SKU-Pack Size | Availability | Size | Price | |
EAB11121-30UL | In Stock | 30ul | €115.70 | |
EAB11121-100UL | In Stock | 100ul | €258.70 | |
EAB11121-200UL | In Stock | 200ul | €440.70 |
Please select the country you are in to find your local distributor. |
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Cambiotech | Phone£º+44 (0) 188 448801 |
Lanwades Business Park, | E-mail£ºinfo@cambiotech.com | |
Ireland | Kobenhavn K, Ireland | Web£ºwww.cambiotech.com |
Product Information | |
Applications | WB, IHC-P, IF, ELISA |
Species Reactivity | Human, Mouse |
Host / Isotype | Rabbit IgG |
Clonality | Polyclonal |
Applications Dilutions | WB=1:500-2000¡¡ IHC-P=1:50-300¡¡ IF=1:50-300 |
MW (kDa) | 22 |
Conjugate | Unconjugate |
Specificity | NDUFB9 Rabbit Polyclonal Antibody detects endogenous levels of NDUFB9 protein. |
Purification | Affinity purification |
Concentration | 1mg/ml |
Format | Liquid |
Formulation | In PBS, pH 7.4, containing 0.02% sodium azide,0.5% BSA and 50% glycerol. |
Shipping | Gel Pack |
Storage | Store at -20¡ãC least 1 year from the date of shipment. avoid repeated freeze/thaw cycles. Aliquots may be stored at +4¡ãC for 1-2 weeks. |
Research Use | For Research Use Only. Not Intended for Diagnostic or Therapeutic Use. |
Application Key WB-Western Blot IP-Immunoprecipitation IHC-Immunohistochemistry IHC-P-Immunohistochemistry-Paraffin |
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Reactivity Key H-Human M-Mouse R-Rat Mk-Monkey B-Bovine Pg-Pig Hm-Hamster Dg-Dog C-Chicken X-Xenopus Z-Zebrafish |
Product Bioinformatics | |
Synonym(s) | NADH:ubiquinone oxidoreductase subunit B9; NDUFB9; B22; LYRM3; CI-B22; UQOR22; MC1DN24 |
Gene Aliases | NDUFB9 |
UniProt ID | |
Entrez Gene ID |
Product Description | |
NDUFB9 (NADH dehydrogenase (ubiquinone) 1 beta subcomplex, 9), also known as LYRM3 or B22, 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. |
Product Image Gallery | |
![]() Western blot analysis of extracts on different cells, using NDUFB9 Rabbit Polyclonal Antibody (EAB11121) at 1:1000 dilution. Secondary antibody Goat Anti-Rabbit IgG (H&L)-HRP (EAB21002) at 1:5000 dilution.
Lane1: HEK293 Lane2: COLO205 ![]() Immunohistochemical analysis of paraffin-embedded Human liver cancer tissue, using NDUFB9 Rabbit Polyclonal Antibody (EAB11121) at 1:200 dilution.
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Specific Protocols | |