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MRP-S22 Rabbit Polyclonal Antibody

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产品基本信息

产品货号
BD-PT2881
产品名称
MRP-S22 Rabbit Polyclonal Antibody
别名
MRPS22; C3orf5; RPMS22; GK002; 28S ribosomal protein S22; mitochondrial; MRP-S22; S22mt
类别
常规抗体
基因名称
MRPS22
蛋白名称
28S ribosomal protein S22 mitochondrial
推荐应用
WB
反应种属
Human,Monkey,Bovine,Hamster,Cow
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
56945
Human Gene Link
http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=56945
Human Swissprot No.
P82650
Human Swissprot Link
http://www.uniprot.org/uniprotkb/P82650/entry
Mouse Swissprot No.
Q9CXW2
Mouse Swissprot Link
http://www.uniprot.org/uniprot/Q9CXW2
免疫原
The antiserum was produced against synthesized peptide derived from human MRPS22. AA range:231-280
特异性
MRP-S22 Polyclonal Antibody detects endogenous levels of MRP-S22 protein.
稀释度
WB 1:500 - 1:2000. IHC 1:100 - 1:300. IF 1:200 - 1:1000. ELISA: 1:40000. Not yet tested in other applications.
预测分子量
41kD
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 does not seem to have a counterpart in prokaryotic and fungal-mitochondrial ribosomes. This gene lies telomeric of and is transcribed in the opposite direction from the forkhead box L2 gene. A pseudogene
组织表达
Brain,Liver cancer,Muscle,Placenta,
细胞定位
Mitochondrion .
功能
disease:Defects in MRPS22 are the cause of combined oxidative phosphorylation deficiency type 5 (COXPD5) [MIM:611719]. COXPD5 is an antenatal mitochondrial disease. Patients show edema, cardiomyopathy, tubulopathy, and hypotonia.,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.

Immunofluorescence analysis of A549 cells, using MRPS22 Antibody. The picture on the right is blocked with the synthesized peptide.

Western blot analysis of lysates from COS cells, using MRPS22 Antibody. The lane on the right is blocked with the synthesized peptide.

Western Blot analysis of various cells using MRP-S22 Polyclonal Antibody

Western blot analysis of mouse-brain 293T lysis using MRP-S22 antibody.

Immunohistochemical analysis of paraffin-embedded Human skeletal muscle. Antibody was diluted at 1:100(4°,overnight). High-pressure and temperature Tris-EDTA,pH8.0 was used for antigen retrieval. Negetive contrl (right) obtaned from antibody was pre-absorbed by immunogen peptide.

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