MFN2 Protein (Transcript Variant 1) (Myc-DYKDDDDK Tag)

Produktnummer ABIN2726077

Produktdetails

Target: MFN2 (Mitofusin 2 (MFN2))

Protein-Typ: Recombinant

Proteineigenschaft: Transcript Variant 1

Spezies: Human

Quelle: HEK-293 Cells

Aufreinigungstag / Konjugat: Dieses MFN2 Protein ist gelabelt mit Myc-DYKDDDDK Tag.

Applikation: Antibody Production (AbP), Standard (STD)

Produktmerkmale:

• Recombinant human Mitofusin-2 (transcript variant 1) protein expressed in HEK293 cells.
• Produced with end-sequenced ORF clone

Reinheit: > 80 % as determined by SDS-PAGE and Coomassie blue staining

Anwendungsinformationen

Applikationshinweise: Recombinant human proteins can be used for:
Native antigens for optimized antibody production
Positive controls in ELISA and other antibody assays

Kommentare:

The tag is located at the C-terminal.

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Konzentration: 50 μg/mL

Buffer: 25 mM Tris.HCl, pH 7.3, 100 mM glycine, 10 % glycerol.

Lagerung: -80 °C

Informationen zur Lagerung: Store at -80°C. Thaw on ice, aliquot to individual single-use tubes, and then re-freeze immediately. Only 2-3 freeze thaw cycles are recommended.

Antigendetails

Target: MFN2 (Mitofusin 2 (MFN2))

Andere Bezeichnung: Mitofusin-2 (MFN2 Produkte)

Synonyme: CG3869 Protein, Dmel\\CG3869 Protein, MARF Protein, Marf-1 Protein, Mfn Protein, anon-WO0125274.3 Protein, dMFN Protein, dMfn Protein, dmfn Protein, marf Protein, mfn Protein, mfn2 Protein, MFN2 Protein, hsg Protein, cmt2a Protein, cprp1 Protein, cmt2a2 Protein, CMT2A Protein, CMT2A2 Protein, CPRP1 Protein, HSG Protein, D630023P19Rik Protein, Fzo Protein, mg:cb01g09 Protein, si:dkeyp-104h9.2 Protein, wu:fb79a11 Protein, mitofusin 2 Protein, Mitochondrial assembly regulatory factor Protein, mitofusin-2 Protein, mitofusin 2 L homeolog Protein, MFN2 Protein, Marf Protein, mfn2 Protein, LOC100186475 Protein, Mfn2 Protein, mfn2.L Protein

Hintergrund: 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.

Molekulargewicht: 86.2 kDa

NCBI Accession: NP_055689

Pathways: Skeletal Muscle Fiber Development