MEF2C 抗体
Quick Overview for MEF2C 抗体 (ABIN7260573)
抗原
See all MEF2C 抗体适用
宿主
克隆类型
标记
应用范围
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产品特性
- Polyclonal Antibody
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纯化方法
- Affinity purification
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免疫原
- Recombinant fusion protein of human MEF2C (NP_001180279.1).
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亚型
- IgG
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anti-Myocyte Enhancer Factor 2C (MEF2C) (AA 1-125) antibody
MEF2C 适用: 人, 小鼠 WB, IHC, ELISA, FACS 宿主: 小鼠 Monoclonal 6H2G2 unconjugated
anti-Myocyte Enhancer Factor 2C (MEF2C) antibodyMEF2C 适用: 人 WB, IHC, IF, IHC (p), ICC, IHC (fro), IP 宿主: 兔 Polyclonal unconjugated
anti-Myocyte Enhancer Factor 2C (MEF2C) (AA 1-125) antibodyMEF2C 适用: 人, 小鼠 WB, IHC, ELISA, FACS 宿主: 小鼠 Monoclonal unconjugated
anti-Myocyte Enhancer Factor 2C (MEF2C) (AA 170-380) antibodyMEF2C 适用: 人 WB, IHC, IF 宿主: 兔 Polyclonal unconjugated
anti-Myocyte Enhancer Factor 2C (MEF2C) (AA 365-394) antibodyMEF2C 适用: 人 WB, IHC, ELISA, IF 宿主: 兔 Polyclonal unconjugated
anti-Myocyte Enhancer Factor 2C (MEF2C) (Ser59) antibodyMEF2C 适用: 人 WB, IHC, IHC (p) 宿主: 兔 Polyclonal unconjugated
anti-Myocyte Enhancer Factor 2C (MEF2C) (Ser396) antibodyMEF2C 适用: 人 WB, IHC, IHC (p) 宿主: 兔 Polyclonal unconjugated
anti-Myocyte Enhancer Factor 2C (MEF2C) (Ser396) antibodyMEF2C 适用: 人 WB, ELISA 宿主: 兔 Polyclonal unconjugated
anti-Myocyte Enhancer Factor 2C (MEF2C) (AA 170-380) antibodyMEF2C 适用: 人 IHC, ELISA 宿主: 兔 Polyclonal unconjugated
anti-Myocyte Enhancer Factor 2C (MEF2C) (AA 170-380) antibodyMEF2C 适用: 人 WB, IHC, ELISA 宿主: 兔 Polyclonal unconjugated
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应用备注
- IHC 1:50-1:200
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限制
- 仅限研究用
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状态
- Liquid
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浓度
- 1 mg/mL
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缓冲液
- PBS with 0.02 % sodium azide, 50 % glycerol, pH 7.3
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储存液
- Sodium azide
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注意事项
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
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储存条件
- -20 °C
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储存方法
- Store at -20°C. Avoid freeze / thaw cycles.
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- MEF2C (Myocyte Enhancer Factor 2C (MEF2C))
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别名
- MEF2C
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背景
- This locus encodes a member of the MADS box transcription enhancer factor 2 (MEF2) family of proteins, which play a role in myogenesis. The encoded protein, MEF2 polypeptide C, has both trans-activating and DNA binding activities. This protein may play a role in maintaining the differentiated state of muscle cells. Mutations and deletions at this locus have been associated with severe mental retardation, stereotypic movements, epilepsy, and cerebral malformation. Alternatively spliced transcript variants have been described.
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基因ID
- 4208
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UniProt
- Q06413
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途径
- Neurotrophin Signaling Pathway, Activation of Innate immune Response, Cellular Response to Molecule of Bacterial Origin, Carbohydrate Homeostasis, Chromatin Binding, Regulation of Muscle Cell Differentiation, Skeletal Muscle Fiber Development, Toll-Like Receptors Cascades, BCR Signaling
抗原
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