COA5 (NM_001008215) Human Mass Spec Standard
CAT#: PH308299
C2orf64 MS Standard C13 and N15-labeled recombinant protein (NP_001008216)
Other products for "COA5"
Specifications
Product Data | |
Tag | C-Myc/DDK |
Species | Human |
Expression Host | HEK293 |
Expression cDNA Clone or AA Sequence | RC208299 |
Predicted MW | 8.4 kDa |
Protein Sequence |
>RC208299 protein sequence
Red=Cloning site Green=Tags(s) MPKYYEDKPQGGACAGLKEDLGACLLQSDCVVQEGKSPRQCLKEGYCNSLKYAFFECKRSVLDNRARFRG RKGY TRTRPLEQKLISEEDLAANDILDYKDDDDKV |
Purity | > 80% as determined by SDS-PAGE and Coomassie blue staining |
Concentration | 50 ug/ml as determined by BCA |
Labeling Method | Labeled with [U- 13C6, 15N4]-L-Arginine and [U- 13C6, 15N2]-L-Lysine |
Buffer | 100 mM glycine, 25 mM Tris-HCl, pH 7.3. Store at -80°C. Avoid repeated freeze-thaw cycles. Stable for 3 months from receipt of products under proper storage and handling conditions. |
Reference Data | |
RefSeq | NP_001008216 |
RefSeq Size | 1767 |
RefSeq ORF | 222 |
Synonyms | 6330578E17Rik; C2orf64; CEMCOX3; Pet191 |
Locus ID | 493753 |
UniProt ID | Q86WW8 |
Cytogenetics | 2q11.2 |
Summary | This gene encodes an ortholog of yeast Pet191, which in yeast is a subunit of a large oligomeric complex associated with the mitochondrial inner membrane, and required for the assembly of the cytochrome c oxidase complex. Mutations in this gene are associated with mitochondrial complex IV deficiency, a disorder of the mitochondrial respiratory chain with heterogeneous clinical manifestations, ranging from isolated myopathy to a severe disease affecting several tissues and organs. [provided by RefSeq, Dec 2011] |
Documents
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Resources
Recombinant Protein Resources |
Other Versions
SKU | Description | Size | Price |
---|---|---|---|
TP308299 | Recombinant protein of human chromosome 2 open reading frame 64 (C2orf64) |
USD 823.00 |
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