MYL3/CMLC1 抗体
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- 抗原 See all MYL3/CMLC1 (MYL3) 抗体
- MYL3/CMLC1 (MYL3) (Myosin, Light Chain 3 (MYL3))
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适用
- 人, 小鼠, 大鼠
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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 MYL3/CMLC1 antibody is un-conjugated
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应用范围
- Western Blotting (WB), Immunohistochemistry (IHC), ELISA
- 产品特性
- Polyclonal Antibody
- 纯化方法
- Affinity purification
- 免疫原
- Recombinant protein of human MYL3
- 亚型
- IgG
- Top Product
- Discover our top product MYL3 Primary Antibody
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anti-Myosin, Light Chain 3 (MYL3) (AA 5-181) antibody
MYL3 适用: 人 WB, IHC, IP, ICC 宿主: 兔 Polyclonal unconjugated
anti-Myosin, Light Chain 3 (MYL3) (AA 8-199) antibodyMYL3 适用: 小鼠 WB, IHC, IP, ICC 宿主: 兔 Polyclonal unconjugated
anti-Myosin, Light Chain 3 (MYL3) (AA 1-195) antibodyMYL3 适用: 人 WB, ELISA 宿主: 小鼠 Monoclonal 4C2 unconjugated
anti-Myosin, Light Chain 3 (MYL3) antibodyMYL3 适用: 人 WB, IHC, ELISA 宿主: 小鼠 Monoclonal 3F8 unconjugated
anti-Myosin, Light Chain 3 (MYL3) (AA 1-195) antibodyMYL3 适用: 人 WB, IHC, ELISA 宿主: 兔 Polyclonal unconjugated
anti-Myosin, Light Chain 3 (MYL3) (Internal Region) antibodyMYL3 适用: 人, 小鼠, 大鼠 WB, IHC, ELISA, ICC, IF 宿主: 兔 Polyclonal unconjugated
anti-Myosin, Light Chain 3 (MYL3) (AA 1-195) antibodyMYL3 适用: 人 WB, IF 宿主: 兔 Polyclonal unconjugated
anti-Myosin, Light Chain 3 (MYL3) antibodyMYL3 适用: 人 WB 宿主: 兔 Polyclonal unconjugated
anti-Myosin, Light Chain 3 (MYL3) (AA 1-195) antibodyMYL3 适用: 人 WB 宿主: 小鼠 Polyclonal unconjugated
anti-Myosin, Light Chain 3 (MYL3) (N-Term) antibodyMYL3 适用: 人, 小鼠, 大鼠 WB 宿主: 兔 Polyclonal unconjugated
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- 应用备注
- WB 1:1000-1:5000, IHC 1:50-1:200
- 限制
- 仅限研究用
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- 状态
- Liquid
- 浓度
- 0.5 mg/mL
- 缓冲液
- PBS with 0.05 % sodium azide and 50 % glycerol, PH7.4
- 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.
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- 抗原
- MYL3/CMLC1 (MYL3) (Myosin, Light Chain 3 (MYL3))
- 别名
- MYL3 (MYL3 产品)
- 背景
- MYL3 encodes myosin light chain 3, an alkali light chain also referred to in the literature as both the ventricular isoform and the slow skeletal muscle isoform. Mutations in MYL3 have been identified as a cause of mid-left ventricular chamber type hypertrophic cardiomyopathy.
- 分子量
- 22 kDa
- UniProt
- P08590
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