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MFN2 Rabbit anti-Human, Mouse, Rat, Polyclonal, Proteintech

Rabbit Polyclonal Antibody
Supplier: Proteintech Group Inc 121861AP150UL

Description
This gene encodes a mitochondrial membrane protein that participates in mitochondrial fusion and contributes to the maintece and operation of the mitochondrial network. This protein is involved in the regulation of vascular smooth muscle cell proliferation, and it may play a role in the pathophysiology of obesity. Mutations in this gene cause Charcot-Marie-Tooth disease type 2A2, and hereditary motor and sensory neuropathy VI, which are both disorders of the peripheral nervous system. Defects in this gene have also been associated with early-onset stroke. Two transcript variants encoding the same protein have been identified.Specifications
MFN2 | |
Polyclonal | |
Unconjugated | |
MFN2 | |
CMT2A, CMT2A2, CPRP1, HSG, KIAA0214, MARF, MFN2, Mitofusin 2, Transmembrane GTPase MFN2 | |
Rabbit | |
Antigen Affinity Chromatography | |
RUO | |
170731, 64476, 9927 | |
-20°C | |
Liquid |
Immunohistochemistry (Paraffin), Immunoprecipitation, Western Blot | |
0.2 mg/mL | |
PBS with 50% glycerol and 0.1% sodium azide; pH 7.3 | |
O95140, Q80U63, Q8R500 | |
Mfn2 | |
MFN2 Fusion Protein Ag2845 | |
150 μL | |
Primary | |
Human, Mouse, Rat | |
Antibody | |
IgG |
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