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Recombinant Human Neutral amino acid transporter A (SLC1A4), Truncated

ACP05534

Number
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High Purity LevelsPrecision and ReliabilityCustomization Options

Specifications


Cat.No ACP05534 Target NameSLC1A4
Target Synonymsmember 4; Solute carrier family 1 member 4FormLyophilized powder
Expression SystemCustom Production. Please inquire and provide the desire expression system.Protein LengthPartial
Purity>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 IDP43007
Background Information
  • Uniprot Id

    P43007

  • Target Species

    Human

  • Target Name

    SLC1A4

  • Target Full Name

    Neutral amino acid transporter A

  • Target Function

    Transporter for alanine, serine, cysteine, and threonine. Exhibits sodium dependence.

  • Target Involvement

    Spastic tetraplegia, thin corpus callosum, and progressive microcephaly (SPATCCM)

  • Target Subcellular Location

    Membrane; Multi-pass membrane protein. Melanosome. Note=Identified by mass spectrometry in melanosome fractions from stage I to stage IV.

  • Target Protein Families

    Dicarboxylate/amino acid:cation symporter (DAACS) (TC 2.A.23) family, SLC1A4 subfamily

  • Target Tissue Specificity

    Expressed mostly in brain, muscle, and pancreas but detected in all tissues examined.

  • Target Synonyms

    Alanine/serine/cysteine/threonine transporter 1; ASCT-1; ASCT1; AW045657; Glutamate/neutral amino acid transporter; Neutral amino acid transporter A; OTTHUMP00000159933; OTTHUMP00000235138; SATT; SATT_HUMAN; SLC1A4; Solute carrier family 1 (glutamate/neutral amino acid transporter), member 4; Solute carrier family 1 member 4

  • Target Background

    The protein encoded by this gene is a sodium-dependent neutral amino acid transporter for alanine, serine, cysteine, and threonine. Defects in this gene have been associated with developmental delay, microcephaly, and intellectual disability.

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