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Invitrogen™ COX3 Polyclonal Antibody

Rabbit Polyclonal Antibody

Supplier:  Invitrogen™ PA597297

Catalog No. PIPA597297


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Description

Description

Immunogen sequence: MTHQTHAYHM VNPSPWPLTG AFSALLLTSG LVMWFHYNSI TLLTLGLLTN ILTMYQWWRD VIREGTYQGH HTPIVQKGLR YGMILFIVSE VFFFAGFFWA; Positive Samples: Mouse liver, Rat liver; Cellular Location: Mitochondrion inner membrane, Multi-pass membrane protein.

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

Specifications

COX3
Polyclonal
Unconjugated
MT-CO3
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
Affinity chromatography
RUO
17710, 26204
-20°C, Avoid Freeze/Thaw Cycles
Liquid
ELISA, Western Blot
0.36 mg/mL
PBS with 50% glycerol and 0.02% sodium azide; pH 7.3
P00416, P05505
MT-CO3
A synthetic peptide corresponding to a sequence within amino acids 1-100 of mouse MT-CO3 (NP_9043341).
100 μL
Primary
Mouse, Rat
Antibody
IgG
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