuronal protein 5 (CLN5)

ACP01155

Number
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Specifications


Cat.No ACP01155 Target NameCLN5
Target Synonyms(Protein CLN5)FormLiquid or Lyophilized powder
Expression SystemE.coliExpression Range47-358aa
Mol Weight43.5 kDaProtein LengthFull Length of Mature Protein
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 IDO75503
Background Information
  • Uniprot Id

    O75503

  • Target Species

    Human

  • Target Name

    CLN5

  • Target Full Name

    Bis(monoacylglycero)phosphate synthase CLN5

  • Target Function

    Plays a role in influencing the retrograde trafficking of lysosomal sorting receptors SORT1 and IGF2R from the endosomes to the trans-Golgi network by controlling the recruitment of retromer complex to the endosomal membrane. Regulates the localization and activation of RAB7A which is required to recruit the retromer complex to the endosomal membrane.

  • Target Involvement

    Ceroid lipofuscinosis, neuronal, 5 (CLN5)

  • Target Subcellular Location

    [Ceroid-lipofuscinosis neuronal protein 5, secreted form]: Lysosome.; [Ceroid-lipofuscinosis neuronal protein 5]: Membrane; Single-pass type II membrane protein.

  • Target Protein Families

    CLN5 family

  • Target Tissue Specificity

    Ubiquitous.

  • Target Research Area

    Others

  • Target Synonyms

    Ceroid lipofuscinosis neuronal 5; Ceroid-lipofuscinosis neuronal protein 5; CLN5; CLN5_HUMAN; NCL; Protein CLN5

  • Target Background

    This gene is one of eight which have been associated with neuronal ceroid lipofuscinoses (NCL). Also referred to as Batten disease, NCL comprises a class of autosomal recessive, neurodegenerative disorders affecting children. The genes responsible likely encode proteins involved in the degradation of post-translationally modified proteins in lysosomes. The primary defect in NCL disorders is thought to be associated with lysosomal storage function.

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