ETFA Antibody
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货号:CSB-PA007844ESR1HU
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规格:¥440
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促销:
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图片:
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Western blot
All lanes: ETFA antibody at 4.34µg/ml
Lane 1: A431 whole cell lysate
Lane 2: Hela whole cell lysate
Lane 3: K562 whole cell lysate
Lane 4: A549 whole cell lysate
Lane 5: HepG2 whole cell lysate
Lane 6: MCF-7 whole cell lysate
Secondary
Goat polyclonal to rabbit IgG at 1/10000 dilution
Predicted band size: 36, 31 kDa
Observed band size: 36 kDa -
Immunohistochemistry of paraffin-embedded human colon cancer using CSB-PA007844ESR1HU at dilution of 1:100
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Immunohistochemistry of paraffin-embedded human kidney tissue using CSB-PA007844ESR1HU at dilution of 1:100
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其他:
产品详情
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产品名称:Rabbit anti-Homo sapiens (Human) ETFA Polyclonal antibody
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Uniprot No.:P13804
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基因名:
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别名:Alpha ETF antibody; Alpha-ETF antibody; Electron transfer flavoprotein alpha polypeptide antibody; Electron transfer flavoprotein alpha subunit antibody; Electron transfer flavoprotein subunit alpha mitochondrial antibody; Electron transfer flavoprotein subunit alpha; mitochondrial antibody; Electron transferring flavoprotein alpha polypeptide antibody; EMA antibody; ETFA antibody; ETFA_HUMAN antibody; GA2 antibody; Glutaric aciduria II antibody
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宿主:Rabbit
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反应种属:Human
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免疫原:Recombinant Human Electron transfer flavoprotein subunit alpha, mitochondrial protein (1-333AA)
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免疫原种属:Homo sapiens (Human)
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标记方式:Non-conjugated
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克隆类型:Polyclonal
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抗体亚型:IgG
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纯化方式:Antigen Affinity Purified
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浓度:It differs from different batches. Please contact us to confirm it.
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保存缓冲液:PBS with 0.02% sodium azide, 50% glycerol, pH7.3.
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产品提供形式:Liquid
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应用范围:ELISA, WB, IHC
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推荐稀释比:
Application Recommended Dilution WB 1:1000-1:5000 IHC 1:20-1:200 -
Protocols:
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储存条件:Upon receipt, store at -20°C or -80°C. Avoid repeated freeze.
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货期:Basically, we can dispatch the products out in 1-3 working days after receiving your orders. Delivery time maybe differs from different purchasing way or location, please kindly consult your local distributors for specific delivery time.
相关产品
靶点详情
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功能:Heterodimeric electron transfer flavoprotein that accepts electrons from several mitochondrial dehydrogenases, including acyl-CoA dehydrogenases, glutaryl-CoA and sarcosine dehydrogenase. It transfers the electrons to the main mitochondrial respiratory chain via ETF-ubiquinone oxidoreductase (ETF dehydrogenase). Required for normal mitochondrial fatty acid oxidation and normal amino acid metabolism.
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基因功能参考文献:
- Data suggest that ETF (heterodimer of ETFA and ETFB) catalyzes irreversible and pH-dependent oxidation of 8alpha-methyl group of FAD to form to 8-formyl-FAD (8f-FAD). PMID: 29301933
- our results indicate that genetic variants in ETFA may modify individual susceptibility to non-GBM of glioma in the Han Chinese population and support the role of the ETFA genes in the occurrence of glioma. PMID: 28320150
- the mechanism of tert-butyl hydroperoxide-induced an apoptosis cascade and endoplasmic reticulum stress in hepatocyte cells by up-regulation of ETFA, providing a new mechanism for liver injury. PMID: 24394546
- These results are consistent with the electron transfer flavoprotein alpha II domain adopting orientations in solution that deviate from the crystal structure of free ETF towards the active, substrate-bound orientation. PMID: 21308847
- investigations are compatible with the notion that the ETFalpha-T171 variant displays an altered conformational landscape that results in reduced protein function under thermal stress PMID: 21219902
- Data established structural hotspots within the ETF fold, and provided a rationale for the prediction of effects of mutations in ETF. PMID: 20674745
- These studies indicate that a series of conformational changes occur during the assembly of the TMADH.ETF electron transfer complex and that the kinetics of assembly observed with mutant TMADH or ETF complexes are much slower PMID: 11756429
- Tissue samples from 16 unrelated patients with ETF deficiency were analysed and the majority of the patients had mutations in the ETFA gene. PMID: 16510302
- No mutations in electron-transfer-flavoprotein but maternal riboflavin deficiency led to multiple acyl-CoA dehydrogenation deficiency PMID: 17689999
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相关疾病:Glutaric aciduria 2A (GA2A)
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亚细胞定位:Mitochondrion matrix.
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蛋白家族:ETF alpha-subunit/FixB family
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数据库链接:
HGNC: 3481
OMIM: 231680
KEGG: hsa:2108
STRING: 9606.ENSP00000452762
UniGene: Hs.39925
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