Recombinant Mitofusine-2 Monoklonale Antilichaam

This gene encodes a mitochondrial membrane protein that participates in mitochondrial fusion and contributes to the maintenance 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.

Mitofusin-2

O95140

Human; Mouse; Rat

Recombinant Human Mitofusin-2 protein

KIAA; Transmembrane GTPase MFN; Hypertension related protein; CMT2A; CMT2A2; CPRP 1; EC 3.6.5.; Fzo; HSG; hyperplasia suppressor gene; Hypertension related protein 1; MARF; MFN 2; Mitochondrial assembly regulatory factor; Mitofusin2; Mitofusin-2; Transmembrane GTPase MFN2; CPRP1; KIAA0214; MFN2; EC 3.6.5.-; Mfn2

7A7

Unconjugated

WB

Neuroscience; Tags & Cell Markers; Signal Transduction; Cell Biology; Metabolism; Cancer

Protein A

0.2 mg/mL

WB 1:2000-1:10000

PBS, 50% glycerol, 0.05% Proclin 300, 0.05% protein protectant.

Ice bag

Store at -20°C Valid for 12 months. Avoid freeze / thaw cycles.

https://789.bio/eb/NQQQGb6n

86 kDa

86 kDa

IgG, κ