Promotion ends on May 1st.
Also for NAA10 (NM_003491)
|Expression cDNA Clone or AA Sequence
Recombinant protein was produced with TrueORF clone, RC201354
. Click on the TrueORF clone link to view cDNA and protein sequences.
||Predicted MW:||26.3 kDa|
|Purity:||> 80% as determined by SDS-PAGE and Coomassie blue staining|
|Mass Spec Validation:
||This protein has been positively validated by MS/MS by Dr. Robert Moritz at The Institute of Systems Biology.
|Concentration:||>50 ug/mL as determined by microplate BCA method|
|Buffer:||25 mM Tris.HCl, pH 7.3, 100 mM glycine, 10% glycerol.|
||Recombinant protein was captured through anti-DDK affinity column followed by conventional chromatography steps.
||Tyrosine metabolismPhenylalanine metabolismGlycerophospholipid metabolismLimonene and pinene degradation
||RefSeq Size: 916
||RefSeq ORF: 708|
|Synonyms : ARD1; ARD1A; ARD1P; DXS707; NATD; TE2|
|Summary: N-alpha-acetylation is among the most common post-translational protein modifications in eukaryotic cells. This process involves the transfer of an acetyl group from acetyl-coenzyme A to the alpha-amino group on a nascent polypeptide and is essential for normal cell function. This gene encodes an N-terminal acetyltransferase that functions as the catalytic subunit of the major amino-terminal acetyltransferase A complex. Mutations in this gene are the cause of Ogden syndrome. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Jan 2012]. |
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for specific inventory information
**: DDK-tag is the same as FLAG tag. Flag® is a registered trademark of Sigma-Aldrich