MIPEP antibody (AA 357-713) (Cy3)

Catalog No. ABIN8010719

This Rabbit Polyclonal antibody specifically detects MIPEP in FACS. It exhibits reactivity toward Human, Rat and Mouse.

Quick Overview for MIPEP antibody (AA 357-713) (Cy3) (ABIN8010719)

Target: MIPEP (Mitochondrial Intermediate Peptidase (MIPEP))

Reactivity: Human, Rat, Mouse

Host: Rabbit

Clonality: Polyclonal

Conjugate: This MIPEP antibody is conjugated to Cy3

Application: Flow Cytometry (FACS)

Product Details anti-MIPEP Antibody (Cy3)

Binding Specificity: AA 357-713

Purpose: Anti-MIPEP Antibody Cy3 Conjugated

Cross-Reactivity (Details): No cross reactivity with other proteins.

Predicted Reactivity: Human MIPEP shares 88%,89.6% amino acid (aa) sequence identity with mouse,rat MIPEP,respectively.

Purification: Immunogen affinity purified.

Immunogen: E.coli-derived human MIPEP recombinant protein (Position: D357-E713). Human MIPEP shares 88% and 89.6% amino acid (aa) sequence identity with mouse and rat MIPEP, respectively.

Isotype: IgG

Application Details

Application Notes: Flow Cytometry, 1-3 μg/1x10⁶ cells

Restrictions: For Research Use only

Handling

Format: Liquid

Buffer: Each vial contains 50 % glycerol, 0.9 % NaCl, 0.2 % Na2HPO4, 0.02 % Sodium azide.

Preservative: Sodium azide

Precaution of Use: This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Storage: -20 °C

Storage Comment: At -20°C for one year from date of receipt. Avoid repeated freezing and thawing. Protect from light.

Expiry Date: 12 months

Target Details for MIPEP

Target: MIPEP (Mitochondrial Intermediate Peptidase (MIPEP))

Alternative Name: MIPEP

Background:

Background: Mitochondrial intermediate peptidase is an enzyme that in humans is encoded by the MIPEP gene. 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 Full Name: mitochondrial intermediate peptidase

Gene ID: 4285

UniProt: Q99797