MEF2A Protein (Transcript Variant 1) (Myc-DYKDDDDK Tag)
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- 抗原 See all MEF2A 蛋白
- MEF2A (Myocyte Enhancer Factor 2A (MEF2A))
- 蛋白类型
- Recombinant
- 产品特性
- Transcript Variant 1
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宿主
- 人
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资源
- HEK-293 Cells
- 标记
- This MEF2A protein is labelled with Myc-DYKDDDDK Tag.
- 应用范围
- Antibody Production (AbP), Standard (STD)
- 产品特性
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- Recombinant human MEF2A (transcript variant 1) protein expressed in HEK293 cells.
- Produced with end-sequenced ORF clone
- 纯度
- > 80 % as determined by SDS-PAGE and Coomassie blue staining
- Top Product
- Discover our top product MEF2A 蛋白
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- 应用备注
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Recombinant human proteins can be used for:
Native antigens for optimized antibody production
Positive controls in ELISA and other antibody assays - 说明
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The tag is located at the C-terminal.
- 限制
- 仅限研究用
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- 浓度
- 50 μg/mL
- 缓冲液
- 25 mM Tris.HCl, pH 7.3, 100 mM glycine, 10 % glycerol.
- 储存条件
- -80 °C
- 储存方法
- Store at -80°C. Thaw on ice, aliquot to individual single-use tubes, and then re-freeze immediately. Only 2-3 freeze thaw cycles are recommended.
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- 抗原
- MEF2A (Myocyte Enhancer Factor 2A (MEF2A))
- 别名
- Mef2a (MEF2A 产品)
- 别名
- ADCAD1 Protein, RSRFC4 Protein, RSRFC9 Protein, mef2 Protein, A430079H05Rik Protein, mef2a Protein, wu:fd19d02 Protein, adcad1 Protein, rsrfc4 Protein, rsrfc9 Protein, sl2 Protein, MEF2A Protein, xmef2a Protein, myocyte enhancer factor 2A Protein, myocyte enhancer factor 2aa Protein, myocyte enhancer factor 2a Protein, myocyte-specific enhancer factor 2A Protein, myocyte-specific enhancer factor 2a, putative Protein, myocyte enhancer factor 2A L homeolog Protein, MEF2A Protein, Mef2a Protein, mef2aa Protein, EDI_092490 Protein, EDI_038250 Protein, Smp_161530 Protein, mef2a.L Protein, mef2a Protein, LOC539054 Protein
- 背景
- The protein encoded by this gene is a DNA-binding transcription factor that activates many muscle-specific, growth factor-induced, and stress-induced genes. The encoded protein can act as a homodimer or as a heterodimer and is involved in several cellular processes, including muscle development, neuronal differentiation, cell growth control, and apoptosis. Defects in this gene could be a cause of autosomal dominant coronary artery disease 1 with myocardial infarction (ADCAD1). Several transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, Jan 2010]
- 分子量
- 53.7 kDa
- NCBI登录号
- NP_005578
- 途径
- Neurotrophin Signaling Pathway, Activation of Innate immune Response, Carbohydrate Homeostasis, Chromatin Binding, Regulation of Muscle Cell Differentiation, Toll-Like Receptors Cascades
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