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TMIE 抗体 (AA 71-100)

TMIE 适用: 人, 小鼠 WB 宿主: 兔 Polyclonal RB24522 unconjugated
产品编号 ABIN653717
发货至: 中国
  • 抗原 See all TMIE 抗体
    TMIE (Transmembrane Inner Ear (TMIE))
    抗原表位
    • 7
    • 6
    • 6
    • 6
    • 1
    • 1
    AA 71-100
    适用
    人, 小鼠
    宿主
    • 14
    • 1
    克隆类型
    • 15
    多克隆
    标记
    • 5
    • 2
    • 2
    • 2
    • 2
    • 2
    This TMIE antibody is un-conjugated
    应用范围
    • 14
    • 14
    • 1
    Western Blotting (WB)
    预测反应
    M
    纯化方法
    This antibody is purified through a protein A column, followed by peptide affinity purification.
    免疫原
    This TMIE antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 71-100 amino acids from the Central region of human TMIE.
    克隆位点
    RB24522
    亚型
    Ig Fraction
    Top Product
    Discover our top product TMIE Primary Antibody
  • 应用备注
    WB: 1:1000. 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
    TMIE (Transmembrane Inner Ear (TMIE))
    别名
    TMIE (TMIE 产品)
    别名
    si:ch211-163f10.1 antibody, DFNB6 antibody, 5131400L21Rik antibody, Mm.87012 antibody, sr antibody, RGD1562523 antibody, transmembrane inner ear antibody, tmie antibody, TMIE antibody, Tmie antibody
    背景
    This gene encodes a transmembrane inner ear protein. Studies in mouse suggest that this gene is required for normal postnatal maturation of sensory hair cells in the cochlea, including correct development of stereocilia bundles. This gene is one of multiple genes responsible for recessive non-syndromic deafness (DFNB), also known as autosomal recessive nonsyndromic hearing loss (ARNSHL), the most common form of congenitally acquired inherited hearing impairment.
    分子量
    17241
    基因ID
    259236
    NCBI登录号
    NP_671729
    UniProt
    Q8NEW7
    途径
    Sensory Perception of Sound
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