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- 抗原 See all Myotilin (MYOT) 抗体
- Myotilin (MYOT)
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抗原表位
- AA 127-155
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适用
- 人
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宿主
- 兔
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克隆类型
- 多克隆
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标记
- This Myotilin antibody is un-conjugated
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应用范围
- 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
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anti-Myotilin (MYOT) (AA 259-314) antibody
MYOT 适用: 人 WB, IF 宿主: 兔 Polyclonal unconjugated
anti-Myotilin (MYOT) (AA 443-498) antibodyMYOT 适用: 人 WB, ELISA, IHC 宿主: 兔 Polyclonal unconjugated
anti-Myotilin (MYOT) antibodyMYOT 适用: 人, 小鼠 WB, ELISA, IHC 宿主: 兔 Polyclonal unconjugated
anti-Myotilin (MYOT) (C-Term) antibodyMYOT 适用: 人 IHC, IHC (p), IHC (fro) 宿主: 小鼠 Monoclonal RSO34 unconjugated
anti-Myotilin (MYOT) (AA 209-221) antibodyVerified MYOT 适用: 人 WB, ELISA 宿主: 山羊 Polyclonal unconjugated
anti-Myotilin (MYOT) antibodyMYOT 适用: 人 WB, IF, IC 宿主: 兔 Polyclonal unconjugated
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- 应用备注
- WB: 1:1000
- 限制
- 仅限研究用
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- 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
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- 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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