Catalog No.
YHH35601
Expression system
E. coli
Species
Homo sapiens (Human)
Protein length
Thr19-Leu99
Predicted molecular weight
21.81 kDa
Nature
Recombinant
Endotoxin level
Please contact with the lab for this information.
Purity
>90% as determined by SDS-PAGE.
Accession
Q16718
Applications
ELISA, Immunogen, SDS-PAGE, WB, Bioactivity testing in progress
Form
Lyophilized
Storage buffer
Lyophilized from a solution in PBS pH 7.4, 0.02% NLS, 1mM EDTA, 4% Trehalose, 1% Mannitol.
Reconstitution
Reconstitute in sterile water for a stock solution. A copy of datasheet will be provided with the products, please refer to it for details.
Shipping
In general, proteins are provided as lyophilized powder/frozen liquid. They are shipped out with dry ice/blue ice unless customers require otherwise.
Stability and Storage
Use a manual defrost freezer and avoid repeated freeze thaw cycles. Store at 2 to 8°C for frequent use. Store at -20 to -80°C for twelve months from the date of receipt.
Alternative Names
Complex I subunit B13, Complex I-13kD-B, CI-13kD-B, NADH dehydrogenase [ubiquinone] 1 alpha subcomplex subunit 5, NDUFA5, NADH-ubiquinone oxidoreductase 13 kDa-B subunit
Shared genes and relevant potential molecular linkages between COVID-19 and chronic thromboembolic pulmonary hypertension (CTEPH)., PMID:39891865
Chemoproteomic profiling by bioorthogonal probes to reveal the novel targets of acrylamide in microglia., PMID:39637805
Proteomic signatures of infiltrative gastric cancer by proteomic and bioinformatic analysis., PMID:36438703
Benzo[a]pyrene inhibits testosterone biosynthesis via NDUFA10-mediated mitochondrial compromise in mouse Leydig cells: Integrating experimental and in silico toxicological approaches., PMID:36108438
Characterization of the liver proteome in dairy cows experiencing negative energy balance at early lactation., PMID:34153542
The impact of blood-processing time on the proteome of human peripheral blood mononuclear cells., PMID:33301959
Proteome alterations associated with the oleic acid and cis-9, trans-11 conjugated linoleic acid content in bovine skeletal muscle., PMID:32335295
Rett Syndrome, a Neurodevelopmental Disorder, Whole-Transcriptome, and Mitochondrial Genome Multiomics Analyses Identify Novel Variations and Disease Pathways., PMID:32105570
Whole Genome Analysis of the Red-Crowned Crane Provides Insight into Avian Longevity., PMID:31940721
Hepatocyte miR-33a mediates mitochondrial dysfunction and hepatosteatosis by suppressing NDUFA5., PMID:30324697
Transcriptional profiles of type 2 diabetes in human skeletal muscle reveal insulin resistance, metabolic defects, apoptosis, and molecular signatures of immune activation in response to infections., PMID:27847319
PPARα modulates gene expression profiles of mitochondrial energy metabolism in oral tumorigenesis., PMID:26869356
Mitochondrial Involvement in Vertebrate Speciation? The Case of Mito-nuclear Genetic Divergence in Chameleons., PMID:26590214
Gene microarray analyses for potential biomarkers of single and recurrent venous thromboembolism., PMID:26397997
Moderate hypoxia induces β-cell dysfunction with HIF-1-independent gene expression changes., PMID:25503986
Supernumerary subunits NDUFA3, NDUFA5 and NDUFA12 are required for the formation of the extramembrane arm of human mitochondrial complex I., PMID:24717771
Mitochondrial proteome remodeling in ischemic heart failure., PMID:24548633
Partial complex I deficiency due to the CNS conditional ablation of Ndufa5 results in a mild chronic encephalopathy but no increase in oxidative damage., PMID:24154540
Downregulation of the expression of mitochondrial electron transport complex genes in autism brains., PMID:23088660
Spatial distribution of cellular function: the partitioning of proteins between mitochondria and the nucleus in MCF7 breast cancer cells., PMID:23051583
Decreased expression of genes involved in oxidative phosphorylation in human pancreatic islets from patients with type 2 diabetes., PMID:21775499
Suggestive evidence on the genetic link between mitochondria dysfunction and autism., PMID:21198452
The NADH-ubiquinone oxidoreductase 1 alpha subcomplex 5 (NDUFA5) gene variants are associated with autism., PMID:20825370
Gene expression patterns of oxidative phosphorylation complex I subunits are organized in clusters., PMID:20376309
A serial analysis of gene expression profile of the Alzheimer's disease Tg2576 mouse model., PMID:19760337
Focusing on genomic and phenomic correlations in respiration of non-melanotic skin cancers., PMID:16594175
Identification of NADH dehydrogenase 1 alpha subcomplex 5 capable to transform murine fibroblasts and overexpressed in human cervical carcinoma cell lines., PMID:16329995
Genomic organization of the human complex I 13-kDa subunit gene NDUFA5., PMID:10343126
For research use only. Not for human or drug use.
