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LIM Homeobox 3 (LHX3) (Middle Region) Peptide

LHX3 Reactivity: Human Host: Synthetic BP, WB
Catalog No. ABIN979300
  • Target See all LHX3 products
    LHX3 (LIM Homeobox 3 (LHX3))
    Protein Region
    Middle Region
    Origin
    Human
    Source
    • 3
    Synthetic
    Application
    Blocking Peptide (BP), Western Blotting (WB)
    Characteristics
    This is a synthetic peptide designed for use in combination with anti-LHX3 antibody (Catalog #: ARP33644_P050). 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
    LHX3 (LIM Homeobox 3 (LHX3))
    Synonyms
    CPHD3 Peptide, LIM3 Peptide, M2-LHX3 Peptide, lim3 Peptide, LIM-3 Peptide, xlim-3 Peptide, lim-3 Peptide, Lim3 Peptide, P-LIM Peptide, mLIM3 Peptide, mLim-3 Peptide, lim homeobox 3 Peptide, LIM/homeobox protein Lhx3 Peptide, LIM homeobox 3 Peptide, LIM homeobox 3 L homeolog Peptide, LIM homeobox protein 3 Peptide, LOC662120 Peptide, LOC100224079 Peptide, LHX3 Peptide, Lhx3 Peptide, lhx3 Peptide, lhx3.L Peptide
    Background
    LHX3 encodes a member a large protein family which carry the LIM domain, a unique cysteine-rich zinc-binding domain. The encoded protein is a transcription factor that is required for pituitary development and motor neuron specification. Mutations in this gene have been associated with a syndrome of combined pituitary hormone deficiency and rigid cervical spine. This gene encodes a member a large protein family which carry the LIM domain, a unique cysteine-rich zinc-binding domain. The encoded protein is a transcription factor that is required for pituitary development and motor neuron specification. Mutations in this gene have been associated with a syndrome of combined pituitary hormone deficiency and rigid cervical spine. Two transcripts variants encoding distinct isoforms have been identified for this gene.

    Alias Symbols: DKFZp762A2013, M2-LHX3, LIM3, CPHD3

    Protein Interaction Partner: CITED2,IFT172,ISL1,ISL2,LDB1,RLIM,CITED2,IFT172,ISL1,ISL2,LHX1,LMX1A,RLIM

    Protein Size: 402
    Molecular Weight
    44 kDa
    Gene ID
    8022
    NCBI Accession
    NM_014564, NP_055379
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