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Name :
Recombinant Human COX20 Protein, Myc/DDK-tagged, C13 and N15-labeled

Specification :
| Description : This gene encodes a protein that plays a role in the assembly of cytochrome C oxidase, an important component of the respiratory pathway. It contains two transmembrane helices and localizes to the mitochondrial membrane. Mutations in this gene can cause mitochondrial complex IV deficiency, which results in ataxia and muscle hypotonia. There are multiple pseudogenes for this gene. Alternative splicing results in multiple transcript variants. | Source : HEK293 | Species : Human | Tag : Myc/DDK | Molecular Mass : 13.3 kDa | AA Sequence : MAAPPEPGEPEERKSLKLLGFLDVE NTPCARHSILYGSLGSVVAGFGHFL FTSRIRRSCDVGVGGFILVTLGCWF HCRYNYAKQRIQERIAREEIKKKIL YEGTHLDPERKHNGSSSNTRTRPLE QKLISEEDLAANDILDYKDDDDKV | Purity : > 80% as determined by SDS-PAGE and Coomassie blue staining | Stability : Stable for 3 months from receipt of products under proper storage and handling conditions. | Storage : Store at -80 centigrade. Avoid repeated freeze-thaw cycles. | Concentration : 50 μg/mL as determined by BCA | Storage Buffer : 100 mM glycine, 25 mM Tris-HCl, pH 7.3.

Gene Information :
| Gene Name : COX20 cytochrome c oxidase assembly factor COX20 [ Homo sapiens (human) ] | Official Symbol : COX20 | Synonyms : COX20; cytochrome c oxidase assembly factor COX20; FAM36A; MC4DN11; cytochrome c oxidase assembly protein COX20, mitochondrial; COX20 Cox2 chaperone homolog; COX20, cytochrome c oxidase assembly factor; cytochrome c oxidase protein 20 homolog; family with sequence similarity 36, member A | Gene ID : 116228 | mRNA Refseq : NM_198076 | Protein Refseq : NP_932342 | MIM : 614698 | UniProt ID : Q5RI15

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Author: Cholesterol Absorption Inhibitors