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LHFPL5 抗体 (C-Term)

LHFPL5 适用: 人, 小鼠 WB 宿主: 兔 Polyclonal RB28242 unconjugated
产品编号 ABIN654373
发货至: 中国
  • 抗原 See all LHFPL5 抗体
    LHFPL5 (Lipoma HMGIC Fusion Partner-Like 5 (LHFPL5))
    抗原表位
    • 7
    • 7
    • 7
    • 5
    AA 186-214, C-Term
    适用
    人, 小鼠
    宿主
    • 19
    克隆类型
    • 19
    多克隆
    标记
    • 5
    • 4
    • 3
    • 3
    • 2
    • 2
    This LHFPL5 antibody is un-conjugated
    应用范围
    • 16
    • 14
    • 1
    • 1
    • 1
    Western Blotting (WB)
    预测反应
    Rat
    纯化方法
    This antibody is purified through a protein A column, followed by peptide affinity purification.
    免疫原
    This LHFPL5 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 186-214 amino acids from the C-terminal region of human LHFPL5.
    克隆位点
    RB28242
    亚型
    Ig Fraction
    Top Product
    Discover our top product LHFPL5 Primary Antibody
  • 应用备注
    WB: 1:1000
    限制
    仅限研究用
  • 状态
    Liquid
    缓冲液
    Purified polyclonal antibody supplied in PBS with 0.09 % (W/V) sodium azide.
    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
    4 °C,-20 °C
    储存方法
    Maintain refrigerated at 2-8 °C for up to 6 months. For long term storage store at -20 °C in small aliquots to prevent freeze-thaw cycles.
    有效期
    6 months
  • 抗原
    LHFPL5 (Lipoma HMGIC Fusion Partner-Like 5 (LHFPL5))
    别名
    LHFPL5 (LHFPL5 产品)
    别名
    DFNB67 antibody, TMHS antibody, dJ510O8.8 antibody, 9330179O15Rik antibody, Tmhs antibody, hscy antibody, PMP22A antibody, lhfpl5 antibody, zgc:171589 antibody, LHFPL tetraspan subfamily member 5 antibody, lipoma HMGIC fusion partner-like 5 antibody, LHFPL tetraspan subfamily member 5b antibody, LHFPL5 antibody, Lhfpl5 antibody, lhfpl5b antibody
    背景
    This gene is a member of the lipoma HMGIC fusion partner (LHFP) gene family, which is a subset of the superfamily of tetraspan transmembrane protein encoding genes. Mutations in this gene result in deafness in humans, and a mutation in a similar gene in mice results in deafness and vestibular dysfunction with severe degeneration of the organ of Corti. It is proposed to function in hair bundle morphogenesis.
    分子量
    24201
    基因ID
    222662
    NCBI登录号
    NP_872354
    UniProt
    Q8TAF8
    途径
    Sensory Perception of Sound
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