OPA1 anticorps

N° du produit ABIN6572036

Détail du produit anti-OPA1 anticorps

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

Reactivité: Humain, Souris, Rat

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp OPA1 est non-conjugé

Application: Western Blotting (WB)

Purification: Affinity purification

Immunogène: Recombinant protein of human OPA1

Isotype: IgG

Information d'application

Indications d'application: WB 1:500 - 1:2000

Restrictions: For Research Use only

Stockage

Concentration: 1 mg/mL

Buffer: Buffer: PBS with 0.02 % sodium azide, 50 % glycerol,  pH 7.3.

Agent conservateur: Sodium azide

Précaution d'utilisation: This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Stock: -20 °C

Stockage commentaire: Store at -20°C. Avoid freeze / thaw cycles.

Détails sur OPA1

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

Autre désignation: OPA1 (OPA1 Produits)

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

Sujet:

Synonyms: Dynamin like 120 kDa protein,Dynamin like 120 kDa protein, mitochondrial,Dynamin-like 120 kDa protein, form S1,FLJ12460,Juvenile kjer type optic atrophy,KIAA0567,KJER type,Large GTP binding protein,largeG,MGM1,Mitochondrial dynamin like 120 kDa protein,Mitochondrial dynamin like GTPase,NPG,NTG,OAK,OPA 1,opa1,OPA1 gene,OPA1,Optic atrophy 1 (autosomal dominant),OPTIC ATROPHY 1,Optic atrophy 1 gene protein,Optic atrophy 1 homolog (human),Optic atrophy protein 1,Optic atrophy protein 1 homolog

Background: 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:

Observed_MW: 112kDa

Calculated_MW: 111kDa/115kDa

ID gène: 4976

UniProt: O60313

Pathways: Tube Formation