OPA1 Protein (Transcript Variant 3) (Myc-DYKDDDDK Tag)

Produktnummer ABIN2727921

Produktdetails

Target: OPA1 (Optic Atrophy 1 (Autosomal Dominant) (OPA1))

Protein-Typ: Recombinant

Proteineigenschaft: Transcript Variant 3

Spezies: Human

Quelle: HEK-293 Cells

Aufreinigungstag / Konjugat: Dieses OPA1 Protein ist gelabelt mit Myc-DYKDDDDK Tag.

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

Produktmerkmale:

• Recombinant human Optic atrophy 1 (autosomal dominant) (OPA1), nuclear gene encoding mitochondrial protein, transcript variant 3 (transcript variant 3) 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: OPA1 (Optic Atrophy 1 (Autosomal Dominant) (OPA1))

Abstract: OPA1 Produkte

Synonyme: 1200011N24Rik Protein, AI225888 Protein, AI847218 Protein, lilr3 Protein, mKIAA0567 Protein, MGM1 Protein, NPG Protein, NTG Protein, largeG Protein, fk62d06 Protein, wu:fb77a10 Protein, wu:fk62d06 Protein, zgc:92092 Protein, OPA1, mitochondrial dynamin like GTPase Protein, optic atrophy 1 (autosomal dominant) Protein, Opa1 Protein, OPA1 Protein, opa1 Protein

Hintergrund: This gene product is a nuclear-encoded mitochondrial protein with similarity to dynamin-related GTPases. It is a component of the mitochondrial network. Mutations in this gene have been associated with optic atrophy type 1, which is a dominantly inherited optic neuropathy resulting in progressive loss of visual acuity, leading in many cases to legal blindness. Multiple transcript variants encoding different isoforms have been found for this gene.

Molekulargewicht: 109.2 kDa

NCBI Accession: NP_570845

Pathways: Tube Formation