Use your antibodies-online credentials, if available.
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 蛋白 (5) 和 EPM2A (Laforin) Interacting Protein 1 试剂盒 (2)和数多这个蛋白质的别的产品。
Showing 10 out of 80 products:
Human Polyclonal EPM2AIP1 Primary Antibody for WB - ABIN1881302
Ianzano, Zhao, Minassian, Scherer: Identification of a novel protein interacting with laforin, the EPM2a progressive myoclonus epilepsy gene product. in Genomics 2003
Show all 3 Pubmed References
Human Monoclonal EPM2AIP1 Primary Antibody for ELISA, WB - ABIN564241
Turnbull, Tiberia, Pereira, Zhao, Pencea, Wheeler, Yu, Ivovic, Naranian, Israelian, Draginov, Piliguian, Frankland, Wang, Ackerley, Giacca, Minassian: Deficiency of a glycogen synthase-associated protein, Epm2aip1, causes decreased glycogen synthesis and hepatic insulin resistance. in The Journal of biological chemistry 2013
The -93G>A polymorphism modifies the efficiency of MLH1 (显示 MLH1 抗体)/EPM2AIP1 transcription.
The EPM2AIP1 gene was identified and characterized in a screen for laforin (显示 EPM2A 抗体)-interacting proteins with a human brain cDNA library; the specificity of the interaction was confirmed; subcellular colocalization of laforin (显示 EPM2A 抗体) and EPM2AIP1 protein was demonstrated
We show that the absence of Epm2aip1 in mice impairs allosteric activation of GS by glucose 6-phosphate, decreases hepatic glycogen (显示 GYS1 抗体) synthesis, increases liver fat, causes hepatic insulin (显示 INS 抗体) 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