Anti-EPM2AIP1抗体The EPM2A gene, which encodes laforin, is mutated in an autosomal recessive form of adolescent progressive myoclonus epilepsy.

产品编号 yb-14612R
英文名称 Anti-EPM2AIP1抗体
中文名称 肌痉挛性癫痫病相互作用蛋白1抗体
别    名 EPM2A (laforin) interacting protein 1; EPM2A (laforin) IP1; EPM2A-interacting protein 1; EPM2AIP 1; Epm2aip1; EPMIP_HUMAN; FLJ11207; KIAA0766; Laforin interacting protein 1; Laforin-interacting protein; My007.
 Anti-EPM2AIP1抗体
说 明 书 0.2ml  
研究领域 细胞生物  神经生物学  信号转导  转录调节因子  
抗体来源 Rabbit
克隆类型 Polyclonal
交叉反应 Human, Mouse, Rat, Dog, Horse, Guinea Pig, 
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 （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 70kDa
性    状 Lyophilized or Liquid
浓    度 1mg/1ml
免 疫 原 KLH conjugated synthetic peptide derived from human EPM2AIP1
亚    型 IgG
纯化方法 affinity purified by Protein A
储 存 液 0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glycerol.
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.
 
PubMed PubMed
产品介绍 background:
The EPM2A gene, which encodes laforin, is mutated in an autosomal recessive form of adolescent progressive myoclonus epilepsy. The protein encoded by this gene binds to laforin, but its function is not known. This gene is intronless. [provided by RefSeq, Oct 2008]

Subunit:
Interacts with EPM2A.

Subcellular Location:
Endoplasmic reticulum.
 
Tissue Specificity:
Expressed in heart, brain, placenta, liver, pancreas, kidney and skeletal muscle.