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TIMP Metallopeptidase Inhibitor 3 (TIMP3) (N-Term) Peptide

TIMP3 适用: 人 宿主: 合成 BP, WB
产品编号 ABIN985101
发货至: 中国
  • 抗原 See all TIMP3 products
    TIMP3 (TIMP Metallopeptidase Inhibitor 3 (TIMP3))
    蛋白结构域
    N-Term
    宿主
    资源
    • 3
    合成
    应用范围
    Blocking Peptide (BP), Western Blotting (WB)
    序列
    MTPWLGLIVL LGSWSLGDWG AEACTCSPSH PQDAFCNSDI VIRAKVVGKK
    产品特性
    This is a synthetic peptide designed for use in combination with anti-TIMP3 Antibody,. 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
    TIMP3 (TIMP Metallopeptidase Inhibitor 3 (TIMP3))
    别名
    TIMP-3 Peptide, TIMP3 Peptide, timp3 Peptide, HSMRK222 Peptide, K222 Peptide, K222TA2 Peptide, SFD Peptide, IMP-3 Peptide, timp3-A Peptide, Timp-3 Peptide, metalloproteinase inhibitor 3 Peptide, TIMP metallopeptidase inhibitor 3 Peptide, Metalloproteinase inhibitor 3 Peptide, TIMP metallopeptidase inhibitor 3 L homeolog Peptide, tissue inhibitor of metalloproteinase 3 Peptide, CpipJ_CPIJ003282 Peptide, TIMP3 Peptide, timp3 Peptide, Timp3 Peptide, timp3.L Peptide
    背景
    This gene belongs to the TIMP gene family. The proteins encoded by this gene family are inhibitors of the matrix metalloproteinases, a group of peptidases involved in degradation of the extracellular matrix (ECM). Expression of this gene is induced in response to mitogenic stimulation and this netrin domain-containing protein is localized to the ECM. Mutations in this gene have been associated with the autosomal dominant disorder Sorsby's fundus dystrophy.

    Alias Symbols: HSMRK222, K222, K222TA2, SFD

    Protein Interaction Partner: ADAM17,EFEMP1,KDR,MMP13,MMP14,MMP2,MMP3,MMP9,ADAM17,MMP2

    Protein Size: 211
    分子量
    22 kDa
    基因ID
    7078
    NCBI登录号
    NM_000362, NP_000353
    UniProt
    P35625
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