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| 货号 (SKU) | 包装规格 | 是否现货 | 价格 | 数量 |
|---|---|---|---|---|
| Ab126844-10μl |
10μl |
现货 ![]() |
| |
| Ab126844-50μl |
50μL |
现货 ![]() |
| |
| Ab126844-100μl |
100μL |
现货 ![]() |
| |
| Ab126844-1ml |
1ml |
期货 ![]() |
|
| 产品名称 | SDHA Mouse mAb |
|---|---|
| 别名 | SDHA抗体 | 鼠抗人SDHA 抗体 | 琥珀酸脱氢酶复合体A亚基(SDHA)单克隆抗体 | SDHA 小鼠 mAb |
| 英文别名 | CMD1GG antibody | DHSA_HUMAN antibody | Flavoprotein subunit of complex II antibody | Fp antibody | PGL5 antibody | SDH 2 antibody | SDH1 antibody | SDH2 antibody | SDHA antibody | SDHF antibody | Succinate dehydrogenase [ubiquinone] flavoprotein subunit |
| 规格或纯度 | 无载体, ExactAb™, 无叠氮钠, 已验证, 高性能, 见COA |
| 宿主种属 | 小鼠(Mouse) |
| 特异性 | SDHA |
| 种属反应性 | 人(Human),大鼠(Rat),小鼠(Mouse) |
| 免疫原 | Recombinant SDHA expressed in E.coli (AA 4-300) |
| 阳性对照 | WB: Hep G2, HeLa, MCF7, A549, LNCaP, HEK293, NIH/3T3 and C6 cell lysates. ICC/IF: HeLa cells. |
| 偶联 | Unconjugated |
| 克隆类型 | 单克隆抗体 |
|---|---|
| 克隆号 | C2 |
| Format | Whole IgG |
| 亚型 | Mouse IgG2a |
| 轻链亚型 | kappa |
| SDS-PAGE | 150 kDa |
| 纯化方法 | Protein A and Protein G purified |
| 物理外观 | Liquid |
| 储存缓冲液 | 10mM PBS, 50% Glycerol, 0.05% Proclin 300, pH7.4 |
| 防腐剂 | 0.05% Proclin 300 |
| 浓度 | 见COA |
| 储存温度 | -20°C储存,避免反复冻融 |
| 运输条件 | 超低温冰袋运输 |
| 稳定性与储存 | 4℃ 短期储存(1-2 周)。-20℃长期保存(24 个月)。收货后建议分装。避免冷冻/解冻循环。 |
| 分子类型 | 抗体 |
| 作用机制 | Action Type | target ID | Target Name | Target Type | Target Organism | Binding Site Name | 参考文献 |
|---|
SDHA Mouse mAb (Ab126844) - Western Blot
All lanes: SDHA Mouse mAb (Ab126844) at 1/1000 dilution
Samples: Lysates at 20 µg per lane
Secondary: Goat Anti-Mouse IgG H&L (HRP) (Ab138040) at 1/20000 dilution
Predicted band size: 70 kDa
Observed band size: 66 kDa
Exposure time: 2.5 s
SDHA Mouse mAb (Ab126844) - IF/ICC
FITC staining on IF
Samples: Human HeLa cells
Primary Ab: 30 µg/mL SDHA Mouse mAb (Ab126844)
Second Ab: 2 µg/mL FITC-Linked Caprine Anti-Mouse IgG Polyclonal Antibody.
| 应用名称 | 稀释比例 |
|---|---|
| IF/ICC |
5-30 µg/mL
|
| WB |
0.01-2 µg/mL
|
通过匹配包装上的批号来查找并下载产品的 COA,每批产品都进行了严格的验证,您可放心使用!
| 批号(Lot Number) | 证书类型 | 货号 |
|---|---|---|
| 分析证书 | Ab126844 | |
| 分析证书 | Ab126844 | |
| 分析证书 | Ab126844 |
| 1. Choudhary C, Kumar C, Gnad F, Nielsen ML, Rehman M, Walther TC, Olsen JV, Mann M. (2009) Lysine acetylation targets protein complexes and co-regulates major cellular functions.. Science, 325 (5942): (834-40). [PMID:19608861] |
| 2. G Herma Renkema,Saskia B Wortmann,Roel J Smeets,Hanka Venselaar,Marion Antoine,Gepke Visser,Tawfeg Ben-Omran,Lambert P van den Heuvel,Henri J L M Timmers,Jan A Smeitink,Richard J T Rodenburg. (2014-05-02) SDHA mutations causing a multisystem mitochondrial disease: novel mutations and genetic overlap with hereditary tumors.. European journal of human genetics : EJHG, 23 ((2)): (202-209). [PMID:24781757] |
| 3. Bourgeron, T T and 7 more authors.. (1995) Mutation of a nuclear succinate dehydrogenase gene results in mitochondrial respiratory chain deficiency.. Nature genetics, [PMID:7550341] |
| 4. Hirawake, H H, Wang, H H, Kuramochi, T T, Kojima, S S and Kita, K K.. (1994) Human complex II (succinate-ubiquinone oxidoreductase): cDNA cloning of the flavoprotein (Fp) subunit of liver mitochondria.. Journal of biochemistry, [PMID:7798181] |
| 5. Morris, A A AA, Farnsworth, L L, Ackrell, B A BA, Turnbull, D M DM and Birch-Machin, M A MA.. (1994) The cDNA sequence of the flavoprotein subunit of human heart succinate dehydrogenase.. Biochimica et biophysica acta, (29): [PMID:8142412] |
| 6. Parfait, B B and 5 more authors.. (2000) Compound heterozygous mutations in the flavoprotein gene of the respiratory chain complex II in a patient with Leigh syndrome.. Human genetics, [PMID:10746566] |
| 7. Birch-Machin, M A MA, Taylor, R W RW, Cochran, B B, Ackrell, B A BA and Turnbull, D M DM.. (2000) Late-onset optic atrophy, ataxia, and myopathy associated with a mutation of a complex II gene.. Annals of neurology, [PMID:10976639] |
| 8. Van Coster, Rudy R and 9 more authors.. (2003) Homozygous Gly555Glu mutation in the nuclear-encoded 70 kDa flavoprotein gene causes instability of the respiratory chain complex II.. American journal of medical genetics. Part A, (1): [PMID:12794685] |
| 9. Aboulaich, Nabila N, Vainonen, Julia P JP, Strålfors, Peter P and Vener, Alexander V AV.. (2004) Vectorial proteomics reveal targeting, phosphorylation and specific fragmentation of polymerase I and transcript release factor (PTRF) at the surface of caveolae in human adipocytes.. The Biochemical journal, (15): [PMID:15242332] |
| 10. Schmutz, Jeremy J and 75 more authors.. (2004) The DNA sequence and comparative analysis of human chromosome 5.. Nature, (16): [PMID:15372022] |
| 11. Hao, Huai-Xiang HX and 13 more authors.. (2009) SDH5, a gene required for flavination of succinate dehydrogenase, is mutated in paraganglioma.. Science (New York, N.Y.), (28): [PMID:19628817] |
| 12. Burnichon, Nelly N and 13 more authors.. (2010) SDHA is a tumor suppressor gene causing paraganglioma.. Human molecular genetics, (1): [PMID:20484225] |
| 13. Levitas, Aviva A and 8 more authors.. (2010) Familial neonatal isolated cardiomyopathy caused by a mutation in the flavoprotein subunit of succinate dehydrogenase.. European journal of human genetics : EJHG, [PMID:20551992] |
| 14. Ogura, Masato; Yamaki, Junko; Homma, Miwako K and Homma, Yoshimi.. (2012) Mitochondrial c-Src regulates cell survival through phosphorylation of respiratory chain components.. The Biochemical journal, (15): [PMID:22823520] |
| 15. Alston, Charlotte L CL and 12 more authors.. (2012) Recessive germline SDHA and SDHB mutations causing leukodystrophy and isolated mitochondrial complex II deficiency.. Journal of medical genetics, [PMID:22972948] |
| 16. Sciacovelli, Marco M and 12 more authors.. (2013) The mitochondrial chaperone TRAP1 promotes neoplastic growth by inhibiting succinate dehydrogenase.. Cell metabolism, (4): [PMID:23747254] |
| 17. Helman, Guy G and 13 more authors.. (2016) Magnetic resonance imaging spectrum of succinate dehydrogenase-related infantile leukoencephalopathy.. Annals of neurology, [PMID:26642834] |
| 18. Courage, Carolina C and 6 more authors.. (2017) SDHA mutation with dominant transmission results in complex II deficiency with ocular, cardiac, and neurologic involvement.. American journal of medical genetics. Part A, [PMID:27683074] |
| 19. Lahiri, Amit A, Hedl, Matija M, Yan, Jie J and Abraham, Clara C.. (2017) Human LACC1 increases innate receptor-induced responses and a LACC1 disease-risk variant modulates these outcomes.. Nature communications, (8): [PMID:28593945] |