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

N° du produit ABIN2727921

Détail du produit

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

Type de proteíne: Recombinant

Attributs du protein: Transcript Variant 3

Origine: Humain

Source: HEK-293 Cells

Purification/Conjugué: Cette OPA1 protéine est marqué à la Myc-DYKDDDDK Tag.

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

Attributs du produit:

• 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

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

Information d'application

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

Commentaires:

The tag is located at the C-terminal.

Restrictions: For Research Use only

Stockage

Concentration: 50 μg/mL

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

Stock: -80 °C

Stockage commentaire: 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.

Détail du antigène

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

Abstract: OPA1 Produits

Synonymes: 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

Sujet: 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.

Poids moléculaire: 109.2 kDa

NCBI Accession: NP_570845

Pathways: Tube Formation