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NDUFB9 Polyclonal Antibody

NDUFB9 Polyclonal Antibody

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Specification

Product name NDUFB9 Polyclonal Antibody
Immunogen Synthesized peptide derived from the Internal region of human NDUFB9 at AA range: 80-160
Host Rabbit
Reactivity Human,Mouse
Applications WB,IHC,IF,ELISA
Applications notes Optimal working dilutions should be determined experimentally by the investigator. Suggested starting dilutions are as follows: WB 1:500-1:2000;IHC 1:100-1:300;ELISA 1:10000;IF 1:50-200
Clonality Polyclonal
Preparation method The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
Alternative NDUFB9; LYRM3; UQOR22; NADH dehydrogenase [ubiquinone] 1 beta subcomplex subunit 9; Complex I-B22; CI-B22; LYR motif-containing protein 3; NADH-ubiquinone oxidoreductase B22 subunit

Product Properties

Formulation Liquid solution
Concentration 1 mg/ml
Molecular weight 22kD
Storage buffer Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
Storage instructions Stable for one year at -20°C from date of shipment. For maximum recovery of product, centrifuge the original vial after thawing and prior to removing the cap. Aliquot to avoid repeated freezing and thawing.
Shipping Gel pack with blue ice.
Precautions The product listed herein is for research use only and is not intended for use in human or clinical diagnosis. Suggested applications of our products are not recommendations to use our products in violation of any patent or as a license. We cannot be responsible for patent infringements or other violations that may occur with the use of this product.

Additional Information

Background NADH dehydrogenase [ubiquinone] 1 beta subcomplex subunit 10 encoded by NDUFB9 is a subunit of the mitochondrial oxidative phosphorylation complex I (nicotinamide adenine dinucleotide: ubiquinone oxidoreductase). Complex I is localized to the inner mitochondrial membrane and functions to dehydrogenate nicotinamide adenine dinucleotide and to shuttle electrons to coenzyme Q. Complex I deficiency is the most common defect found in oxidative phosphorylation disorders and results in a range of conditions, including lethal neonatal disease, hypertrophic cardiomyopathy, liver disease, and adult-onset neurodegenerative disorders. Pseudogenes of this gene are found on chromosomes five, seven and eight. Alternative splicing results in multiple transcript variants.
Gene ID 4715
Alternative NDUFB9; LYRM3; UQOR22; NADH dehydrogenase [ubiquinone] 1 beta subcomplex subunit 9; Complex I-B22; CI-B22; LYR motif-containing protein 3; NADH-ubiquinone oxidoreductase B22 subunit
Others NDUFB9 Polyclonal Antibody detects endogenous levels of NDUFB9 protein.
Accession Q9Y6M9
Observed Band(KD) 22

Image & description

Fig.1. Western Blot analysis of various cells using NDUFB9 Polyclonal Antibody diluted at 1:500.

Fig.1. Western Blot analysis of various cells using NDUFB9 Polyclonal Antibody diluted at 1:500.

Fig.2. Western Blot analysis of 293 cells using NDUFB9 Polyclonal Antibody diluted at 1:500.

Fig.2. Western Blot analysis of 293 cells using NDUFB9 Polyclonal Antibody diluted at 1:500.

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