OPA3 antibody

Product Graph
Contáctenos para saber el precio

Por favor contáctenos para obtener información detallada sobre el precio y disponibilidad.

935106861
info@markelab.com
name
OPA3 antibody
category
Primary Antibodies
provider
FineTest
reference
FNab05995
tested applications
ELISA, WB, IHC, IF

Description

The mouse ortholog of this protein co-purifies with the mitochondrial inner membrane. Mutations in this gene have been shown to result in 3-methylglutaconic aciduria type III and autosomal dominant optic atrophy and cataract. Multiple transcript variants encoding different isoforms have been found for this gene.

Documents del producto

Instrucciones
Descargar
Data sheet
Descargar

Product specifications

Category
Primary Antibodies
Immunogen Target
optic atrophy 3 (autosomal recessive, with chorea and spastic paraplegia) (OPA3)
Host
Rabbit
Reactivity
Human, Mouse, Rat
Recommended Dilution
WB: 1:500 - 1:2000; IHC: 1:50 - 1:100; IF: 1:50 - 1:100
Clonality
polyclonal
Conjugation
Unconjugated
Isotype
IgG
Observed MW
20 kDa
Purity
≥95% as determined by SDS-PAGE
Purification
Immunogen affinity purified
Size 1
100µg
Form
liquid
Tested Applications
ELISA, WB, IHC, IF
Storage
PBS with 0.02% sodium azide and 50% glycerol pH 7.3, -20℃ for 12 months (Avoid repeated freeze / thaw cycles.)
UniProt ID
Q9H6K4
Gene ID
80207
Alias
Optic atrophy 3 protein,OPA3
Background
Antibody anti-OPA3
Status
RUO
Note
Mol. Weight 20 kDa

Descripción

Related Products

FNab05995

OPA3 antibody

The mouse ortholog of this protein co-purifies with the mitochondrial inner membrane. Mutations in this gene have been shown to result in 3-methylglutaconic aciduria type III and autosomal dominant optic atrophy and cataract. Multiple transcript variants encoding different isoforms have been found for this gene.

Ver Producto
P8369

Recombinant Human OPA3

Ver Producto
abx003811

OPA3, Outer Mitochondrial Membrane Lipid Metabolism Regulator (OPA3) Antibody

OPA3 Antibody is a Rabbit Polyclonal antibody against OPA3. The mouse ortholog of this protein co-purifies with the mitochondrial inner membrane. Mutations in this gene have been shown to result in 3-methylglutaconic aciduria type III and autosomal dominant optic atrophy and cataract. Multiple transcript variants encoding different isoforms have been found for this gene.

Ver Producto