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Immunoglobulin lambda-Like Polypeptide 1 (IGLL1) Peptide

IGLL1 Reactivity: Human Host: Synthetic WB, BP
Catalog No. ABIN978447

Quick Overview for Immunoglobulin lambda-Like Polypeptide 1 (IGLL1) Peptide (ABIN978447)

Target

IGLL1 (Immunoglobulin lambda-Like Polypeptide 1 (IGLL1))

Origin

Human

Source

  • 3
  • 1
Synthetic

Application

Western Blotting (WB), Blocking Peptide (BP)
  • Characteristics

    This is a synthetic peptide designed for use in combination with anti-IGLL1 antibody (Catalog #: ARP42547_T100). It may block above mentioned antibody from binding to its target protein in western blot and/or immunohistochecmistry under proper experimental settings. There is no guarantee for its use in other applications.

    Purification

    Purified
  • Application Notes

    Each Investigator should determine their own optimal working dilution for specific applications.

    Restrictions

    For Research Use only
  • Format

    Lyophilized

    Reconstitution

    Add 100 μL of sterile PBS. Final peptide concentration is 1 mg/mL in PBS.

    Concentration

    1 mg/mL

    Buffer

    Final peptide concentration is 1 mg/mL in PBS.

    Handling Advice

    Avoid repeated freeze-thaw cycles.

    Storage

    -20 °C

    Storage Comment

    For longer periods of storage, store at -20°C. Avoid repeat freeze-thaw cycles.
  • Target

    IGLL1 (Immunoglobulin lambda-Like Polypeptide 1 (IGLL1))

    Background

    The preB cell receptor is found on the surface of proB and preB cells, where it is involved in transduction of signals for cellular proliferation, differentiation from the proB cell to the preB cell stage, allelic exclusion at the Ig heavy chain gene locus, and promotion of Ig light chain gene rearrangements. The preB cell receptor is composed of a membrane-bound Ig mu heavy chain in association with a heterodimeric surrogate light chain. IGLL1 is one of the surrogate light chain subunits and is a member of the immunoglobulin gene superfamily. Mutations in its gene can result in B cell deficiency and agammaglobulinemia, an autosomal recessive disease in which few or no gamma globulins or antibodies are made.The preB cell receptor is found on the surface of proB and preB cells, where it is involved in transduction of signals for cellular proliferation, differentiation from the proB cell to the preB cell stage, allelic exclusion at the Ig heavy chain gene locus, and promotion of Ig light chain gene rearrangements. The preB cell receptor is composed of a membrane-bound Ig mu heavy chain in association with a heterodimeric surrogate light chain. This gene encodes one of the surrogate light chain subunits and is a member of the immunoglobulin gene superfamily. This gene does not undergo rearrangement. Mutations in this gene can result in B cell deficiency and agammaglobulinemia, an autosomal recessive disease in which few or no gamma globulins or antibodies are made. Two transcript variants encoding different isoforms have been found for this gene.

    Alias Symbols: 14.1, CD179b, IGL1, IGL5, IGLJ14.1, IGLL, IGO, IGVPB, VPREB2, AGM2

    Protein Interaction Partner: IGLL1,MYOC

    Protein Size: 213

    Molecular Weight

    19 kDa

    Gene ID

    3543

    NCBI Accession

    NM_020070, NP_064455

    UniProt

    P15814
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