Catalog No.
YHC03301
Expression system
E. coli
Species
Homo sapiens (Human)
Protein length
Phe19-Leu84
Predicted molecular weight
34.13 kDa
Nature
Recombinant
Endotoxin level
Please contact with the lab for this information.
Purity
>90% as determined by SDS-PAGE.
Accession
P03886
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
MT-ND1, NADH1, MTND1, NADH-ubiquinone oxidoreductase chain 1, ND1, NADH dehydrogenase subunit 1
Protective Effects of Rat Bone Marrow Mesenchymal Stem Cells-Derived Fusogenic Plasma Membrane Vesicles Containing VSVG Protein Mediated Mitochondrial Transfer on Myocardial Injury In Vitro., PMID:40330432
Ellagic acid maintains post-thaw goat sperm quality via protecting mitochondrial function from ROS damage., PMID:40132303
Q-Der: a next-generation CoQ10 analogue supercharging neuroprotection by combating oxidative stress and enhancing mitochondrial function., PMID:40070687
A high-resolution bovine mitochondrial co-expression network., PMID:39898529
Research on the mechanism of eugenol in the treatment of liver cancer based on network pharmacology, molecular docking technology, and in vitro experiments., PMID:39786976
Respiratory Chain Complex I Deficiency in Leber Hereditary Optic Neuropathy: Insights from Ophthalmologic and Molecular Investigations in Tunisia., PMID:39578757
Diabetes mellitus disrupts lncRNA Malat1 regulation of cardiac mitochondrial genome-encoded protein expression., PMID:39453425
Bladder cancer associated with elevated heavy metals: Investigation of probable carcinogenic pathways through mitochondrial dysfunction, oxidative stress and mitogen-activated protein kinase., PMID:39379209
Dysregulation of mitochondria, apoptosis and mitophagy in Leber's hereditary optic neuropathy with MT-ND1 3635G>A mutation., PMID:39147111
The predictive value of peripheral blood cell mitochondrial gene expression in identifying the prognosis in pediatric sepsis at preschool age., PMID:39113822
Vibration Emissions Reduce Boar Sperm Quality via Disrupting Its Metabolism., PMID:38927250
Cell-free DNA in patients with sepsis: long term trajectory and association with 28-day mortality and sepsis-associated acute kidney injury., PMID:38803503
Cardioprotective Potential of Cymbopogon citratus Essential Oil against Isoproterenol-induced Cardiomyocyte Hypertrophy: Possible Involvement of NLRP3 Inflammasome and Oxidative Phosphorylation Complex Subunits., PMID:38639827
Mitochondrial variants of complex I genes associated with leprosy clinical subtypes., PMID:38493220
Digenic Leigh syndrome on the background of the m.11778G>A Leber hereditary optic neuropathy variant., PMID:38478578
Ribosome Profiling and Mass Spectrometry Reveal Widespread Mitochondrial Translation Defects in a Striatal Cell Model of Huntington Disease., PMID:38447791
Alterations in leukocyte telomere length and mitochondrial DNA copy number in benzene poisoning patients., PMID:38372835
Dramatic genome-wide reprogramming of mRNA in hypometabolic muscle., PMID:38355035
Mitochonic Acid 5 Increases Ram Sperm Quality by Improving Mitochondrial Function during Storage at 4 °C., PMID:38338011
Genetic variants affecting NQO1 protein levels impact the efficacy of idebenone treatment in Leber hereditary optic neuropathy., PMID:38272025
Differential Modulation of Mouse Intestinal Organoids with Fecal Luminal Factors from Obese, Allergic, Asthmatic Children., PMID:38255939
Pyrroloquinoline Quinone Improves Ram Sperm Quality through Its Antioxidative Ability during Storage at 4 °C., PMID:38247528
Multi-level profiling unravels mitochondrial dysfunction in myotonic dystrophy type 2., PMID:38240888
Jianpi-Yangxue-Jiedu decoction improves the energy metabolism of psoriasis mice by regulating the electron transfer of oxidative phosphorylation., PMID:38184027
Dangua Fang regulating tricarboxylic acid cycle and respiratory chain and its mechanism in diabetic rats., PMID:37946477
Effect of prolactin on cytotoxicity and oxidative stress in ovine ovarian granulosa cells., PMID:37456891
Mitochondria-wide association study observed significant interactions of mitochondrial respiratory and the inflammatory in the development of anxiety and depression., PMID:37344456
Identification of a New RNA and Protein Integrated Biomarker Panel Associated with Kidney Function Impairment in DKD: Translational Implications., PMID:37298364
Cardiovascular-related proteomic changes in ECFCs exposed to the serum of COVID-19 patients., PMID:37063416
Mitochondria and cytochrome components released into the plasma of severe COVID-19 and ICU acute respiratory distress syndrome patients., PMID:37031181
De novo frameshift variant in MT-ND1 causes a mitochondrial complex I deficiency associated with MELAS syndrome., PMID:36717040
Mitochondrial mutations in protein coding genes of respiratory chain including complexes IV, V, and mt-tRNA genes are associated risk factors for congenital heart disease., PMID:36483916
Down regulation of NDUFS1 is involved in the progression of parenteral-nutrition-associated liver disease by increasing Oxidative stress., PMID:36402252
Aberrant RNA processing contributes to the pathogenesis of mitochondrial diseases in trans-mitochondrial mouse model carrying mitochondrial tRNALeu(UUR) with a pathogenic A2748G mutation., PMID:35998911
REM-Sleep Deprivation Induces Mitochondrial Biogenesis in the Rat Hippocampus., PMID:35738625
Co-expression analysis to identify key modules and hub genes associated with COVID-19 in platelets., PMID:35421970
miR-669a-5p promotes adipogenic differentiation and induces browning in preadipocytes., PMID:35094659
The serotonin reuptake transporter modulates mitochondrial copy number and mitochondrial respiratory complex gene expression in the frontal cortex and cerebellum in a sexually dimorphic manner., PMID:35043462
[Risk of Multiple Sclerosis: Analysis of Interactions Between Variants of Nuclear and Mitochondrial Genomes]., PMID:34837699
Identification of a novel m.3955G > A variant in MT-ND1 associated with Leigh syndrome., PMID:34656796
Leber's hereditary optic neuropathy: Current approaches and future perspectives on Mesenchymal stem cell-mediated rescue., PMID:34454075
Pathogenic SLIRP variants as a novel cause of autosomal recessive mitochondrial encephalomyopathy with complex I and IV deficiency., PMID:34426662
Lipotoxicity-induced STING1 activation stimulates MTORC1 and restricts hepatic lipophagy., PMID:34382907
Transcriptional Changes after Enniatins A, A1, B and B1 Ingestion in Rat Stomach, Liver, Kidney and Lower Intestine., PMID:34359500
Assocation Between Leber's Hereditary Optic Neuropathy and MT-ND1 3460G>A Mutation-Induced Alterations in Mitochondrial Function, Apoptosis, and Mitophagy., PMID:34311469
Dysfunction in Mitochondrial Electron Transport Chain Complex I, Pyruvate Dehydrogenase Activity, and Mutations in ND1 and ND4 Gene in Autism Spectrum Disorder Subjects from Tamil Nadu Population, India., PMID:34279772
Biochemical consequences of two clinically relevant ND-gene mutations in Escherichia coli respiratory complex I., PMID:34135385
Mitochondrial disease patients with novel ND4 12058A > C and ND1 m.3911A > G variations: implications for a role in the phenotype following a bioinformatic investigation., PMID:34089464
NGS-based mtDNA Profiling Could Reveal Genetic Alterations in Schizophrenia., PMID:34060999
Iterative Reanalysis of Hypertrophic Cardiomyopathy Exome Data Reveals Causative Pathogenic Mitochondrial DNA Variants., PMID:33970670
For research use only. Not for human or drug use.
