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Recombinant Human Profilin-1 (PFN1)

ACP22201

Number
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High Purity LevelsPrecision and ReliabilityCustomization Options

Specifications


Cat.No ACP22201 Target NamePFN1
Target SynonymsActin binding protein ; ALS18; Epididymis tissue protein Li 184a; OTTHUMP00000125244; PFN 1; Pfn; PFN1; PROF1_HUMAN; Profilin I; Profilin-1; Profilin1; ProfilinIFormLyophilized powder
Expression SystemCustom Production. Please inquire and provide the desire expression system.Expression Range2-140
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 IDP07737
Background Information
  • Uniprot Id

    P07737

  • Target Species

    Human

  • Target Name

    PFN1

  • Target Full Name

    Profilin-1

  • Target Function

    Binds to actin and affects the structure of the cytoskeleton. At high concentrations, profilin prevents the polymerization of actin, whereas it enhances it at low concentrations. By binding to PIP2, it inhibits the formation of IP3 and DG. Inhibits androgen receptor (AR) and HTT aggregation and binding of G-actin is essential for its inhibition of AR.

  • Target Involvement

    Amyotrophic lateral sclerosis 18 (ALS18)

  • Target Subcellular Location

    Cytoplasm, cytoskeleton.

  • Target Protein Families

    Profilin family

  • Target Tissue Specificity

    Expressed in epididymis (at protein level).

  • Target Research Area

    Neuroscience

  • Target Synonyms

    Actin binding protein ; ALS18; Epididymis tissue protein Li 184a; OTTHUMP00000125244; PFN 1; Pfn; PFN1; PROF1_HUMAN; Profilin I; Profilin-1; Profilin1; ProfilinI

  • Target Background

    This gene encodes a member of the profilin family of small actin-binding proteins. The encoded protein plays an important role in actin dynamics by regulating actin polymerization in response to extracellular signals. Deletion of this gene is associated with Miller-Dieker syndrome, and the encoded protein may also play a role in Huntington disease. Multiple pseudogenes of this gene are located on chromosome 1.

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