missing translation for 'onlineSavingsMsg'
Learn More
Learn More
Invitrogen™ COX3 Polyclonal Antibody

Rabbit Polyclonal Antibody
Brand: Invitrogen™ PA5148300
This item is not returnable.
View return policy
Description
COX3 Polyclonal Antibody for ICC/IF, IHC (P)
COX3 is a multi-pass membrane protein. It belongs to the cytochrome c oxidase subunit 3 family. Defects in COX3 are a cause of Leber hereditary optic neuropathy (LHON) and cytochrome c oxidase deficiency (COX deficiency). Defects in MT-CO3 are also found in mitochondrial encephalomyopathy with lactic acidosis and stroke-like episodes (MELAS) syndrome and recurrent myoglobinuria.
Specifications
| COX3 | |
| Polyclonal | |
| Unconjugated | |
| COX3 | |
| ACI60_gp01; Co3; Coiii; COX3; COXIII; cytchrome c oxidase sububnit 3; Cytochrome c oxidase polypeptide III; Cytochrome c oxidase subunit 3; cytochrome c oxidase subunit III; mitochondrially encoded cytochrome c oxidase III; Mtco3; mt-Co3; OXI2; Q0275 | |
| Rabbit | |
| Antigen Affinity Chromatography, Protein A | |
| RUO | |
| 139542, 4514 | |
| Store at 4°C short term. For long term storage, store at -20°C, avoiding freeze/thaw cycles. | |
| Liquid |
| Immunohistochemistry (Paraffin), Immunocytochemistry | |
| 100 μg/mL | |
| PBS with 0.03% ProClin 300; pH 7 | |
| P00414 | |
| COX3, MT-CO3 | |
| E. coli-derived Human MTCO3 fragment. | |
| 100 μL | |
| Primary | |
| Human | |
| Antibody | |
| IgG |
Product Content Correction
Your input is important to us. Please complete this form to provide feedback related to the content on this product.
Product Title
Spot an opportunity for improvement?Share a Content Correction