MFN2 Antibody

NSJ Bioreagents
Product Code: NSJ-R31678
Product Group: Primary Antibodies
Supplier: NSJ Bioreagents
CodeSizePrice
NSJ-R31678-100ug100 ug£535.00
Quantity:
Prices exclude any Taxes / VAT

Overview

Host Type: Rabbit
Antibody Isotype: Rabbit IgG
Antibody Clonality: Polyclonal
Regulatory Status: RUO
Target Species:
  • Human
  • Mouse
  • Rat
Application: Western Blot (WB)
Storage:
After reconstitution, the MFN2 antibody can be stored for up to one month at 40. For long-term, aliquot and store at -200. Avoid repeated freezing and thawing.

Images

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Western blot testing of MFN2 antibody and Lane 1: HeLa; 2: A549. Predicted/observed size ~86KD
2 / 3
Western blot testing of MFN2 antibody and recombinant human protein (0.5ng)
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Western blot testing of rat 1) brain, 2) heart, 3) kidney and mouse 4) brain, 5) heart, 6) kidney, 7) small intestine and 8) NIH3T3 lysate with MFN2 antibody. Predicted molecular weight ~86 kDa.

Western blot testing of MFN2 antibody and Lane 1: HeLa; 2: A549. Predicted/observed size ~86KD
Western blot testing of MFN2 antibody and recombinant human protein (0.5ng)
Western blot testing of rat 1) brain, 2) heart, 3) kidney and mouse 4) brain, 5) heart, 6) kidney, 7) small intestine and 8) NIH3T3 lysate with MFN2 antibody. Predicted molecular weight ~86 kDa.

Further Information

Application Details :
Western blot: 0.5-1ug/ml
Application Note:
The stated application concentrations are suggested starting amounts. Titration of the MFN2 antibody may be required due to differences in protocols and secondary/substrate sensitivity.
Description:
Mitofusin-2 is a protein that in humans is encoded by the MFN2 gene. It is mapped to chromosome 1 and encodes a 757-amino acid protein that contains an ATP/GTP-binding site motif. This gene is expressed in many tissues and cell lines such as brain and KG-1 with the highest expression in heart and skeletal muscle. It has been found that MFN2 triggers mitochondrial energization, at least in part, by regulating OXPHOS expression through signals that are independent of its role as a mitochondrial fusion protein. And it contributes to the maintenance and operation of the mitochondrial network. Axonal CMT type 2A and autosomal dominant HMSN VI are caused by MFN2 and mutations of, which emphasizes its important role of mitochondrial function for both optic atrophies and peripheral neuropathies.
Format :
Antigen affinity purified
Formulation :
0.5mg/ml if reconstituted with 0.2ml sterile DI water
Gene ID #:
9927
Immunogen:
Human partial recombinant protein (AA 601-757) was used as the immunogen for this MFN2 antibody.
Limitation:
This MFN2 antibody is available for research use only.
Purity:
Antigen affinity
Species Reactivity :
Human, Mouse, Rat