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MRP-S16 Rabbit Polyclonal Antibody

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产品基本信息

产品货号
BD-PT2875
产品名称
MRP-S16 Rabbit Polyclonal Antibody
别名
MRPS16; RPMS16; CGI-132; 28S ribosomal protein S16; mitochondrial; MRP-S16; S16mt
类别
常规抗体
基因名称
MRPS16
蛋白名称
28S ribosomal protein S16 mitochondrial
推荐应用
WB
反应种属
Human,Mouse
浓度
1 mg/ml
存储缓冲液
Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% New type preservative N.
Human Gene ID
51021
Human Gene Link
http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=51021
Human Swissprot No.
Q9Y3D3
Human Swissprot Link
http://www.uniprot.org/uniprotkb/Q9Y3D3/entry
Mouse Gene ID
66242
Mouse Gene Link
http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=66242
Mouse Swissprot No.
Q9CPX7
Mouse Swissprot Link
http://www.uniprot.org/uniprot/Q9CPX7
免疫原
The antiserum was produced against synthesized peptide derived from human MRPS16. AA range:81-130
特异性
MRP-S16 Polyclonal Antibody detects endogenous levels of MRP-S16 protein.
稀释度
WB 1:500 - 1:2000. IHC 1:100 - 1:300. ELISA: 1:40000.. IF 1:50-200
预测分子量
15kD
运输及保存条件
-20°C/1 year
宿主
Polyclonal, Rabbit,IgG
背景介绍
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 S16P family. The encoded protein is one of the most highly conserved ribosomal proteins between mammalian and yeast mitochondria. Three pseudogenes (located at 8q21.3, 20
组织表达
Muscle,
细胞定位
Mitochondrion .
功能
disease:Defects in MRPS16 are the cause of combined oxidative phosphorylation deficiency type 2 (COXPD2) [MIM:610498]. Defects in the mitochondrial oxidative phosphorylation system result in devastating, mainly multisystem, diseases. COXPD2 symptoms include fatal neonatal metabolic acidosis with agenesis of the corpus callosum.,similarity:Belongs to the ribosomal protein S16P family.,subunit:Component of the mitochondrial ribosome small subunit (28S) which comprises a 12S rRNA and about 30 distinct proteins.,
期货
现货
纯化
The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.

Immunohistochemistry analysis of paraffin-embedded human tonsil tissue, using MRPS16 Antibody. The picture on the right is blocked with the synthesized peptide.

Western blot analysis of lysates from HepG2 cells, using MRPS16 Antibody. The lane on the right is blocked with the synthesized peptide.

Western blot analysis of the lysates from COLO205 cells using MRPS16 antibody.

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