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SDHA Mouse mAb

    应用:
  • IF/ICC
  • WB
  • 宿主种属: 小鼠(Mouse)
  • 种属反应性: 人(Human), 大鼠(Rat), 小鼠(Mouse)
  • 亚型: Mouse IgG2a
  • 克隆号: C2
  • 偶联: Unconjugated
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库存信息

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货号 (SKU) 包装规格 是否现货 价格 数量
Ab126844-10μl
10μl 现货 Stock Image
Ab126844-50μl
50μL 现货 Stock Image
Ab126844-100μl
100μL 现货 Stock Image
Ab126844-1ml
1ml 期货 Stock Image

基本信息

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

产品属性

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

关联靶点(人)

SDHA Tbio 琥珀酸脱氢酶[泛醌]黄素蛋白亚基,线粒体(Succinate dehydrogenase [ubiquinone] flavoprotein subunit, mitochondrial) (0 活性数据)
活性类型 活性值-log(M) 作用机制 期刊 参考文献(PubMed IDs)

作用机制

作用机制 Action Type target ID Target Name Target Type Target Organism Binding Site Name 参考文献

图片

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

应用名称 稀释比例
IF/ICC

5-30 µg/mL

WB

0.01-2 µg/mL

质检证书(CoA,COO,BSE/TSE 和分析图谱)

C of A & Other Certificates(BSE/TSE, COO):
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找到3个结果

批号(Lot Number) 证书类型 货号
ZJ23F0901138 分析证书 Ab126844
ZJ23F0901139 分析证书 Ab126844
ZJ24F0505914 分析证书 Ab126844

引用文献

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]

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