MRPS22 Antibody

Code CSB-PA785563
Size US$297
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  • Western blot analysis of extracts from COS cells, using MRPS22 antibody.
  • Immunofluorescence analysis of A549 cells, using MRPS22 antibody.
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Product Details

Full Product Name
Rabbit anti-Homo sapiens (Human) MRPS22 Polyclonal antibody
Uniprot No.
Target Names
MRPS22
Alternative Names
28S ribosomal protein S22 antibody; C3orf5 antibody; COXPD5 antibody; GIBT antibody; GK002 antibody; mitochondrial antibody; Mitochondrial ribosomal protein S22 antibody; MRP-S22 antibody; MRPS22 antibody; RPM S22 antibody; RPMS22 antibody; RT22_HUMAN antibody; S22mt antibody
Raised in
Rabbit
Species Reactivity
Human
Immunogen
Synthesized peptide derived from internal of Human MRPS22.
Immunogen Species
Homo sapiens (Human)
Clonality
Polyclonal
Purification Method
The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
Concentration
It differs from different batches. Please contact us to confirm it.
Form
Rabbit IgG in phosphate buffered saline (without Mg2+ and Ca2+), pH 7.4, 150mM NaCl, 0.02% sodium azide and 50% glycerol.
Tested Applications
ELISA,WB,IF
Recommended Dilution
Application Recommended Dilution
WB 1:500-1:3000
IF 1:100-1:500
Troubleshooting and FAQs
Storage
Upon receipt, store at -20°C or -80°C. Avoid repeated freeze.
Lead Time
Basically, we can dispatch the products out in 1-3 working days after receiving your orders. Delivery time maybe differs from different purchasing way or location, please kindly consult your local distributors for specific delivery time.
Usage
For Research Use Only. Not for use in diagnostic or therapeutic procedures.

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Target Background

Gene References into Functions
  1. hypertrophic cardiomyopathy and tubulopathy may not be considered as constant features of MRPS22 PMID: 28752220
  2. A mutation in the MRPS22 gene led to reduction of 12sRNA in fibroblasts and fatal neonatal hypertrophic cardiomyopathy & kidney tubulopathy. PMID: 17873122
  3. The effect of mutated MRPS22 on the assembly of the small and large ribosomal subunits in human mitochondria is reported. PMID: 18539099
Involvement in disease
Combined oxidative phosphorylation deficiency 5 (COXPD5)
Subcellular Location
Mitochondrion.
Protein Families
Mitochondrion-specific ribosomal protein mS22 family
Database Links

HGNC: 14508

OMIM: 605810

KEGG: hsa:56945

STRING: 9606.ENSP00000310785

UniGene: Hs.745001

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