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MVK Monoclonal antibody

MVK Monoclonal Antibody for WB, ELISA
Cat No. 67820-1-Ig

产品说明书

CloneNo. 2F1D3

宿主/亚型

Mouse / IgG2b

种属反应性

human

应用

WB, ELISA

2F1D3, EC:2.7.1.36, LRBP, Mevalonate kinase, MK

缓冲液配方:  PBS, Azide, Glycerol
PBS, Azide, Glycerol
PBS Only
偶联物:  Unconjugated
Unconjugated
CoraLite® Plus 488
规格价格库存


经过测试的应用

Positive WB detected inLNCaP cells, U2OS cells, HepG2 cells, Jurkat cells, K-562 cells
Planning an IF experiment? We recommend our CoraLite® Plus 488 conjugated versions of this antibody.

推荐稀释比

应用推荐稀释比
Western Blot (WB)WB : 1:5000-1:50000
It is recommended that this reagent should be titrated in each testing system to obtain optimal results.
Sample-dependent, Check data in validation data gallery.

产品信息

67820-1-Ig targets MVK in WB, ELISA applications and shows reactivity with human samples.

经测试应用 WB, ELISA Application Description
经测试反应性 human
免疫原

CatNo: Ag28887

Product name: Recombinant human MVK protein

Source: e coli.-derived, PET28a

Tag: 6*His

Domain: 1-396 aa of BC016140

Sequence: MLSEVLLVSAPGKVILHGEHAVVHGKVALAVSLNLRTFLRLQPHSNGKVDLSLPNIGIKRAWDVARLQSLDTSFLEQGDVTTPTSEQVEKLKEVAGLPDDCAVTERLAVLAFLYLYLSICRKQRALPSLDIVVWSELPPGAGLGSSAAYSVCLAAALLTVCEEIPNPLKDGDCVNRWTKEDLELINKWAFQGERMIHGNPSGVDNAVSTWGGALRYHQGKISSLKRSPALQILLTNTKVPRNTRALVAGVRNRLLKFPEIVAPLLTSIDAISLECERVLGEMGEAPAPEQYLVLEELIDMNQHHLNALGVGHASLDQLCQVTRARGLHSKLTGAGGGGCGITLLKPGLEQPEVEATKQALTSCGFDCLETSIGAPGVSIHSATSLDSRVQQALDGL

种属同源性预测
宿主/亚型 Mouse / IgG2b
抗体类别 Monoclonal
产品类型 Antibody
全称 mevalonate kinase
别名 2F1D3, EC:2.7.1.36, LRBP, Mevalonate kinase, MK
计算分子量 396 aa, 42 kDa
观测分子量 42 kDa
GenBank蛋白编号BC016140
基因名称 MVK
Gene ID (NCBI) 4598
RRIDAB_2918583
偶联类型 Unconjugated
形式Liquid
纯化方式Protein A purification
UNIPROT IDQ03426
储存缓冲液 PBS with 0.02% sodium azide and 50% glycerol, pH 7.3.
储存条件Store at -20°C. Stable for one year after shipment. Aliquoting is unnecessary for -20oC storage.

背景介绍

MVK (Mevalonate kinase) is a 42 kDa cytoplasmic protein that belongs to the GHMP kinase family. Mevalonate kinase catalyzes the ATP-dependent phosphorylation of mevalonic acid to form mevalonate 5-phosphate. Defects in mevalonate kinase can cause mevalonic aciduria (MEVA). It is an accumulation of mevalonic acid which causes a variety of symptoms such as psychomotor retardation, dysmorphic features, cataracts, hepatosplenomegaly, lymphadenopathy, anemia, hypotonia, myopathy and ataxia.

实验方案

Product Specific Protocols
WB protocol for MVK antibody 67820-1-IgDownload protocol
Standard Protocols
Click here to view our Standard Protocols
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