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TRIOBP 抗体

TRIOBP 适用: 人, 小鼠 WB 宿主: 兔 Polyclonal unconjugated
产品编号 ABIN6569705
发货至: 中国
  • 抗原 See all TRIOBP 抗体
    TRIOBP (TRIO and F-Actin Binding Protein (TRIOBP))
    适用
    • 8
    • 3
    • 2
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    人, 小鼠
    宿主
    • 8
    克隆类型
    • 8
    多克隆
    标记
    • 8
    This TRIOBP antibody is un-conjugated
    应用范围
    • 8
    • 4
    • 2
    • 2
    • 1
    • 1
    Western Blotting (WB)
    纯化方法
    Affinity purification
    免疫原
    Recombinant protein of human TRIOBP
    亚型
    IgG
    Top Product
    Discover our top product TRIOBP Primary Antibody
  • 应用备注
    WB 1:500 - 1:2000
    限制
    仅限研究用
  • 浓度
    1 mg/mL
    缓冲液
    Buffer: PBS with 0.02 % sodium azide, 50 % glycerol,  pH 7.3.
    储存液
    Sodium azide
    注意事项
    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
    储存条件
    -20 °C
    储存方法
    Store at -20°C. Avoid freeze / thaw cycles.
  • 抗原
    TRIOBP (TRIO and F-Actin Binding Protein (TRIOBP))
    别名
    TRIOBP (TRIOBP 产品)
    别名
    tara antibody, DFNB28 antibody, TARA antibody, dJ37E16.4 antibody, AI428493 antibody, EST478828 antibody, Tara antibody, mKIAA1662 antibody, TRIO and F-actin binding protein antibody, TRIO and F-actin-binding protein antibody, TRIO and F-actin binding protein L homeolog antibody, TRIO and F-actin binding protein-like antibody, TRIOBP antibody, LOC100354753 antibody, triobp.L antibody, TRIOBPL antibody, Triobp antibody
    背景

    Synonyms: DFNB28,KIAA1662,Protein TARA,TARA,Tara like protein,TRIO and F actin binding protein,Trio and filamentous actin binding protein,Trio associated repeat on actin

    Background: This gene encodes a protein with an N-terminal pleckstrin homology domain and a C-terminal coiled-coil region. The protein interacts with trio, which is involved with neural tissue development and controlling actin cytoskeleton organization, cell motility and cell growth. The protein also associates with F-actin and stabilizes F-actin structures. Mutations in this gene have been associated with a form of autosomal recessive nonsyndromic deafness. Multiple alternatively spliced transcript variants that would encode different isoforms have been found for this gene, however some transcripts may be subject to nonsense-mediated decay (NMD).

    分子量

    Observed_MW: 70kDa

    Calculated_MW: 47kDa/68kDa/74kDa/125kDa/243kDa/250kDa/261kDa

    基因ID
    11078
    UniProt
    Q9H2D6
    途径
    Regulation of Actin Filament Polymerization
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