EF-1 Alpha1/2 (Acetyl Lys41) Polyclonal Antibody, 50ul Cell Dissociation Defects in this gene are

Defects in this gene are a cause of neurofibromatosis type 1-like syndrome (NFLS)

The protein product of this gene also plays a role in the differentiation and survival of midbrain dopaminergic neurons

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Homozygous conditional knockout mice for PPP2R3C exhibit reduced numbers and impaired proliferation of immune system B cells

Alternative splicing plays a role in modulating the subcellular localization and physiological function of this gene

EF-1 Alpha1/2 (Acetyl Lys41) Polyclonal Antibody, 50ul Cell Dissociation Defects in this gene areEEF1A1 encodes an isoform of the alpha subunit of the elongation factor 1 complex, which is responsible for the enzymatic delivery of aminoacyl tRNAs to the ribosome. This isoform (alpha 1) is expressed in brain, placenta, lung, liver, kidney, and pancreas, and the other isoform (alpha 2) is expressed in brain, heart and skeletal muscle. eukaryotic translation elongation factor 1 alpha 1 is identified as an autoantigen in 66% of patients with Felty