Anti-MRPS12 Polyclonal Antibody北京索莱宝科技有限公司

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产品名称: Anti-MRPS12 Polyclonal Antibody
英文名称: Anti-MRPS12 Polyclonal Antibody
抗体货号: K107321P
产品规格: 50ul/100ul
级    别: ,
产品产地: 北京
品牌商标: Solarbio
价    格: 900/50ul;1600/100ul元
抗原: A synthetic peptide of human MRPS12
抗原来源: 
抗体来源: Rabbit
适用物种: Human Mouse
应用范围: IHC
更新时间: 2019/9/5 14:07:00
详细资料:  实验方法技术资料
浏览人数:7
诚信指数:1279点
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使用范围:仅限科研使用,不能应用于临床
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北京索莱宝科技有限公司
地址:
北京市通州区马驹桥镇联东U谷景盛南四街15号85A三层
邮编:
101102
电话:
18435223305
传真:
010-56371281
联系人:
郭倩
所在区域:
北京·北京
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公司展台:
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产品详细描述

 

Anti-MRPS12 Polyclonal Antibody  

品牌:Solarbio | 货号:K107321P

商品货号:商品品牌:规格基本售价:选择规格
K107301P-50ulSolarbio50ul960.00元
K107301P-100ulSolarbio100ul1600.00元

英文名称Anti-MRPS12 Polyclonal Antibody
宿主Rabbit
别名MPR-S12;MT-RPS12;RPMS12;RPS12;RPSM12;
mitochondrial ribosomal protein S12
应用IHC
稀释比例IHC 1:50-200.
交叉反应Human Mouse
蛋白分子量15kDa
保存Store at -20°C. Avoid freeze / thaw cycles.
储存液Buffer: PBS with 0.03% Proclin300, 50% glycerol, pH7.3.
纯化方法Affinity purification
亚型IgG
免疫原A synthetic peptide of human MRPS12
Subcellular
Locations
Cytoplasm
Swiss ProtO15235
克隆类型Polyclonal Antibody
背景资料Mammalian mitochondrial ribosomal proteins are encoded
by nuclear genes and help in protein synthesis within the
mitochondrion. Mitochondrial ribosomes (mitoribosomes)
consist of a small 28S subunit and a large 39S subunit.
They have an estimated 75% protein to rRNA composition
compared to prokaryotic ribosomes, where this ratio is
reversed. Another difference between mammalian
mitoribosomes and prokaryotic ribosomes is that the latter
contain a 5S rRNA. Among different species, the proteins
comprising the mitoribosome differ greatly in sequence,
and sometimes in biochemical properties, which prevents
easy recognition by sequence homology. This gene encodes
a 28S subunit protein that belongs to the
ribosomal protein S12P family. The encoded protein is a
key component of the ribosomal small subunit and
controls the decoding fidelity and susceptibility to
aminoglycoside antibiotics. The gene for mitochondrial
seryl-tRNA synthetase is located upstream and adjacent to
this gene, and both genes are possible candidates for the
autosomal dominant deafness gene (DFNA4). Splice
variants that differ in the 5' UTR have been found for this
gene; all three variants encode the same protein.



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