Loading...
Products:Neuroscience >> Sensory System >> Visual system
MSCatalog No. MS995
If your product does not perform as described on this datasheet, we will refund or replace your product...
Read our guarantee »Anti-OPA1 antibody [1E81D9]
See all OPA1 products (5) ...
Mouse monoclonal [1E81D9] to OPA1
Reacts with
Mouse, Rat, Human
Human, full-length, corresponding to short form of isoform 1
Liquid
Store at +4°C. Do not freeze.
Preservative: 0.02% Sodium azide
Constituent: 99% HBS
Concentration information loading...
Ammonium Sulphate Precipitation
Purity is near homogeneity as judged by SDS-PAGE. ab119685 was produced in vitro using hybridomas grown in serum-free medium, and then concentrated by ammonium sulfate precipitation.
Monoclonal
1E81D9
IgG1
kappa
Metabolism >> Mitochondrial Metabolism >> Mitophagy fission and fusion
Neuroscience >> Neurology process >> Neurodegenerative disease >> Other
Neuroscience >> Sensory System >> Visual system
Western blot - Anti-OPA1 antibody [1E81D9] (ab119685)
(enlarge)
Our Abpromise guarantee covers the use of ab119685 in the following tested applications.
The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.
WB: Use a concentration of 1 µg/mlPredicted molecular weight: 112 kDa.
Dynamin-related GTPase required for mitochondrial fusion and regulation of apoptosis. May form a diffusion barrier for proteins stored in mitochondrial cristae. Proteolytic processing in response to intrinsic apoptotic signals may lead to disassembly of OPA1 oligomers and release of the caspase activator cytochrome C (CYCS) into the mitochondrial intermembrane space.
Highly expressed in retina. Also expressed in brain, testis, heart and skeletal muscle. Isoform 1 expressed in retina, skeletal muscle, heart, lung, ovary, colon, thyroid gland, leukocytes and fetal brain. Isoform 2 expressed in colon, liver, kidney, thyroid gland and leukocytes. Low levels of all isoforms expressed in a variety of tissues.
Defects in OPA1 are a cause of optic atrophy type 1 (OPA1) [MIM:165500]. OPA1 is a dominantly inherited optic neuropathy occurring in 1 in 50,000 individuals that features progressive loss in visual acuity leading, in many cases, to legal blindness.
Defects in OPA1 are the cause of optic atrophy 1 with deafness (OPA1D) [MIM:125250]. Some individuals with mutations in OPA1 manifest also ophthalmoplegia and myopathy.
Belongs to the dynamin family.
PARL-dependent proteolytic processing releases an antiapoptotic soluble form not required for mitochondrial fusion.
Mitochondrion inner membrane. Mitochondrion intermembrane space.
Target information above from: UniProt accessionO60313
The UniProt Consortium
The Universal Protein Resource (UniProt) in 2010
Nucleic Acids Res. 38:D142-D148 (2010).
Western blot - Anti-OPA1 antibody [1E81D9] (ab119685)
![Western blot - Anti-OPA1 antibody [1E81D9] (ab119685)](/ps/datasheet/images/119/ab119685/OPA1-Primary-antibodies-ab119685-2.jpg)
All lanes : Anti-OPA1 antibody [1E81D9] (ab119685) at 1 µg/ml
Lane 1 : whole cell lysates from HeLa cells(human)
Lane 2 : whole cell lysates from H4IIE cells(rat)
Lane 3 : whole cell lysates from MEF cells(mouse)
Lysates/proteins at 30 µg per lane.
Secondary
HRP goat anti-mouse at 1/5000 dilution
developed using the ECL technique
Performed under reducing conditions.
Predicted band size : 112 kDa
ab119685 has not yet been referenced specifically in any publications.
Publishing research using ab119685? Please let us know so that we can cite the reference in this datasheet
Concentration of lot no. is
Concentration not available for this lot.
Find concentration of your lot:
Please note: All products are "FOR RESEARCH USE ONLY AND ARE NOT INTENDED FOR DIAGNOSTIC OR THERAPEUTIC USE"
Call 01223 696 000 or contact us
