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Mitofusin 2 Antibody

Catalog # Availability Size / Price Inquiry
APR08456G 100 μg / $495

Mitofusin 2 Antibody

Brand

Leading Biology

Catalog Number

APR08456G

Product Type

Polyclonal Antibodies

Field of Research

Product Overview

We constantly strive to ensure we provide our customers with the best antibodies. As a result of this work we offer this antibody in purified format. We are in the process of updating our datasheets. If you have any questions regarding this update, please feel free to contact our technical support team. This product is a high quality Mitofusin 2 antibody.

Molecular Weight

86402 Da

Cellular Localization

Antigen Cellular Localization: Mitochondrion outer membrane; Multi- pass membrane protein. Note=Colocalizes with BAX during apoptosis

Host

Rabbit

Species Reactivity

Human, Mouse, Rat

Target

Mitofusin 2

Isotype

Rabbit IgG

Symbol

CPRP1, KIAA0214

GeneID

UniProt ID

Function

Essential transmembrane GTPase, which mediates mitochondrial fusion. Fusion of mitochondria occurs in many cell types and constitutes an important step in mitochondria morphology, which is balanced between fusion and fission. MFN2 acts independently of the cytoskeleton. It therefore plays a central role in mitochondrial metabolism and may be associated with obesity and/or apoptosis processes. Overexpression induces the formation of mitochondrial networks. Plays an important role in the regulation of vascular smooth muscle cell proliferation. Involved in the clearance of damaged mitochondria via selective autophagy (mitophagy). Is required for PARK2 recruitment to dysfunctional mitochondria. Involved in the control of unfolded protein response (UPR) upon ER stress including activation of apoptosis and autophagy during ER stress. Acts as an upstream regulator of EIF2AK3 and suppresses EIF2AK3 activation under basal conditions.

Summary

Mitofusin 2 (Mfn 2) is mostly expressed in the heart and muscle tissues. It is a transmembrane protein that mediates mitochondria fusion and plays a central role in the maintenance of mitochondrial morphology. A GTPase domain is required for the function of Mitofusin proteins. Mutations in Mfn2 can lead to Charcot-Marie-Tooth disease, a common inherited disorder of the peripheral nervous system. Mfn2 may also be associated with obesity and/or apoptosis.

Form

Liquid

Storage & Stability

Store at +4°C short term. For long-term storage, aliquot and store at -20°C or below. Stable for 12 months at -20°C. Avoid repeated freeze-thaw cycles.

Applications

WB

Synonyms

mitofusin2, mitofusin 2, mitofusin-2, MFN2, CMT2A, CMT2A2, CPRP1, HSG, KIAA0214, MARF

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