ARG42814
anti-NDUFB9 antibody
anti-NDUFB9 antibody for Western blot,IHC-Formalin-fixed paraffin-embedded sections,ICC/IF,Flow cytometry,Immunoprecipitation and Human,Mouse,Rat
Overview
Product Description | Rabbit Polyclonal antibody recognizes NDUFB9 |
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Tested Reactivity | Hu, Ms, Rat |
Tested Application | FACS, ICC/IF, IHC-P, IP, WB |
Host | Rabbit |
Clonality | Polyclonal |
Isotype | IgG |
Target Name | NDUFB9 |
Antigen Species | Human |
Immunogen | Recombinant protein of Human NDUFB9. |
Conjugation | Un-conjugated |
Alternate Names | NADH-ubiquinone oxidoreductase B22 subunit; CI-B22; LYR motif-containing protein 3; B22; NADH dehydrogenase [ubiquinone] 1 beta subcomplex subunit 9; LYRM3; UQOR22; Complex I-B22 |
Application Instructions
Application Suggestion |
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Application Note | * The dilutions indicate recommended starting dilutions and the optimal dilutions or concentrations should be determined by the scientist. | ||||||||||||
Positive Control | Rat brain | ||||||||||||
Observed Size | ~ 23 kDa |
Properties
Form | Liquid |
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Purification | Affinity purified. |
Buffer | 50 nM Tris-Glycine (pH 7.4), 0.15 M NaCl, 0.01% Sodium azide, 40% Glycerol and 0.05% BSA. |
Preservative | 0.01% Sodium azide |
Stabilizer | 40% Glycerol and 0.05% BSA |
Storage Instruction | For continuous use, store undiluted antibody at 2-8°C for up to a week. For long-term storage, aliquot and store at -20°C. Storage in frost free freezers is not recommended. Avoid repeated freeze/thaw cycles. Suggest spin the vial prior to opening. The antibody solution should be gently mixed before use. |
Note | For laboratory research only, not for drug, diagnostic or other use. |
Bioinformation
Database Links |
Swiss-port # Q9CQJ8 Mouse NADH dehydrogenase [ubiquinone] 1 beta subcomplex subunit 9 Swiss-port # Q9Y6M9 Human NADH dehydrogenase [ubiquinone] 1 beta subcomplex subunit 9 |
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Gene Symbol | NDUFB9 |
Gene Full Name | NADH dehydrogenase (ubiquinone) 1 beta subcomplex, 9, 22kDa |
Background | 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 | 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. [UniProt] |
Cellular Localization | Mitochondrion inner membrane; Peripheral membrane protein; Matrix side. [UniProt] |
Calculated MW | 22 kDa |