Products Antibodies Monoclonal Antibodies Anti-NDUFB9 Rabbit Monoclonal Antibody for WB, IHC-P, ELISA - Q9Y6M9
Anti-NDUFB9 Rabbit Monoclonal Antibody for WB, IHC-P, ELISA - Q9Y6M9

Monoclonal Antibodies

Anti-NDUFB9 Rabbit Monoclonal Antibody for WB, IHC-P, ELISA - Q9Y6M9

Item Number : CM0002250

Price varies based on specs and customizations


Application
WB, IHC-P, ELISA
Cross Reactivity
Human, Mouse, Rat
Protein Weight
22kDa
ISO & CE icon

Shipping:

Contact us to get shipping details Enjoy On-time Dispatch Guarantee.

View Specs

Why Choose Us

Easy ordering process, quality products, and dedicated support for your business success.

Easy Process Quality Assured Dedicated Support

Core Product Specifications and Parameters

Parameter Value
Product Name NDUFB9 Rabbit mAb
Remarks/Alias B22; LYRM3; CI-B22; UQOR22; NDUFB9
Species Human
GeneID (Human) 4715
GeneID 4715
Immunogen Recombinant protein corresponding to amino acids 80-170 of human NDUFB9 (Q9Y6M9)
Source Rabbit
Category Monoclonal Antibodies
Application WB, IHC-P, ELISA
Cross Reactivity Human, Mouse, Rat
SWISS Q9Y6M9
Protein Weight 22kDa
Shipping Ice bag

Biological Background: NDUFB9 Function and Localization

  • NDUFB9, also known as CI-B22 or LYRM3, is a nuclear-encoded accessory subunit of the mitochondrial NADH dehydrogenase complex (Complex I) that is not directly involved in catalysis but is essential for complex assembly or stability.
  • Complex I transfers electrons from NADH to ubiquinone in the respiratory chain, coupling this process to proton translocation across the inner mitochondrial membrane; NDUFB9 assists in maintaining this electron transfer chain.
  • As a member of the LYR motif-containing protein family, NDUFB9 features a conserved LYR domain that may mediate protein-protein interactions within the complex.
  • The protein is anchored to the mitochondrial inner membrane, where Complex I is embedded, positioning it within the oxidative phosphorylation machinery.
  • Post-translational modifications include acetylation and phosphorylation, which may regulate Complex I activity or assembly dynamics under metabolic conditions.
  • Mutations in NDUFB9 have been associated with primary mitochondrial disease, specifically Complex I deficiency, underscoring its clinical relevance in metabolic disorders.

Experimental Guidance and Technical Tips

  • The immunogen corresponds to residues 80-170 of human NDUFB9, a region that is likely well-conserved across species, consistent with reported cross-reactivity with mouse and rat. Consider Western blot sample preparation with mitochondrial-enriched fractions to enhance signal.
  • For IHC-P, antigen retrieval methods and tissue fixation conditions may impact antibody binding; validate in both frozen and paraffin-embedded sections from relevant tissues.
  • In ELISA, the antibody can be used as a capture or detection reagent; pairing with a compatible secondary antibody is recommended, and optimal dilutions should be determined empirically.

CamelBio: Your One-Stop Sourcing Bridge

CamelBio connects diagnostic manufacturers and researchers with validated raw materials for mitochondrial biology and metabolic research. We offer this anti-NDUFB9 rabbit monoclonal antibody alongside complementary reagents—including antibody pairs, bulk ancillary proteins, and custom sourcing for rare targets—to streamline your assay development pipeline.

View more faqs for this product

Product Datasheet

Anti-NDUFB9 Rabbit Monoclonal Antibody for WB, IHC-P, ELISA - Q9Y6M9


REQUEST A QUOTE

Our professional team will reply to you within one business day. Please feel free to contact us!