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Myotilin 抗体 (AA 127-155)

MYOT 适用: 人 WB 宿主: 兔 Polyclonal RB36975 unconjugated
产品编号 ABIN1537809
发货至: 中国
  • 抗原 See all Myotilin (MYOT) 抗体
    Myotilin (MYOT)
    抗原表位
    • 15
    • 6
    • 6
    • 6
    • 6
    • 2
    • 2
    • 1
    • 1
    • 1
    AA 127-155
    适用
    • 39
    • 6
    • 4
    • 2
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    宿主
    • 37
    • 1
    • 1
    克隆类型
    • 39
    多克隆
    标记
    • 15
    • 3
    • 3
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This Myotilin antibody is un-conjugated
    应用范围
    • 24
    • 20
    • 13
    • 13
    • 5
    • 4
    • 4
    • 3
    • 1
    • 1
    Western Blotting (WB)
    纯化方法
    This antibody is purified through a protein A column, followed by peptide affinity purification.
    免疫原
    This MYOT antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 127-155 amino acids from the Central region of human MYOT.
    克隆位点
    RB36975
    亚型
    Ig Fraction
    Top Product
    Discover our top product MYOT 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
    MYOT Antibody (Center) can be refrigerated at 2-8 °C for up to 6 months. For long term storage, keep at -20 °C.
    有效期
    6 months
  • 抗原
    Myotilin (MYOT)
    别名
    MYOT (MYOT 产品)
    别名
    LGMD1 antibody, LGMD1A antibody, MFM3 antibody, TTID antibody, TTOD antibody, 5530402I04Rik antibody, Ttid antibody, MYOT antibody, ttid antibody, myotilin antibody, MYOT antibody, Myot antibody, myot antibody
    背景
    This gene encodes a cystoskeletal protein which plays a significant role in the stability of thin filaments during muscle contraction. This protein binds F-actin, crosslinks actin filaments, and prevents latrunculin A-induced filament disassembly. Mutations in this gene have been associated with limb-girdle muscular dystrophy and myofibrillar myopathies. Several alternatively spliced transcript variants of this gene have been described, but the full-length nature of some of these variants has not been determined.
    分子量
    55395
    基因ID
    9499
    NCBI登录号
    NP_001129412, NP_006781
    UniProt
    Q9UBF9
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