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MEF2C 抗体
MEF2C
适用: 人, 小鼠, 大鼠
IHC, IF
宿主: 兔
Polyclonal
unconjugated
MEF2C抗体详情
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抗原
See all MEF2C 抗体
MEF2C
(Myocyte Enhancer Factor 2C (MEF2C))
适用
All reactivities for MEF2C 抗体
人, 小鼠, 大鼠
宿主
All hosts for MEF2C 抗体
兔
克隆类型
All clonalities for MEF2C 抗体
多克隆
标记
All conjugates for MEF2C 抗体
This MEF2C antibody is un-conjugated
应用范围
All applications for MEF2C 抗体
Immunohistochemistry (IHC), Immunofluorescence (IF)
产品特性
Polyclonal Antibody
纯化方法
Affinity purification
免疫原
Recombinant fusion protein of human MEF2C (NP_001180279.1).
亚型
IgG
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Discover our top product MEF2C Primary Antibody
Alternatives
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使用细节
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应用备注
IHC 1:50-1:100 IF 1:50-1:100
限制
仅限研究用
贮存及处理
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状态
Liquid
浓度
1 mg/mL
缓冲液
PBS with 0.02 % sodium azide, 50 % glycerol, pH 7.3
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.
MEF2C目标详情
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抗原
MEF2C
(Myocyte Enhancer Factor 2C (MEF2C))
别名
MEF2C (MEF2C 产品 )
别名
MEF2C antibody, XMEF2C antibody, si:ch211-202e12.2 antibody, C5DELq14.3 antibody, DEL5q14.3 antibody, 5430401D19Rik antibody, 9930028G15Rik antibody, AV011172 antibody, Mef2 antibody, RGD1563119 antibody, id:ibd5026 antibody, mef2c antibody, wu:fc05b06 antibody, zgc:64184 antibody, zgc:85726 antibody, myocyte enhancer factor 2C antibody, MADS box transcription enhancer factor 2, polypeptide C (myocyte enhancer factor 2C) antibody, myocyte enhancer factor 2cb antibody, MADS box transcription enhancer factor 2, polypeptide C (myocyte enhancer factor 2C) L homeolog antibody, myocyte enhancer factor 2ca antibody, MEF2C antibody, mef2c antibody, mef2cb antibody, mef2c.L antibody, Mef2c antibody, mef2ca antibody
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.
基因ID
4208
UniProt
Q06413
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
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