NDUFS1 (NM_005006) Human Mass Spec Standard

CAT#: PH305506

NDUFS1 MS Standard C13 and N15-labeled recombinant protein (NP_004997)



  View other "NDUFS1" 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 1, 75kDa (NADH-coenzyme Q reductase) (NDUFS1), nuclear gene encoding mitochondrial protein
    • 100 ug

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Rabbit Polyclonal Anti-NDUFS1 Antibody
    • 100 ul

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Specifications

Product Data
Description NDUFS1 MS Standard C13 and N15-labeled recombinant protein (NP_004997)
Species Human
Expression Host HEK293
Expression cDNA Clone or AA Sequence RC205506
Predicted MW 79.44 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_004997
RefSeq Size 3417
RefSeq ORF 2181
Synonyms CI-75k; CI-75Kd; MC1DN5; PRO1304
Locus ID 4719
Cytogenetics 2q33.3
Summary The protein encoded by this gene belongs to the complex I 75 kDa subunit family. Mammalian complex I is composed of 45 different subunits. It locates at the mitochondrial inner membrane. This protein has NADH dehydrogenase activity and oxidoreductase activity. It transfers electrons from NADH to the respiratory chain. The immediate electron acceptor for the enzyme is believed to be ubiquinone. This protein is the largest subunit of complex I and it is a component of the iron-sulfur (IP) fragment of the enzyme. It may form part of the active site crevice where NADH is oxidized. Mutations in this gene are associated with complex I deficiency. Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jan 2011]
Protein Pathways Alzheimer's disease, Huntington's disease, Metabolic pathways, Oxidative phosphorylation, Parkinson's disease
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