MTCO2 Monoclonal antibody, PBS Only

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  WB analysis of 143B.TK.P0 using 68527-1-Ig (same clone as 68527-1-PBS)

  WB result of MTCO2 antibody (MTCO2; 1:1000; incubated at room temperature for 1.5 hours) with 143B and 143B.TK.ρ0 cell. 143B is wild-type cell line, 143B.TK.ρ0 is mtDNA deletion cell line. This data was developed using the same antibody clone with 68527-1-PBS in a different storage buffer formulation.

• 

  WB analysis using 68527-1-Ig (same clone as 68527-1-PBS)

  Various lysates were subjected to SDS PAGE followed by western blot with 68527-1-Ig (MTCO2 antibody) at dilution of 1:10000 incubated at room temperature for 1.5 hours. This data was developed using the same antibody clone with 68527-1-PBS in a different storage buffer formulation.

• Featured Product
• KD/KO Validated

MTCO2 Monoclonal Antibody for WB, Indirect ELISA

Cat No. 68527-1-PBS

Clone No.10G14F4

Host / Isotype

Mouse / IgG1

Reactivity

human

Applications

WB, Indirect ELISA

Synonyms

COX2, MT CO2, COXII, COX 2, COII

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Product Information

68527-1-PBS targets MTCO2 in WB, Indirect ELISA applications and shows reactivity with human samples.

• Tested Reactivity: human
• Host / Isotype: Mouse / IgG1
• Class: Monoclonal
• Type: Antibody
• Immunogen: Peptide
• Full Name: cytochrome c oxidase II
• Calculated Molecular Weight: 26 kDa
• Observed Molecular Weight: 23-26 kDa
• GenBank Accession Number: YP_003024029
• Gene Symbol: MTCO2
• Gene ID (NCBI): 4513
• Conjugate: Unconjugated
• Form: Liquid
• Purification Method: Protein A purification
• UNIPROT ID: P00403
• Storage Buffer: PBS Only
• Storage Conditions: Store at -80°C.

Background Information

MTCO2, also named as COII, COXII, and COX2, belongs to the cytochrome c oxidase subunit 2 family. It is the component of the respiratory chain that catalyzes the reduction of oxygen to water. Subunits 1-3 form the functional core of the enzyme complex. Subunit 2 transfers the electrons from cytochrome c via its binuclear copper A center to the bimetallic center of the catalytic subunit 1. Defects in COX2 are a cause of mitochondrial complex IV deficiency (MT-C4D).