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Recombinant Human Neuroligin-4, X-linked (NLGN4X), Truncated

ACP13726

Number
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Specifications


Cat.No ACP13726 Target NameNLGN4X
Target SynonymsASPGX2; AUTSX2; HLNX; HNL4X; HNLX; KIAA1260; neuroligin 4, X-linked; Neuroligin X; Neuroligin-4; NL4; NLGN; NLGN4; NLGN4X; NLGNX_HUMAN; OTTHUMP00000022863; OTTHUMP00000022864; OTTHUMP00000022865; X-linkedFormLyophilized 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 IDQ8N0W4
Background Information
  • Uniprot Id

    Q8N0W4

  • Target Species

    Human

  • Target Name

    NLGN4X

  • Target Full Name

    Neuroligin-4, X-linked

  • Target Function

    Putative neuronal cell surface protein involved in cell-cell-interactions.

  • Target Involvement

    Autism, X-linked 2 (AUTSX2); Asperger syndrome, X-linked, 2 (ASPGX2)

  • Target Subcellular Location

    Cell membrane; Single-pass type I membrane protein. Cell junction, synapse, postsynaptic density membrane.

  • Target Protein Families

    Type-B carboxylesterase/lipase family

  • Target Tissue Specificity

    Expressed at highest levels in heart. Expressed at lower levels in liver, skeletal muscle and pancreas and at very low levels in brain.

  • Target Synonyms

    ASPGX2; AUTSX2; HLNX; HNL4X; HNLX; KIAA1260; neuroligin 4, X-linked; Neuroligin X; Neuroligin-4; NL4; NLGN; NLGN4; NLGN4X; NLGNX_HUMAN; OTTHUMP00000022863; OTTHUMP00000022864; OTTHUMP00000022865; X-linked

  • Target Background

    This gene encodes a member of the type-B carboxylesterase/lipase protein family. The encoded protein belongs to a family of neuronal cell surface proteins. Members of this family may act as splice site-specific ligands for beta-neurexins and may be involved in the formation and remodeling of central nervous system synapses. The encoded protein interacts with discs large homolog 4 (DLG4). Mutations in this gene have been associated with autism and Asperger syndrome. Alternative splicing results in multiple transcript variants.

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