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Major intrinsic protein is a member of the water-transporting aquaporins as well as the original member of the MIP family of channel proteins. Zusätzlich bieten wir Ihnen Mitochondrial Intermediate Peptidase Antikörper (70) und Mitochondrial Intermediate Peptidase Proteine (3) und viele weitere Produktgruppen zu diesem Protein an.
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The data evidence a broad lipidation profile of AQP0 (zeige MIP ELISA Kits) that is both species and site independent, suggesting a chemical-based ester aminolysis mechanism to explain such modifications.
MIPEP recessive variants cause a syndrome of left ventricular non-compaction, hypotonia, and infantile death.
A novel MIP (zeige TNPO1 ELISA Kits) frame-shift mutation in familial congenital nuclear cataract patient
defects in AQP-0 (zeige MIP ELISA Kits) permeability may be a cause for presbyopia.
the p.D150H mutation is a novel disease-causing mutation in MIP (zeige TNPO1 ELISA Kits), which leads to congenital progressive cortical punctate cataract by impairing the trafficking mechanism of AQP0 (zeige MIP ELISA Kits).
Authors identified a novel nonsense mutation in MIP (zeige TNPO1 ELISA Kits) (c.657 C>G; p.Y219*) (major intrinsic protein gene) that segregates with congenital posterior polar cataract in a Chinese family.
Functional evidence linking the new MIP (zeige TNPO1 ELISA Kits) mutation of G215D to autosomal dominant congenital cataracts.
A novel donor splice-site mutation (c.606+1G>A) in the MIP (zeige TNPO1 ELISA Kits) gene causes congenital cataract in a Chinese family.
the first nonsense mutation of MIP (zeige TNPO1 ELISA Kits) identified in autosomal dominant congenital cataracts
Mutation of this conserved glycine residue leads to improper trafficking of AQP0 (zeige MIP ELISA Kits)-G165D and loss of water channel (zeige AQP4 ELISA Kits) function.
The product of this gene performs the final step in processing a specific class of nuclear-encoded proteins targeted to the mitochondrial matrix or inner membrane. This protein is primarily involved in the maturation of oxidative phosphorylation (OXPHOS)-related proteins. This gene may contribute to the functional effects of frataxin deficiency and the clinical manifestations of Friedreich ataxia.
mitochondrial intermediate peptidase
, Mitochondrial intermediate peptidase
, aquaporin 0
, lens fiber major intrinsic protein
, Mitochondrial intermediate peptidase, mitochondrial