Mitochondrial Intermediate Peptidase (MIPEP) ELISA Kits

Major intrinsic protein is a member of the water-transporting aquaporins as well as the original member of the MIP family of channel proteins. Additionally we are shipping Mitochondrial Intermediate Peptidase Antibodies (70) and Mitochondrial Intermediate Peptidase Proteins (3) and many more products for this protein.

list all ELISA KIts Gene Name GeneID UniProt
MIPEP 4284 P30301
MIPEP 70478 A6H611
MIPEP 81684 Q01992
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More ELISA Kits for Mitochondrial Intermediate Peptidase Interaction Partners

Human Mitochondrial Intermediate Peptidase (MIPEP) interaction partners

  1. The data evidence a broad lipidation profile of AQP0 (show MIP ELISA Kits) that is both species and site independent, suggesting a chemical-based ester aminolysis mechanism to explain such modifications.

  2. MIPEP recessive variants cause a syndrome of left ventricular non-compaction, hypotonia, and infantile death.

  3. A novel MIP (show TNPO1 ELISA Kits) frame-shift mutation in familial congenital nuclear cataract patient

  4. defects in AQP-0 (show MIP ELISA Kits) permeability may be a cause for presbyopia.

  5. the p.D150H mutation is a novel disease-causing mutation in MIP (show TNPO1 ELISA Kits), which leads to congenital progressive cortical punctate cataract by impairing the trafficking mechanism of AQP0 (show MIP ELISA Kits).

  6. Authors identified a novel nonsense mutation in MIP (show TNPO1 ELISA Kits) (c.657 C>G; p.Y219*) (major intrinsic protein gene) that segregates with congenital posterior polar cataract in a Chinese family.

  7. Functional evidence linking the new MIP (show TNPO1 ELISA Kits) mutation of G215D to autosomal dominant congenital cataracts.

  8. A novel donor splice-site mutation (c.606+1G>A) in the MIP (show TNPO1 ELISA Kits) gene causes congenital cataract in a Chinese family.

  9. the first nonsense mutation of MIP (show TNPO1 ELISA Kits) identified in autosomal dominant congenital cataracts

  10. Mutation of this conserved glycine residue leads to improper trafficking of AQP0 (show MIP ELISA Kits)-G165D and loss of water channel (show AQP4 ELISA Kits) function.

Mitochondrial Intermediate Peptidase (MIPEP) Antigen Profile

Antigen Summary

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.

Gene names and symbols associated with MIPEP

  • mitochondrial intermediate peptidase (MIPEP) antibody
  • zincin-like metalloproteases family protein (AT5G51540) antibody
  • mitochondrial intermediate peptidase (CHLREDRAFT_141176) antibody
  • mitochondrial intermediate peptidase (mip) antibody
  • mitochondrial intermediate peptidase (POSPLDRAFT_43376) antibody
  • Mitochondrial intermediate peptidase (PAS_chr2-1_0435) antibody
  • major intrinsic protein of lens fiber (MIP) antibody
  • mitochondrial intermediate peptidase (Mipep) antibody
  • 5730405E07Rik antibody
  • AQP0 antibody
  • CTRCT15 antibody
  • HMIP antibody
  • K17N15.9 antibody
  • K17N15_9 antibody
  • LIM1 antibody
  • MIP antibody
  • MIP26 antibody
  • MP26 antibody

Protein level used designations for MIPEP

mitochondrial intermediate peptidase , Mitochondrial intermediate peptidase , aquaporin 0 , lens fiber major intrinsic protein , MIP , Mitochondrial intermediate peptidase, mitochondrial

418942 Gallus gallus
517531 Bos taurus
835228 Arabidopsis thaliana
5727159 Chlamydomonas reinhardtii
6069018 Laccaria bicolor S238N-H82
8142875 Postia placenta Mad-698-R
8146343 Postia placenta Mad-698-R
8198961 Komagataella pastoris GS115
4284 Homo sapiens
4285 Homo sapiens
70478 Mus musculus
81684 Rattus norvegicus
100171586 Pongo abelii
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