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Recombinant Human Presenilins-associated rhomboid-like protein, mitochondrial (PARL), Truncated

ACP07276

Number
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Specifications


Cat.No ACP07276 Target NamePARL
Target Synonymsmitochondrial; Mitochondrial intramembrane cleaving protease PARL, PARL; PSARL; PRO2207; Presenilins-associated rhomboid-like proteinFormLyophilized powder
Expression SystemCustom Production. Please inquire and provide the desire expression system.Protein LengthPartial
Purity>85% (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 IDQ9H300
Background Information
  • Uniprot Id

    Q9H300

  • Target Species

    Human

  • Target Name

    PARL

  • Target Full Name

    Presenilin-associated rhomboid-like protein, mitochondrial

  • Target Function

    Required for the control of apoptosis during postnatal growth. Essential for proteolytic processing of an antiapoptotic form of OPA1 which prevents the release of mitochondrial cytochrome c in response to intrinsic apoptotic signals. Required for the maturation of PINK1 into its 52kDa mature form after its cleavage by mitochondrial-processing peptidase (MPP). Promotes changes in mitochondria morphology regulated by phosphorylation of P-beta domain.

  • Target Subcellular Location

    Mitochondrion inner membrane; Multi-pass membrane protein.; [P-beta]: Nucleus.

  • Target Protein Families

    Peptidase S54 family

  • Target Synonyms

    PARL; PSARL; PRO2207; Presenilins-associated rhomboid-like protein, mitochondrial; Mitochondrial intramembrane cleaving protease PARL

  • Target Background

    This gene encodes a member of the rhomboid family of intramembrane serine proteases that is localized to the inner mitochondrial membrane. The encoded protein regulates mitochondrial remodeling and apoptosis through regulated substrate proteolysis. Proteolytic processing of the encoded protein results in the release of a small peptide, P-beta, which may transit to the nucleus. Mutations in this gene may be associated with Parkinson's disease.

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