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Recombinant Human Protein DGCR6L (DGCR6L)

ACP11052

Number
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High Purity LevelsPrecision and ReliabilityCustomization Options

Specifications


Cat.No ACP11052 Target NameDGCR6L
Target SynonymsDGC6L_HUMAN; DGCR6L; DiGeorge syndrome critical region 6-like protein; Protein DGCR6LFormLyophilized powder
Expression SystemCustom Production. Please inquire and provide the desire expression system.Expression Range1-220
Protein LengthFull length 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 IDQ9BY27
Background Information
  • Uniprot Id

    Q9BY27

  • Target Species

    Human

  • Target Name

    DGCR6L

  • Target Full Name

    Protein DGCR6L

  • Target Function

    May play a role in neural crest cell migration into the third and fourth pharyngeal pouches.

  • Target Subcellular Location

    Nucleus. Note=Predominantly nuclear.

  • Target Protein Families

    Gonadal family

  • Target Tissue Specificity

    Widely expressed in fetal and adult tissues. Highest expression in liver, heart and skeletal muscle. Lower levels in pancreas and placenta. Weak expression in brain.

  • Target Research Area

    Cell Biology

  • Target Synonyms

    DGC6L_HUMAN; DGCR6L; DiGeorge syndrome critical region 6-like protein; Protein DGCR6L

  • Target Background

    This gene, the result of a duplication at this locus, is one of two functional genes encoding nearly identical proteins that have similar expression patterns. The product of this gene is a protein that shares homology with the Drosophila gonadal protein, expressed in gonadal tissues and germ cells, and with the human laminin gamma-1 chain that functions in cell attachment and migration. This gene is located in a region of chromosome 22 implicated in the DiGeorge syndrome, one facet of a broader collection of anomalies referred to as the CATCH 22 syndrome.

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