NDUF3 (NDUFAF3) (NM_199073) Human Mass Spec Standard

SKU PH317754

NDUFAF3 MS Standard C13 and N15-labeled recombinant protein (NP_951047)

Product Data

• Tag: C-Myc/DDK
• Species: Human
• Expression Host: HEK293
• Expression cDNA Clone or AA Sequence: [RC217754]
• Predicted MW: 20.4 kDa
• Protein Sequence:
  Protein Sequence

  >RC217754 protein sequence; Red=Cloning site Green=Tags(s); ; MATALALRSLYRARPSLRCPPVELPWAPRRGHRLSPADDELYQRTRISLLQREAAQAMYIDSYNSRGFMI; NGNRVLGPCALLPHSVVQWNVGSHQDITEDSFSLFWLLEPRIEIVVVGTGDRTERLQSQVLQAMRQRGIA; VEVQDTPNACATFNFLCHEGRVTGAALIPPPGGTSLTSLGQAAQ; ; TRTRPLEQKLISEEDLAANDILDYKDDDDKV
• Purity: > 80% as determined by SDS-PAGE and Coomassie blue staining
• Concentration: >0.05 µg/µL as determined by microplate BCA method
• Labeling Method: Labeled with [U- 13C6, 15N4]-L-Arginine and [U- 13C6, 15N2]-L-Lysine
• Buffer: 25 mM Tris-HCl, 100 mM glycine, pH 7.3
• Storage: Store at -80°C. Avoid repeated freeze-thaw cycles.
• Stability: Stable for 3 months from receipt of products under proper storage and handling conditions.
• Shipping: Dry Ice

Reference Data

• RefSeq: NP_951047
• RefSeq Size: 1021
• RefSeq ORF: 552
• Synonyms: 2P1; C3orf60; E3-3; MC1DN18
• Locus ID: 25915
• UniProt ID: A4FU71
• Cytogenetics: 3p21.31
• Summary: This gene encodes a mitochondrial complex I assembly protein that interacts with complex I subunits. Mutations in this gene cause mitochondrial complex I deficiency, a fatal neonatal disorder of the oxidative phosphorylation system. Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Jul 2009]