Description
| 抗体名: | NDUFB9 Antibody (PACO06674) |
| 抗体コード: | PACO06674 |
| サイズ: | 50ug |
| 宿主種: | Rabbit |
| 申し込み: | ELISA, WB, IHC |
| 推奨される希釈: | ELISA:1:10000, WB:1:500-1:2000, IHC:1:100-1:300 |
| 反応性: | Human |
| 免疫原: | Synthesized peptide derived from the Internal region of human NDUFB9. |
| 憲法: | Liquid |
| ストレージバッファ: | Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide. |
| 精製方法: | The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen. |
| 抗体のクローン性: | Polyclonal |
| アイソタイプ: | IgG |
| Conjugate: | Non-conjugated |
 | Western Blot analysis of HELA cells using NDUFB9 Polyclonal Antibody. |
 | Western Blot analysis of 293 cells using NDUFB9 Polyclonal Antibody. |
| シノニム: | NDUFB9; LYRM3; UQOR22; NADH dehydrogenase [ubiquinone] 1 β subcomplex subunit 9; Complex I-B22; CI-B22; LYR motif-containing protein 3; NADH-ubiquinone oxidoreductase B22 subunit |
| UniProt Protein Function: | NDUFB9: 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. Belongs to the complex I LYR family. |
| UniProt Protein Details: | Protein type:Mitochondrial; EC 1.6.5.3; Oxidoreductase; Energy Metabolism - oxidative phosphorylation; EC 1.6.99.3 Chromosomal Location of Human Ortholog: 8q13.3 Cellular Component: mitochondrion; mitochondrial inner membrane; mitochondrial respiratory chain complex I Molecular Function:NADH dehydrogenase (ubiquinone) activity Biological Process: cellular metabolic process; sensory perception of sound; mitochondrial electron transport, NADH to ubiquinone Disease: Mitochondrial Complex I Deficiency |
| NCBI Summary: | 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] |
| UniProt Code: | Q9Y6M9 |
| NCBI GenInfo Identifier: | 8134589 |
| NCBI Gene ID: | 4715 |
| NCBI Accession: | Q9Y6M9.3 |
| UniProt Secondary Accession: | Q9Y6M9,Q9UQE8, B2R8M6, |
| UniProt Related Accession: | Q9Y6M9 |
| Molecular Weight: | 21,831 Da |
| NCBI Full Name: | NADH dehydrogenase |
| NCBI Synonym Full Names: | NADH dehydrogenase (ubiquinone) 1 beta subcomplex, 9, 22kDa |
| NCBI Official Symbol: | NDUFB9 |
| NCBI Official Synonym Symbols: | B22; LYRM3; CI-B22; UQOR22 |
| NCBI Protein Information: | NADH dehydrogenase [ubiquinone] 1 beta subcomplex subunit 9; NADH dehydrogenase [ubiquinone] 1 beta subcomplex subunit 9; complex I-B22; complex I B22 subunit; LYR motif-containing protein 3; NADH-ubiquinone oxidoreductase B22 subunit |
| UniProt Protein Name: | NADH dehydrogenase [ubiquinone] 1 beta subcomplex subunit 9 |
| UniProt Synonym Protein Names: | Complex I-B22; CI-B22; LYR motif-containing protein 3; NADH-ubiquinone oxidoreductase B22 subunit |
| Protein Family: | NADH dehydrogenase |
| UniProt Gene Name: | NDUFB9 |
| UniProt Entry Name: | NDUB9_HUMAN |
