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Recombinant Human Semaphorin-3C (SEMA3C)

ACP12375

Number
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High Purity LevelsPrecision and ReliabilityCustomization Options

Specifications


Cat.No ACP12375 Target NameSEMA3C
Target SynonymsSEMA3C; SEMAE; Semaphorin-3C; Semaphorin-E; Sema EFormLyophilized powder
Expression SystemCustom Production. Please inquire and provide the desire expression system.Expression Range21-751
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 IDQ99985
Background Information
  • Uniprot Id

    Q99985

  • Target Species

    Human

  • Target Name

    SEMA3C

  • Target Full Name

    Semaphorin-3C

  • Target Function

    Binds to plexin family members and plays an important role in the regulation of developmental processes. Required for normal cardiovascular development during embryogenesis. Functions as attractant for growing axons, and thereby plays an important role in axon growth and axon guidance.

  • Target Subcellular Location

    Secreted.

  • Target Protein Families

    Semaphorin family

  • Target Tissue Specificity

    Expressed intensely in the heart, skeletal muscle, colon, small intestine, ovary, testis, and prostate. Faint expression ubiquitously among other organs, including brain.

  • Target Synonyms

    SEMA3C; SEMAE; Semaphorin-3C; Semaphorin-E; Sema E

  • Target Background

    This gene encodes a secreted glycoprotein that belongs to the semaphorin class 3 family of neuronal guidance cues. The encoded protein contains an N-terminal sema domain, integrin and immunoglobulin-like domains, and a C-terminal basic domain. Homodimerization and proteolytic cleavage of the C-terminal propeptide are necessary for the function of the encoded protein. It binds a neuropilin co-receptor before forming a heterotrimeric complex with an associated plexin. An increase in the expression of this gene correlates with an increase in cancer cell invasion and adhesion. Naturally occurring mutations in this gene are associated with Hirschsprung disease.

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