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Mouse Monoclonal COX4I2 antibody (STJ98479)
Supplier: St John’s Laboratory Ltd.
Recommended applications: WB, FC, IF
Recommended dilution: WB 1:1000-1:2000; FC 1:100-1:200; IF 1:100-1:500
Recommended protocols: check protocols
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Check alternative names for the antibodyExpand
COX4I2 antibody, COX4L2 antibody,|COX IV-2 antibody|COX4 2 antibody|COX4 antibody|COX42_HUMAN antibody|COX4B antibody|Cox4i2 antibody|COX4L2 antibody|COXIV 2 antibody|Cytochrome c oxidase subunit 4 isoform 2 antibody|Cytochrome c oxidase subunit 4 isoform 2 mitochondrial [Precursor] antibody|cytochrome c oxidase subunit IV isoform 2 (lung) antibody|Cytochrome c oxidase subunit IV isoform 2 antibody|dJ857M17.2 antibody|mitochondrial antibody|RP23 106A3.3 antibody|Anti-COXIV Isoform 2 antibody (ab70112)
SCBT cat No: sc-100522|sc-86386|
COX4I2 Monoclonal Antibody
|Catalogue No.|| |
COX4I2 Monoclonal Antibody detects endogenous levels of COX4I2 protein.
Purified recombinant human COX4I2 (C-terminus) protein fragments expressed in Ecoli
WB, FC, IF
|Recommended dilution|| |
WB 1:1000-1:2000; FC 1:100-1:200; IF 1:100-1:500
COX4I2 Antibody was tube-contained. Purified in buffer containing 0.1M Tris-Glycine (pH 7.4, 150 mM NaCl) with 0.2% sodium azide, 50% glycerol.
COX4I2 Antibody was purified using affinity purification.
-20 Celsius degree. Avoid repeated freeze/thaw cycles.
|Alternative antibody names|| |
Cytochrome c oxidase subunit 4 isoform 2, mitochondrial antibody, Cytochrome c oxidase subunit IV isoform 2 antibody, COX IV-2 antibody
|Protein names|| |
Cytochrome c oxidase subunit 4 isoform 2, mitochondrial , Cytochrome c oxidase subunit IV isoform 2 , COX IV-2
|Protein function|| |
This protein is one of the nuclear-coded polypeptide chains of cytochrome c oxidase, the terminal oxidase in mitochondrial electron transport.
|Protein tissue specificity|| |
Highly expressed in lung.
|Involvement in disease|| |
Exocrine pancreatic insufficiency dyserythropoietic anemia and calvarial hyperostosis (EPIDACH) [MIM:612714]: Patients present with pancreatic insufficiency, intestinal malabsorption, failure to thrive, and anemia soon after birth. . Note: The disease is caused by mutations affecting the gene represented in this entry.
|Protein sequence and domain|| |
Belongs to the cytochrome c oxidase IV family.
|Protein cellular localization|| |
Mitochondrion inner membrane
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St John’s Laboratory Ltd.
|Product type|| |
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