Total OXPHOS Rodent WB抗体Cocktail (ab110413)
Key features and details
- Assay type: Semi-quantitative
概述
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产品名称
Total OXPHOS Rodent WB抗体Cocktail -
检测类型
Semi-quantitative -
种属反应性
与反应: Mouse, Rat, Cow, Human, Cynomolgus monkey -
产品概述
Total OXPHOS Rodent WB Antibody Cocktail ab110413 is an optimized cocktail of high quality antibodies for analyzing relative levels of OXPHOS complexes in rat or mouse mitochondria by western blot.
This OXPHOS cocktail contains 5 mouse mAbs, one each against CI subunit NDUFB8 (ab110242), CII-30kDa (ab14714), CIII-Core protein 2 (ab14745), CIV subunit I (ab14705) and CV alpha subunit (ab14748) as an optimized premixed cocktail. The kit is suitable for Western Blotting analysis of the relative levels of the 5 OXPHOS complexes in mitochondrial preparations from mouse, rat, human, or bovine sources. The positive control supplied with the cocktail is ab110341.
Altered levels of assembly can arise from mutations in individual subunits, mutations in assembly factors for the complex(es), mtDNA depletion or as a result of physiological and or pathological changes e.g. hormone treatment, exercise, diet or oxidative stress.
The mAbs in the cocktail were chosen because they are each against a subunit that is labile when its complex is not assembled. Also, the different subunits are easily resolved in SDS-PAGE (see protocols).
Note: Mouse tissue samples can easily be contaminated with antibodies from the animal's blood. To avoid background bands, use ab110413 with an anti-mouse secondary against native antibodies. Also, COXI is a highly hydrophobic protein and appears as a broad band at ~35 kDa (not at its true molecular weight at 57 kDa). It is very sensitive to heating. Therefore, the samples, including the positive control, should not be heated over 50°C before loaded on the gel.
The Western blot cocktail is supplied at a concentration of 1.5 mg/mL.
We recommend using a high pH CAPS / PVDF transfer protocol when using this antibody for Western blot.
Store the antibody cocktail at 4°C and the control sample at -80°C.
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说明
Related products
Review the mitochondrial assay guide, or the full metabolism assay guide to learn about more assays for metabolites, metabolic enzymes, mitochondrial function, and oxidative stress, and also how to assay metabolic function in live cells using your plate reader.
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经测试应用
适用于: WBmore details
性能
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存放说明
Store at -80°C. Please refer to protocols. -
组件 300 µg Cocktail of 5 Antibodies 1 x 300µg Rat Heart Mitochondria Western Blot Control 1 x 50µg -
研究领域
相关产品
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Positive Controls
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Related Products
应用
The Abpromise guarantee
Abpromise™承诺保证使用ab110413于以下的经测试应用
“应用说明”部分 下显示的仅为推荐的起始稀释度；实际最佳的稀释度/浓度应由使用者检定。
| 应用 | Ab评论 | 说明 |
|---|---|---|
| WB |
Use at an assay dependent concentration.
The antibody cocktail (1.5 mg/mL) should be diluted 250x to a final working concentration of 6.0 µg/mL for Western blotting. We recommend using PBS with 1% milk as the antibody diluent. Store the antibody cocktail at 4°C and the control sample at -80°C. We recommend using a high pH CAPS / PVDF transfer protocol when using this antibody for Western blot. Please contact us for more details. |
| 说明 |
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WB
Use at an assay dependent concentration. The antibody cocktail (1.5 mg/mL) should be diluted 250x to a final working concentration of 6.0 µg/mL for Western blotting. We recommend using PBS with 1% milk as the antibody diluent. Store the antibody cocktail at 4°C and the control sample at -80°C. We recommend using a high pH CAPS / PVDF transfer protocol when using this antibody for Western blot. Please contact us for more details. |
图片
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Western blot - MitoProfile® Total OXPHOS Rodent WB Antibody Cocktail (ab110413)
Rat liver mitochondria labeled with ab110413 (MS604). The sample in lane 1 was kept at room temperature, whereas the remaining three samples were heated to 37°C, 50°C, and 100°C, respectively. This blot shows that boiling of samples leads to a decrease in signal due to aggregation of proteins therefore heating samples at or close to boiling is not recommended.
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AbReviewThis image is courtesy of Aida AdlimoghaddamIsolated mitochondria from mice brain (control and Alzheimer’s disease (AD)) labeled with ab110413 at 1/1000 dilution in 5% BSA.
This image shows NADH dehydrogenase beta subcomplex subunit 8 of Complex I (NDUFB8), succinate dehydrogenase subunit B of Complex II (SDHB), cytochrome c oxidase subunit 1 of Complex IV (MTCO1), cytochrome b-c1 complex subunit 2 of Complex III (UQCRC2) and ATP synthase subunit alpha of Complex V (ATP5A).
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CI subunit NDUFB8 (ab110242)Isolated mitochondria from heart of human (5 µg - Lane 1), cow (1 ug - Lane 2), rat (10 µg - Lane 3), mouse (10 µg - Lane 4) labeling CI subunit NDUFB8 with ab110242 at 0.5 ug/ml.
Extra bands in the mouse sample (lane 4) are due to the reaction of the IgG-specific goat anti-mouse secondary antibody with residual mouse blood in the heart tissue, as it is very difficult to entirely remove the blood from these small organs.
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CII-30kDa (ab14714)Isolated mitochondria from heart of human (5 µg - Lane 1), cow (1 ug - Lane 2), rat (10 µg - Lane 3), mouse (10 µg - Lane 4), HepG2 (human liver hepatocellular carcinoma cell line) whole cell lysate (20 µg -Lane 5) labeling CII-30kDa with ab14714 at 5 µg/mL. Secondary antibody is a goat anti-mouse antibody.
Extra bands in the mouse sample (lane 4) are due to the reaction of the IgG-specific goat anti-mouse secondary antibody with residual mouse blood in the heart tissue, as it is very difficult to entirely remove the blood from these small organs.
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CIII-Core protein 2 (ab14745)Human skeletal muscle tissue lysate, (10 µg - Lane 1) and Ramos (human Burkitt's lymphoma cell line) whole cell lysate (10 µg - Lane 2) labeling CIII-Core protein 2 with ab14745 at 5 µg/mL. Secondary antibody is a goat polyclonal to Mouse IgG - H&L - Pre-Adsorbed (HRP), 1/3000 dilution.
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CIV subunit I (ab14705)Isolated mitochondria from heart of human (5 µg - Lane 1), cow (1 ug - Lane 2), rat (10 µg - Lane 3), mouse (5 µg - Lane 4) labeling CIV subunit I with ab14705 at 0.5 µg/mL. Secondary antibody is a goat anti-mouse antibody.
Extra bands in the mouse sample (lane 4) are due to the reaction of the IgG-specific goat anti-mouse secondary antibody with residual mouse blood in the heart tissue, as it is very difficult to entirely remove the blood from these small organs.
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CV alpha subunit (ab14748)Isolated mitochondria from heart of human (10 µg - Lane 1), cow (4 µg - Lane 2), rat (10 µg - Lane 3), mouse (10 µg - Lane 4), HepG2 (human liver hepatocellular carcinoma cell line) whole cell lysate (20 µg -Lane 5) labeling CV alpha subunit with ab14748 at 1 µg/mL
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CV alpha subunit (ab14748)Human liver tissue lysate, (10 µg - Lane 1) and HepG2 (human liver hepatocellular carcinoma cell line) whole cell lysate (10 µg - Lane 2) labeling CV alpha subunit with ab14748 at 1 µg/mL. Secondary antibody is a goat polyclonal to Mouse IgG - H&L - Pre-Adsorbed (HRP), 1/3000 dilution.
实验方案
To our knowledge, customised protocols are not required for this product. Please try the standard protocols listed below and let us know how you get on.
数据表及文件
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SDS download
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Datasheet download
文献 (1208)
ab110413 被引用在 1208 文献中.
- Kosik B et al. Actovegin improves skeletal muscle mitochondrial respiration and functional aerobic capacity in a type 1 diabetic male murine model. Appl Physiol Nutr Metab 49:265-272 (2024). WB ; Mouse . PubMed: 37913525
- Zhu F et al. Hypomethylating agent decitabine sensitizes diffuse large B-cell lymphoma to venetoclax. Haematologica 109:186-199 (2024). PubMed: 37534528
- Eisenbaum M et al. ApoE4 expression disrupts tau uptake, trafficking, and clearance in astrocytes. Glia 72:184-205 (2024). PubMed: 37668005
- Moschandrea C et al. Mitochondrial dysfunction abrogates dietary lipid processing in enterocytes. Nature 625:385-392 (2024). PubMed: 38123683
- Brownstein AJ et al. Mitochondria isolated from lipid droplets of white adipose tissue reveal functional differences based on lipid droplet size. Life Sci Alliance 7:N/A (2024). PubMed: 38056907