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MFN2, Mouse, Clone: 4H8, Abnova™
Mouse monoclonal antibody raised against a full-length recombinant MFN2.
Supplier: Abnova Corporation H00009927M03J
Description
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. [provided by RefSeq
Sequence: FKRQFVEHASEKLQLVISYTGSNCSHQVQQELSGTFAHLCQQVDVTRENLEQEIAAMNKKIEVLDSLQSKAKLLRNKAGWLDSELNMFTHQYLQPSRSpécifications
| MFN2, | |
| Monoclonal | |
| Unconjugated | |
| PBS with no preservative; pH 7.4 | |
| NM_014874 | |
| MFN2 | |
| MFN2 (NP_055689, 661 a.a. ∼ 757 a.a) full-length recombinant protein with GST tag. MW of the GST tag alone is 26 KDa. | |
| 100 μg | |
| Primary | |
| Human | |
| Antibody | |
| IgG2a κ |
| ELISA, Western Blot | |
| 4H8 | |
| Mouse monoclonal antibody raised against a full length recombinant MFN2. | |
| MFN2 | |
| CMT2A/CMT2A2/CPRP1/HSG/KIAA0214/MARF | |
| Mouse | |
| Affinity chromatography | |
| RUO | |
| 9927 | |
| Store at -20°C or lower. Aliquot to avoid repeated freezing and thawing. | |
| Liquid |