MYL3/CMLC1 抗体 (N-Term)
Quick Overview for MYL3/CMLC1 抗体 (N-Term) (ABIN2798613)
抗原
See all MYL3/CMLC1 (MYL3) 抗体适用
宿主
克隆类型
标记
应用范围
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抗原表位
- AA 1-30, N-Term
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原理
- Rabbit Anti-Human MYL3 (N-term) Antibody
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免疫原
- This MYL3 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 1-30 amino acids from the N-terminal region of human MYL3.
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亚型
- Ig Fraction
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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) antibodyMYL3 适用: 人, 小鼠, 大鼠 WB, IHC, ELISA 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
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应用备注
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Western Blot, Immunohistochemistry
Recommended Dilutions
WB: 1:1000, IHC: 1:10-50Western blot analysis of lysates from human skeletal muscle and heart tissue lysates (from left to right), using MYL3 Antibody (N-term) for immunohistochemistry. Clinical relevance has not been evaluated. -
限制
- 仅限研究用
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状态
- Liquid
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浓度
- 0.400 mg/mL
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储存条件
- 4 °C,-20 °C
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储存方法
- 2-8°C (short-term), -20°C (long-term)
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- MYL3/CMLC1 (MYL3) (Myosin, Light Chain 3 (MYL3))
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别名
- MYL3
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背景
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Target Description: 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.
Gene Symbol: MYL3
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分子量
- 21932 Da
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基因ID
- 4634
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UniProt
- P08590
抗原
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