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The antibody against MIPEP was raised in rabbit using the Recombinant Human Mitochondrial intermediate peptidase protein (504-713AA) as the immunogen. This antibody exists as a non-conjugated isotype IgG, Antigen affinity purified. This antibody has been validated on ELISA, IHC.
The antibody against MIPEP was raised in rabbit using the Recombinant Human Mitochondrial intermediate peptidase protein (504-713AA) as the immunogen. This antibody exists as a non-conjugated isotype IgG, Antigen affinity purified. This antibody has been validated on ELISA, IHC.
$299.00
| Cat.No | ADC-16650A | Clonality | Polyclonal |
|---|---|---|---|
| Host Species | Rabbit | Target Name | MIPEP |
| Form | Liquid | Species Reactivity | Human |
| Isotype | IgG | Storage Buffer | 50% Glycerol, PBS with 0.02% sodium azide, pH7.3. |
| Purification Method | Antigen affinity purified | Conjugate | Non-conjugated |
| Application | ELISA, IHC | Storage | Upon receipt |
| Immunogen Description | Recombinant Human Mitochondrial intermediate peptidase protein (504-713AA) | Target Species | Human |
|---|---|---|---|
| Immunogen Sequence | Complete sequences for the immunogen, target protein, and peptides are available upon request. | Uniprot ID | Q99797 |
Uniprot Id
Q99797
Target Species
Human
Target Name
MIPEP
Target Full Name
Mitochondrial intermediate peptidase
Target Function
Cleaves proteins, imported into the mitochondrion, to their mature size.
Target Involvement
Combined oxidative phosphorylation deficiency 31 (COXPD31)
Target Subcellular Location
Mitochondrion matrix.
Target Protein Families
Peptidase M3 family
Target Synonyms
EC 3.4.24.59 ; HMIP; MIP; Mipep; MIPEP_HUMAN; Mitochondrial intermediate peptidase; Mitochondrial intermedieate peptide; OTTHUMP00000018121; OTTHUMP00000042292
Target Background
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.
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