Mitofusin 2 Monoclonal Antibody
Product Specifications
Background
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, Jul 2008].
Synonyms
CMT2A; CMT2A2; MARF; CPRP 1; CPRP1; Fzo; HSG; hyperplasia suppressor gene; Hypertension related protein 1; MFN 2; Mfn2; MFN2_HUMAN; Mitochondrial assembly regulatory factor; Mitofusin-2; Mitofusin2; Transmembrane GTPase MFN2.
Gene ID
9927
Swiss Prot
O95140
Cellular Locus
Cytoplasm, Cell membrane
Host
Mouse
Cross Reactivity
Human, Mouse
Target
Mitofusin 2
Clonality
Monoclonal
Isotype
IgG2a
Clone
G8D3
Conjugation
Unconjugated
Source
KLH conjugated synthetic peptide derived from human Mitofusin 2
Applications
WB
Purification
Purified by Protein A.
Concentration
1mg/ml
Dilution
WB (WB=1:1000)
Buffer
0.01M TBS (pH7.4) with 1% BSA, 0.02% Proclin300 and 50% Glycerol.
Modification
Unmodified
Storage Conditions
Shipped at 4°C. Store at -20°C for one year. Avoid repeated freeze/thaw cycles.
Gene ID URL
9927
Curated Selection
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