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脆性X综合征相关蛋白AFF2抗体

脆性X综合征相关蛋白AFF2抗体

价格: 面议

品牌:R&D

供货周期: 现货

货号:hz-11703R

规格:g/mg

英文名称    AFF2    

中文名称    脆性X综合征相关蛋白AFF2抗体    

别    名    FMR2; AF4/FMR2 family member 2; AF4/FMR2 family, member 2; AFF2; AFF2_HUMAN; FMR2; FMR2P; Fragile X E mental retardation syndrome protein; fragile X mental retardation 2; Fragile X mental retardation 2 protein; fragile X mental retardation gene associated with FRAXE; FRAXE; mild or borderline mental retardation; MRX2; OX19; Protein FMR-2; Protein Ox19.    

说 明 书    0.1ml  0.2ml      

研究领域    神经生物学      

抗体来源    Rabbit    

克隆类型    Polyclonal    

交叉反应    Human, Mouse, Rat, Dog, Pig, Cow, Horse,     

产品应用    WB=1:100-500 ELISA=1:500-1000 IHC-P=1:100-500 IHC-F=1:100-500 ICC=1:100-500 IF=1:100-500 脆性X综合征相关蛋白AFF2抗体(石蜡切片需做抗原修复) 
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.    

分 子 量    145kDa    

细胞定位    细胞核     

性    状    Lyophilized or Liquid    

浓    度    1mg/1ml    

免 疫 原    KLH conjugated synthetic peptide derived from human AFF2 (1-80aa)    

亚    型    IgG    

纯化方法    affinity purified by Protein A    

储 存 液    Preservative: 15mM Sodium Azide, Constituents: 1% BSA, 0.01M PBS, pH 7.4    

保存条件    Store at -20 °C for one year. Avoid repeated freeze/thaw cycles. The lyophilized antibody is stable at room temperature for at least one month and for greater than a year when kept at -20°C. When reconstituted in sterile pH 7.4 0.01M PBS or diluent of antibody the antibody is stable for at least two weeks at 2-4 °C.    

脆性X综合征相关蛋白AFF2抗体产品介绍    background:

FMR2 is a 1311 amino acid nuclear protein belonging to the AF4 family. Expressed in the brain, placenta and lung, FMR2 exists as two isoforms produced by alternative splicing. Defects in the gene that encodes FMR2 have been found to be a cause of FRAXE, an X-linked form of mental retardation. Individuals expressing the FRAXE site also have more than two-hundred copies of a GCC repeat adjacent to CpG island, compared to six to thirty-five copies of the GCC repeat in a normal individual. It is believed that loss of FMR2 expression causes this GCC expansion of the FRAXE site. 

Function:
RNA-binding protein. Might be involved in alternative splicing regulation through an interaction with G-quartet RNA structure.

Subcellular Location:
Nucleus speckle. When splicing is inhibited, accumlates in enlarged speckles.

Tissue Specificity:
Brain (most abundant in hippocampus and amygdala), placenta and lung.

DISEASE:
Defects in AFF2 are the cause of fragile X-E mental retardation syndrome (FRAXE) [MIM:309548]. FRAXE is an X-linked form of mental retardation. Loss of FMR2 expression is correlated with FRAXE CCG(N) expansion. Normal individuals have 6-35 copies of the repeat, whereas cytogenetically positive, developmentally delayed males have more than 200 copies and show methylation of the associated CPG island.

Similarity:
Belongs to the AF4 family.

Database links:

Entrez Gene: 2334 Human

Omim: 309548 Human

SwissProt: P51816 Human

Unigene: 496911 Human


Important Note:
This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.     

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生化试剂 脆性X综合征相关蛋白AFF2抗体 由上海沪震生物科技有限公司为您提供,如想了解更多关于抗体/抗原 脆性X综合征相关蛋白AFF2抗体 的报价、规格、厂家等信息,欢迎来电或留言咨询。除供应脆性X综合征相关蛋白AFF2抗体 外,上海沪震生物科技有限公司还可为您提供: 猴子巨噬细胞移动抑制因子(MIF)ELISA试剂盒、 豚鼠γ干扰素(IFN-γ)ELISA试剂盒 、 山羊丙酮检测(acetone)ELISA试剂盒
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