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Recombinant Human Prokineticin-2 (PROK2)

ACP11245

Number
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High Purity LevelsPrecision and ReliabilityCustomization Options

Specifications


Cat.No ACP11245 Target NamePROK2
Target SynonymsBV8; Bv8 homolog ; MIT1 ; PK2; PROK2; PROK2_HUMAN; Prokineticin-2; Protein Bv8 homologFormLyophilized powder
Expression SystemCustom Production. Please inquire and provide the desire expression system.Expression Range28-129
Protein LengthFull Length of Mature ProteinPurity>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 IDQ9HC23
Background Information
  • Uniprot Id

    Q9HC23

  • Target Species

    Human

  • Target Name

    PROK2

  • Target Full Name

    Prokineticin-2

  • Target Function

    May function as an output molecule from the suprachiasmatic nucleus (SCN) that transmits behavioral circadian rhythm. May also function locally within the SCN to synchronize output. Potently contracts gastrointestinal (GI) smooth muscle.

  • Target Involvement

    Hypogonadotropic hypogonadism 4 with or without anosmia (HH4)

  • Target Subcellular Location

    Secreted.

  • Target Protein Families

    AVIT (prokineticin) family

  • Target Tissue Specificity

    Expressed in the testis and, at low levels, in the small intestine.

  • Target Synonyms

    BV8; Bv8 homolog ; MIT1 ; PK2; PROK2; PROK2_HUMAN; Prokineticin-2; Protein Bv8 homolog

  • Target Background

    This gene encodes a protein expressed in the suprachiasmatic nucleus (SCN) circadian clock that may function as the output component of the circadian clock. The secreted form of the encoded protein may also serve as a chemoattractant for neuronal precursor cells in the olfactory bulb. Proteins from other vertebrates which are similar to this gene product were isolated based on homology to snake venom and secretions from frog skin, and have been shown to have diverse functions. Mutations in this gene are associated with Kallmann syndrome 4. Multiple transcript variants encoding different isoforms have been found for this gene.

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