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MRP-S22 Polyclonal Antibody
MRP-S22 Polyclonal Antibody
MRP-S22 Polyclonal Antibody
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经销商客户: ¥440.0
实验室客户: ¥600.0
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Target:MRP-S22

Gene Name:MRPS22

Protein Name:28S ribosomal protein S22 mitochondrial

Human Gene Id:56945

Human Swiss Prot No:P82650

Mouse Swiss Prot No:Q9CXW2

Immunogen:The antiserum was produced against synthesized peptide derived from human MRPS22. AA range:231-280

Specificity:MRP-S22 Polyclonal Antibody detects endogenous levels of MRP-S22 protein.

Formulation:Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.

Source:Polyclonal, Rabbit,IgG

Dilution:WB 1:500 - 1:2000. IHC 1:100 - 1:300. IF 1:200 - 1:1000. ELISA: 1:40000. Not yet tested in other applications.

Purification:The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.

Concentration:1 mg/ml

Storage Stability:-15°C to -25°C/1 year(Do not lower than -25°C)

Other Name:MRPS22;C3orf5;RPMS22;GK002;28S ribosomal protein S22; mitochondrial;MRP-S22;S22mt

Observed Band(KD):41kD

Background: 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

Function: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.,

Subcellular Location:Mitochondrion .

Expression: Brain,Liver cancer,Muscle,Placenta,

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