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MVK 抗体
MVK
适用: 人, 小鼠, 大鼠
WB, IHC, ELISA
宿主: 兔
Polyclonal
unconjugated
MVK抗体详情
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抗原
See all MVK 抗体
MVK
(Mevalonate Kinase (MVK))
适用
All reactivities for MVK 抗体
人, 小鼠, 大鼠
宿主
All hosts for MVK 抗体
兔
克隆类型
All clonalities for MVK 抗体
多克隆
标记
All conjugates for MVK 抗体
This MVK antibody is un-conjugated
应用范围
All applications for MVK 抗体
Western Blotting (WB), Immunohistochemistry (IHC), ELISA
产品特性
Polyclonal Antibody
纯化方法
Affinity purification
免疫原
Recombinant protein of human MVK
亚型
IgG
Top Product
Discover our top product MVK Primary Antibody
Alternatives
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使用细节
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应用备注
WB 1:200-1:1000, IHC 1:100-1:300
限制
仅限研究用
贮存及处理
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状态
Liquid
浓度
0.4 mg/mL
缓冲液
PBS with 0.05 % sodium azide and 50 % glycerol, PH7.4
储存液
Sodium azide
注意事项
This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
储存条件
-20 °C
储存方法
Store at -20°C. Avoid freeze / thaw cycles.
MVK目标详情
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抗原
MVK
(Mevalonate Kinase (MVK))
别名
MVK (MVK 产品 )
别名
F21A20.160 antibody, F21A20_160 antibody, MEVALONATE KINASE antibody, MVK antibody, mevalonate kinase antibody, DDBDRAFT_0168621 antibody, DDBDRAFT_0302479 antibody, DDB_0168621 antibody, DDB_0302479 antibody, LRBP antibody, MK antibody, MVLK antibody, POROK3 antibody, 2310010A05Rik antibody, AI256848 antibody, AI414037 antibody, zgc:103473 antibody, mevalonate kinase antibody, mvk antibody, hypothetical protein antibody, MVK antibody, MK antibody, MA_RS03165 antibody, PAB_RS02890 antibody, LMOf2365_0011 antibody, mvk antibody, RCI_RS14145 antibody, TGAM_RS08735 antibody, MMAH_RS07705 antibody, TAGG_RS01605 antibody, SHELL_RS02965 antibody, MVOL_RS03085 antibody, Igag_1464 antibody, VDIS_RS11260 antibody, MFER_RS04560 antibody, DESMU_RS01555 antibody, ARCVE_RS02955 antibody, MZHIL_RS05110 antibody, Mvk antibody
背景
This gene encodes the peroxisomal enzyme mevalonate kinase. Mevalonate is a key intermediate, and mevalonate kinase a key early enzyme, in isoprenoid and sterol synthesis. Mevalonate kinase deficiency caused by mutation of this gene results in mevalonic aciduria, a disease characterized psychomotor retardation, failure to thrive, hepatosplenomegaly, anemia and recurrent febrile crises. Defects in this gene also cause hyperimmunoglobulinaemia D and periodic fever syndrome, a disorder characterized by recurrent episodes of fever associated with lymphadenopathy, arthralgia, gastrointestinal dismay and skin rash.
分子量
42 kDa
UniProt
Q03426
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