Anti-MTCO3 抗体 [DA5BC4] (ab110259)
Key features and details
- Mouse monoclonal [DA5BC4] to MTCO3
- Suitable for: WB
- Reacts with: Mouse, Rat, Human, Saccharomyces cerevisiae
- Isotype: IgG2a
製品の概要
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製品名
Anti-MTCO3 antibody [DA5BC4] -
製品の詳細
Mouse monoclonal [DA5BC4] to MTCO3 -
由来種
Mouse -
アプリケーション
適用あり: WBmore details -
種交差性
交差種: Mouse, Rat, Human, Saccharomyces cerevisiae -
免疫原
Full length native protein (purified). This information is considered to be commercially sensitive.
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ポジティブ・コントロール
- Isolated mitochondria from Human , Rat and Mouse hearts.
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特記事項
This antibody clone is manufactured by Abcam. If you require a custom buffer formulation or conjugation for your experiments, please contact orders@abcam.com.
The Life Science industry has been in the grips of a reproducibility crisis for a number of years. Abcam is leading the way in addressing this with our range of recombinant monoclonal antibodies and knockout edited cell lines for gold-standard validation. Please check that this product meets your needs before purchasing.
If you have any questions, special requirements or concerns, please send us an inquiry and/or contact our Support team ahead of purchase. Recommended alternatives for this product can be found below, along with publications, customer reviews and Q&As
Product was previously marketed under the MitoSciences sub-brand.
製品の特性
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製品の状態
Liquid -
保存方法
Shipped at 4°C. Store at +4°C. Do Not Freeze. -
バッファー
pH: 7.5
Preservative: 0.02% Sodium azide
Constituent: HEPES buffered saline -
Concentration information loading...
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精製度
IgG fraction -
特記事項(精製)
ab110259 was produced in vitro using hybridomas grown in serum-free medium, and then purified by biochemical fractionation. Near homogeneity ab110259 was judged as near homogeneity by SDS-PAGE. -
ポリ/モノ
モノクローナル -
クローン名
DA5BC4 -
アイソタイプ
IgG2a -
軽鎖の種類
kappa -
研究分野
関連製品
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Compatible Secondaries
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Isotype control
アプリケーション
The Abpromise guarantee
Abpromise保証は、 次のテスト済みアプリケーションにおけるab110259の使用に適用されます
アプリケーションノートには、推奨の開始希釈率がありますが、適切な希釈率につきましてはご検討ください。
アプリケーション | Abreviews | 特記事項 |
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WB | (3) |
Use a concentration of 2 - 4 µg/ml. Predicted molecular weight: 30 kDa.
Due to the hydrophobic nature of this protein, it is recommended that the WB is performed on a PVDF membrane with a 90 minute CAPS-buffer transfer. |
特記事項 |
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WB
Use a concentration of 2 - 4 µg/ml. Predicted molecular weight: 30 kDa. Due to the hydrophobic nature of this protein, it is recommended that the WB is performed on a PVDF membrane with a 90 minute CAPS-buffer transfer. |
ターゲット情報
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機能
Subunits I, II and III form the functional core of the enzyme complex. -
関連疾患
Defects in MT-CO3 are a cause of Leber hereditary optic neuropathy (LHON) [MIM:535000]. LHON is a maternally inherited disease resulting in acute or subacute loss of central vision, due to optic nerve dysfunction. Cardiac conduction defects and neurological defects have also been described in some patients. LHON results from primary mitochondrial DNA mutations affecting the respiratory chain complexes.
Defects in MT-CO3 are a cause of mitochondrial complex IV deficiency (MT-C4D) [MIM:220110]; also known as cytochrome c oxidase deficiency. A disorder of the mitochondrial respiratory chain with heterogeneous clinical manifestations, ranging from isolated myopathy to severe multisystem disease affecting several tissues and organs. Features include hypertrophic cardiomyopathy, hepatomegaly and liver dysfunction, hypotonia, muscle weakness, excercise intolerance, developmental delay, delayed motor development and mental retardation. A subset of patients manifest Leigh syndrome.
Defects in MT-CO3 are associated with recurrent myoglobinuria mitochondrial (RM-MT) [MIM:550500]. Recurrent myoglobinuria is characterized by recurrent attacks of rhabdomyolysis (necrosis or disintegration of skeletal muscle) associated with muscle pain and weakness, and followed by excretion of myoglobin in the urine. -
配列類似性
Belongs to the cytochrome c oxidase subunit 3 family. -
細胞内局在
Mitochondrion inner membrane. - Information by UniProt
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参照データベース
- Entrez Gene: 4514 Human
- Entrez Gene: 17710 Mouse
- Entrez Gene: 26204 Rat
- Omim: 516050 Human
- SwissProt: P00414 Human
- SwissProt: P00416 Mouse
- SwissProt: P05505 Rat
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別名
- COIII antibody
- COX3 antibody
- COX3_HUMAN antibody
see all
画像
データシートおよび資料
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SDS download
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Datasheet download
参考文献 (42)
ab110259 は 42 報の論文で使用されています。
- Xu M et al. Identification of a Novel Variant in MT-CO3 Causing MELAS. Front Genet 12:638749 (2021). PubMed: 34054915
- Verma Y et al. MRX8, the conserved mitochondrial YihA GTPase family member, is required for de novo Cox1 synthesis at suboptimal temperatures in Saccharomyces cerevisiae. Mol Biol Cell 32:ar16 (2021). PubMed: 34432493
- Dietz JV et al. Mitochondrial contact site and cristae organizing system (MICOS) machinery supports heme biosynthesis by enabling optimal performance of ferrochelatase. Redox Biol 46:102125 (2021). PubMed: 34517185
- Fan W et al. FARS2 deficiency in Drosophila reveals the developmental delay and seizure manifested by aberrant mitochondrial tRNA metabolism. Nucleic Acids Res 49:13108-13121 (2021). PubMed: 34878141
- Esparza-Moltó PB et al. Generation of mitochondrial reactive oxygen species is controlled by ATPase inhibitory factor 1 and regulates cognition. PLoS Biol 19:e3001252 (2021). PubMed: 33983919