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Recombinant Human Rho guanine nucleotide exchange factor 3 (ARHGEF3)

ACP11205

Number
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High Purity LevelsPrecision and ReliabilityCustomization Options

Specifications


Cat.No ACP11205 Target NameARHGEF3
Target SynonymsARHGEF3; Rho guanine nucleotide exchange factor 3; Exchange factor found in platelets and leukemic and neuronal tissues; XPLNFormLyophilized powder
Expression SystemCustom Production. Please inquire and provide the desire expression system.Expression Range1-526
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 IDQ9NR81
Background Information
  • Uniprot Id

    Q9NR81

  • Target Species

    Human

  • Target Name

    ARHGEF3

  • Target Full Name

    Rho guanine nucleotide exchange factor 3

  • Target Function

    Acts as guanine nucleotide exchange factor (GEF) for RhoA and RhoB GTPases.

  • Target Subcellular Location

    Cytoplasm.

  • Target Tissue Specificity

    Widely expressed. Highest levels are found in adult brain and skeletal muscle. Lower levels are found in heart and kidney.

  • Target Synonyms

    ARHGEF3; Rho guanine nucleotide exchange factor 3; Exchange factor found in platelets and leukemic and neuronal tissues; XPLN

  • Target Background

    Rho-like GTPases are involved in a variety of cellular processes, and they are activated by binding GTP and inactivated by conversion of GTP to GDP by their intrinsic GTPase activity. Guanine nucleotide exchange factors (GEFs) accelerate the GTPase activity of Rho GTPases by catalyzing their release of bound GDP. This gene encodes a guanine nucleotide exchange factor, which specifically activates two members of the Rho GTPase family: RHOA and RHOB, both of which have a role in bone cell biology. It has been identified that genetic variation in this gene plays a role in the determination of bone mineral density (BMD), indicating the implication of this gene in postmenopausal osteoporosis. Alternatively spliced transcript variants encoding different isoforms have been found for this gene.

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