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IMMP2L encodes a protein involved in processing the signal peptide sequences used to direct mitochondrial proteins to the mitochondria. Additionally we are shipping IMMP2L Antibodies (27) and IMMP2L Kits (1) and many more products for this protein.
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Deficiency of IMMP2L in cells cultured under hypoxia and high glucose, exacerbated neuronal death.
Chromosomal breakpoints involved the IMMP2L gene in 7q31 is associated with Diffuse Large B-Cell Lymphomas.
IMMP2L transcription requires Topoisomerase I (show TOP1 Proteins) in human primary astrocytes
genomic rearrangements affecting IMMP2L may be one of the predisposing factors involved in Tourette syndrome and overlapping neurodevelopmental disorders.
AUTS1/AUTS5 linkage to immp2l-dock4 may be involved in autism susceptibility
data suggest that respiratory deficiency is not the cause of the observed Immp2l mutant phenotypes.
provides evidence for a causal role of oxidative stress in neurodegeneration of Immp2l mutant mice
IMP2 as a developmental stage-dependent regulator of the differentiation potentials of NPCs in the mouse neocortex.
This study demomistrated that Immp2l deficiency increases ischemic brain damage by enhancing O(2)(-) production and damaging mitochondrial functional performance.
Mitochondrial peptidase IMMP2L mutation causes early onset of age-associated disorders and impairs adult stem cell self-renewal
This gene encodes a protein involved in processing the signal peptide sequences used to direct mitochondrial proteins to the mitochondria. The encoded protein resides in the mitochondria and is one of the necessary proteins for the catalytic activity of the mitochondrial inner membrane peptidase (IMP) complex. Two variants that encode the same protein have been described for this gene.
mitochondrial inner membrane protease subunit 2
, inner mitochondrial membrane peptidase 2 like
, IMP2-like protein