NDUFS2 (NM_004550) Human Mass Spec Standard

CAT#: PH303485

NDUFS2 MS Standard C13 and N15-labeled recombinant protein (NP_004541)



  View other "NDUFS2" proteins (3)

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CNY 19,520.00


货期*
4周

规格
    • 10 ug

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经常一起买 (2)
Transient overexpression lysate of NADH dehydrogenase (ubiquinone) Fe-S protein 2, 49kDa (NADH-coenzyme Q reductase) (NDUFS2), nuclear gene encoding mitochondrial protein, transcript variant 1
    • 100 ug

CNY 3,080.00


NDUFS2 mouse monoclonal antibody,clone OTI1D5
    • 100 ul

CNY 1,999.00
CNY 2,700.00

Specifications

Product Data
Description NDUFS2 MS Standard C13 and N15-labeled recombinant protein (NP_004541)
Species Human
Expression Host HEK293
Expression cDNA Clone or AA Sequence RC203485
Predicted MW 52.5 kDa
Protein Sequence
Tag C-Myc/DDK
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
Reference Data
RefSeq NP_004541
RefSeq Size 2059
RefSeq ORF 1389
Synonyms CI-49; MC1DN6
Locus ID 4720
Cytogenetics 1q23.3
Summary The protein encoded by this gene is a core subunit of the mitochondrial membrane respiratory chain NADH dehydrogenase (complex I). Mammalian mitochondrial complex I is composed of at least 43 different subunits, 7 of which are encoded by the mitochondrial genome, and the rest are the products of nuclear genes. The iron-sulfur protein fraction of complex I is made up of 7 subunits, including this gene product. Complex I catalyzes the NADH oxidation with concomitant ubiquinone reduction and proton ejection out of the mitochondria. Mutations in this gene are associated with mitochondrial complex I deficiency. Alternatively spliced transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, Oct 2009]
Protein Pathways Alzheimer's disease, Huntington's disease, Metabolic pathways, Oxidative phosphorylation, Parkinson's disease
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