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NDUFB9 Polyclonal Antibody
Datasheet   

  • Catalog Number:

    E20-73014

  • Amount:

    100ul

  • Molecular Weight:

    21831Da

  • Applications:

    WB;IHC-p;IF(paraffin section);ELISA

  • Reactivity:

    Human;Rat;Mouse;

  • Purification:

    The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.

  • Immunogen:

    The antiserum was produced against synthesized peptide derived from human NDUFB9. AA range:102-151

  • Source:

    Polyclonal, Rabbit

  • Western Blot analysis of 293 cells using NDUFB9 Polyclonal Antibody diluted at 1:500

  • Gene Name:

    NDUFB9

  • Dilution:

    Western Blot: 1/500 - 1/2000. Immunohistochemistry: 1/100 - 1/300. ELISA: 1/10000. Not yet tested in other applications.

  • Protein Name:

    NADH dehydrogenase [ubiquinone] 1 beta subcomplex subunit 9

  • Human Gene Id:

    4715

  • Human Swiss Prot No:

    Q9Y6M9

  • Mouse Swiss Prot No:

    Q9CQJ8

  • Specificity:

    NDUFB9 Polyclonal Antibody detects endogenous levels of NDUFB9 protein.

  • Formulation:

    Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.

  • Concentration:

    1 mg/ml

  • Storage Stability:

    -20°C/1 year

  • Other Name:

    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

  • Observed Band(KD):

    22

  • Background:

    NADH:ubiquinone oxidoreductase subunit B9(NDUFB9) Homo sapiens The protein encoded by this gene 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. [provided by RefSeq, Jul 2015],

  • Function:

    function:Accessory subunit of the mitochondrial membrane respiratory chain NADH dehydrogenase (Complex I), that is believed to be not involved in 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.,similarity:Belongs to the complex I LYR family.,subunit:Mammalian complex I is composed of 45 different subunits.,

  • Subcellular Location:

    Mitochondrion inner membrane ; Peripheral membrane protein ; Matrix side .

  • Expression:

    Astrocytoma,Brain,Colon adenocarcinoma,Kidney,Placenta,Umbi

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