Anti-MT-ND5 Rabbit Polyclonal Antibody

Product#: SB-GB112639
$779.20
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Anti-MT-ND5 Rabbit Polyclonal Antibody

 

General information 

Cat. No. SB-GB112639
Size :100 uL
Protein full name NADH-ubiquinone oxidoreductase chain 5
Synonym NADH dehydrogenase subunit 5, Mtnd5, mt-Nd5, Nd5
Immunogen KLH conjugated Synthetic peptide corresponding to Mouse MT-ND5
Isotype IgG
Purity Affinity purification
Subcellular location Mitochondrion
Predicted MW. 68 kDa
Observed MW. 68 kDa
Uniprot ID P03921P11661
Long Term Storage -20 ℃ or below 
Shipping Condition  Dry Ice
Storage Buffer PBS with 0.02% sodium azide,100 μg/ml BSA and 50% glycerol.


Application
 
Applications Species Dilution Positive Tissue
WB Mouse, Rat 1: 1000-1: 2000

liver, brain

IF Human, Rat 1: 400-1: 800

lung, kidney, para-cancer lung



Description


ND5 belongs to the complex I subunit 1 family. ND5 is a core subunit of the mitochondrial membrane respiratory chain NADH dehydrogenase (Complex I) that is believed to belong to the minimal assembly required for catalysis. Complex I functions in the transfer of electrons from NADH to the respiratory chain. The immediate electron acceptor for the enzyme is believed to be ubiquinone.

 
GB112639-1.png

Western blot analysis of MT-ND5 (GB112639) at dilution of 1: 2000

Lane 1: Mouse liver tissue lysate

Lane 2: Mouse brain tissue lysate

Lane 3: Rat liver tissue lysate

GB112639-2.png
Immunofluorescent analysis of paraformaldehyde-fixed human para-cancer lung using MT-ND5 (GB112639) at dilution of 1: 800
GB112639-3.png

Immunofluorescent analysis of paraformaldehyde-fixed rat lung using MT-ND5 (GB112639) at dilution of 1: 800

GB112639-4.png

Immunofluorescent analysis of paraformaldehyde-fixed rat kidney using MT-ND5 (GB112639) at dilution of 1: 800

 

Antigen Characterization 
  • Type: Primary
  • Application: ELISA,Western Blot,IF
  • Species: Human
  • Recombinant: Yes

Human Diseases
  • Leber Hereditary Optic Neuropathy (LHON): A genetic condition leading to vision loss due to mitochondrial dysfunction.
  • Mitochondrial Myopathy: Disorders affecting muscle function due to impaired energy production.
  • Leigh Syndrome: A severe neurological disorder characterized by progressive loss of mental and movement abilities.
  • MELAS Syndrome: Mitochondrial Encephalomyopathy, Lactic Acidosis, and Stroke-like episodes

Cellular Signaling Pathways
  • Respiratory Electron Transport Chain: Integral to ATP production through oxidative phosphorylation.
  • Complex I Biogenesis: Involvement in the assembly and maintenance of mitochondrial complex I, crucial for cellular energy metabolism.
  • NADH to Ubiquinone Activity: Facilitates electron transfer essential for metabolic processes.

Aliases for MT-ND5 Gene
  • Mitochondrially Encoded NADH:Ubiquinone Oxidoreductase Core Subunit 5 2 5
  • ND5 2 3 4 5
  • MTND5 3 4 5
  • NADH-Ubiquinone Oxidoreductase Chain 5 2 4
  • NADH Dehydrogenase Subunit 5 3 4
  • NAD5 2 5
  • Mitochondrially Encoded NADH Dehydrogenase 5 2
  • Complex I ND5 Subunit 2
  • NADH Dehydrogenase 5 2
  • EC 7.1.1.2 4
  • EC 1.6.5.3 48
  • NADH5 4
References 
  • MT-ND5 Mitochondrially Encoded NADH Dehydrogenase 5 [Homo Sapiens (Human)] - Gene - NCBI.” National Center for Biotechnology Information, U.S. National Library of Medicine, www.ncbi.nlm.nih.gov/gene?Cmd=DetailsSearch&Db=gene&Term=4540. 
  • MT-ND5 NADH Dehydrogenase 5, Mitochondrial [Mus Musculus (House Mouse)] - Gene - NCBI.” National Center for Biotechnology Information, U.S. National Library of Medicine, www.ncbi.nlm.nih.gov/gene?Cmd=DetailsSearch&Db=gene&Term=17721. 
  • MT-ND5 Mutation Exhibits Highly Variable Neurological Manifestations at Low Mutant Load - Ebiomedicine, www.thelancet.com/article/S2352-3964(18)30064-1/fulltext. 
  • Database, Rat Genome. MT-ND5 (NADH Dehydrogenase 5, Mitochondrial) - Rat Genome Database, rgd.mcw.edu/rgdweb/report/gene/main.html?id=736401. 
  • Pignataro, Daniela, et al. “A Missense MT-ND5 Mutation in Differentiated Parkinson Disease Cytoplasmic Hybrid Induces ROS-Dependent DNA Damage Response Amplified by Drosha.” Nature News, Nature Publishing Group, 25 Aug. 2017, www.nature.com/articles/s41598-017-09910-x. 
 

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