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The EPM2A gene, which encodes laforin, is mutated in an autosomal recessive form of adolescent progressive myoclonus epilepsy. 再加上，我们可以发EPM2A (Laforin) Interacting Protein 1 抗体 (96) 和 EPM2A (Laforin) Interacting Protein 1 蛋白 (5)和数多这个蛋白质的别的产品。
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The -93G>A polymorphism modifies the efficiency of MLH1 (显示 MLH1 ELISA试剂盒)/EPM2AIP1 transcription.
The EPM2AIP1 gene was identified and characterized in a screen for laforin (显示 EPM2A ELISA试剂盒)-interacting proteins with a human brain cDNA library; the specificity of the interaction was confirmed; subcellular colocalization of laforin (显示 EPM2A ELISA试剂盒) and EPM2AIP1 protein was demonstrated
The authors conclude that laforin's principle function is to control glycogen (显示 GYS1 ELISA试剂盒) chain lengths, in a malin (显示 NHLRC1 ELISA试剂盒)-dependent fashion, and that loss of this control underlies Lafora disease.
We show that the absence of Epm2aip1 in mice impairs allosteric activation of GS by glucose 6-phosphate, decreases hepatic glycogen (显示 GYS1 ELISA试剂盒) synthesis, increases liver fat, causes hepatic insulin (显示 INS ELISA试剂盒) resistance, and protects against age-related obesity
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.
EPM2A (laforin) interacting protein 1
, EPM2A interacting protein 1
, EPM2A-interacting protein 1
, laforin-interacting protein