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Recombinant Human Septin-6 (41523)

ACP17748

Number
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High Purity LevelsPrecision and ReliabilityCustomization Options

Specifications


Cat.No ACP17748 Target NameSEPT6
Target SynonymsKIAA0128; Nkrf; RCG53214; isoform CRA_d; RP5-876A24.2; SEP2 ; SEPT2; SEPT6; SEPT6/MLL FUSION GENE; SEPT6_HUMAN; Septin 2 ; Septin 6; Septin-6FormLyophilized powder
Expression SystemCustom Production. Please inquire and provide the desire expression system.Expression Range2-434
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 IDQ14141
Background Information
  • Uniprot Id

    Q14141

  • Target Species

    Human

  • Target Name

    SEPT6

  • Target Full Name

    Septin-6

  • Target Function

    Filament-forming cytoskeletal GTPase. Required for normal organization of the actin cytoskeleton. Involved in cytokinesis. May play a role in HCV RNA replication. Forms a filamentous structure with SEPTIN12, SEPTIN6, SEPTIN2 and probably SEPTIN4 at the sperm annulus which is required for the structural integrity and motility of the sperm tail during postmeiotic differentiation.

  • Target Subcellular Location

    Cytoplasm. Cytoplasm, cytoskeleton, spindle. Chromosome, centromere, kinetochore. Cleavage furrow. Midbody. Cell projection, cilium, flagellum.

  • Target Protein Families

    TRAFAC class TrmE-Era-EngA-EngB-Septin-like GTPase superfamily, Septin GTPase family

  • Target Tissue Specificity

    Widely expressed.

  • Target Synonyms

    KIAA0128; Nkrf; RCG53214; isoform CRA_d; RP5-876A24.2; SEP2 ; SEPT2; SEPT6; SEPT6/MLL FUSION GENE; SEPT6_HUMAN; Septin 2 ; Septin 6; Septin-6

  • Target Background

    This gene is a member of the septin family of GTPases. Members of this family are required for cytokinesis. One version of pediatric acute myeloid leukemia is the result of a reciprocal translocation between chromosomes 11 and X, with the breakpoint associated with the genes encoding the mixed-lineage leukemia and septin 2 proteins. This gene encodes four transcript variants encoding three distinct isoforms. An additional transcript variant has been identified, but its biological validity has not been determined.

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