ATP5D Antibody
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货号:CSB-PA002355GA01HU
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规格:¥3,900
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其他:
产品详情
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Uniprot No.:P30049
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基因名:
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别名:ATP synthase subunit delta; mitochondrial antibody; ATP synthase subunit delta; mitochondrial antibody; ATP synthase; H+ transporting; mitochondrial F1 complex; delta subunit antibody; ATP5D antibody; ATPD_HUMAN antibody; F ATPase delta subunit antibody; F-ATPase delta subunit antibody; Mitochondrial ATP synthase complex delta subunit precusor antibody; Mitochondrial ATP synthase delta subunit antibody
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宿主:Rabbit
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反应种属:Human,Mouse,Rat
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免疫原:Human ATP5D
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免疫原种属:Homo sapiens (Human)
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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 0.1% Sodium Azide, 50% Glycerol, pH 7.3. -20°C, Avoid freeze / thaw cycles.
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产品提供形式:Liquid
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应用范围:ELISA,WB
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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.
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靶点详情
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功能:Mitochondrial membrane ATP synthase (F(1)F(0) ATP synthase or Complex V) produces ATP from ADP in the presence of a proton gradient across the membrane which is generated by electron transport complexes of the respiratory chain. F-type ATPases consist of two structural domains, F(1) - containing the extramembraneous catalytic core, and F(0) - containing the membrane proton channel, linked together by a central stalk and a peripheral stalk. During catalysis, ATP turnover in the catalytic domain of F(1) is coupled via a rotary mechanism of the central stalk subunits to proton translocation. Part of the complex F(1) domain and of the central stalk which is part of the complex rotary element. Rotation of the central stalk against the surrounding alpha(3)beta(3) subunits leads to hydrolysis of ATP in three separate catalytic sites on the beta subunits.
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基因功能参考文献:
- These data establish c.245C>T (p.Pro82Leu) and c.317T>G (p.Val106Gly) in ATP5F1D as pathogenic variants leading to a Mendelian mitochondrial disease featuring episodic metabolic decompensation. PMID: 29478781
- Immunohistochemical and immunofluorescent double staining of ATP5D and synaptophysin showed that the reduction of ATP5D was most pronounced at synapses in amyotrophic lateral sclerosis PMID: 27899032
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亚细胞定位:Mitochondrion. Mitochondrion inner membrane.
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蛋白家族:ATPase epsilon chain family
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数据库链接:
HGNC: 837
OMIM: 603150
KEGG: hsa:513
STRING: 9606.ENSP00000215375
UniGene: Hs.418668
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