MDH2 Antibody
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中文名稱:MDH2兔多克隆抗體
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貨號(hào):CSB-PA013623ESR2HU
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規(guī)格:¥440
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圖片:
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其他:
產(chǎn)品詳情
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產(chǎn)品名稱:Rabbit anti-Homo sapiens (Human) MDH2 Polyclonal antibody
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Uniprot No.:
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基因名:MDH2
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別名:M MDH antibody; Malate dehydrogenase 2; NAD (mitochondrial) antibody; Malate dehydrogenase antibody; Malate dehydrogenase; mitochondrial antibody; MDH antibody; mdh2 antibody; MDHM_HUMAN antibody; MGC:3559 antibody; mitochondrial antibody; Mitochondrial malate dehydrogenase 2; NAD antibody; Mor 1 antibody; MOR1 antibody
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宿主:Rabbit
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反應(yīng)種屬:Human, Mouse
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免疫原:Recombinant Human Malate dehydrogenase, mitochondrial protein (59-338AA)
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免疫原種屬:Homo sapiens (Human)
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標(biāo)記方式:Non-conjugated
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克隆類型:Polyclonal
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抗體亞型:IgG
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純化方式:Antigen Affinity Purified
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濃度:It differs from different batches. Please contact us to confirm it.
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保存緩沖液:PBS with 0.02% sodium azide, 50% glycerol, pH7.3.
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產(chǎn)品提供形式:Liquid
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應(yīng)用范圍:ELISA, WB
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推薦稀釋比:
Application Recommended Dilution WB 1:500-1:5000 -
Protocols:
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儲(chǔ)存條件:Upon receipt, store at -20°C or -80°C. Avoid repeated freeze.
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貨期: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.
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用途:For Research Use Only. Not for use in diagnostic or therapeutic procedures.
相關(guān)產(chǎn)品
靶點(diǎn)詳情
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基因功能參考文獻(xiàn):
- these data suggest that MDH2, functioning as an RNA-binding protein, is involved in the posttranscriptional downregulation of SCN1A expression under seizure condition. PMID: 28433711
- loss-of-function mutations in MDH2 are also associated with severe neurological clinical presentations in children PMID: 27989324
- Data indicate that acetyl-CoA acetyltransferase (ACAT1) and malate dehydrogenase (MDH2) are involved in various drug-resistance-forming mechanisms. PMID: 25639359
- Segregation of the mutation with disease and absence of MDH2 in mutated tumors revealed MDH2 as a novel pheochromocytoma/paraganglioma susceptibility gene. PMID: 25766404
- L-2-hydroxyglutarate accumulates as a result of a deficiency in FAD-linked L-2-hydroxyglutarate dehydrogenase. mitochondrial L-malate dehydrogenase is responsible for the excretion of L-2-hydroxyglutarate in this condition. PMID: 17603759
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相關(guān)疾?。?/div>Epileptic encephalopathy, early infantile, 51 (EIEE51)亞細(xì)胞定位:Mitochondrion matrix.蛋白家族:LDH/MDH superfamily, MDH type 1 family數(shù)據(jù)庫鏈接:
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