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LIM Homeobox 4 (LHX4) (Middle Region) Peptide

LHX4 适用: 人 宿主: 合成 BP, WB
产品编号 ABIN979301
发货至: 中国
  • 抗原 See all LHX4 products
    LHX4 (LIM Homeobox 4 (LHX4))
    蛋白结构域
    Middle Region
    宿主
    资源
    合成
    应用范围
    Blocking Peptide (BP), Western Blotting (WB)
    产品特性
    This is a synthetic peptide designed for use in combination with anti-LHX4 antibody (Catalog #: ARP32424_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.
    纯化方法
    Purified
  • 应用备注
    Each Investigator should determine their own optimal working dilution for specific applications.
    限制
    仅限研究用
  • 状态
    Lyophilized
    溶解方式
    Add 100 μL of sterile PBS. Final peptide concentration is 1 mg/mL in PBS.
    浓度
    1 mg/mL
    缓冲液
    Final peptide concentration is 1 mg/mL in PBS.
    注意事项
    Avoid repeated freeze-thaw cycles.
    储存条件
    -20 °C
    储存方法
    For longer periods of storage, store at -20°C. Avoid repeat freeze-thaw cycles.
  • 抗原
    LHX4 (LIM Homeobox 4 (LHX4))
    别名
    LHX4 Peptide, si:dkeyp-35f11.3 Peptide, CPHD4 Peptide, A330062J17Rik Peptide, Gsh-4 Peptide, Gsh4 Peptide, LIM homeobox 4 Peptide, LIM homeobox protein 4 Peptide, LHX4 Peptide, lhx4 Peptide, Lhx4 Peptide
    背景
    LHX4 is a member of a large protein family which contains the LIM domain, a unique cysteine-rich zinc-binding domain. The encoded protein may function as a transcriptional regulator and be involved in control of differentiation and development of the pituitary gland. Mutations in this gene are associated with syndromic short stature and pituitary and hindbrain defects.This gene encodes a member of a large protein family which contains the LIM domain, a unique cysteine-rich zinc-binding domain. The encoded protein may function as a transcriptional regulator and be involved in control of differentiation and development of the pituitary gland. Mutations in this gene are associated with syndromic short stature and pituitary and hindbrain defects. An alternative splice variant has been described but its biological nature has not been determined. Publication Note: This RefSeq record includes a subset of the publications that are available for this gene. Please see the Entrez Gene record to access additional publications.

    Alias Symbols: Gsh-4, Gsh4, CPHD4

    Protein Interaction Partner: IFT172,IFT172

    Protein Size: 390
    分子量
    43 kDa
    基因ID
    89884
    NCBI登录号
    NM_033343, NP_203129
    UniProt
    P53776
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